NZ749198B2 - Method for producing dna library and method for analyzing genomic dna using the dna library - Google Patents

Abstract

According to the present invention, a DNA library exhibiting excellent reproducibility is easily produced. A nucleic acid amplification reaction is carried out in a reaction solution containing a genomic DNA and a high concentration of a random primer, and a fragment of the DNA obtained by the nucleic acid amplification reaction is obtained by using the genomic DNA as a template. ic acid amplification reaction is obtained by using the genomic DNA as a template.

Description

DESCRIPTION Title of Invention: METHOD FOR PRODUCING DNA LIBRARY AND METHOD FOR ANALYZING GENOMIC DNA USING THE DNA LIBRARY Technical Field The present invention relates to a method for producing a DNA library that can be used for analyzing a DNA marker, for example, and a method for genomic DNA analysis using such DNA library.

Background Art In general, genomic analysis is performed to conduct comprehensive analysis of genetic information contained in the genome, such as nucleotide sequence information.

However, an analysis aimed at determination of the nucleotide sequence for whole genome is disadvantageous in terms of the number of processes and the cost. In cases of organisms with large genomic sizes, in addition, genomic analysis based on nucleotide sequence analysis has limitations because of genome complexity.

Patent Literature 1 discloses an amplified fragment length polymorphism (AFLP) marker technique wherein a sample-specific index is incorporated into a restriction-enzyme- treated fragment that had been ligated to an adapter and only a part of the sequence of the restriction-enzyme-treated fragment is to be determined. According to the technique disclosed in Patent Literature 1, the complexity of genomic DNA is reduced by treating genomic DNA with a restriction enzyme, the nucleotide sequence of a target part of the restriction-enzyme-treated fragment is determined, and the target restriction-enzyme-treated fragment is thus determined sufficiently. The technique disclosed in Patent Literature 1, however, requires processes such as treatment of genomic DNA with a restriction enzyme and ligation reaction with the use of an adapter. Thus, it is difficult to achieve a cost reduction.

Meanwhile, Patent Literature 2 discloses as follows. That is, a DNA marker for identification that is highly correlated with the results of taste evaluation was found from among DNA bands obtained by amplifying DNAs extracted from a rice sample via PCR in the presence of adequate primers by the so-called RAPD (randomly amplified polymorphic DNA) technique. The method disclosed in Patent Literature 2 involves the use of a plurality of sequence-tagged sites (STSs, which are primers) identified by particular sequences.

According to the method disclosed in Patent Literature 2, a DNA marker for identification amplified with the use of an STS primer is detected via electrophoresis. However, the RAPD technique disclosed in Patent Literature 2 yields significantly poor reproducibility of PCR amplification, and, accordingly, such technique cannot be generally adopted as a DNA marker technique.

Patent Literature 3 discloses a method for producing a genomic library wherein PCR is carried out with the use of a single type of primer designed on the basis of a sequence that appears relatively frequently in the target genome, the entire genomic region is substantially uniformly amplified, and a genomic library can be thus produced. While Patent Literature 3 describes that a genomic library can be produced by conducting PCR with the use of a random primer containing a random sequence, it does not describe any actual procedures or results of experimentation. Accordingly, the method described in Patent Literature 3 is deduced to require nucleotide sequence information of the genome so as to identify the genome appearing frequency, which would increase the number of procedures and the cost. According to the method described in Patent Literature 3, in addition, the entire genome is to be amplified, and complexity of genomic DNA cannot be reduced, disadvantageously.

Citation List Patent Literature Patent Literature 1: JP Patent No. 5389638 Patent Literature 2: JP Patent Publication (Kokai) No. 2003-79375 A Patent Literature 3: JP Patent No. 3972106 Summary of Invention Technical Problem For a technique for genome information analysis, such as genetic linkage analysis conducted with the use of a DNA marker, production of a DNA library in a more convenient and highly reproducible manner is desired. As described above, a wide variety of techniques for producing a DNA library are known. To date, however, there have been no techniques known to be sufficient in terms of convenience and/or reproducibility. Under the above circumstances, it is an object of the present invention to provide a method for producing a DNA library with more convenience and higher reproducibility, and it is another object to provide a method for analyzing genomic DNA with the use of such DNA library.

Solution to Problem The present inventors have conducted concentrated studies in order to attain the above objects. As a result, they discovered that high reproducibility could be achieved by conducting PCR with the use of a random primer while designating the concentration of such random primer within a designated range in a reaction solution. This has led to the completion of the present invention. [0008a] According to a first aspect, the present invention provides a method for analyzing genomic DNA, comprising steps of: preparing a DNA library, which is produced by the method comprising conducting a nucleic acid amplification reaction in a reaction solution containing genomic DNA and a random primer comprising 9 to 30 nucleotides using genomic DNA as a template to obtain DNA fragments by the nucleic acid amplification reaction, wherein when the random primer contains 9 to 10 nucleotides, the concentration of the random primer is set to 40 to 60 μM; when the random primer contains 10 to 14 nucleotides, the concentration of the random primer is set to 100 μM or less, and said concentration is defined by the formula -6.974 y > 3E + 08x , provided that the nucleotide length of the random primer is represented by "y" and the concentration of the random primer is represented by "x"; when the random primer contains 14 to 18 nucleotides, the concentration of the random primer is set to 4 to 100 μM; when the random primer contains 18 to 28 nucleotides, the concentration of the random primer is set to 4 μM or more, and said concentration is defined by the formula y -5.533 < 8E + 08x ; when the random primer contains 28 to 29 nucleotides, the concentration of the random primer is set to 6 to 10 μM; and when the random primer contains 30 nucleotides, the concentration of the random primer is set to 6 μM; determining the nucleotide sequence of DNA fragments contained in the DNA library produced; and confirming the presence or absence of specific DNA fragments based on the nucleotide sequence. [0008b] According to a second aspect, the present invention provides a method for analyzing genomic DNA, comprising steps of: conducting a nucleic acid amplification reaction in a first reaction solution comprising genomic DNA and a random primer comprising 9 to 30 nucleotides at a high concentration to obtain first DNA fragments by the nucleic acid amplification reaction using the genomic DNA as a template, wherein when the random primer contains 9 to 10 nucleotides, the concentration of the random primer is set to 40 to 60 μM; when the random primer contains 10 to 14 nucleotides, the concentration of the random primer is set to 100 μM or less, and said concentration is defined by the formula -6.974 y > 3E + 08x , provided that the nucleotide length of the random primer is represented by "y" and the concentration of the random primer is represented by "x"; when the random primer contains 14 to 18 nucleotides, the concentration of the random primer is set to 4 to 100 μM; when the random primer contains 18 to 28 nucleotides, the concentration of the random primer is set to 4 μM or more, and said concentration is defined by the formula y -5.533 < 8E + 08x ; when the random primer contains 28 to 29 nucleotides, the concentration of the random primer is set to 6 to 10 μM; and when the random primer contains 30 nucleotides, the concentration of the random primer is set to 6 μM; conducting a nucleic acid amplification reaction in a second reaction solution comprising the obtained first DNA fragments and a primer, which has a 3'-end nucleotide sequence capable of hybridizing to a 5'-end nucleotide sequence of the first DNA fragments to obtain second DNA fragments; preparing a DNA library with the second DNA fragments or DNA fragments obtained by a nucleic acid amplification reaction using the second DNA fragments as templates or a nucleic acid amplification reaction to be conducted repeatedly; determining the nucleotide sequence of DNA fragments contained in the DNA library prepared; and confirming the presence or absence of specific DNA fragments based on the nucleotide sequence. [0008c] According to a third aspect, the present invention provides the method according to the invention, substantially as herein described with reference to any one or more of the examples but excluding comparative examples.

The present invention includes the following. 3b followed by page 4 (1) A method for producing a DNA library, comprising conducting a nucleic acid amplification reaction in a reaction solution containing genomic DNA and a random primer at a high concentration using genomic DNA as a template to obtain DNA fragments. (2) The method for producing a DNA library according to (1), wherein the reaction solution comprises the random primer at a concentration of 4 to 200 µM. (3) The method for producing a DNA library according to (1), wherein the reaction solution comprises the random primer at a concentration of 4 to 100 µM. (4) The method for producing a DNA library according to (1), wherein the random primer comprises 9 to 30 nucleotides. (5) The method for producing a DNA library according to (1), wherein the DNA fragments each comprise 100 to 500 nucleotides. (6) A method for analyzing genomic DNA, comprising using a DNA library produced by the method for producing a DNA library according to any one of (1) to (5) as a DNA marker. (7) The method for analyzing genomic DNA according to (6), which comprises determining the nucleotide sequence of the DNA library produced by the method for producing a DNA library according to any one of (1) to (5) and confirming the presence or absence of the DNA marker based on the nucleotide sequence. (8) The method for analyzing genomic DNA according to (7), wherein the presence or absence of the DNA marker is confirmed based on the number of reads of the nucleotide sequence of the DNA library in the step of confirming the presence or absence of the DNA marker. (9) The method for analyzing genomic DNA according to (7), wherein the nucleotide sequence of the DNA library is compared with known sequence information or with the nucleotide sequence of a DNA library produced using genomic DNA from a different organism or tissue, and the presence or absence of the DNA marker is confirmed based on differences in the nucleotide sequences. (10) The method for analyzing genomic DNA according to (6), which comprises: a step of preparing a pair of primers for specifically amplifying the DNA marker based on the nucleotide sequence of the DNA marker; a step of conducting a nucleic acid amplification reaction using genomic DNA extracted from a target organism as a template and the pair of primers; and a step of confirming the presence or absence of the DNA marker in the genomic DNA based on the results of the nucleic acid amplification reaction. (11) A method for producing a DNA library, comprising: a step of conducting a nucleic acid amplification reaction in a first reaction solution comprising genomic DNA and a random primer at a high concentration to obtain first DNA fragments by the nucleic acid amplification reaction using the genomic DNA as a template; a step of conducting a nucleic acid amplification reaction in a second reaction solution comprising the obtained first DNA fragments and a nucleotide, as a primer, which has a 3'-end nucleotide sequence having 70% identity to at least a 5'-end nucleotide sequence of the random primer to ligate the nucleotides to the first DNA fragments, thereby obtaining second DNA fragments. (12) The method for producing a DNA library according to (11), wherein the first reaction solution comprises the random primer at a concentration of 4 to 100 µM. (13) The method for producing a DNA library according to (11), wherein the first reaction solution comprises the random primer at a concentration of 4 to 100 µM. (14) The method for producing a DNA library according to (11), wherein the random primer comprises 9 to 30 nucleotides. (15) The method for producing a DNA library according to (11), wherein the first DNA fragments each comprise 100 to 500 nucleotides. (16) The method for producing a DNA library according to (11), wherein the primer for amplifying the second DNA fragments comprises a region used for a nucleotide sequencing reaction, or the primer used for a nucleic acid amplification reaction using the second DNA fragments as templates or a nucleic acid amplification reaction to be conducted repeatedly comprises a region used for a nucleotide sequencing reaction. (17) A method for analyzing a DNA library, comprising a step of determining a nucleotide sequence for a second DNA fragment obtained by the method for producing a DNA library according to any one of (11) to (15) or a DNA fragment obtained using a primer comprising a region complementary to a sequencer primer to be used in a nucleotide sequencing reaction in the method for producing a DNA library according to (16). (18) A method for analyzing genomic DNA, comprising using a DNA library produced by the method for producing a DNA library according to any one of (11) to (17) as a DNA marker. (19) The method for analyzing genomic DNA according to (18), which comprises determining the nucleotide sequence of the DNA library produced by the method for producing a DNA library according to any one of (11) to (17) and confirming the presence or absence of the DNA marker based on the nucleotide sequence. (20) The method for analyzing genomic DNA according to (19), wherein the presence or absence of the DNA marker is confirmed based on the number of reads of the nucleotide sequence of the DNA library in the step of confirming the presence or absence of the DNA marker. (21) The method for analyzing genomic DNA according to (19), wherein the nucleotide sequence of the DNA library is compared with known sequence information or with the nucleotide sequence of a DNA library produced using genomic DNA from a different organism or tissue, and the presence or absence of the DNA marker is confirmed based on differences in the nucleotide sequences. (22) The method for analyzing genomic DNA according to (18), which comprises: a step of preparing a pair of primers for specifically amplifying the DNA marker based on the nucleotide sequence of the DNA marker; a step of conducting a nucleic acid amplification reaction using genomic DNA extracted from a target organism as a template and the pair of primers; and a step of confirming the presence or absence of the DNA marker in the genomic DNA based on the results of the nucleic acid amplification reaction. (23) A DNA library, which is produced by the method for producing a DNA library according to any one of (1) to (5) and (11) to (16).

The present description includes part or all of the contents as disclosed in the descriptions and/or drawings of Japanese Patent Application Nos. 2016-129048, 2016- 178528, and 2017-071020, which are priority documents of the present application.

Advantageous Effects of Invention A DNA library can be produced in a very convenient manner by the method for producing a DNA library according to the present invention because the method is based on a nucleic acid amplification method using random primers. In addition, reproducibility of a nucleic acid fragment to be amplified is excellent in the method for producing a DNA library according to the present invention even though the method is a nucleic acid amplification method using random primers. Therefore, according to the method for producing a DNA library of the present invention, the produced DNA library can be used as a DNA marker and thus can be used for genomic DNA analysis such as genetic linkage analysis.

The method for analyzing genomic DNA with the use of a DNA library according to the present invention involves the use of a DNA library produced in a simple manner with excellent reproducibility. Accordingly, genomic DNA can be analyzed in a cost- effective manner with high accuracy.

Brief Description of Drawings Fig. 1 shows a flow chart demonstrating the method for producing a DNA library and the method for genomic DNA analysis with the use of the DNA library according to the present invention.

Fig. 2 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern of the DNA library amplified via PCR using DNA of the sugarcane variety NiF8 as a template under general conditions.

Fig. 3 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template at an annealing temperature of 45°C.

Fig. 4 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template at an annealing temperature of 40℃.

Fig. 5 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template at an annealing temperature of 37℃.

Fig. 6 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and 2.5 units of an enzyme.

Fig. 7 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and 12.5 units of an enzyme.

Fig. 8 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and MgCl at the concentration doubled from the original level.

Fig. 9 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and MgCl at the concentration tripled from the original level.

Fig. 10 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and MgCl at the concentration quadrupled from the original level.

Fig. 11 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer comprising 8 nucleotides.

Fig. 12 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer comprising 9 nucleotides.

Fig. 13 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer comprising 11 nucleotides.

Fig. 14 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer comprising 12 nucleotides.

Fig. 15 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer comprising 14 nucleotides.

Fig. 16 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer comprising 16 nucleotides.

Fig. 17 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer comprising 18 nucleotides.

Fig. 18 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer comprising 20 nucleotides.

Fig. 19 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 2 µM.

Fig. 20 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 4 µM.

Fig. 21 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 6 µM.

Fig. 22 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 6 µM.

Fig. 23 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 8 µM.

Fig. 24 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 8 µM.

Fig. 25 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 10 µM.

Fig. 26 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 10 µM.

Fig. 27 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 20 µM.

Fig. 28 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 20 µM.

Fig. 29 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 40 µM.

Fig. 30 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 40 µM.

Fig. 31 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 60 µM.

Fig. 32 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 60 µM.

Fig. 33 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 100 µM.

Fig. 34 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 100 µM.

Fig. 35 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 200 µM.

Fig. 36 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 200 µM.

Fig. 37 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 300 µM.

Fig. 38 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 300 µM.

Fig. 39 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 400 µM.

Fig. 40 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 400 µM.

Fig. 41 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 500 µM.

Fig. 42 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 500 µM.

Fig. 43 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 600 µM.

Fig. 44 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 700 µM.

Fig. 45 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 800 µM.

Fig. 46 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 900 µM.

Fig. 47 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer at a concentration of 1000 µM.

Fig. 48 shows a characteristic diagram demonstrating the results of MiSeq analysis of a DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer.

Fig. 49 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the rice variety Nipponbare as a template and a random primer.

Fig. 50 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the rice variety Nipponbare as a template and a random primer.

Fig. 51 shows a characteristic diagram demonstrating the results of MiSeq analysis of a DNA library amplified using DNA of the rice variety Nipponbare as a template and a random primer.

Fig. 52 shows a characteristic diagram demonstrating positions of MiSeq read patterns in the genome information of the rice variety Nipponbare.

Fig. 53 shows a characteristic diagram demonstrating the frequency distribution of the number of mismatched nucleotides between the random primer and the rice genome.

Fig. 54 shows a characteristic diagram demonstrating the number of reads of the sugarcane varieties NiF8 and Ni9 and hybrid progeny lines thereof at the marker N80521152.

Fig. 55 shows a photograph demonstrating electrophoretic patterns of the sugarcane varietiesNiF8 and Ni9 and hybrid progeny lines thereof at the PCR marker N80521152.

Fig. 56 shows a characteristic diagram demonstrating the number of reads of the sugarcane varieties NiF8 and Ni9 and hybrid progeny lines thereof at the marker N80997192.

Fig. 57 shows a photograph demonstrating electrophoretic patterns of the sugarcane varietiesNiF8 and Ni9 and hybrid progeny lines thereof at the PCR marker N80997192.

Fig. 58 shows a characteristic diagram demonstrating the number of reads of the sugarcane varieties NiF8 and Ni9 and hybrid progeny lines thereof at the marker N80533142.

Fig. 59 shows a photograph demonstrating electrophoretic patterns of the sugarcane varietiesNiF8 and Ni9 and hybrid progeny lines thereof at the PCR marker N80533142.

Fig. 60 shows a characteristic diagram demonstrating the number of reads of the sugarcane varieties NiF8 and Ni9 and hybrid progeny lines thereof at the marker N91552391.

Fig. 61 shows a photograph demonstrating electrophoretic patterns of the sugarcane varieties NiF8 and Ni9 and hybrid progeny lines thereof at the PCR marker N91552391.

Fig. 62 shows a characteristic diagram demonstrating the number of reads of the sugarcane varieties NiF8 and Ni9 and hybrid progeny lines thereof at the marker N91653962.

Fig. 63 shows a photograph demonstrating electrophoretic patterns of the sugarcane varietiesNiF8 and Ni9 and hybrid progeny lines thereof at the PCR marker N91653962.

Fig. 64 shows a characteristic diagram demonstrating the number of reads of the sugarcane varieties NiF8 and Ni9 and hybrid progeny lines thereof at the marker N91124801.

Fig. 65 shows a photograph demonstrating electrophoretic patterns of the sugarcane varietiesNiF8 and Ni9 and hybrid progeny lines thereof at the PCR marker N91124801.

Fig. 66 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer comprising 9 nucleotides.

Fig. 67 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer comprising 9 nucleotides.

Fig. 68 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer comprising 10 nucleotides.

Fig. 69 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer comprising 10 nucleotides.

Fig. 70 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer comprising 11 nucleotides.

Fig. 71 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer comprising 11 nucleotides.

Fig. 72 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer comprising 12 nucleotides.

Fig. 73 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer comprising 12 nucleotides.

Fig. 74 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer comprising 14 nucleotides.

Fig. 75 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer comprising 14 nucleotides.

Fig. 76 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer comprising 16 nucleotides.

Fig. 77 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer comprising 16 nucleotides.

Fig. 78 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer comprising 18 nucleotides.

Fig. 79 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer comprising 18 nucleotides.

Fig. 80 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer comprising 20 nucleotides.

Fig. 81 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer comprising 20 nucleotides.

Fig. 82 shows a characteristic diagram demonstrating the results of investigating the reproducibility of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and random primers each comprising 8 to 35 nucleotides used at a concentration of 0.6 to 300 µM.

Fig. 83 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and 1 type of random primer.

Fig. 84 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and 1 type of random primer.

Fig. 85 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and 2 types of random primers.

Fig. 86 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and 2 types of random primers.

Fig. 87 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and 3 types of random primers.

Fig. 88 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and 3 types of random primers.

Fig. 89 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and 12 types of random primers.

Fig. 90 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and 12 types of random primers.

Fig. 91 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and 24 types of random primers.

Fig. 92 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and 24 types of random primers.

Fig. 93 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and 48 types of random primers.

Fig. 94 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and 48 types of random primers.

Fig. 95 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer B comprising 10 nucleotides.

Fig. 96 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer B comprising 10 nucleotides.

Fig. 97 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer C comprising 10 nucleotides.

Fig. 98 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer C comprising 10 nucleotides.

Fig. 99 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer D comprising 10 nucleotides.

Fig. 100 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer D comprising 10 nucleotides.

Fig. 101 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer E comprising 10 nucleotides.

Fig. 102 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer E comprising 10 nucleotides.

Fig. 103 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer F comprising 10 nucleotides.

Fig. 104 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer F comprising 10 nucleotides.

Fig. 105 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using human genomic DNA as a template and a random primer A comprising 10 nucleotides.

Fig. 106 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using human genomic DNA as a template and a random primer A comprising 10 nucleotides.

Fig. 107 schematically shows a characteristic diagram of a method for producing a DNA library applied to a next-generation sequencer.

Fig. 108 schematically shows a characteristic diagram of a method for producing a DNA library applied to a next-generation sequencer.

Fig. 109 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer G comprising 10 nucleotides.

Fig. 110 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer G comprising 10 nucleotides.

Fig. 111 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using a DNA library of the sugarcane variety NiF8 produced using a random primer G comprising 10 nucleotides as a template and a next-generation sequencer.

Fig. 112 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using a DNA library of the sugarcane variety NiF8 produced using a random primer G comprising 10 nucleotides as a template and a next-generation sequencer.

Fig. 113 shows a characteristic diagram demonstrating the results of MiSeq analysis of a DNA library amplified using DNA of the sugarcane variety NiF8 as a template and a random primer G comprising 10 nucleotides.

Fig. 114 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using DNA of the rice variety Nipponbare as a template and a random primer B comprising 12 nucleotides.

Fig. 115 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using DNA of the rice variety Nipponbare as a template and a random primer B comprising 12 nucleotides.

Fig. 116 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the first time) of the DNA library amplified using a DNA library of the rice variety Nipponbare produced using a random primer B comprising 12 nucleotides as a template and a next-generation sequencer.

Fig. 117 shows a characteristic diagram demonstrating a correlation between an amplified fragment length and a fluorescence unit (FU) in which the amplified fragment length is determined based on an electrophoretic pattern (appeared for the second time) of the DNA library amplified using a DNA library of the rice variety Nipponbare produced using a random primer B comprising 12 nucleotides as a template and a next-generation sequencer.

Fig. 118 shows a characteristic diagram demonstrating a distribution of the read pattern obtained by MiSeq analysis of a DNA library amplified using DNA of the rice variety Nipponbare as a template and a random primer B comprising 12 nucleotides and the degree of consistency between the random primer sequence and the reference sequence of rice variety Nipponbare.

Fig. 119 shows a characteristic diagram demonstrating the results of MiSeq analysis of a DNA library amplified using DNA of the rice variety Nipponbare as a template and a random primer B comprising 12 nucleotides.

Description of Embodiments Hereafter, the present invention is described in detail.

According to the method for producing a DNA library of the present invention, a nucleic acid amplification reaction is conducted in a reaction solution, which is prepared to contain a primer having an arbitrary nucleotide sequence (hereafter, referred to as "random primer") at a high concentration, and the amplified nucleic acid fragment is determined to be a DNA library. The expression "high concentration" used herein means that the concentration is higher than the primer concentration in a general nucleic acid amplification reaction. Specifically, the method for producing a DNA library of the present invention is characterized in that a random primer is used at a higher concentration than a primer used in a general nucleic acid amplification reaction. As a template contained in a reaction solution, genomic DNA prepared from a target organism for which a DNA library is produced can be used.

In the method for producing a DNA library of the present invention, a target organism species is not particularly limited, and a target organism species can be any organism species such as an animal including a human, a plant, a microorganism, or a virus.

In other words, according to the method for producing a DNA library of the present invention, a DNA library can be produced from any organism species.

In the method for producing a DNA library of the present invention, the concentration of a random primer is specified as described above. Thus, a nucleic acid fragment (or nucleic acid fragments) can be amplified with high reproducibility. The term "reproducibility" used herein means an extent of concordance among nucleic acid fragments amplified by a plurality of nucleic acid amplification reactions carried out with the use of the same template and the same random primer. That is, the term "high reproducibility (or the expression "reproducibility is high")" means that the extent of concordance among nucleic acid fragments amplified by a plurality of nucleic acid amplification reactions carried out with the use of the same template and the same random primer is high.

The extent of reproducibility can be evaluated by, for example, conducting a plurality of nucleic acid amplification reactions with the use of the same template and the same random primer, calculating the Spearman's rank correlation coefficient for the fluorescence unit (FU) obtained as a result of electrophoresis of the resulting amplified fragments, and evaluating the extent of reproducibility on the basis of such coefficient. The Spearman's rank correlation coefficient is generally represented by the symbol ρ. When ρ is greater than 0.9, for example, the reproducibility of the amplification reaction of interest can be evaluated to be sufficient.

[Random primer] A sequence constituting a random primer that can be used in the method for producing a DNA library according to the present invention is not particularly limited. For example, a random primer comprising nucleotides comprising 9 to 30 nucleotides can be used. In particular, a random primer may be composed of any nucleotide sequence comprising 9 to 30 nucleotides, a nucleotide type (i.e., a sequence type) is not particularly limited, and a random primer may be composed of 1 or more types of nucleotide sequences, preferably 1 to 10,000 types of nucleotide sequences, more preferably 1 to 1,000 types of nucleotide sequences, further preferably 1 to 100 types of nucleotide sequences, and most preferably 1 to 96 types of nucleotide sequences. With the use of nucleotides (or a group of nucleotides)within the range mentioned above for a random primer, an amplified nucleic acid fragment can be obtained with higher reproducibility. When a random primer comprises a plurality of nucleotide sequences, it is not necessary that all nucleotide sequences comprise the same number of nucleotides (9 to 30 nucleotides). A random primer may comprise a plurality of nucleotide sequences composed of a different number of nucleotides.

In general, in order to obtain a specific amplicon by a nucleic acid amplification reaction, the nucleotide sequence of a primer corresponding to the amplicon is designed.

For example, a pair of primers are designed such that the primers sandwich a site corresponding to an amplicon of a template DNA of genomic DNA or the like. In such case, as the primers are designed to be hybridized to a specific region included in a template, they may be referred to as "specific primers." Meanwhile, a random primer is different from a primer that is designed to obtain a specific amplicon, and it is designed to obtain a random amplicon but not to be hybridized to a specific region of a template DNA. A random primer may have any nucleotide sequence and can contribute to random amplicon amplification when it is incidentally hybridized to a region included in template DNA.

In other words, a random primer can be regarded as nucleotides involved in random amplicon amplification comprsing an arbitrary sequence as described above. Here, such arbitrary sequence is not particularly limited. However, it may be designed as, for example, a nucleotide sequence randomly selected from the group consisting of adenine, guanine, cytosine, and thymine or a specific nucleotide sequence. Examples of a specific nucleotide sequence include a nucleotide sequence including a restriction enzyme recognition sequence or a nucleotide sequence having an adapter sequence used for a next- generation sequencer.

When designing plural types of nucleotides for random primers, it is possible to use a method for designing a plurality of nucleotide sequences having certain lengths by randomly selecting from the group consisting of adenine, guanine, cytosine, and thymine.

In addition, when designing different types of nucleotides for random primers, it is also possible to use a method for designing a plurality of nucleotide sequences each comprising a common part consisting of a specific nucleotide sequence and a non-common part consisting of an arbitrary nucleotide sequence. Here, the non-common part may consist of a nucleotide sequence randomly selected from the group consisting of adenine, guanine, cytosine, and thymine or all or one of combinations of four types of nucleotides which are adenine, guanine, cytosine, and thymine. The common part is not particularly limited, and it may consist of any nucleotide sequence. It may consist of, for example, a nucleotide sequence including a restriction enzyme recognition sequence, a nucleotide sequence having an adapter sequence used for a next-generation sequencer, or a nucleotide sequence common in a specific gene family.

When designing plural types of nucleotide sequences having certain lengths by randomly selecting nucleotides from four types of nucleotides for a plurality of random primers, 30% or more, preferably 50% or more, more preferably 70% or more, and further preferably 90% or more of the entire such sequences exhibit 70% or less, preferably 60% or less, more preferably 50% or less, and most preferably 40% or less identity. By designing different types of nucleotide sequences having certain lengths by randomly selecting nucleotides from different types of nucleotides for a plurality of random primers exhibiting the identity within such range, an amplified fragment can be obtained over the entire genomic DNA of the target organism species. Thus, uniformity of the amplified fragment can be enhanced.

When designing a plurality of nucleotide sequences each comprising a common part consisting of a specific nucleotide sequence and a non-common part consisting of an arbitrary nucleotide sequence for a plurality of random primers, it is possible to design, for example, a nucleotide sequence comprising a non-common part consisting of several nucleotides on the 3’ end side and a common part consisting of the remaining nucleotides on the 5’ end side. By allowing a non-common part to consist of n number of nucleotides on the 3’ end side, it is possible to design 4 types of random primers. Here, the expression "n number" may refer to 1 to 5, preferably 2 to 4, and more preferably 2 to 3.

For example, it is possible to design, as a random primer comprising a common part and a non-common part, 16 types of random primers in total, each of which has an adapter sequence (common part) used for a next-generation sequencer on the 5’ end side and two nucleotides (non-common part) on the 3’ end side in total. It is possible to design 64 types of random primers in total by setting the number of nucleotides on the 3’end side to 3 nucleotides (non-common part). The more types of random primers, the more comprehensively the amplified fragments can be obtained throughout the genomic DNA of the target organism species. Therefore, when designing a random primer consisting of a common part and a non-common part, it is preferable that 3 nucleotides exist on the 3 'end side.

However, for example, after designing 64 types of nucleotide sequences each comprising a common part and a non-common part consisting of 3 nucleotides, not more than 63 types of random primers selected from these 64 types of nucleotide sequences may be used. In other words, as compared with the case of using all 64 types of random primers, in the case of using not more than 63 types of random primers, excellent results can be obtained in a nucleic acid amplification reaction or analysis using a next generation sequencer. Specifically, when 64 types of random primers are used, the number of reads of a specific nucleic acid amplification fragment might become remarkably large. In such case, favorable analysis results can be obtained by using the remaining 63 random primers excluding one or more random primers involved in the amplification of the specific nucleic acid amplification fragment from 64 types of random primers.

Similarly, in the case of designing 16 types of random primers each comprising a common part and a non-common part of 2 nucleotides, when not more than 15 types of random primers selected from 16 types of random primers are used, favorable analysis results may be obtained in a nucleic acid amplification reaction or analysis using a next generation sequencer.

Nucleotides constituting a random primer are preferably designed such that the G- C content is 5% to 95%, more preferably 10% to 90%, further preferably 15% to 80%, and most preferably 20% to 70%. With the use of a set of nucleotides having a G-C content within the above range as a random primer, amplified nucleic acid fragments can be obtained with enhanced reproducibility. The G-C content is the percentage of guanine and cytosine contained in the whole nucleotide chain.

Further, nucleotides constituting a random primer are designed such that consecutive nucleotides account for preferably 80% or less, more preferably 70% or less, further preferably 60% or less, and most preferably 50% or less with respect to the entire sequence length. Alternatively, nucleotides constituting a random primer are designed such that the number of consecutive nucleotides is preferably 8 or less, more preferably 7 or less, further preferably 6 or less, and most preferably 5 or less. An amplified nucleic acid fragment can be obtained with enhanced reproducibility with the use of a set of nucleotides constituting a random primer, for which the number of consecutive nucleotides falls within the above range.

In addition, it is preferable that nucleotides constituting a random primer be designed not to constitute a complementary region of 6 or more, more preferably 5 or more, and further preferably 4 or more nucleotides in a molecule. When the nucleotides designed not to constitute a complementary region within the above range, double strand formation occurring in a molecule can be prevented, and amplified nucleic acid fragments can be obtained with enhanced reproducibility.

Further, when plural types of nucleotides are designed for a random primer, in particular, it is preferable that a plurality of nucleotides be designed not to constitute a complementary region of 6 or more, more preferably 5 or more, and further preferably 4 or more nucleotides while forming a plurality of nucleotide sequences. When different types of nucleotide sequences are designed Thus, double strand formation occurring between nucleotide sequences can be prevented, and amplified nucleic acid fragments can be obtained with enhanced reproducibility.

When plural types of nucleotides are designed for random primers, it is preferable that the nucleotides be designed not to constitute a complementary sequence of 6 or more, more preferably 5 or more, and further preferably 4 or more nucleotides at the 3’ end side.

When they are designed not to form a complementary sequence within the above range at the 3' end side, double strand formation occurring between nucleotide sequences can be prevented, and amplified nucleic acid fragments can be obtained with enhanced reproducibility.

The terms "complementary region" and "complementary sequence" refer to, for example, a region and a sequence exhibiting 80% to 100% identity (e.g., a region and a sequence each comprising 5 nucleotides in which 4 or 5 nucleotides are complementary to each other) or a region and a sequence exhibiting 90% to 100% identity (e.g., a region and a sequence each comprising 5 nucleotides in which 5 nucleotides are complementary to each other).

Further, nucleotides constituting a random primer are preferably designed to have a Tm value suitable for thermal cycle conditions (in particular, an annealing temperature) in a nucleic acid amplification reaction. A Tm value can be calculated by a conventional method, such as the nearest neighbor base pair approach, the Wallace method, or the GC% method, although a method of calculation is not particularly limited thereto. Specifically, nucleotides used for a random primer are preferably designed to have a Tm value of 10°C to 85°C, more preferably 12°C to 75°C, further preferably 14°C to 70°C, and most preferably 16°C to 65°C. By designing Tm values for nucleotides within the above range, amplified nucleic acid fragments can be obtained with enhanced reproducibility under given thermal cycle conditions (in particular, at a given annealing temperature) in a nucleic acid amplification reaction.

Furthermore, when different types of nucleotides constituting a random primer are designed, in particular, a variation for Tm among a plurality of nucleotides is preferably 50°C or less, more preferably 45°C or less, further preferably 40°C or less, and most preferably 35°C or less. When the nucleotides are designed such that a variation for Tm among a plurality of nucleotides falls within the above range, amplified nucleic acid fragments can be obtained with enhanced reproducibility under given thermal cycle conditions (in particular, at a given annealing temperature) in a nucleic acid amplification reaction.

[Nucleic acid amplification reaction] According to the method for producing a DNA library of the present invention, many amplification fragments are obtained via a nucleic acid amplification reaction conducted with the use of the random primer and genomic DNA as a template described above. In particular, in such a nucleic acid amplification reaction, the concentration of a random prime in a reaction solution is set higher than the primer concentration in a usual nucleic acid amplification reaction. Thus, many amplification fragments can be obtained using genomic DNA as a template while achieving high reproducibility. The thus obtained many amplification fragments can be used for a DNA library that can be applied to genotyping and the like.

A nucleic acid amplification reaction is a reaction for synthesizing amplification fragments in a reaction solution containing genomic DNA as a template, the above- mentioned random primers, DNA polymerase, deoxynucleoside triphosphate as a substrate (i.e., dNTP, which is a mixture of dATP, dCTP, dTTP, and dGTP), and a buffer under given thermal cycle conditions. As it is necessary to add Mg at a given concentration to a reaction solution in a nucleic acid amplification reaction, the buffer of the above composition contains MgCl . When the buffer does not contain MgCl , MgCl is further 2 2 2 added to the above composition.

In particular, in a nucleic acid amplification reaction, it is preferable to adequately set the concentration of a random primer in accordance with the nucleotide length of the random primer. When different types of nucleotides constitute random primers with different nucleotide lengths, the average of nucleotide lengths of random primers may be set as the nucleotide length (the average may be a simple average or the weight average taking the amount of nucleotides into account).

Specifically, a nucleic acid amplification reaction is conducted using a random primer comprising 9 to 30 nucleotides at a random primer concentration of 4 to 200 μM and preferably at 4 to 100 μM. Under such conditions, many amplified fragments, and in particular, many amplified fragments comprising 100 to 500 nucleotides via a nucleic acid amplification reaction can be obtained while achieving high reproducibility.

More specifically, when a random primer comprises 9 to 10 nucleotides, the random primer concentration is preferably 40 to 60 μM. When a random primer comprises 10 to 14 nucleotides, it is preferable that the random primer concentration satisfy 100 μM or less and y > -6.974 3E + 08x , provided that the nucleotide length of the random primer is represented by "x" and the concentration of the random primer is represented by "y." When a random primer comprises 14 to 18 nucleotides, the random primer concentration is preferably 4 to 100 μM. When a random primer comprises 18 to 28 nucleotides, the random primer concentration satisfies -5.533 preferably 4 μM or more and y < 8E + 08x . When a random primer comprises 28 to 29 nucleotides, the random primer concentration is preferably 6 to 10 μM. By setting the random primer concentration in accordance with the nucleotide length of a random primer as described above, many amplified fragments can be obtained with improved certainty while achieving high reproducibility. -6.974 As described in the Examples below, the above inequations (y > 3E + 08x and y < 8E -5.533 + 08x ) are developed to be able to represent the random primer concentration at which many DNA fragments comprising 100 to 500 nucleotides can be obtained with favorable reproducibility as a result of thorough inspection of the correlation between the random primer length and the random primer concentration.

The amount of genomic DNA as a template in a nucleic acid amplification reaction is not particularly limited. However, it is preferably 0.1 to 1000 ng, more preferably 1 to 500 ng, further preferably 5 to 200 ng, and most preferably 10 to 100 ng, when the amount of the reaction solution is 50 µl. By setting the amount of genomic DNA as a template within the above range, many amplified fragments can be obtained without inhibiting the amplification reaction with a random primer, while achieving high reproducibility.

Genomic DNA can be prepared in accordance with a conventional technique without particular limitations. With the use of a commercially available kit, genomic DNA can be easily prepared from a target organism species. Genomic DNA extracted from an organism in accordance with a conventional technique or with the use of a commercially available kit may be used as is, genomic DNA extracted from an organism and purified may be used, or genomic DNA subjected to restriction enzyme treatment or ultrasonic treatment may be used.

DNA polymerase used in a nucleic acid amplification reaction is not particularly limited, and an enzyme having DNA polymerase activity under thermal cycle conditions for a nucleic acid amplification reaction can be used. Specifically, heat-stable DNA polymerase used for a general nucleic acid amplification reaction can be used. Examples of DNA polymerase include thermophilic bacteria-derived DNA polymerase such as Taq DNA polymerase, and hyperthermophilic Archaea-derived DNA polymerase such as KOD DNA polymerase or Pfu DNA polymerase. In a nucleic acid amplification reaction, it is particularly preferable to use Pfu DNA polymerase as DNA polymerase in combination with the random primer described above. With the use of such DNA polymerases, many amplified fragments can be obtained with improved certainty while achieving high reproducibility.

In a nucleic acid amplification reaction, the concentration of deoxynucleoside triphosphate as a substrate (i.e., dNTP, which is a mixture of dATP, dCTP, dTTP, and dGTP) is not particularly limited, and it can be 5 µM to 0.6 mM, preferably 10 µM to 0.4 mM, and more preferably 20 µM to 0.2 mM. By setting the concentration of dNTP as a substrate within such range, errors caused by incorrect incorporation by DNA polymerase can be prevented, and many amplified fragments can be obtained while achieving high reproducibility.

A buffer used in a nucleic acid amplification reaction is not particularly limited.

For example, a solution comprising MgCl as described above, Tris-HCl (pH 8.3), and KCl can be used. The concentration of Mg is not particularly limited. For example, it can be 0.1 to 4.0 mM, preferably 0.2 to 3.0 mM, more preferably 0.3 to 2.0 mM, and further preferably 0.5 to 1.5 mM. By designating the concentration of Mg in the reaction solution within such range, many amplified fragments can be obtained while achieving high reproducibility.

Thermal cycling conditions of a nucleic acid amplification reaction are not particularly limited, and a common thermal cycle can be adopted. A specific example of a thermal cycle comprises a first step of thermal denaturation in which genomic DNA as a template is dissociated into single strands, a cycle comprising thermal denaturation, annealing, and extension repeated a plurality of times (e.g., 20 to 40 times), a step of extension for a given period of time according to need, and the final step of storage.

Thermal denaturation can be performed at, for example, 93°C to 99°C, preferably 95°C to 98°C, and more preferably 97°C to 98°C. Annealing can be performed at, for example, 30°C to 70°C, preferably 35°C to 68°C, and more preferably 37°C to 65°C, although it varies depending on the Tm value of a random primer. Extension can be performed at, for example, 70°C to 76°C, preferably 71°C to 75°C, and more preferably 72°C to 74°C. Storage can be performed at, for example, 4°C.

The first step of thermal denaturation can be performed within the temperature range described above for a period of, for example, 5 seconds to 10 minutes, preferably 10 seconds to 5 minutes, and more preferably 30 seconds to 2 minutes. In the cycle comprising "thermal denaturation, annealing, and extension," thermal denaturation can be carried out within the temperature range described above for a period of, for example, 2 seconds to 5 minutes, preferably5 seconds to 2 minutes, and more preferably 10 seconds to 1 minute. In the cycle comprising "thermal denaturation, annealing, and extension," annealing can be carried out within the temperature range described above for a period of, for example, 1 second to 3 minutes, preferably 3 seconds to 2 minutes, and more preferably 5 seconds to 1 minute. In the cycle comprising "thermal denaturation, annealing, and extension," extension can be carried out within the temperature range described above for a period of, for example, 1 second to 3 minutes, preferably 3 seconds to 2 minutes, and more preferably seconds to 1 minute.

According to the method for producing a DNA library of the present invention, amplified fragments may be obtained by a nucleic acid amplification reaction that employs a hot start method. The hot start method is intended to prevent mis-priming or non-specific amplification caused by primer-dimer formation prior the cycle comprising "thermal denaturation, annealing, and extension." The hot start method involves the use of an enzyme in which DNA polymerase activity has been suppressed by binding an anti-DNA polymerase antibody thereto or chemical modification thereof. Thus, DNA polymerase activity can be suppressed and a non-specific reaction prior to the thermal cycle can be prevented. According to the hot start method, a temperature is set high in the first thermal cycle, DNA polymerase activity is thus recovered, and the subsequent nucleic acid amplification reaction is then allowed to proceed.

As described above, many amplified fragments can be obtained with the use of genomic DNA as a template and a random primer by conducting a nucleic acid amplification reaction with the use of a random primer comprising 9 to 30 nucleotides and setting the concentration thereof to 4 to 200 µM in a reaction solution. With the use of the random primer comprising 9 to 30 nucleotides while setting the concentration thereof to 4 to 200 µM in a reaction solution, a nucleic acid amplification reaction can be performed with very high reproducibility. According to the nucleic acid amplification reaction, specifically, many amplified fragments can be obtained while achieving very high reproducibility.

Therefore, the thus obtained many amplified fragments can be used for a DNA library in genetic analysis targeting genomic DNA.

By performing a nucleic acid amplification reaction with the use of the random primer comprising 9 to 30 nucleotides and setting the concentration thereof in a reaction solution to 4 to 200 µM, in particular, many amplified fragments comprising about 100 to 500 nucleotides can be obtained with the use of genomic DNA as a template. Such many amplified fragments comprising about 100 to 500 nucleotides are suitable for mass analysis of nucleotide sequences with the use of, for example, a next-generation sequencer, and highly accurate sequence information can thus be obtained. According to the present invention, a DNA library including DNA fragments comprising about 100 to 500 nucleotides can be produced.

By performing a nucleic acid amplification reaction with the use of the random primer comprising 9 to 30 nucleotides and setting the concentration thereof to 4 to 200 µM in a reaction solution, in particular, amplified fragments can be obtained uniformly across genomic DNA. In other words, DNA fragments are amplified in a distributed manner across the genome but not in a localized manner in a specific region of genomic DNA in a nucleic acid amplification reaction with the use of such random primer. That is, according to the present invention, a DNA library can be produced uniformly across the entire genome.

After performing the nucleic acid amplification reaction using the above- mentioned random primer, restriction enzyme treatment, size selection treatment, sequence capture treatment, and the like can be performed on the obtained amplified fragments. By carrying out restriction enzyme treatment, size selection treatment, and sequence capture treatment on the amplified fragments, specific amplified fragments (a fragment having a specific restriction enzyme site, an amplified fragment with a specific size range, and an amplified fragment having a specific sequence) can be obtained from among the obtained amplified fragments. Then, specific amplified fragments obtained by these treatments can be used for a DNA library.

[Method of genomic DNA analysis] With the use of the DNA library produced in the manner described above, genomic DNA analysis such as genotyping can be performed. Such DNA library has very high reproducibility, the size thereof is suitable for a next-generation sequencer, and it has uniformity across the entire genome. Accordingly, the DNA library can be used as a DNA marker (also referred to as "genetic marker" or "gene marker"). The term "DNA marker" refers to a wide range of characteristic nucleotide sequences present in genomic DNA. In addition, a DNA marker may be especially a nucleotide sequence on the genome serving as a marker associated with genetic traits. A DNA marker can be used for, for example, genotype identification, linkage mapping, gene mapping, breeding comprising a step of selection with the use of a marker, back crossing using a marker, quantitative trait locus mapping, bulked segregant analysis, variety identification, or discontinuous imbalance mapping.

For example, the nucleotide sequence of a DNA library prepared as described above is determined using a next generation sequencer or the like, and the presence or absence of a DNA marker can be confirmed based on the obtained nucleotide sequence.

As an example, the presence or absence of a DNA marker can be confirmed from the number of reads of the obtained nucleotide sequence. While a next-generation sequencer is not particularly limited, such sequencer is also referred to as a "second- generation sequencer," and such sequencer is an apparatus for nucleotide sequencing that allows simultaneous determination of nucleotide sequences of several tens of millions of DNA fragments. The sequencing principle of a next-generation sequencer is not particularly limited. For example, sequencing can be carried out in accordance with a method in which sequencing is carried out while amplifying and synthesizing target DNA on flow cells by bridge PCR method and the sequencing-by-synthesis method, or in accordance with a method in which sequencing is carried out by emulsion PCR and the pyrosequencing method for assaying the amount of pyrophosphoric acids released upon DNA synthesis. More specific examples of next-generation sequencers include MiniSeq, MiSeq, NextSeq, HiSeq, and HiSeq X Series (Illumina, Inc.) and Roche 454 GS FLX sequencers (Roche).

In another example, the presence or absence of a DNA marker can be confirmed by comparing the nucleotide sequence obtained for the DNA library prepared as described above with the reference nucleotide sequence. Here, the reference nucleotide sequence means a known sequence as a reference, and it can be, for example, a known sequence stored in a database. That is, a DNA library is prepared as described above for a given organism, its nucleotide sequence is determined, and the nucleotide sequence of the DNA library is compared with the reference nucleotide sequence. A nucleotide sequence that differs from the reference nucleotide sequence can be designated as a DNA marker (a characteristic nucleotide sequence existing in the genomic DNA) related to the organism.

For each specified DNA marker, the relevance to the genetic trait (phenotype) can be determined by further analysis according to a conventional method. In other words, a DNA marker related to a phenotype (sometimes referred to as a "selective marker") can be identified from among the DNA markers identified as described above.

Furthermore, in another example, the presence or absence of a DNA marker can be confirmed by comparing the nucleotide sequence obtained for the DNA library prepared as described above with the nucleotide sequence of a DNA library prepared as described above using genomic DNA from a different organism or tissue. In other words, a DNA library is prepared as described above for each of two or more organisms or two different tissues, the nucleotide sequences thereof are determined, and the nucleotide sequences of the DNA libraries are compared with each other. Then, a nucleotide sequence that differs between the DNA libraries can be designated as a DNA marker (a characteristic nucleotide sequence existing in the genomic DNA) related to the sampled organism or tissue. For each specified DNA marker, the relevance to the genetic trait (phenotype) can be determined by further analysis according to a conventional method. In other words, a DNA marker related to a phenotype (sometimes referred to as a "selective marker") can be identified from among the DNA markers identified as described above.

As an aside, it is also possible to design a pair of primers which specifically amplify the DNA marker based on the obtained nucleotide sequence. It is also possible to confirm the presence or absence of the DNA marker in the extracted genomic DNA by performing a nucleic acid amplification reaction using a pair of designed primers and genomic DNA extracted from a target organism as a template.

Alternatively, DNA libraries prepared as described above can be used for metagenomic analysis for examining a wide variety of microorganisms and the like, genome mutation analysis of somatic cells of tumor tissue or the like, genotyping using microarrays, determination and analysis of ploidy, calculation and analysis of the number of chromosomes, analysis of the increase and decrease of chromosomes, analysis of partial insertion/deletion/replication/translocation of chromosomes, analysis of contamination with foreign genome, parentage discrimination analysis, and testing and analysis of crossed seed purity.

[Application to next generation sequencing technology] As described above, by conducting a nucleic acid amplification reaction with a random primer contained at a high concentration in a reaction solution, it is possible to obtain many amplified fragments with favorable reproducibility using genomic DNA as a template. Since each obtained amplified fragment has nucleotide sequence at both ends thereof which are the same as those of the random primer, it can be easily applied to the next generation sequence technology by utilizing the nucleotide sequence.

Specifically, as described above, a nucleic acid amplification reaction is conducted in a reaction solution (first reaction solution) containing genomic DNA and a random primer at a high concentration to obtain many amplified fragments (first DNA fragments) using the genomic DNA as a template. Next, a nucleic acid amplification reaction is conducted in a reaction solution (second reaction solution) containing the obtained many amplified fragments (first DNA fragments) and a primer designed based on the nucleotide sequence of the random primer (referred to as "next generation sequencer primer"). A next generation sequencer primer to be used herein is a nucleotide sequence including a region used for a nucleotide sequencing reaction. More specifically, for example, the next- generation sequencer primer may be a nucleotide sequence having a region necessary for a nucleotide sequencing reaction (sequence reaction) by a next-generation sequencer, in which the nucleotide sequence at the 3' end of the primer is a nucleotide sequence having 70% or more identity, preferably 80% or more identity, more preferably 90% or more identity, still more preferably 95% or more identity, further preferably 97% or more identity, and most preferably 100% identity to the nucleotide sequence on the 5' end side of the first DNA fragment.

Here, the "region used for a nucleotide sequencing reaction" included in a next- generation sequencer primer is not particularly limited because it varies depending on type of the next-generation sequencer. However, in the case of conducting a nucleotide sequencing reaction using a next-generation sequencer with a sequence primer, such region may be, for example, a nucleotide sequence complementary to the nucleotide sequence of the sequence primer. In a case in which a sequencing reaction is conducted by a next- generation sequencer using capture beads bound to given DNA, the "region used for a nucleotide sequencing reaction" refers to a nucleotide sequence complementary to the nucleotide sequence of the DNA bound to capture beads. Further, in a case in which a next- generation sequencer reads a sequence based on a current change when a DNA chain having a terminal hairpin loop passes through a protein having nano-sized pores, the "region used for a nucleotide sequencing reaction" may be a nucleotide sequence complementary to the nucleotide sequence forming the hairpin loop.

By designing the nucleotide sequence at the 3 'end of a next-generation sequencer primer as described above, the next-generation sequencer primer can be hybridized to the 3' end of the first DNA fragment under stringent conditions, and the second DNA fragment can be amplified using the first DNA fragment as a template. Stringent conditions mean conditions under which a so-called specific hybrid is formed while a nonspecific hybrid is not formed. For example, such conditions can be appropriately determined with reference to Molecular Cloning: A Laboratory Manual (Third Edition). Specifically, stringency can be determined by setting the temperature and the salt concentration in a solution upon Southern hybridization, and the temperature and the salt concentration in a solution in the washing step of Southern hybridization. More specifically, for example, the sodium concentration is set to 25 to 500 mM and preferably 25 to 300 mM and the temperature is set to 42°C to 68°C and preferably 42°C to 65°C under stringent conditions. More specifically, the sodium concentration is 5 × SSC (83 mM NaCl, 83 mM sodium citrate) and the temperature is 42°C.

In particular, when different types of random primers are used to obtain a first DNA fragment, next-generation sequencer primers may be prepared to correspond to all or some of random primers.

For example, in a case in which a set of different types of random primers (each having an arbitrary 3'-end sequence of several nucleotides) each comprising a common nucleotide sequence except several nucleotides (e.g., about 1 to 3 nucleotides) at the 3' end is used, all of the obtained many first DNA fragments have a common 5'-end sequence.

Accordingly, the 3'-end nucleotide sequence of a next generation sequencer primer is designated to be a nucleotide sequence having 70% or more identity to the 5'-end nucleotide sequence common to the first DNA fragments. By designing next-generation sequencer primers as described above, it is possible to obtain next generation sequencer primers corresponding to all random primers. By using such next generation sequencer primers, it is possible to amplify second DNA fragments using all of the first DNA fragments as templates.

Similarly, even in a case in which a set of different types of random primers (each having an arbitrary 3'-end sequence of several nucleotides) each comprising a common nucleotide sequence except several nucleotides (e.g., about 1 to 3 nucleotides) at the 3' end is used, it is also possible to obtain second DNA fragments using some of the obtained many first DNA fragments as templates. Specifically, the 3'-end nucleotide sequence of a next generation sequencer primer is designated to be a nucleotide sequence having 70% or more identity to the 5'-end nucleotide sequence common to the first DNA fragments and the sequence comprising several nucleotides following the nucleotide sequence (corresponding to several nucleotides (arbitrary sequence) at the 3' end of the random primer) such that second DNA fragments can be amplified using some of the first DNA fragments as templates.

Meanwhile, in a case in which first DNA fragments are obtained using different types of random primers each consisting of an arbitrary nucleotide sequence, it is possible to obtain second DNA fragments using different types of next-generation sequencer primers such that the second DNA fragments correspond to all of the first DNA fragments, or it is also possible to obtain second DNA fragments using different types of next-generation sequencer primers such that the second DNA fragments correspond to some of the first DNA fragments.

As described above, the second DNA fragments amplified using next-generation sequencer primers have a region necessary for a nucleotide sequencing reaction (sequence reaction) by a next-generation sequencer, which is included in the next-generation sequencer primers. The region necessary for a sequence reaction is not particularly limited as it varies depending on a next generation sequencer. For example, when a next-generation sequencer primer is used in a next-generation sequencer based on the principle that sequencing is carried out while amplifying and synthesizing target DNA on flow cells by bridge PCR method and the sequencing-by-synthesis method, the next-generation sequencer primer needs to contain a region necessary for bridge PCR and a region necessary for the sequencing-by-synthesis method. The region necessary for bridge PCR is a region that is hybridized to an oligonucleotide immobilized on flow cells and has a length of 9 nucleotides including the 5 'end of the next generation sequencer primer. In addition, a region necessary for the sequencing-by-synthesis method is a region to which a sequence primer used in a sequence reaction is hybridized, and is a region in the middle of the next generation sequencer primer.

In addition, a next-generation sequencer may be an Ion Torrent sequencer. In the case of using the Ion Torrent sequencer, a next-generation sequencer primer has a so-called ion adapter on the 5 'end side and binds to a particle for conducting emulsion PCR. In addition, in the Ion Torrent sequencer, particles coated with a template amplified by emulsion PCR are placed on an ion chip and subjected to a sequence reaction.

Here, a nucleic acid amplification reaction using a next-generation sequencer primer and a second reaction solution containing the first DNA is not particularly limited, and conventional conditions for nucleic acid amplification reaction can be applied. That is, the conditions in [Nucleic acid amplification reaction] described above can be used. For example, the second reaction solution contains first DNA fragments as templates, the above-described next-generation sequencer primer, DNA polymerase, deoxynucleoside triphosphate as a substrate (i.e., dNTP, which is a mixture of dATP, dCTP, dTTP, and dGTP), and a buffer.

In particular, the concentration of the next-generation sequencer primer can be set to 0.01 to 5.0 µM, preferably 0.1 to 2.5 µM, and most preferably 0.3 to 0.7 µM.

While the amount of the first DNA fragments serving as templates in a nucleic acid amplification reaction is not particularly limited, it is preferably 0.1 to 1000 ng, more preferably 1 to 500 ng, further preferably 5 to 200 ng, and most preferably 10 to 100 ng when the amount of the reaction solution is 50 µl.

A method for preparing first DNA fragments as templates is not particularly limited. In the method, the reaction solution obtained after the completion of the nucleic acid amplification reaction using the above-described random primers may be used as is, or the reaction solution may be used after purifying the first DNA fragments therefrom.

Regarding the type of DNA polymerase, the concentration of deoxynucleoside triphosphate as a substrate (dNTP, i.e., a mixture of dATP, dCTP, dTTP and dGTP), the buffer composition, and temperature cycle conditions used for the nucleic acid amplification reaction, the conditions in [Nucleic acid amplification reaction] described above can be used. In addition, in a nucleic acid amplification reaction using next-generation sequencer primers, a hot start method may be employed, or amplified fragments may be obtained by a nucleic acid amplification reaction.

As described above, by using the first DNA fragments obtained using random primers as templates and using the second DNA fragments amplified using next-generation sequencer primers, it is possible to readily prepare a DNA library that can be applied to a next-generation sequencer.

In the above examples, a DNA library is prepared using the first DNA fragments obtained using random primers as templates and amplifying the second DNA fragments using next-generation sequencer primers. However, the scope of the present invention is not limited to Such examples. For example, the DNA library according to the present invention may be prepared by amplifying second DNA fragments using first DNA fragments obtained using random primers as templates and further obtaining third DNA fragments using the second DNA fragments as templates and next-generation sequencer primers, thereby obtaining a DNA library of the third DNA fragments applicable to a next generation sequencer.

Similarly, in order to prepare a DNA library applicable to a next-generation sequencer, after a nucleic acid amplification reaction using second DNA fragments as templates, a nucleic acid amplification reaction is repeatedly conducted using the obtained DNA fragments as templates, and next-generation sequencer primers are used for the final nucleic acid amplification reaction. In such case, the number of nucleic acid amplification reactions to be repeated is not particularly limited, but it is 2 to 10 times, preferably 2 to 5 times, and more preferably 2 to 3 times.

Examples Hereafter, the present invention is described in greater detail with reference to the Examples below, although the scope of the present invention is not limited to these Examples.

[Example 1] 1. Flowchart In this Example, a DNA library was prepared via PCR using genomic DNAs extracted from various types of organism species as templates and various sets of random primers in accordance with the flow chart shown in Fig. 1. In addition, with the use of the prepared DNA library, sequence analysis was performed by a so-called next-generation sequencer, and the genotype was analyzed based on the obtained read data. 2. Materials In this Example, genomic DNAs were extracted from the sugarcane varieties NiF8 and Ni9, 22 hybrid progeny lines thereof, and the rice variety Nipponbare using the DNeasy Plant Mini Kit (QIAGEN), and the extracted genomic DNAs were purified. The purified genomic DNAs were used as NiF8-derived genomic DNA, Ni9-derived genomic DNA, genomic DNAs from 22 hybrid progeny lines, and Nipponbare-derived genomic DNA, respectively. In this Example, Human Genomic DNA was purchased as human DNA from TakaraBio and used as human-derived genomic DNA. 3. Method 3.1 Correlation between PCR conditions and DNA fragment sizes 3.1.1 Random primer designing In order to design random primers, the GC content was set between 20% and 70%, and the number of consecutive nucleotides was adjusted to 5 or less. The nucleotide length was set at 16 levels (i.e., 8, 9, 10, 11, 12, 14, 16, 18, 20, 22, 24, 26, 28, 29, 30, and 35 nucleotides). For each nucleotide length, 96 types of nucleotide sequences were designed, and a set of 96 types of random primers was prepared for each nucleotide length.

Concerning 10-nucleotide primers, 6 sets (each comprising 96 types of random primers) were designed (these 6 sets are referred to as 10-nucleotide primer A to 10-nucleotide primer F). In this Example, specifically, 21 different sets of random primers were prepared.

Tables 1 to 21 show nucleotide sequences of random primers contained in these 21 different sets of random primers.

[Table 1-1] Table 1. Random primer list (10-nucleotide A) No. Primer sequence SEQ ID NO: No. Primer sequence SEQ ID NO: 33 GCCGAATAGT 33 1 AGACGTCGTT 1 34 GTACCTAGGC 34 2 GAGGCGATAT 2 GCTTACATGA 35 3 GTGCGAACGT 3 36 TCCACGTAGT 36 4 TTATACTGCC 4 37 AGAGGCCATC 37 CAAGTTCGCA 5 38 CGGTGATGCT 38 6 ACAAGGTAGT 6 39 CACTGTGCTT 39 7 ACACAGCGAC 7 40 CATGATGGCT 40 8 TTACCGATGT 8 41 GCCACACATG 41 9 CACAGAGTCG 9 42 CACACACTGT 42 TTCAGCGCGT 10 43 CAGAATCATA 43 11 AGGACCGTGA 11 44 ATCGTCTACG 44 12 GTCTGTTCGC 12 45 CGAGCAATAC 45 13 ACCTGTCCAC 13 46 ACAAGCGCAC 46 14 CCGCAATGAC 14 47 GCTTAGATGT 47 CTGCCGATCA 15 48 TGCATTCTGG 48 16 TACACGGAGC 16 49 TGTCGGACCA 49 17 CCGCATTCAT 17 50 AGGCACTCGT 50 18 GACTCTAGAC 18 51 CTGCATGTGA 51 19 GGAGAACTTA 19 52 ACCACGCCTA 52 TCCGGTATGC 20 53 GAGGTCGTAC 53 21 GGTCAGGAGT 21 54 AATACTCTGT 54 22 ACATTGGCAG 22 55 TGCCAACTGA 55 23 CGTAGACTGC 23 56 CCTGTTCGGT 56 24 AGACTGTACT 24 57 GTAGAGAGTT 57 TAGACGCAGT 25 58 TACAGCGTAA 58 26 CCGATAATCT 26 59 TGACGTGATG 59 27 GAGAGCTAGT 27 60 AGACGTCGGT 60 28 GTACCGCGTT 28 61 CGCTAGGTTC 61 29 GACTTGCGCA 29 62 GCCTTATAGC 62 CGTGATTGCG 30 63 CCTTCGATCT 63 31 ATCGTCTCTG 31 64 AGGCAACGTG 64 32 CGTAGCTACG 32 [Table 1-2] No. Primer sequence SEQ ID NO: 65 TGAGCGGTGT 65 66 GTGTCGAACG 66 67 CGATGTTGCG 67 68 AACAAGACAC 68 69 GATGCTGGTT 69 70 ACCGGTAGTC 70 71 GTGACTAGCA 71 72 AGCCTATATT 72 73 TCGTGAGCTT 73 74 ACACTATGGC 74 75 GACTCTGTCG 75 76 TCGATGATGC 76 77 CTTGGACACT 77 78 GGCTGATCGT 78 79 ACTCACAGGC 79 80 ATGTGCGTAC 80 81 CACCATCGAT 81 82 AGCCATTAAC 82 83 AATCGACTGT 83 84 AATACTAGCG 84 85 TCGTCACTGA 85 86 CAGGCTCTTA 86 87 GGTCGGTGAT 87 88 CATTAGGCGT 88 89 ACTCGCGAGT 89 90 TTCCGAATAA 90 91 TGAGCATCGT 91 92 GCCACGTAAC 92 93 GAACTACATG 93 94 TCGTGAGGAC 94 95 GCGGCCTTAA 95 96 GCTAAGGACC 96 [Table 2-1] Table 2. Random primer list (10-nucleotide B) No. Primer sequence SEQ ID NO: No. Primer sequence SEQ ID NO: 1 ATAGCCATTA 97 33 GGTATAGTAC 129 2 CAGTAATCAT 98 34 CTAATCCACA 130 3 ACTCCTTAAT 99 35 GCACCTTATT 131 4 TCGAACATTA 100 36 ATTGACGGTA 132 ATTATGAGGT 101 37 GACATATGGT 133 6 AATCTTAGAG 102 38 GATAGTCGTA 134 7 TTAGATGATG 103 39 CAATTATCGC 135 8 TACATATCTG 104 40 CTTAGGTGAT 136 9 TCCTTAATCA 105 41 CATACTACTG 137 GTTGAGATTA 106 42 TAACGCGAAT 138 11 TGTTAACGTA 107 43 CAAGTTACGA 139 12 CATACAGTAA 108 44 AATCTCAAGG 140 13 CTTATACGAA 109 45 GCAATCATCA 141 14 AGATCTATGT 110 46 TGTAACGTTC 142 AAGACTTAGT 111 47 TATCGTTGGT 143 16 TGCGCAATAA 112 48 CGCTTAAGAT 144 17 TTGGCCATAT 113 49 TTAGAACTGG 145 18 TATTACGAGG 114 50 GTCATAACGT 146 19 TTATGATCGC 115 51 AGAGCAGTAT 147 AACTTAGGAG 116 52 CAACATCACT 148 21 TCACAATCGT 117 53 CAGAAGCTTA 149 22 GAGTATATGG 118 54 AACTAACGTG 150 23 ATCAGGACAA 119 55 TTATACCGCT 151 24 GTACTGATAG 120 56 GAATTCGAGA 152 CTTATACTCG 121 57 TTACGTAACC 153 26 TAACGGACTA 122 58 GCATGGTTAA 154 27 GCGTTGTATA 123 59 GCACCTAATT 155 28 CTTAAGTGCT 124 60 TGTAGGTTGT 156 29 ATACGACTGT 125 61 CCATCTGGAA 157 ACTGTTATCG 126 62 TTCGCGTTGA 158 31 AATCTTGACG 127 63 AACCGAGGTT 159 32 ACATCACCTT 128 64 GTACGCTGTT 160 [Table 2-2] No. Primer sequence SEQ ID NO: 65 AGTATCCTGG 161 66 GGTTGTACAG 162 67 ACGTACACCA 163 68 TGTCGAGCAA 164 69 GTCGTGTTAC 165 70 GTGCAATAGG 166 71 ACTCGATGCT 167 72 GAATCGCGTA 168 73 CGGTCATTGT 169 74 ATCAGGCGAT 170 75 GTAAGATGCG 171 76 GGTCTCTTGA 172 77 TCCTCGCTAA 173 78 CTGCGTGATA 174 79 CATACTCGTC 175 80 ATCTGAGCTC 176 81 ACGGATAGTG 177 82 ACTGCAATGC 178 83 TAACGACGTG 179 84 TAGACTGTCG 180 85 CAGCACTTCA 181 86 AACATTCGCC 182 87 ACTAGTGCGT 183 88 ACGCTGTTCT 184 89 CGTCGAATGC 185 90 CTCTGACGGT 186 91 GTCGCCATGT 187 92 GGTCCACGTT 188 93 CGAGCGACTT 189 94 TTGACGCGTG 190 95 CTGAGAGCCT 191 96 CGCGCTAACT 192 [Table 3-1] Table 3. Random primer list (10-nucleotide C) No. Primer sequence SEQ ID NO: No. Primer sequence SEQ ID NO: 1 GGTCGTCAAG 193 33 TGAGGCAACC 225 2 AGGTTGACCA 194 34 CAACTGCAGT 226 3 TAACGGCAAC 195 35 CGGAGATACG 227 4 GAGGCTGGAT 196 36 CTTCGCAAGT 228 GTGCACACCT 197 37 CTGGCATACG 229 6 TGAGGACCAG 198 38 TAACGTTCGC 230 7 TACTTGCGAG 199 39 CCGGCGTTAA 231 8 AACTGTGAGA 200 40 ACAAGACGCC 232 9 CTCCATCAAC 201 41 CCATTAGACT 233 CGGACTGTTA 202 42 GTCTGTGACA 234 11 TAGGACAGTC 203 43 GGCATTGGAC 235 12 AGAGGACACA 204 44 TCTTCGCACG 236 13 ACATTCGCGG 205 45 TAGCCTGTGC 237 14 GCTTACTGCA 206 46 CACTGACCTA 238 CAATACGTAA 207 47 CCGCACGATT 239 16 AGACTTGCGC 208 48 ATAGCACACG 240 17 GAGCGGTGTT 209 49 GCACGTCATA 241 18 CGTGAGAGGT 210 50 AAGCCGTTGG 242 19 AATCCGTCAG 211 51 CGGACCGTTA 243 ATACGTACCG 212 52 TACACAGCGT 244 21 AACTGATTCC 213 53 CGGACTTCAG 245 22 CTGAGCGTAC 214 54 TAGAACGTCA 246 23 GTCGGATTCG 215 55 GGCATTGGAG 247 24 GCCGACCATA 216 56 GGCACTCGTT 248 GCAGAACTAA 217 57 GTACCGTTAA 249 26 CTAACGACCG 218 58 AATACGTGTC 250 27 GCTGGACCAT 219 59 CCATTGACGT 251 28 GACGCGGTTA 220 60 CGTGAATCGC 252 29 AGTGGTGAGC 221 61 ATCAACGCGG 253 CAGGCAGTCA 222 62 CGCCAAGGTA 254 31 TCTGACGTCA 223 63 AGAAGACGCC 255 32 TACATGACGT 224 64 CCGCATAGTC 256 [Table 3-2] No. Primer sequence SEQ ID NO: 65 CTTATATGTG 257 66 GGTCTCATCG 258 67 CCACCATGTC 259 68 ACGAATGTGT 260 69 GGTAGTAACA 261 70 GCCACTTAAT 262 71 ATATTGCGCC 263 72 GACCAATAGT 264 73 AACAACACGG 265 74 ATAGCCGATG 266 75 CGAGAGCATA 267 76 CGAGACATGA 268 77 CGCCAAGTTA 269 78 TTATAATCGC 270 79 TAGAAGTGCA 271 80 GGAGGCATGT 272 81 GCCACTTCGA 273 82 TCCACGGTAC 274 83 CAACTATGCA 275 84 CAAGGAGGAC 276 85 GAGGTACCTA 277 86 GAGCGCATAA 278 87 TCGTCACGTG 279 88 AACTGTGACA 280 89 TCCACGTGAG 281 90 ACACTGCTCT 282 91 TACGGTGAGC 283 92 CGGACTAAGT 284 93 AAGCCACGTT 285 94 CAATTACTCG 286 95 TCTGGCCATA 287 96 TCAGGCTAGT 288 [Table 4-1] Table 4. Random primer list (10-nucleotide D) No. Primer sequence SEQ ID NO: No. Primer sequence SEQ ID NO: 1 TTGACCCGGA 289 33 CAAGTCAGGA 321 2 TTTTTATGGT 290 34 GGGTCGCAAT 322 3 ATGTGGTGCG 291 35 CAGCAACCTA 323 4 AAGGCGCTAG 292 36 TTCCCGCCAC 324 TCCAACTTTG 293 37 TGTGCATTTT 325 6 CCATCCCATC 294 38 ATCAACGACG 326 7 CAATACGAGG 295 39 GTGACGTCCA 327 8 GAGTGTTACC 296 40 CGATCTAGTC 328 9 GCCTCCTGTA 297 41 TTACATCCTG 329 CGAAGGTTGC 298 42 AGCCTTCAAT 330 11 GAGGTGCTAT 299 43 TCCATCCGAT 331 12 TAGGATAATT 300 44 GACTGGGTCT 332 13 CGTTGTCCTC 301 45 TTCGGTGGAG 333 14 TGAGACCAGC 302 46 GACCAGCACA 334 TGCCCAAGCT 303 47 CATTAACGGA 335 16 TACTGAATCG 304 48 TTTTTCTTGA 336 17 TTACATAGTC 305 49 CATTGCACTG 337 18 ACAAAGGAAA 306 50 TGCGGCGATC 338 19 CTCGCTTGGG 307 51 ATATTGCGGT 339 CCTTGCGTCA 308 52 GACGTCGCTC 340 21 TAATTCCGAA 309 53 TCGCTTATCG 341 22 GTGAGCTTGA 310 54 GCGCAGACAC 342 23 ATGCCGATTC 311 55 CATGTATTGT 343 24 GCTTGGGCTT 312 56 TCTATAACCT 344 ACAAAGCGCC 313 57 GTGGAGACAA 345 26 GAAAGCTCTA 314 58 CGAAGATTAT 346 27 TACCGACCGT 315 59 TAGCAACTGC 347 28 TCGAAGAGAC 316 60 ATAATCGGTA 348 29 GTCGCTTACG 317 61 CAGGATGGGT 349 GGGCTCTCCA 318 62 GACGATTCCC 350 31 GCGCCCTTGT 319 63 CACGCCTTAC 351 32 GGCAATAGGC 320 64 AGTTGGTTCC 352 [Table 4-2] No. Primer sequence SEQ ID NO: 65 TCTTATCAGG 353 66 CGAGAAGTTC 354 67 GTGGTAGAAT 355 68 TAGGCTTGTG 356 69 ATGCGTTACG 357 70 ACTACCGAGG 358 71 CGAGTTGGTG 359 72 GGACGATCAA 360 73 AACAGTATGC 361 74 TTGGCTGATC 362 75 AGGATTGGAA 363 76 CATATGGAGA 364 77 CTGCAGGTTT 365 78 CTCTCTTTTT 366 79 AGTAGGGGTC 367 80 ACACCGCAAG 368 81 GAAGCGGGAG 369 82 GATACGGACT 370 83 TACGACGTGT 371 84 GTGCCTCCTT 372 85 GGTGACTGAT 373 86 ATATCTTACG 374 87 AATCATACGG 375 88 CTCTTGGGAC 376 89 GACGACAAAT 377 90 GTTGCGAGGT 378 91 AAACCGCACC 379 92 GCTAACACGT 380 93 ATCATGAGGG 381 94 GATTCACGTA 382 95 TCTCGAAAAG 383 96 CTCGTAACCA 384 [Table 5-1] Table 5. Random primer list (10-nucleotide E) No. Primer sequence SEQ ID NO: No. Primer sequence SEQ ID NO: 1 GTTACACACG 385 33 TTCCGGTTAT 417 2 CGTGAAGGGT 386 34 GATAAACTGT 418 3 ACGAGCATCT 387 35 TACAGTTGCC 419 4 ACGAGGGATT 388 36 CGATGGCGAA 420 GCAACGTCGG 389 37 CCGACGTCAG 421 6 CACGGCTAGG 390 38 TATGGTGCAA 422 7 CGTGACTCTC 391 39 GACGACAGTC 423 8 TCTAGACGCA 392 40 GTCACCGTCC 424 9 CTGCGCACAT 393 41 GGTTTTAACA 425 ATGCTTGACA 394 42 GAGGACAGTA 426 11 TTTGTCGACA 395 43 GTTACCTAAG 427 12 ACGTGTCAGC 396 44 ATCACGTGTT 428 13 GAAAACATTA 397 45 TAAGGCCTGG 429 14 ACATTAACGG 398 46 TGTTCGTAGC 430 GTACAGGTCC 399 47 TGAGGACGTG 431 16 CTATGTGTAC 400 48 GTGCTGTGTA 432 17 GCGTACATTA 401 49 GAGGGTACGC 433 18 GATTTGTGGC 402 50 CCGTGATTGT 434 19 TCGCGCGCTA 403 51 AAAATCGCCT 435 ACAAGGGCGA 404 52 CGATCGCAGT 436 21 AACGCGCGAT 405 53 ACGCAATAAG 437 22 CGTAAATGCG 406 54 AAGGTGCATC 438 23 TAGGCACTAC 407 55 CGCGTAGATA 439 24 GCGAGGATCG 408 56 CGAGCAGTGC 440 CACGTTTACT 409 57 ATACGTGACG 441 26 TACCACCACG 410 58 AGATTGCGCG 442 27 TTAACAGGAC 411 59 ACGTGATGCC 443 28 GCTGTATAAC 412 60 GTACGCATCG 444 29 GTTGCTGGCA 413 61 TCCCGACTTA 445 AGTGTGGCCA 414 62 GTTTTTACAC 446 31 CTGCGGTTGT 415 63 CCTGAGCGTG 447 32 TAGATCAGCG 416 64 CGGCATTGTA 448 [Table 5-2] No. Primer sequence SEQ ID NO: 65 TAGAGTGCGT 449 66 ATGGCCAGAC 450 67 CTTAGCATGC 451 68 ACAACACCTG 452 69 AGTGACTATC 453 70 CATGCTACAC 454 71 AAAGCGGGCG 455 72 AGATCGCCGT 456 73 CGTAGATATT 457 74 AATGGCAGAC 458 75 GTATAACGTG 459 76 ATGTGCGTCA 460 77 CCTGCCAACT 461 78 TTTATAACTC 462 79 ACGGTTACGC 463 80 TAGCCTCTTG 464 81 TCGCGAAGTT 465 82 GTCTACAACC 466 83 GTCTACTGCG 467 84 GTTGCGTCTC 468 85 GGGCCGCTAA 469 86 GTACGTCGGA 470 87 AGCGAGAGAC 471 88 TGGCTACGGT 472 89 AGGCATCACG 473 90 TAGCTCCTCG 474 91 GGCTAGTCAG 475 92 CTCACTTTAT 476 93 ACGGCCACGT 477 94 AGCGTATATC 478 95 GACACGTCTA 479 96 GCCAGCGTAC 480 [Table 6-1] Table 6. Random primer list (10-nucleotide F) No. Primer sequence SEQ ID NO: No. Primer sequence SEQ ID NO: 1 AACATTAGCG 481 33 CAACCGACGT 513 2 AGTGTGCTAT 482 34 TGGTAACGCG 514 3 CACGAGCGTT 483 35 GTGCAGACAT 515 4 GTAACGCCTA 484 36 GTCTAGTTGC 516 CACATAGTAC 485 37 CAATTCGACG 517 6 CGCGATATCG 486 38 CTTAGCACCT 518 7 CGTTCTGTGC 487 39 TAATGTCGCA 519 8 CTGATCGCAT 488 40 CAATCGGTAC 520 9 TGGCGTGAGA 489 41 AGCACGCATT 521 TTGCCAGGCT 490 42 AGGTCCTCGT 522 11 GTTATACACA 491 43 TTGTGCCTGC 523 12 AGTGCCAACT 492 44 ACCGCCTGTA 524 13 TCACGTAGCA 493 45 GTACGTCAGG 525 14 TAATTCAGCG 494 46 GCACACAACT 526 AAGTATCGTC 495 47 TGAGCACTTA 527 16 CACAGTTACT 496 48 GTGCCGCATA 528 17 CCTTACCGTG 497 49 ATGTTTTCGC 529 18 ACGGTGTCGT 498 50 ACACTTAGGT 530 19 CGCGTAAGAC 499 51 CGTGCCGTGA 531 TTCGCACCAG 500 52 TTACTAATCA 532 21 CACGAACAGA 501 53 GTGGCAGGTA 533 22 GTTGGACATT 502 54 GCGCGATATG 534 23 GGTGCTTAAG 503 55 GAACGACGTT 535 24 TCGGTCTCGT 504 56 ATCAGGAGTG 536 TCTAGTACGC 505 57 GCCAGTAAGT 537 26 TTAGGCCGAG 506 58 GCAAGAAGCA 538 27 CGTCAAGAGC 507 59 AACTCCGCCA 539 28 ACATGTCTAC 508 60 ACTTGAGCCT 540 29 ATCGTTACGT 509 61 CGTGATCGTG 541 ACGGATCGTT 510 62 AATTAGCGAA 542 31 AATCTTGGCG 511 63 ACTTCCTTAG 543 32 AGTATCTGGT 512 64 TGTGCTGATA 544 [Table 6-2] No. Primer sequence SEQ ID NO: 65 AGGCGGCTGA 545 66 CGTTTAGAGC 546 67 ACGCGTCTAA 547 68 GCGAATGTAC 548 69 CGTGATCCAA 549 70 CAACCAGATG 550 71 ACCATTAACC 551 72 CGATTCACGT 552 73 CTAGAACCTG 553 74 CCTAACGACA 554 75 GACGTGCATG 555 76 ATGTAACCTT 556 77 GATACAGTCG 557 78 CGTATGTCTC 558 79 AGATTATCGA 559 80 ATACTGGTAA 560 81 GTTGAGTAGC 561 82 ACCATTATCA 562 83 CACACTTCAG 563 84 GACTAGCGGT 564 85 AATTGTCGAG 565 86 CTAAGGACGT 566 87 ATTACGATGA 567 88 ATTGAAGACT 568 89 GCTTGTACGT 569 90 CCTACGTCAC 570 91 CACAACTTAG 571 92 GCGGTTCATC 572 93 GTACTCATCT 573 94 GTGCATCAGT 574 95 TCACATCCTA 575 96 CACGCGCTAT 576 [Table 7-1] Table 7. Random primer list (8-nucleotide) No. Primer sequence SEQ ID NO: No. Primer sequence SEQ ID NO: 1 CTATCTTG 577 33 CGTCAAGT 609 2 AAGTGCGT 578 34 AAGTAGAC 610 3 ACATGCGA 579 35 TCAGACAA 611 4 ACCAATGG 580 36 TCCTTGAC 612 TGCGTTGA 581 37 GTAGCTGT 613 6 GACATGTC 582 38 CGTCGTAA 614 7 TTGTGCGT 583 39 CCAATGGA 615 8 ACATCGCA 584 40 TTGAGAGA 616 9 GAAGACGA 585 41 ACAACACC 617 TCGATAGA 586 42 TCTAGTAC 618 11 TCTTGCAA 587 43 GAGGAAGT 619 12 AGCAAGTT 588 44 GCGTATTG 620 13 TTCATGGA 589 45 AAGTAGCT 621 14 TCAATTCG 590 46 TGAACCTT 622 CGGTATGT 591 47 TGTGTTAC 623 16 ACCACTAC 592 48 TAACCTGA 624 17 TCGCTTAT 593 49 GCTATTCC 625 18 TCTCGACT 594 50 GTTAGATG 626 19 GAATCGGT 595 51 CAGGATAA 627 GTTACAAG 596 52 ACCGTAGT 628 21 CTGTGTAG 597 53 CCGTGTAT 629 22 TGGTAGAA 598 54 TCCACTCT 630 23 ATACTGCG 599 55 TAGCTCAT 631 24 AACTCGTC 600 56 CGCTAATA 632 ATATGTGC 601 57 TACCTCTG 633 26 AAGTTGCG 602 58 TGCACTAC 634 27 GATCATGT 603 59 CTTGGAAG 635 28 TTGTTGCT 604 60 AATGCACG 636 29 CCTCTTAG 605 61 CACTGTTA 637 TCACAGCT 606 62 TCGACTAG 638 31 AGATTGAC 607 63 CTAGGTTA 639 32 AGCCTGAT 608 64 GCAGATGT 640 [Table 7-2] No. Primer sequence SEQ ID NO: 65 AGTTCAGA 641 66 CTCCATCA 642 67 TGGTTACG 643 68 ACGTAGCA 644 69 CTCTTCCA 645 70 CGTCAGAT 646 71 TGGATCAT 647 72 ATATCGAC 648 73 TTGTGGAG 649 74 TTAGAGCA 650 75 TAACTACC 651 76 CTATGAGG 652 77 CTTCTCAC 653 78 CGTTCTCT 654 79 GTCACTAT 655 80 TCGTTAGC 656 81 ATCGTGTA 657 82 GAGAGCAA 658 83 AGACGCAA 659 84 TCCAGTTA 660 85 AATGCCAC 661 86 ATCACGTG 662 87 ACTGTGCA 663 88 TCACTGCA 664 89 GCATCCAA 665 90 AGCACTAT 666 91 CGAAGGAT 667 92 CCTTGTGT 668 93 TGCGGATA 669 94 AGGAATGG 670 95 ATCGTAAC 671 96 GAATGTCT 672 [Table 8-1] Table 8. Random primer list (9-nucleotide) No. Primer sequence SEQ ID NO: No. Primer sequence SEQ ID NO: 1 TTGCTACAT 673 33 TGCGACTTA 705 2 TAACGTATG 674 34 TGTCCGTAA 706 3 CAGTATGTA 675 35 GTAATCGAG 707 4 TCAATAACG 676 36 GTACCTTAG 708 CACACTTAT 677 37 ATCACGTGT 709 6 GACTGTAAT 678 38 ACTTAGCGT 710 7 TATACACTG 679 39 GTAATCGTG 711 8 ACTGCATTA 680 40 ATGCCGTTA 712 9 ACATTAAGC 681 41 ATAACGTGC 713 CATATTACG 682 42 CTACGTTGT 714 11 ATATCTACG 683 43 TATGACGCA 715 12 AGTAACTGT 684 44 CCGATAACA 716 13 ATGACGTTA 685 45 ATGCGCATA 717 14 ATTATGCGA 686 46 GATAAGCGT 718 AGTATACAC 687 47 ATATCTGCG 719 16 TTAGCGTTA 688 48 ACTTAGACG 720 17 TATGACACT 689 49 ATCACCGTA 721 18 ATTAACGCT 690 50 TAAGACACG 722 19 TAGGACAAT 691 51 AATGCCGTA 723 AAGACGTTA 692 52 AATCACGTG 724 21 TATAAGCGT 693 53 TCGTTAGTC 725 22 ATACCTGGC 694 54 CATCATGTC 726 23 CTCGAGATC 695 55 TAAGACGGT 727 24 ATGGTGAGG 696 56 TGCATAGTG 728 ATGTCGACG 697 57 GAGCGTTAT 729 26 GACGTCTGA 698 58 TGCCTTACA 730 27 TACACTGCG 699 59 TTCGCGTTA 731 28 ATCGTCAGG 700 60 GTGTTAACG 732 29 TGCACGTAC 701 61 GACACTGAA 733 GTCGTGCAT 702 62 CTGTTATCG 734 31 GAGTGTTAC 703 63 GGTCGTTAT 735 32 AGACTGTAC 704 64 CGAGAGTAT 736 [Table 8-2] No. Primer sequence SEQ ID NO: 65 ATACAGTCC 737 66 AATTCACGC 738 67 TATGTGCAC 739 68 GATGACGTA 740 69 GATGCGATA 741 70 GAGCGATTA 742 71 TGTCACAGA 743 72 TACTAACCG 744 73 CATAACGAG 745 74 CGTATACCT 746 75 TATCACGTG 747 76 GAACGTTAC 748 77 GTCGTATAC 749 78 ATGTCGACA 750 79 ATACAGCAC 751 80 TACTTACGC 752 81 AACTACGGT 753 82 TAGAACGGT 754 83 GAATGTCAC 755 84 TGTACGTCT 756 85 AACATTGCG 757 86 TTGAACGCT 758 87 AATCAGGAC 759 88 ATTCGCACA 760 89 CCATGTACT 761 90 TGTCCTGTT 762 91 TAATTGCGC 763 92 GATAGTGTG 764 93 ATAGACGCA 765 94 TGTACCGTT 766 95 ATTGTCGCA 767 96 GTCACGTAA 768 [Table 9-1] Table 9. Random primer list (11-nucleotide) No. Primer sequence SEQ ID NO: No. Primer sequence SEQ ID NO: 1 TTACACTATGC 769 33 CAGTCACGACA 801 2 GCGATAGTCGT 770 34 TTACTCGACGT 802 3 CTATTCACAGT 771 35 GCAATGTTGAA 803 4 AGAGTCACTGT 772 36 GACACGAGCAA 804 AGAGTCGAAGC 773 37 CGAGATTACAA 805 6 CTGAATATGTG 774 38 TACCGACTACA 806 7 ACTCCACAGGA 775 39 ACCGTTGCCAT 807 8 ATCCTCGTAAG 776 40 ATGTAATCGCC 808 9 TACCATCGCCT 777 41 AAGCCTGATGT 809 AACGCCTATAA 778 42 AAGTAACGTGG 810 11 CTGTCGAACTT 779 43 GTAGAGGTTGG 811 12 TCAGATGTCCG 780 44 CTCTTGCCTCA 812 13 CTGCTTATCGT 781 45 ATCGTGAAGTG 813 14 ACATTCGCACA 782 46 ACCAGCACTAT 814 CCTTAATGCAT 783 47 CACCAGAATGT 815 16 GGCTAGCTACT 784 48 GAGTGAACAAC 816 17 TTCCAGTTGGC 785 49 TAACGTTACGC 817 18 GAGTCACAAGG 786 50 CTTGGATCTTG 818 19 CAGAAGGTTCA 787 51 GTTCCAACGTT 819 TCAACGTGCAG 788 52 CAAGGACCGTA 820 21 CAAGCTTACTA 789 53 GACTTCACGCA 821 22 AGAACTCGTTG 790 54 CACACTACTGG 822 23 CCGATACAGAG 791 55 TCAGATGAATC 823 24 GTACGCTGATC 792 56 TATGGATCTGG 824 TCCTCAGTGAA 793 57 TCTTAGGTGTG 825 26 GAGCCAACATT 794 58 TGTCAGCGTCA 826 27 GAGATCGATGG 795 59 GTCTAGGACAG 827 28 ATCGTCAGCTG 796 60 GCCTCTTCATA 828 29 GAAGCACACGT 797 61 AGAAGTGTTAC 829 ATCACGCAACC 798 62 CATGAGGCTTG 830 31 TCGAATAGTCG 799 63 TGGATTGCTCA 831 32 TATTACCGTCT 800 64 ATCTACCTAAG 832 [Table 9-2] No. Primer sequence SEQ ID NO: 65 ATGAGCAGTGA 833 66 CCAGGAGATAC 834 67 CCGTTATACTT 835 68 CTCAGTACAAG 836 69 GGTGATCGTAG 837 70 CGAACGAGACA 838 71 ACTACGAGCTT 839 72 TTGCCACAGCA 840 73 GTCAACTCTAC 841 74 TGGACTGTGTC 842 75 GGAATGGACTT 843 76 CGAGAACATAA 844 77 ACCTGGTCAGT 845 78 CGAACGACACA 846 79 AGTCTAGCCAT 847 80 AGGCCTAGATG 848 81 GGTGCGTTAGT 849 82 ATTGTGTCCGA 850 83 GCAGACATTAA 851 84 ATTGGCTCATG 852 85 GAGGTTACATG 853 86 CCTATAGGACC 854 87 TTAGACGGTCT 855 88 GATTGACGCAC 856 89 AAGACACCTCG 857 90 TCGAATAATCG 858 91 TCTATGTCGGA 859 92 TCGCATGAACC 860 93 TGTTATGTCTC 861 94 TGGATCCTACA 862 95 ATCGTTCAGCC 863 96 TACCGCAAGCA 864 [Table 10-1] Table 10. Random primer list (12-nucleotide) No. Primer sequence SEQ ID NO: No. Primer sequence SEQ ID NO: 1 GCTGTTGAACCG 865 33 ACTGAGGCGTTC 897 2 ATACTCCGAGAT 866 34 TAAGGCTGACAT 898 3 CTTAAGGAGCGC 867 35 AGTTCGCATACA 899 4 TATACTACAAGC 868 36 GCAGAATTGCGA 900 TAGTGGTCGTCA 869 37 GGTTATGAAGAA 901 6 GTGCTTCAGGAG 870 38 AGAAGTCGCCTC 902 7 GACGCATACCTC 871 39 TTCGCGTTATTG 903 8 CCTACCTGTGGA 872 40 TACCTGGTCGGT 904 9 GCGGTCACATAT 873 41 GGTTACCGAGGA 905 CTGCATTCACGA 874 42 ACACACTTCTAG 906 11 TGGATCCTTCAT 875 43 GGAAGTGATTAA 907 12 TTGTGCTGGACT 876 44 TCCATCAGATAA 908 13 ATTGAGAGCTAT 877 45 TGTCTGTATCAT 909 14 TCGCTAATGTAG 878 46 AATTGGCTATAG 910 CTACTGGCACAA 879 47 ACGTCGGAAGGT 911 16 AGAGCCAGTCGT 880 48 AGGCATCCGTTG 912 17 AATACTGGCTAA 881 49 ACCGTCGCTTGA 913 18 CTGCATGCATAA 882 50 TACCGTCAAGTG 914 19 TTGTCACAACTC 883 51 CTCGATATAGTT 915 TGCTAACTCTCC 884 52 CGTCAACGTGGT 916 21 TCTCTAGTTCGG 885 53 TAGTCAACGTAG 917 22 TTACGTCCGCAA 886 54 TGAGTAGGTCAG 918 23 GTGTTGCTACCA 887 55 CTTGGCATGTAC 919 24 CGCATGTATGCC 888 56 TGCCGAGACTTC 920 CCTGTTCTGATT 889 57 CTAAGACTTAAG 921 26 TAAGATGCTTGA 890 58 TTCTCGTGTGCG 922 27 ATATATCTCAGC 891 59 CACCTGCACGAT 923 28 TTCCTCGTGGTT 892 60 ATTAAGCCTAAG 924 29 ATGTCGATCTAG 893 61 GGTGGAACCATG 925 CATCCACTAATC 894 62 ACTAACGCGACT 926 31 GCCTCTGGTAAC 895 63 CAGTTGTGCTAT 927 32 AGTCAAGAGATT 896 64 ACGCTGTTAGCA 928 [Table 10-2] No. Primer sequence SEQ ID NO: 65 GTCAACGCTAAG 929 66 AGCTTAGGTATG 930 67 CGCAGGACGATT 931 68 AACCGGCTGTCT 932 69 GTTGCTCACGTG 933 70 GAATCTTCCGCG 934 71 AGAGCGTACACG 935 72 AAGGCTAATGTC 936 73 TCTATGTAGACG 937 74 AGACGGTCTAGT 938 75 TTGGTCACACGC 939 76 GTCGATATATGG 940 77 AACATGGATACG 941 78 TTCGCAGTTCCT 942 79 CGCATGTTGTGC 943 80 TGTTAAGTTGGA 944 81 CAAGTGTGATGA 945 82 CTGGTACCACGT 946 83 CGCTAGGATCAC 947 84 TGCTCATTACGG 948 85 TGCTCAGTAACA 949 86 ACGATCATAGCC 950 87 ACGATACGTGGA 951 88 GTTCGATGATGG 952 89 AAGAGCTGTGCC 953 90 GGTTGGATCAAC 954 91 GCGCGCTTATGA 955 92 CGTCGATCATCA 956 93 GAGACTGCACTC 957 94 GATAGATCGCAT 958 95 GGCCATCATCAG 959 96 GGTGTTCCACTG 960 [Table 11-1] Table 11. Random primer list (14-nucleotide) No. Primer sequence SEQ ID NO: No. Primer sequence SEQ ID NO: 1 AGCTATACAGAGGT 961 33 GGTTGGAATCTTGC 993 2 AGGCCGTTCTGTCT 962 34 CATCGGTGCACTCA 994 3 CATTGGTCTGCTAT 963 35 AATGCACTAGACGT 995 4 CTACATACGCGCCA 964 36 TACAGTCAGGCTCG 996 GCTTAACGGCGCTT 965 37 AGAGAAGCTTAGCC 997 6 TACGATACTCCACC 966 38 CCATAGGATCGTAT 998 7 ACCGGCATAAGAAG 967 39 TTGTGCTACACCTG 999 8 GGATGCTTCGATAA 968 40 CTCCAGTAATACTA 1000 9 GTGTACCTGAATGT 969 41 TGATGCCGATGTGG 1001 CGCGGATACACAGA 970 42 GTCATACCGCTTAA 1002 11 TTCCACGGCACTGT 971 43 ACGTTCTCTTGAGA 1003 12 TAGCCAGGCAACAA 972 44 CAGCCATATCGTGT 1004 13 AGCGTCAACACGTA 973 45 TTGAACGTAGCAAT 1005 14 TAACGCTACTCGCG 974 46 ACAATCGCGGTAAT 1006 TAGATAGACGATCT 975 47 GTTCCTGTAGATCC 1007 16 ACTCTTGCAATGCT 976 48 AGAGCCTTACGGCA 1008 17 ACTCGGTTAGGTCG 977 49 AATATGGCGCCACC 1009 18 CATTATCTACGCAT 978 50 ACCATATAGGTTCG 1010 19 CACACCGGCGATTA 979 51 ATGCACCACAGCTG 1011 TACGCAGTACTGTG 980 52 CTACTATTGAACAG 1012 21 CAAGCGCGTGAATG 981 53 TGCCATCACTCTAG 1013 22 GAATGGACTGACGA 982 54 GCGAACGAGAATCG 1014 23 CTAGCGCTGAAGTT 983 55 GAATCAAGGAGACC 1015 24 TGCGGCAGACCAAT 984 56 CAACATCTATGCAG 1016 AAGGCATAGAGATT 985 57 CAATCCGTCATGGA 1017 26 TTCTCCTCGCCATG 986 58 AGCTCTTAGCCATA 1018 27 TCATTGGTCGTGAA 987 59 AACAAGGCAACTGG 1019 28 ATTACGCTATACGA 988 60 GTCGTCGCTCCTAT 1020 29 ATGATCCTCCACGG 989 61 GTCATCATTAGATG 1021 CGTCGTTAGTAATC 990 62 GCACTAAGTAGCAG 1022 31 TGCACATAGTCTCA 991 63 ACCTTACCGGACCT 1023 32 GTCAAGGAGTCACG 992 64 GCTCAGGTATGTCA 1024 [Table 11-2] No. Primer sequence SEQ ID NO: 65 TGTCACGAGTTAGT 1025 66 CAGATGACTTACGT 1026 67 GAAGTAGCGATTGA 1027 68 GCAGGCAATCTGTA 1028 69 CCTTATACAACAAG 1029 70 CCTTAGATTGATTG 1030 71 AGCCACGAGTGATA 1031 72 GGATGACTCGTGAC 1032 73 CTTCGTTCGCCATT 1033 74 TCTTGCGTATTGAT 1034 75 CTTAACGTGGTGGC 1035 76 TGCTGTTACGGAAG 1036 77 CTGAATTAGTTCTC 1037 78 CCTCCAAGTACAGA 1038 79 CTGGTAATTCGCGG 1039 80 CGACTGCAATCTGG 1040 81 TGGATCGCGATTGG 1041 82 CGACTATTCCTGCG 1042 83 CAAGTAGGTCCGTC 1043 84 AGTAATCAGTGTTC 1044 85 TTATTCTCACTACG 1045 86 CATGTCTTCTTCGT 1046 87 AGGCACATACCATC 1047 88 AGGTTAGAGGATGT 1048 89 CAACTGGCAAGTGC 1049 90 CGCTCACATAGAGG 1050 91 GCAATGTCGAGATC 1051 92 GTTCTGTGGTGCTC 1052 93 AAGTGATCAGACTA 1053 94 ATTGAAGGATTCCA 1054 95 ACGCCATGCTACTA 1055 96 CTGAAGATGTCTGC 1056 [Table 12-1] Table 12. Random primer list (16-nucleotide) No. Primer sequence SEQ ID NO: No. Primer sequence SEQ ID NO: 1 GACAATCTCTGCCGAT 1057 33 AATGACGTTGAAGCCT 1089 2 GGTCCGCCTAATGTAA 1058 34 TCGATTCTATAGGAGT 1090 3 AGCCACAGGCAATTCC 1059 35 CGATAGGTTCAGCTAT 1091 4 ATCTCAAGTTCTCAAC 1060 36 CCATGTTGATAGAATA 1092 TGTAACGCATACGACG 1061 37 GAGCCACTTCTACAGG 1093 6 TATCTCGAATACCAGC 1062 38 GCGAACTCTCGGTAAT 1094 7 ACCGCAACACAGGCAA 1063 39 GACCTGAGTAGCTGGT 1095 8 GGCCAGTAACATGACT 1064 40 CGAGTCTATTAGCCTG 1096 9 GTGAACAGTTAAGGTG 1065 41 GTAGTGCCATACACCT 1097 CCAGGATCCGTATTGC 1066 42 CCAGTGGTCTATAGCA 1098 11 GACCTAGCACTAGACC 1067 43 GTCAGTGCGTTATTGC 1099 12 CGCCATCCTATTCACG 1068 44 AGTGTCGGAGTGACGA 1100 13 AAGTGCAGTAATGGAA 1069 45 AATCTCCGCTATAGTT 1101 14 TCAACGCGTTCGTCTA 1070 46 CGAGTAGGTCTGACTT 1102 AGCGGCCACTATCTAA 1071 47 CTGTCGCTCTAATAAC 1103 16 CTCGGCGCCATATAGA 1072 48 GCTGTCAATATAACTG 1104 17 CGATAACTTAGAAGAA 1073 49 AGCTCAAGTTGAATCC 1105 18 CATAGGATGTGACGCC 1074 50 AATTCATGCTCCTAAC 1106 19 GGCTTGTCGTCGTATC 1075 51 CCAAGGTCTGGTGATA 1107 CTTGTCTGAATATTAG 1076 52 CTCCACGTATCTTGAA 1108 21 ACAGTTCGAGTGTCGG 1077 53 TAGCCGAACAACACTT 1109 22 CTCTAACCTGTGACGT 1078 54 AGTACACGACATATGC 1110 23 CGCGCTAATTCAACAA 1079 55 ACGTTCTAGACTCCTG 1111 24 ACTCACGAATGCGGCA 1080 56 CGACTCAAGCACTGCT 1112 AATCTTCGGCATTCAT 1081 57 TGAAGCTCACGATTAA 1113 26 AAGTATCAGGATCGCG 1082 58 TATCTAACGTATGGTA 1114 27 AGTAACTCTGCAGACA 1083 59 TATACCATGTTCCTTG 1115 28 GGATTGAACATTGTGC 1084 60 TTCCTACGATGACTTC 1116 29 GTGATGCTCACGCATC 1085 61 CTCTCCAATATGTGCC 1117 CGTAGCGTAACGGATA 1086 62 GAGTAGAGTCTTGCCA 1118 31 TGCGATGCACCGTTAG 1087 63 GCGAGATGTGGTCCTA 1119 32 CCAGTATGCTCTCAGG 1088 64 AAGCTACACGGACCAC 1120 [Table 12-2] No. Primer sequence SEQ ID NO: 65 ATACAACTGGCAACCG 1121 66 CGGTAGATGCTATGCT 1122 67 TCTTGACCGGTCATCA 1123 68 AGATCGTGCATGCGAT 1124 69 TCCTCGAGACAGCCTT 1125 70 TAGCCGGTACCACTTA 1126 71 GTAAGGCAGCGTGCAA 1127 72 TAGTCTGCTCCTGGTC 1128 73 TGGATTATAGCAGCAG 1129 74 AAGAATGATCAGACAT 1130 75 CAGCGCTATATACCTC 1131 76 GAGTAGTACCTCCACC 1132 77 GACGTGATCCTCTAGA 1133 78 GTTCCGTTCACTACGA 1134 79 TGCAAGCACCAGGATG 1135 80 TTAGTTGGCGGCTGAG 1136 81 CAGATGCAGACATACG 1137 82 GACGCTTGATGATTAT 1138 83 TGGATCACGACTAGGA 1139 84 CTCGTCGGTATAACGC 1140 85 AAGCACGGATGCGATT 1141 86 AGATCTTCCGGTGAAC 1142 87 GGACAATAGCAACCTG 1143 88 GATAATCGGTTCCAAT 1144 89 CTCAAGCTACAGTTGT 1145 90 GTTGGCATGATGTAGA 1146 91 CAGCATGAGGTAAGTG 1147 92 GCCTCATCACACGTCA 1148 93 TCGATACTACACATCG 1149 94 TACACGAGGCTTGATC 1150 95 TTCTCGTGTCCGCATT 1151 96 GGTGAAGCAACAGCAT 1152 [Table 13-1] Table 13. Random primer list (18-nucleotide) No. Primer sequence SEQ ID NO: No. Primer sequence SEQ ID NO: 1 CGAACCGACTGTACAGTT 1153 33 ATGTTCAGTCACAAGCGA 1185 2 CCGACTGCGGATAAGTTA 1154 34 TAGGAAGTGTGTAATAGC 1186 3 CGACAGGTAGGTAAGCAG 1155 35 AATCCATGTAGCTGTACG 1187 4 TGATACGTTGGTATACAG 1156 36 CCAGATTCACTGGCATAG 1188 CTACTATAGAATACGTAG 1157 37 TTGTCTCTACGTAATATC 1189 6 AGACTGTGGCAATGGCAT 1158 38 GTGGTGCTTGTGACAATT 1190 7 GGAAGACTGATACAACGA 1159 39 CAGCCTACTTGGCTGAGA 1191 8 TATGCACATATAGCGCTT 1160 40 TACTCAATGCATCTGTGT 1192 9 CATGGTAATCGACCGAGG 1161 41 TGTAGAGAGACGAATATA 1193 GTCATTGCCGTCATTGCC 1162 42 GCCTACAACCATCCTACT 1194 11 CCTAAGAACTCCGAAGCT 1163 43 GCGTGGCATTGAGATTCA 1195 12 TCGCTCACCGTACTAGGA 1164 44 GCATGCCAGCTAACTGAG 1196 13 TATTACTGTCACAGCAGG 1165 45 GCGAGTAATCCGGTTGGA 1197 14 TGAGACAGGCTACGAGTC 1166 46 GCCTCTACCAGAACGTCA 1198 AAGCTATGCGAACACGTT 1167 47 GTCAGCAGAAGACTGACC 1199 16 AACGGAGGAGTGAGCCAA 1168 48 GATAACAGACGTAGCAGG 1200 17 CCACTATGGACATCATGG 1169 49 CAGGAGATCGCATGTCGT 1201 18 ATGGTGGTGGATAGCTCG 1170 50 CTGGAAGGAATGGAGCCA 1202 19 TCACCGGTTACACATCGC 1171 51 ATTGGTTCTCTACCACAA 1203 AAGATACTGAGATATGGA 1172 52 CTCATTGTTGACGGCTCA 1204 21 GACCTGTTCTTGAACTAG 1173 53 TTCAGGACTGTAGTTCAT 1205 22 AAGTAGAGCTCTCGGTTA 1174 54 AGACCGCACTAACTCAAG 1206 23 CTATGTTCTTACTCTCTT 1175 55 GGAATATTGTGCAGACCG 1207 24 CAAGGCTATAAGCGGTTA 1176 56 CCTATTACTAATAGCTCA 1208 GAAGCTAATTAACCGATA 1177 57 ATGGCATGAGTACTTCGG 1209 26 TTCACGTCTGCCAAGCAC 1178 58 GACACGTATGCGTCTAGC 1210 27 ATCGTATAGATCGAGACA 1179 59 GAAGGTACGGAATCTGTT 1211 28 GTCACAGATTCACATCAT 1180 60 TATAACGTCCGACACTGT 1212 29 GTGCCTGTGAACTATCAG 1181 61 GCTAATACATTACCGCCG 1213 CAGCGTACAAGATAGTCG 1182 62 GAAGCCAACACTCCTGAC 1214 31 GCATGGCATGGTAGACCT 1183 63 CGAATAACGAGCTGTGAT 1215 32 GGTATGCTACTCTTCGCA 1184 64 GCCTACCGATCGCACTTA 1216 [Table 13-2] No. Primer sequence SEQ ID NO: 65 CTGAGGAGAATAGCCTGC 1217 66 CAGCATGGACAGTACTTC 1218 67 GGTATAGAGCCTTCCTTA 1219 68 CGCTCTGCATATATAGCA 1220 69 CGGCTCTACTATGCTCGT 1221 70 CCTAATGCGAAGCTCACC 1222 71 ACAACCGGTGAGGCAGTA 1223 72 TTGGTTCGAACCAACCGC 1224 73 ATACTAGGTTGAACTAAG 1225 74 GCGTTGAGAGTAACATAT 1226 75 AGTTGTATAATAAGCGTC 1227 76 GTATGATGCCGTCCAATT 1228 77 GGACTCTCTGAAGAGTCT 1229 78 GGACTCTCTTGACTTGAA 1230 79 GATAACAGTGCTTCGTCC 1231 80 GGCCATTATAGATGAACT 1232 81 ATAGAGAGCACAGAGCAG 1233 82 GTGTGAGTGTATCATAAC 1234 83 ATAACCTTAGTGCGCGTC 1235 84 CCGACTGATATGCATGGA 1236 85 GGATATCTGATCGCATCA 1237 86 CAGCATTAACGAGGCGAA 1238 87 GCGAGGCCTACATATTCG 1239 88 CGATAAGTGGTAAGGTCT 1240 89 AGATCCTGAGTCGAGCAA 1241 90 AAGATATAACGAGACCGA 1242 91 CCGACTGATTGAGAACGT 1243 92 TCGGCTTATATGACACGT 1244 93 AATAACGTACGCCGGAGG 1245 94 AACACAGCATTGCGCACG 1246 95 GTAGTCTGACAGCAACAA 1247 96 AGAATGACTTGAGCTGCT 1248 [Table 14-1] Table 14. Random primer list (20-nucleotide) No. Primer sequence SEQ ID NO: No. Primer sequence SEQ ID NO: 1 ACTGGTAGTAACGTCCACCT 1249 33 CACTTAAGTGTGATATAGAT 1281 2 AGACTGGTTGTTATTCGCCT 1250 34 ATCGGTATGCTGACCTAGAC 1282 3 TATCATTGACAGCGAGCTCA 1251 35 TACAATCTCGAATGCAGGAT 1283 4 TGGAGTCTGAAGAAGGACTC 1252 36 CCATATGAAGCGCAGCCGTC 1284 CATCTGGACTACGGCAACGA 1253 37 CGTCTCGTGGACATTCGAGG 1285 6 AACTGTCATAAGACAGACAA 1254 38 CCGAGTACAGAAGCGTGGAA 1286 7 CCTCAACATGACATACACCG 1255 39 TTACGTGGTCGACAGGCAGT 1287 8 CAATACCGTTCGCGATTCTA 1256 40 AGCTGCAATCTGCATGATTA 1288 9 GCGTCTACGTTGATTCGGCC 1257 41 ACCTGCCGAAGCAGCCTACA 1289 TGAACAGAGGCACTTGCAGG 1258 42 AACATGATAACCACATGGTT 1290 11 CGACTAGAACCTACTACTGC 1259 43 ATCCGACTGATTGAATTACC 1291 12 GCACCGCACGTGGAGAGATA 1260 44 TCACGCTGACTCTTATCAGG 1292 13 CTGAGAGACCGACTGATGCG 1261 45 GCGCGCTCGAAGTACAACAT 1293 14 TCGTCCTTCTACTTAATGAT 1262 46 ACAGCCAGATGCGTTGTTCC 1294 CAAGCTATACCATCCGAATT 1263 47 GGAGCTCTGACCTGCAAGAA 1295 16 CAATACGTATAGTCTTAGAT 1264 48 AACATTAGCCTCAAGTAAGA 1296 17 CCATCCACAGTGACCTATGT 1265 49 TGTGATTATGCCGAATGAGG 1297 18 TATCCGTTGGAGAAGGTTCA 1266 50 GAGTAATAATCCAATCAGTA 1298 19 CGCCTAGGTACCTGAGTACG 1267 51 CTCCTTGGCGACAGCTGAAC 1299 CAGAGTGCTCGTGTTCGCGA 1268 52 TTACGCACACATACACAGAC 1300 21 CGCTTGGACATCCTTAAGAA 1269 53 ACGCCGTATGGCGACTTAGG 1301 22 GACCGCATGATTAGTCTTAC 1270 54 AGAACGACAATTACGATGGC 1302 23 CTTGGCCGTAGTCACTCAGT 1271 55 TGCTAACGTACCACTGCCAC 1303 24 GATAGCGATATTCAGTTCGC 1272 56 CATCCAGAATGTCTATCATA 1304 ATCCAACACTAAGACAACCA 1273 57 GGAGAACGCCTATAGCACTC 1305 26 CCATTCTGTTGCGTGTCCTC 1274 58 ACCTCTTGTGACGGCCAGTC 1306 27 ACATTCTGTACGCTTGCAGC 1275 59 TGCCATAACTTGGCATAAGA 1307 28 TGCTGAACGCCAATCGCTTA 1276 60 ACAATTGTCTGACCACGCTC 1308 29 TCCTCTACAAGAATATTGCG 1277 61 TCGTCACCTTCACAGAACGA 1309 CGACCAACGCAGCCTGATTC 1278 62 AGCAGCAGATGATGATCCAA 1310 31 ATTGCGAGCTTGAGTAGCGC 1279 63 TCGTGCCTTGGATTCCAGGA 1311 32 AAGGTGCGAGCATAGGAATC 1280 64 TGTTATAGCCACGATACTAT 1312 [Table 14-2] No. Primer sequence SEQ ID NO: 65 AATCTCACCTGTACCTTCCG 1313 66 GAGTAGCGGAAGCGTTAGCG 1314 67 AATACTCCGGCGAGGTATAC 1315 68 TTCGCATCCTTGCACGAACA 1316 69 AACCGGCTAATACTACTGGC 1317 70 CTAGCATCTTAGACACCAGA 1318 71 TAGTTGCGTGATACAAGATA 1319 72 TCGTCTCGACACAGTTGGTC 1320 73 TCCGTTCGCGTGCGAACTGA 1321 74 TCTGACTCTGGTGTACAGTC 1322 75 ACAGCGCAATTATATCCTGT 1323 76 AGATCCGTACGTGAGACTAG 1324 77 TACATTGAAGCATCCGAACA 1325 78 CTCCTGAGAGATCAACGCCA 1326 79 TCACCTCGAATGAGTTCGTT 1327 80 TAGCGACTTAAGGTCCAAGC 1328 81 AGTACGTATTGCCGTGCAAG 1329 82 AGCCACGAACCGACGTCATA 1330 83 TGATGTGTACGCTACTACTA 1331 84 CCACTGTGTGCAGCAGACGA 1332 85 CTATTGTACAGCGAACGCTG 1333 86 CTCCGATATCGCACGGATCG 1334 87 AACTTATCGTCGGACGCATG 1335 88 TATCCTAATTCGTGCCGGTC 1336 89 ACAGCCTTCCTGTGTGGACT 1337 90 CCTCCGTGAGGATCGTACCA 1338 91 GCTCTAAGTAACAGAACTAA 1339 92 GACTTACCGCGCGTTCTGGT 1340 93 TCTGAGGATACACATGTGGA 1341 94 TGTAATCACACTGGTGTCGG 1342 95 CACTAGGCGGCAGACATACA 1343 96 CTAGAGCACAGTACCACGTT 1344 [Table 15-1] Table 15. Random primer list (22-nucleotide) No. Primer sequence SEQ ID NO: 1 TTCAGAGGTCTACGCTTCCGGT 1345 2 AACACAGACTGCGTTATGCCAA 1346 3 TGCTGAGTTCTATACAGCAGTG 1347 4 ACCTATTATATGATAGCGTCAT 1348 ATCGTGAGCTACAGTGAATGCA 1349 6 CGTGATGTATCCGGCCTTGCAG 1350 7 TCTTCTGGTCCTAGAGTTGTGC 1351 8 TGATGTCGGCGGCGGATCAGAT 1352 9 TCGGCCTTAGCGTTCAGCATCC 1353 TTAAGTAGGTCAGCCACTGCAC 1354 11 CCAGGTGAGTTGATCTGACACC 1355 12 TATACTATTACTGTGTTCGATC 1356 13 CCGCAGTATGTCTAGTGTTGTC 1357 14 GTCTACCGCGTACGAAGCTCTC 1358 ATGCGAGTCCGTGGTCGATCCT 1359 16 TGGTAGATTGGTGTGAGAACTA 1360 17 AGGTTCGTCGATCAACTGCTAA 1361 18 ACGACAAGCATCCTGCGATATC 1362 19 TTGAATCACAGAGAGCGTGATT 1363 GTACTTAGTGCTTACGTCAGCT 1364 21 GATTATTAAGGCCAAGCTCATA 1365 22 GCATGCAGAGACGTACTCATCG 1366 23 TAGCGGATGGTGTCCTGGCACT 1367 24 TACGGCTGCCAACTTAATAACT 1368 CTCATATGACAACTTCTATAGT 1369 26 CAAGCAATAGTTGTCGGCCACC 1370 27 TTCAGCAATCCGTACTGCTAGA 1371 28 TGAGACGTTGCTGACATTCTCC 1372 29 GTTCCGATGAGTTAGATGTATA 1373 TTGACGCTTGGAGGAGTACAAG 1374 31 TTCATGTTACCTCCACATTGTG 1375 32 GAGCACGTGCCAGATTGCAACC 1376 [Table 15-2] No. Primer sequence SEQ ID NO: 33 GGTCGACAAGCACAAGCCTTCT 1377 34 TAGGCAGGTAAGATGACCGACT 1378 CGAGGCATGCCAAGTCGCCAAT 1379 36 AGTGTTGATAGGCGGATGAGAG 1380 37 TTCGGTCTAGACCTCTCACAAT 1381 38 GTGACGCTCATATCTTGCCACC 1382 39 GATGTAATTCTACGCGCGGACT 1383 40 GATGGCGATGTTGCATTACATG 1384 41 TATGCTCTGAATTAACGTAGAA 1385 42 AGGCAATATGGTGATCCGTAGC 1386 43 TGACAGCGATGCATACAGTAGT 1387 44 TTCTGCTAACGGTATCCAATAC 1388 45 GAGTCGTCCATACGATCTAGGA 1389 46 AGACGGACTCAACGCCAATTCC 1390 47 GTAGTGTTGAGCGGACCGAGCT 1391 48 AATATAACTAGATCATAGCCAG 1392 49 TCAATCGGAGAATACAGAACGT 1393 50 ATCTCCGTCGTCCGAACCAACA 1394 51 TAGGCGTTCAGCGGTATGCTTA 1395 52 TGCGTGCTATACAACCTATACG 1396 53 ATGGCCGGCATACATCTGTATG 1397 54 TGATGCTGACATAACACTGAAT 1398 55 ATCCAAGGTACCTGAACATCCT 1399 56 TAGTGACGACCAGGTGAGCCTC 1400 57 AGGAGGATCCGTCAAGTCGACC 1401 58 AGAGTATGCCAGATCGTGAGGC 1402 59 CCACTCACTAGGATGGCTGCGT 1403 60 TATCCAACCTGTTATAGCGATT 1404 61 TCTTGCAGTGAGTTGAGTCTGC 1405 62 CCACTGTTGTACATACACCTGG 1406 63 ATGCGCGTAGGCCACTAAGTCC 1407 64 ACAGCGGTCTACAACCGACTGC 1408 [Table 15-3] No. Primer sequence SEQ ID NO: 65 TCGCGCTCCAGACAATTGCAGC 1409 66 CCGGTAGACCAGGAGTGGTCAT 1410 67 ATCTCCTAACCTAGAGCCATCT 1411 68 CCACATCGAATCTAACAACTAC 1412 69 TAGTCTTATTGAATACGTCCTA 1413 70 TCCTTAAGCCTTGGAACTGGCG 1414 71 CCGTGATGGATTGACGTAGAGG 1415 72 GCCTGGATAACAGATGTCTTAG 1416 73 CTCGACCTATAATCTTCTGCCA 1417 74 AGCTACTTCTCCTTCCTAATCA 1418 75 ACACGCTATTGCCTTCCAGTTA 1419 76 AAGCCTGTGCATGCAATGAGAA 1420 77 TCGTTGGTTATAGCACAACTTC 1421 78 GCGATGCCTTCCAACATACCAA 1422 79 CCACCGTTAGCACGTGCTACGT 1423 80 GTTACCACAATGCCGCCATCAA 1424 81 GGTGCATTAAGAACGAACTACC 1425 82 TCCTTCCGGATAATGCCGATTC 1426 83 AACCGCAACTTCTAGCGGAAGA 1427 84 TCCTTAAGCAGTTGAACCTAGG 1428 85 TACTAAGTCAGATAAGATCAGA 1429 86 TTCGCCATAACTAGATGAATGC 1430 87 AAGAAGTTAGACGCGGTGGCTG 1431 88 GTATCTGATCGAAGAGCGGTGG 1432 89 TCAAGAGCTACGAAGTAAGTCC 1433 90 CGAGTACACAGCAGCATACCTA 1434 91 CTCGATAAGTTACTCTGCTAGA 1435 92 ATGGTGCTGGTTCTCCGTCTGT 1436 93 TCAAGCGGTCCAAGGCTGAGAC 1437 94 TGTCCTGCTCTGTTGCTACCGT 1438 95 AGTCATATCGCGTCACACGTTG 1439 96 GGTGAATAAGGACATGAGAAGC 1440 [Table 16-1] Table 16. Random primer list (24-nucleotide) No. Primer sequence SEQ ID NO: 1 CCTGATCTTATCTAGTAGAGACTC 1441 2 TTCTGTGTAGGTGTGCCAATCACC 1442 3 GACTTCCAGATGCTTAAGACGACA 1443 4 GTCCTTCGACGGAGAACATCCGAG 1444 CTTGGTTAGTGTACCGTCAACGTC 1445 6 AAGCGGCATGTGCCTAATCGACGT 1446 7 CGACCGTCGTTACACGGAATCCGA 1447 8 TCGCAAGTGTGCCGTTCTGTTCAT 1448 9 CGTACTGAAGTTCGGAGTCGCCGT 1449 CCACTACAGAATGGTAGCAGATCA 1450 11 AGTAGGAGAGAGGCCTACACAACA 1451 12 AGCCAAGATACTCGTTCGGTATGG 1452 13 GTTCCGAGTACATTGAATCCTGGC 1453 14 AGGCGTACGAGTTATTGCCAGAGG 1454 GTGGCATCACACATATCTCAGCAT 1455 16 GAGACCGATATGTTGATGCCAGAA 1456 17 CAACTGTAGCCAGTCGATTGCTAT 1457 18 TATCAATGCAATGAGAGGATGCAG 1458 19 GTATGCTCGGCTCCAAGTACTGTT 1459 AGAGACTCTTATAGGCTTGACGGA 1460 21 ACTTAACAGATATGGATCATCGCC 1461 22 AATCAGAGCGAGTCTCGCTTCAGG 1462 23 ACCACCGAGGAACAGGTGCGACAA 1463 24 TGGTACATGTCAACCGTAAGCCTG 1464 CGTGCCGCGGTGTTCTTGTATATG 1465 26 GACAAGCGCGCGTGAGACATATCA 1466 27 AGTGCACTCCGAACAAGAGTTAGT 1467 28 CCTCATTACCGCGTTAGGAGTCCG 1468 29 TGCTTATTGCTTAGTTGCTATCTC 1469 GCGTGATCCTGTTCTATTCGTTAG 1470 31 GGCCAGAACTATGACGAGTATAAG 1471 32 GATGGCGACTATCTAATTGCAATG 1472 [Table 16-2] No. Primer sequence SEQ ID NO: 33 TAGTAACCATAGCTCTGTACAACT 1473 34 CGTGATCGCCAATACACATGTCGC 1474 TAATAACGGATCGATATGCACGCG 1475 36 ATCATCGCGCTAATACTATCTGAA 1476 37 CACGTGCGTGCAGGTCACTAGTAT 1477 38 AGGTCCAATGCCGAGCGATCAGAA 1478 39 CAGCATAACAACGAGCCAGGTCAG 1479 40 ATGGCGTCCAATACTCCGACCTAT 1480 41 AGGAACATCGTGAATAATGAAGAC 1481 42 TCTCGACGTTCATGTAATTAAGGA 1482 43 TCGCGGTTAACCTTACTTAGACGA 1483 44 ATCATATCTACGGCTCTGGCGCCG 1484 45 GCAGATGGAGACCAGAGGTACAGG 1485 46 AGACAGAAGATTACCACGTGCTAT 1486 47 CCACGGACAACATGCCGCTTAACT 1487 48 CTTGAAGTCTCAAGCTATGAGAGA 1488 49 ACAGCAGTCGTGCTTAGGTCACTG 1489 50 AGGTGTTAATGAACGTAGGTGAGA 1490 51 AGCCACTATGTTCAAGGCTGAGCC 1491 52 GCAGGCGGTGTCGTGTGACAATGA 1492 53 AGCCATTGCTACAGAGGTTACTTA 1493 54 ACAATCGAACCTACACTGAGTCCG 1494 55 CCGATCTCAATAGGTACCACGAAC 1495 56 GATACGTGGCGCTATGCTAATTAA 1496 57 AGAGAGATGGCACACATTGACGTC 1497 58 CTCAACTCATCCTTGTAGCCGATG 1498 59 GTGGAATAACGCGATACGACTCTT 1499 60 ATCTACCATGCGAATGCTCTCTAG 1500 61 ATACGCACGCCTGACACAAGGACC 1501 62 GTCCACTCTCAGTGTGTAGAGTCC 1502 63 AATATATCCAGATTCTCTGTGCAG 1503 64 CCTTCCGCCACATGTTCGACAAGG 1504 [Table 16-3] No. Primer sequence SEQ ID NO: 65 ACTGTGCCATCATCCGAGGAGCCA 1505 66 TCTATGCCGCTATGGCGTCGTGTA 1506 67 CGTAACCTAAGGTAATATGTCTGC 1507 68 TACTGACCGTATCAAGATTACTAA 1508 69 TCATCGGAGCGCCATACGGTACGT 1509 70 GCAAGAGGAATGAACGAAGTGATT 1510 71 GGCTGATTGACATCCTGACTTAGT 1511 72 AAGGCGCTAGATTGGATTAACGTA 1512 73 GCTAGCTAGAAGAATAGGATTCGT 1513 74 CAGGTGACGGCCTCTATAACTCAT 1514 75 CAGGTTACACATACCACTATCTTC 1515 76 TTGCTACGTACCGTCTTAATCCGT 1516 77 CTCAACATGTCTTGCAAGCTTCGA 1517 78 GGTGCGGTACGTAGAACCAGATCA 1518 79 AATGCTCTCCAAGATCCTGACCTA 1519 80 GCTTCGCAGGTCTGGATGATGGAG 1520 81 ACATTGACCAGACAGCACCTTGCG 1521 82 AGGTATCAATGTGCTTAATAGGCG 1522 83 TCCGGACACACGATTAGTAACGGA 1523 84 TACGAAGTACTACAGATCGGTCAG 1524 85 AATTGTCAGACGAATACTGCTGGA 1525 86 TGAATCATGAGCCAGAGGTTATGC 1526 87 CACAAGACACGTCATTAACATCAA 1527 88 GAATGACTACATTACTCCGCCAGG 1528 89 AGCCAGAGATACTGGAACTTGACT 1529 90 TATCAGACACATCACAATGGATAC 1530 91 CTAGGACACCGCTAGTCGGTTGAA 1531 92 GTATAACTGCGTGTCCTGGTGTAT 1532 93 ATGCAATACTAAGGTGGACCTCCG 1533 94 ATGCAGACGCTTGCGATAAGTCAT 1534 95 TTGCTCGATACACGTAGACCAGTG 1535 96 TACTGGAGGACGATTGTCTATCAT 1536 [Table 17-1] Table 17. Random primer list (26-nucleotide) No. Primer sequence SEQ ID NO: 1 ACTAAGGCACGCTGATTCGAGCATTA 1537 2 CGGATTCTGGCACGTACAAGTAGCAG 1538 3 TTATGGCTCCAGATCTAGTCACCAGC 1539 4 CATACACTCCAGGCATGTATGATAGG 1540 AGTTGTAAGCCAACGAGTGTAGCGTA 1541 6 GTATCAGCTCCTTCCTCTGATTCCGG 1542 7 AACATACAGAATGTCTATGGTCAGCT 1543 8 GACTCATATTCATGTTCAGTATAGAG 1544 9 AGAGTGAACGAACGTGACCGACGCTC 1545 AATTGGCGTCCTTGCCACAACATCTT 1546 11 TCGTAGACGCCTCGTACATCCGAGAT 1547 12 CCGGCTCGTGAGGCGATAATCATATA 1548 13 AGTCCTGATCACGACCACGACTCACG 1549 14 GGCACTCAATCCTCCATGGAGAAGCT 1550 TCATCATTCCTCACGTTCACCGGTGA 1551 16 TCAACTCTGTGCTAACCGGTCGTACA 1552 17 TGTTCTTATGCATTAATGCCAGGCTT 1553 18 GATTCACGACCTCAACAGCATCACTC 1554 19 GGCGAGTTCGACCAGAATGCTGGACA 1555 TTCCGTATACAATGCGATTAAGATCT 1556 21 GAGTAATCCGTAACCGGCCAACGTTG 1557 22 CGCTTCCATCATGGTACGGTACGTAT 1558 23 CCGTCGTGGTGTGTTGACTGGTCAAC 1559 24 TATTCGCATCTCCGTATTAGTTGTAG 1560 TATTATTGTATTCTAGGCGGTGCAAC 1561 26 AGGCTGCCTACTTCCTCGTCATCTCG 1562 27 GTAACATACGGCTCATCGAATGCATC 1563 28 TTATGGCACGGATATTACCGTACGCC 1564 29 ATAGCACTTCCTCTAATGCTCTGCTG 1565 TCACAGGCAATAGCCTAATATTATAT 1566 31 GGCGGATGTTCGTTAATATTATAAGG 1567 32 TGCAATAGCCGTTGTCTCTGCCAGCG 1568 [Table 17-2] No. Primer sequence SEQ ID NO: 33 TACAGCGCGTTGGCGAGTACTGATAG 1569 34 TGCAGTTAGTACCTTCTCACGCCAAC 1570 CCATTGGCTACCTAGCAGACTCTACC 1571 36 AACAGTAGCTCGCGTCTTGCTCTCGT 1572 37 GCAGTCCATCAGCTCTCGCTTATAGA 1573 38 TATCTCTCTGTCGCCAGCTTGACCAA 1574 39 CAGACTGTTCAAGCTTGCTGTAGGAG 1575 40 TAACCGGAACTCGTTCAGCAACATTC 1576 41 TCAATTATGCATGTCGTCCGATCTCT 1577 42 TTGTCTAAGTCAACCTGTGGATAATC 1578 43 TCTAAGAGTGGTATGACCAGGAGTCC 1579 44 TCGTAGTACTACTGGAACAGGTAATC 1580 45 ATGTCAACATTCTAATCATCTCTCGG 1581 46 AGCGCGCAACTGTTACGGTGATCCGA 1582 47 GCGATAGAATAATGGTGTCACACACG 1583 48 AAGGCTGCGATGAGAGGCGTACATCG 1584 49 GGTTCATGGTCTCAGTCGTGATCGCG 1585 50 TAGTGACTCTATGTCACCTCGGAGCC 1586 51 ATGTGATAGCAATGGCACCTCTAGTC 1587 52 TCGCGAAGTGTAATGCATCATCCGCT 1588 53 ATGTGGCGACGATCCAAGTTCAACGC 1589 54 ACCTTGTATGAGTCGGAGTGTCCGGC 1590 55 ACCTCAAGAGAGTAGACAGTTGAGTT 1591 56 GGTGTAATCCTGTGTGCGAAGCTGGT 1592 57 ATAGCGGAACTGTACGACGCTCCAGT 1593 58 AAGCACGAGTCGACCATTAGCCTGGA 1594 59 ATTCCGGTAACATCAGAAGGTACAAT 1595 60 GTGCAACGGCAGTCCAGTATCCTGGT 1596 61 CCATCTTATACACGGTGACCGAAGAT 1597 62 GCACTTAATCAAGCTTGAGTGATGCT 1598 63 AGTATTACGTGAGTACGAAGATAGCA 1599 64 TTCTTAGGTTAAGTTCCTTCTGGACC 1600 [Table 17-3] No. Primer sequence SEQ ID NO: 65 GTCCTTGCTAGACACTGACCGTTGCT 1601 66 GCCGCTATGTGTGCTGCATCCTAAGC 1602 67 CCATCAATAACAGACTTATGTTGTGA 1603 68 CGCGTGTGCTTACAAGTGCTAACAAG 1604 69 CGATATGTGTTCGCAATAAGAGAGCC 1605 70 CGCGGATGTGAGCGGCTCAATTAGCA 1606 71 GCTGCATGACTATCGGATGGAGGCAT 1607 72 CTATGCCGTGTATGGTACGAGTGGCG 1608 73 CCGGCTGGAGTTCATTACGTAGGCTG 1609 74 TGTAGGCCTACTGAGCTAGTATTAGA 1610 75 CCGTCAAGTGACTATTCTTCTAATCT 1611 76 GGTCTTACGCCAGAGACTGCGCTTCT 1612 77 CGAAGTGTGATTATTAACTGTAATCT 1613 78 GCACGCGTGGCCGTAAGCATCGATTA 1614 79 ATCCTGCGTCGGAACGTACTATAGCT 1615 80 AGTATCATCATATCCATTCGCAGTAC 1616 81 AGTCCTGACGTTCATATATAGACTCC 1617 82 CTTGCAGTAATCTGAATCTGAAGGTT 1618 83 ATAACTTGGTTCCAGTAACGCATAGT 1619 84 GATAAGGATATGGCTGTAGCGAAGTG 1620 85 GTGGAGCGTTACAGACATGCTGAACA 1621 86 CGCTTCCGGCAGGCGTCATATAAGTC 1622 87 ATAACATTCTAACCTCTATAAGCCGA 1623 88 ACGATCTATGATCCATATGGACTTCC 1624 89 TGAAGCTCAGATATCATGCCTCGAGC 1625 90 AGACTTCACCGCAATAACTCGTAGAT 1626 91 AGACTAAGACATACGCCATCACCGCT 1627 92 TGTAGCGTGATGTATCGTAATTCTGT 1628 93 TGTGCTATTGGCACCTCACGCTGACC 1629 94 TGTAGATAAGTATCCAGCGACTCTCT 1630 95 AATTCGCCAATTGTGTGTAGGCGCAA 1631 96 CGATTATGAGTACTTGTAGACCAGCT 1632 [Table 18-1] Table 18. Random primer list (28-nucleotide) No. Primer sequence SEQ ID NO: 1 TTGCAAGAACAACGTATCTCATATGAAC 1633 2 CACCGTGCTGTTATTACTTGGTATTCGG 1634 3 CACGTGTATTGTTGCACCAGAACGACAA 1635 4 ATGCACGTAATTACTTCCGGAGAAGACG 1636 TATGTTGTCTGATATGGTTCATGTGGCA 1637 6 AGCGCGACTAGTTGATGCCAACATTGTA 1638 7 ATAGGCAGGTCCAGGCTCGGAACAAGTC 1639 8 GCGGTAGTCGGTCAAGAACTAGAACCGT 1640 9 ACTATACACTCTAGCTATTAGGAAGCAT 1641 GATCATCTTGCTTCTCCTGTGGAGATAA 1642 11 CTACTACGAGTCCATAACTGATAGCCTC 1643 12 GCACAGACACCTGTCCTATCTAGCAGGA 1644 13 AAGCGAGGCGCGAAGGAGATGGAAGGAT 1645 14 CTGAAGACGCCAGTCTGGATAGGTGCCT 1646 GTAAGCTCTGTCCTTCGAGATTGATAAG 1647 16 GGTTAGAGAGATTATTGTGCGCATCCAT 1648 17 CCAGGAGGACCTATGATCTTGCCGCCAT 1649 18 ACTATTCGAGCTACTGTATGTGTATCCG 1650 19 GACATCGCGATACGTAACTCCGGAGTGT 1651 CCGCAATTCGTCTATATATTCTAGCATA 1652 21 CTACACTTGAGGTTGATGCTCAAGATCA 1653 22 CGATCAGTTCTAGTTCACCGCGGACAAT 1654 23 AAGAATGATGATTGGCCGCGAACCAAGC 1655 24 CACGACCGGAACTAGACTCCTACCAATT 1656 AGTTGCCTGTGAGTGAGGCTACTATCTC 1657 26 GATTCTTCCGATGATCATGCCACTACAA 1658 27 CGCTGAAGTGAACTATGCAAGCACCGCA 1659 28 ATTATCGTGATGGTGAGACTGAGCTCGT 1660 29 CGAGGCCACTCTGAGCCAGGTAAGTATC 1661 TGCCGAGGACAGCCGATCACATCTTCGT 1662 31 GTTGACATGAAGGTTATCGTCGATATTC 1663 32 GTGGTCCAGGTCAAGCTCTGATCGAATG 1664 [Table 18-2] No. Primer sequence SEQ ID NO: 33 CCAGTCCGGTGTACTCAGACCTAATAAC 1665 34 CGAGACACTGCATGAGCGTAGTCTTATT 1666 GACGGCTTGTATACTTCTCTACGGTCTG 1667 36 TTAGCTGGATGGAAGCCATATTCCGTAG 1668 37 CAGCCTACACTTGATTACTCAACAACTC 1669 38 GTACGTAGTGTCACGCGCCTACGTTCGT 1670 39 CTACAACTTCTCAATCATGCCTCTGTTG 1671 40 CGAGGACAGAATTCGACATAAGGAGAGA 1672 41 GCCGAACGACACAGTGAGTTGATAGGTA 1673 42 GAACACTATATGCTGTCGCTGTCTGAGG 1674 43 GTTAAGTTCTTCGGCGGTCATGCTCATT 1675 44 TTGCTTACAGATCGCGTATCCATAGTAT 1676 45 GAGGACCACCTCTGCGAAGTTCACTGTG 1677 46 AATCCTAGCATATCGAGAACGACACTGA 1678 47 TGAATACTATAGCCATAGTCGACTTCCG 1679 48 GACATCCACGAAGCTGGTAATCGGAACC 1680 49 TTAGCCGTCTTAGAAGTGTCTGACCGGC 1681 50 CTATTCTGCCGTAATTGATTCCTTCGTT 1682 51 ACGCCTCTGGTCGAAGGTAGATTAGCTC 1683 52 CAGCCTATTGATCGTAAGTAGATGGTCC 1684 53 TTAAGTGAGGTGGACAACCATCAACTTC 1685 54 AAGGCCTTGCGGCTAAGTAGTATTCATC 1686 55 TTGTGATACTAATTCTTCTCAAGAGTCA 1687 56 GCATTAGGTGACGACCTTAGTCCATCAC 1688 57 GCGGATGGACGTATACAGTGAGTCGTGC 1689 58 GAACATGCCAGCCTCAACTAGGCTAAGA 1690 59 TCCGTCATTAGAGTATGAGTGACTACTA 1691 60 AACACTTAGTAACCAGTTCGGACTGGAC 1692 61 CGCTAACTATTGCGTATATTCGCGGCTT 1693 62 GCCATCTACGATCTTCGGCTTATCCTAG 1694 63 CCTGAGAATGTTGACTAAGATCTTGTGA 1695 64 TCGGTTAGTCTAATCATCACGCAACGGA 1696 [Table 18-3] No. Primer sequence SEQ ID NO: 65 ATTATCTATTGAAGCAGTGACAGCGATC 1697 66 GAGGAGAATCACGGAACACGGTCACATG 1698 67 GCTGCAAGCATTATGACCATGGCATCTG 1699 68 GAACAACCTATAACGACGTTGTGGACAA 1700 69 TTAATCATCGATAGACGACATGGAATCA 1701 70 TCGAGTGTAAGCACACTACGATCTGGAA 1702 71 GCTACGCACAGTCTCTGCACAGCTACAC 1703 72 CCTGTATGTACGTTCTGGCTAATACCTT 1704 73 TGAAGCACCGGTACATGGTGTATCCGGA 1705 74 TGCTGGAACCTAACTCGGTGATGACGAT 1706 75 CGCTATCTTACTGCCAAGTTCTCATATA 1707 76 AACGCGCGCGTATCGGCAATAATCTCAA 1708 77 CCATTAGGATGACCATCGACTATTAGAG 1709 78 TACTGCTAGACTGCGTGCATTCATGGCG 1710 79 CATTGCGCGCTCCACGAACTCTATTGTC 1711 80 GACGCGCCTAGAACTGTATAGCTCTACG 1712 81 CATTGCAACTTGTCGGTGATGGCAATCC 1713 82 TTAATGCACATGCAGTACGGCACCACAG 1714 83 AGCGGTACGTGGACGAGTGGTAATTAAT 1715 84 GACGTATTGCTATGCATTGGAAGATGCT 1716 85 AACACTTCGACCATTGCGCCTCAATGGT 1717 86 CGGTACGCTCTAGCGGTCATAAGATGCA 1718 87 CCTGAATAACAGCCGCGCCTAATTAGAT 1719 88 AAGCGTCTAATGTGCCTTAAGTCACATG 1720 89 GCTCTCCAAGAACCAGAAGTAAGCATCG 1721 90 GAGGAGAGTTGTCCGAGTGGTGTGATGT 1722 91 TAACGAGTGGTGCGTCTAAGCAATTGAG 1723 92 CCAACAGTATGCTGACATAACTATGATA 1724 93 GATCCTTGCCACGCCTATGAGATATCGC 1725 94 AACGCGCTACCGTCCTTGTGCATAGAGG 1726 95 CTACATGTGCCTTATAGTACAGAGGAAC 1727 96 CAGCCTCGTAGTTAGCGTGATTCATGCG 1728 [Table 19-1] Table 19. Random primer list (29-nucleotide) No. Primer sequence SEQ ID NO: 1 CTCCTCGCCGATTGAAGTGCGTAGAACTA 1729 2 CAGCAGGCCTCAATAGGATAAGCCAACTA 1730 3 GACCATCAATCTCGAAGACTACGCTCTGT 1731 4 GGTTGCTCCGTCTGTTCAGCACACTGTTA 1732 AATGTCGACTGGCCATTATCGCCAAGTGT 1733 6 GATAGCTTGCCATGCGAATGGATCTCCAG 1734 7 CCAGACCGGAGCCAATTGGCTGCCAATAT 1735 8 AACGTCGCTCCATACGTTACCTAATGCAG 1736 9 GAATATGACGCGAACAGTCTATTCGGATC 1737 GACGAGAATGTATTAAGGATAAGCAAGGT 1738 11 AAGTCGTATGAATCGCTATCACATGAGTC 1739 12 GTCGTGGAGACTACAATTCTCCTCACGTT 1740 13 GTTGCCACCGTTACACGACTATCGACAGT 1741 14 AGGATAGGCTACGCCTTACTCTCCTAAGC 1742 TAATCATCCTGTTCGCCTCGAGGTTGTTA 1743 16 GACAAGCAGTAATAATTACTGAGTGGACG 1744 17 TACAGCGTTACGCAGGTATATCAAGGTAG 1745 18 CTAACATCACTTACTATTAGCGGTCTCGT 1746 19 CCGCGCTTCTTGACACGTTCTCCACTAGG 1747 CAAGTAACATGAGATGCTATCGGTACATT 1748 21 CGACCACTAGGCTGTGACCACGATACGCT 1749 22 CAGGTCATGTGACGCAGTCGGCAGTCAAC 1750 23 ACTCCATCGTTAGTTCTTCCGCCGTGCTG 1751 24 CTCACCACGTATGCGTCACTCGGTTACGT 1752 TGCCTATGCTATGGACCTTGCGCGACTCT 1753 26 AATGAAGGTCAACGCTCTGTAGTTACGCG 1754 27 CACCATTGATTCATGGCTTCCATCACTGC 1755 28 GACACGCAAGGTAATTCGAGATTGCAGCA 1756 29 CACCGAGAGGAAGGTTCGATCGCTTCTCG 1757 CAGTTATCGGATTGTGATATTCACTCCTG 1758 31 ATACTGTAACGCCTCAACCTATGCTGACT 1759 32 ATCTGTCTTATTCTGGCACACTCAGACTT 1760 [Table 19-2] No. Primer sequence SEQ ID NO: 33 TCCAACCGGTGACGTGCTCTTGATCCAAC 1761 34 CACACTCAGTTCGGCTATCTCTGCGATAG 1762 AGCTGTAAGTCAGGTCTACGACTCGTACT 1763 36 GTCGGCGGCACGCACAGCTAACATTCGTA 1764 37 ATATGGTAGCCAGCCACGTATACTGAACA 1765 38 TGGACAATCCGACTCTAACACAGAGGTAG 1766 39 TCCGCCGCTGACAGTTCAATCTATCAATT 1767 40 GGTTCCTTAGAATATGCACCTATCAGCGA 1768 41 CGGCTGTACGACATGGATCATAAGAGTGT 1769 42 TGCAGATGTACGCTGTGGCCAGTGGAGAG 1770 43 CCTACTCACTTAACAATAATCGGTTCGGT 1771 44 CGCTTCCTACTGCCTGTGCCGCGACATAA 1772 45 CTAGACCGACCGGTTATGCGCTATTGTTC 1773 46 TTGTGAGCACGTCTGCGGCAAGCCTATGG 1774 47 TCATCGGCCGGCGCTGTTGTTGTTACCAT 1775 48 GCGGTTAGGTGCAGTTAGGAAGACTATCA 1776 49 TATGCGGTCGTGAGGCGTAGCATTCTAGA 1777 50 CCATCTATTCGTCGAACTCTCAGCTCGTA 1778 51 ATCAGATCTACTGATCGCGGTAGAGTATC 1779 52 TACACATAGGCGGCGCAGCCTTCTAATTA 1780 53 TTAACCGTAGTTCTTAGCTTACGCCGCTC 1781 54 ACTATAGAGGACATGGCACTCCTCTTCTA 1782 55 CAGTTCGTATTAAGATTGAATGTAGCGGT 1783 56 AGTTATCGGTATCCGCTTATCCGTACGTA 1784 57 AGCTTATTCATACACTGCACCACAGCAAG 1785 58 CCGTCGGCTAGTCTATCCTCTAATTAGAA 1786 59 GTCCGCTTCCATGCCTGCTGTACGAACAC 1787 60 TCTCTTCCTCCTTCATTGTTCGCTAGCTC 1788 61 TCTCTTGAGCGGTCCTCATACAGGTCTGC 1789 62 GACCAAGTGTAGGTGATATCACCGGTACT 1790 63 AAGATTGTGATAGGTTGGTAGTTACCACA 1791 64 TCGCCTCCGAAGAGTATAGCATCGGCAGA 1792 [Table 19-3] No. Primer sequence SEQ ID NO: 65 GAGGTAGTTATGAGCATCGAGGTCCTGTT 1793 66 GGACGCAAGATCGCAGGTACTTGTAAGCT 1794 67 ACTCGTACACGTCATCGTGCAGGTCTCAG 1795 68 TAATCCGTCAGGAGTGAGATGGCTCGACA 1796 69 AAGATGGTTCCGCGCATTGACTAGCAAGT 1797 70 TCCGCGATCTGCGGATCTTGAATGCTCAC 1798 71 TTCACGAGAGTCAACTGCTAGTATCCTAG 1799 72 TTCCAACTGGATTCTTCCAACTCCTCGAA 1800 73 CACTACTACTCAAGTTATACGGTGTTGAC 1801 74 CAACTGGATTCTCAGGATGCGTCTCTAGC 1802 75 TGGACTAGAGTGGAGCGATTACGTAATAT 1803 76 GAGGTCATTCAACTGGACTCGCCACGGAC 1804 77 CAGGTGTGTAACGCTGCAATCACATGAAT 1805 78 TATGCTGAGGTATTAGTTCTAACTATGCG 1806 79 CGTCTGAGTCGGATAAGGAAGGTTACCGC 1807 80 GTACTATCGTCGCAGGCACTATCTCTGCC 1808 81 GCTTCCTCCTTGCAACTTCATTGCTTCGA 1809 82 TGTCTACGAAGTAGAAGACACGAATAATG 1810 83 CCGTCATCTAAGGCAGAGTACATCCGCGA 1811 84 CCGGAGGCGTACTAACTGACCACAACACC 1812 85 AACTCGTCGCTGCCTGAATAGGTCAGAGT 1813 86 TTATAAGATTAATGTCGGTCAGTGTCGGA 1814 87 CGTCTCGATGGATCCACACGAACCTGTTG 1815 88 ATGCCATCATGGTCGTCCTATCTTAAGGC 1816 89 GCGCTTCAGCGATTCGTCATGCAAGGCAC 1817 90 CCAAGCGATACCGAGGTACGGTTAACGAG 1818 91 ATATGACAGACAGGTGGACCTAAGCAAGC 1819 92 CACTACATCGTCAGGCCTGGAAGCCTCAG 1820 93 GCCGTGTAGACGAGGACATTATGTCGTAT 1821 94 CAACGTATATACACACCTTGTGAAGAGAA 1822 95 TCCAACGTAATTCCGCCGTCTGTCGAGAC 1823 96 AATTCGTGCTTCGATCACCGTAGACTCAG 1824 [Table 20-1] Table 20. Random primer list (30-nucleotide) No. Primer sequence SEQ ID NO: 1 ACTATATTGTATTCACGTCCGACGACTCGC 1825 2 GACGAGCTTGTGGTACACTATACCTATGAG 1826 3 TGATTCAAGCACCAGGCATGCTTAAGCTAG 1827 4 CGGTCTCCTATAGGAAGGCTCATTCTGACG 1828 AGTCAGTGTCGAATCAATCAAGGCGTCCTT 1829 6 CGAACGTAATGGCCATCACGCGCTGGCCTA 1830 7 CGAACCTGGACCACCTGGCATTACCATTAC 1831 8 ACATTAGGTTCCTGTAATGTCTTATCAACG 1832 9 CGTCTAATGCACCGTATCGTCTTCGCGCAT 1833 TCTATGACTTACAACGGAATCTTACTTCGT 1834 11 GTAACCGATCGGTACCGTCTGCTATTGTTC 1835 12 GGTGATTGATAAGCAACACATATTAGGAGG 1836 13 AATTATCGACGCTAATAGGCGAGCTGTTCA 1837 14 GGAGGTACATGACGAGTGGACAGACAGACC 1838 CTCTAATCCGTTATGCGGTGATGTAATCCG 1839 16 GCAAGCACGCGGCTTGGCGAACTTCTATGC 1840 17 TAGATGTAGGCCTGGTAGGCAGAGGAGTAA 1841 18 CCGAGTGGCGACCACACAGGTACGCATTAA 1842 19 GTCCTGGCTCAGATTAGTGCACTTAGTTAT 1843 GCGGTACCTACATGTTATGACTCAGACGAC 1844 21 TCTCTGCCAATGCTGGTCTCATCGAATCCA 1845 22 TCTCTACACAGCTACATACTATACTGTAAC 1846 23 TACGACGGACGCTGGTGGTGTAAGAGAAGG 1847 24 GCCTCGATATATCTACGTATAGTTCAAGTT 1848 GGCTCCTGCATTCATTGAAGGTCGGCCTTG 1849 26 CAGTTCGGTGATTCAAGAGAACAATGGTGG 1850 27 TATAACGAAGCCGGCTGGAACGGTAACTCA 1851 28 CTGTATCAATTCAAGTGACAGTGGCACGTC 1852 29 AGCAATTGCGGTTCATAGGCGTAATTATAT 1853 CATATGGACCTGGAGATCACCGTTCAGTCC 1854 31 GAAGGCCGTTGGTCTATCTCTTACTGGAGC 1855 32 GTGCGTTCATCTAGCCTAAGACGCTGACCT 1856 [Table 20-2] No. Primer sequence SEQ ID NO: 33 GAGTAACTTATATCCTCTCTACGACATCGA 1857 34 ATTCTACGCTGATGTCTCCGCTGAACAGGA 1858 TCATCAACGTTACTCACTAGTACCACGGCT 1859 36 AACCATTCTTGAACGTTGAGAACCTGGTGG 1860 37 ACGACACCTCCGCGGAACATACCTGATTAG 1861 38 GCGCACTTATTGAAGTAATCTCATGGCCAA 1862 39 GCGCCAATTCAGCCAGTTAGCGTCTCCGTG 1863 40 AGCAACAAGTCGCTGTATATCGACTGGCCG 1864 41 CCTTACAATAGACCTCGCGGCGTTCATGCC 1865 42 GGATCCAACTTCAGCGAAGCACCAACGTCG 1866 43 GCGCCAGTTCTCGTACTCTCGAGAAGCGAC 1867 44 GAGTGCGGCCAATCTGGAACTCATGACGTT 1868 45 CCTGAGAGTGATTCGTGTCTGCGAAGATGC 1869 46 GTGACTGGTTAAGGCAATATTGGTCGACCG 1870 47 CTATCAAGCCTTACAAGGTCACGTCCACTA 1871 48 ACTGCGTCCTTGCGTCGGAACTCCTTGTGT 1872 49 TGCAACTCAGTGGCGGCGACACCAAGAGCT 1873 50 TTCGGTTCTACTAGGATCTCTATCTGAGCT 1874 51 AGCTAATCTATTAAGACAGATTAGACAGGA 1875 52 GGACCGCTCTTAGGTTATGCACCTGCGTAT 1876 53 CTCTAATACTAGTCCACAGGTTAGTACGAA 1877 54 ATCCATATATGCTCGTCGTCAGCCAGTGTT 1878 55 GCTATTACTGTGTTGATGTCCACAGGAGAA 1879 56 GCTACGGCGCAGATCTAGACAACTGGAAGT 1880 57 GCCTCTTGTGTTAGCCGAATACCAATGACC 1881 58 TGAGGACGATAACATTACCTCTCGAGTCGC 1882 59 CGATTACCAATCCGACGACTTCGCAGCAGC 1883 60 ATGACACGAGTCCAGTACATATGCGAAGAC 1884 61 GCGCTCGCATGCACTAGTGTAGACTGACGA 1885 62 GCACATCTCAGAATTGATGGTCTATGTCGC 1886 63 TTCTTCGACGCCGCGTACTAATAGGTCAAT 1887 64 GGAAGCGCCTCTAACAACCGATGCTTGTGG 1888 [Table 20-3] No. Primer sequence SEQ ID NO: 65 CTCTAGACGCGTCGTGACTCCAATCTGTTG 1889 66 GTAGTTCGTCGGAGTGACCTCGTACTCACT 1890 67 ATGCTGTCGAGTGTCCGGCATAGAGCACAC 1891 68 GCGCATCTTGCAGCGTCCTGTAGTTCTGAA 1892 69 GCGATTGTTGAGGAACCACAGCGGCACCTA 1893 70 CACGCGTACTCTGCTTGCTGTGTGGTCGGT 1894 71 CATCCAACGCAGGACCTAGTAGTCATGCTT 1895 72 TTCTAGTTGTGATGAGAATCGCTAGCGTGC 1896 73 CATTCTGAATCTGGTCTCTCTCGATCATCC 1897 74 ATTAATGTAGAGGATAGTTCCGTTCTCTCC 1898 75 GTATCGCGCTTACGAATGAGGTGTGGCTTC 1899 76 GCTGGTGAGAGAGCCAGATTATCGGTGGAG 1900 77 GGCACGAGCAGGTAGAACTAGAACCTAGAT 1901 78 TGTATTATCTCGAAGCGGTGCGTTAGAGTC 1902 79 CACGTGTTCTAGCTACTAATGGCGTCAATT 1903 80 CGCGCTACATTACTTCCTACACCATGCGTA 1904 81 TGAGGCAACTAGTGTTCGCAAGATGACGGA 1905 82 TTATTATTGTCTGTGGAACGCACGCCAGTC 1906 83 GCTATAGTATTATCCATGAATTCCGTCGGC 1907 84 GTATCAATAGCTCAATTCGTCAGAGTTGTG 1908 85 TAGTCCATGCGTGGATATATTGAGAGCTGA 1909 86 GCACAGTACGACTTATAACAGGTCTAGATC 1910 87 ACTCAATGGTGGCACGCTCGGCGCAGCATA 1911 88 GTAGTACCACTCCGCCTTAGGCAGCTTAAG 1912 89 CGCTCAACTGATGCGTGCAACCAATGTTAT 1913 90 GCAGCTTGACTGCCTAGACAGCAGTTACAG 1914 91 GCAACTTCTTAGTACGAATTCATCGTCCAA 1915 92 ATCCGTATGCTGCGGCAGTGGAGGTGGCTT 1916 93 TGCGGATCAATCCAGTTCTGTGTACTGTGA 1917 94 TTATGATTATCACCGGCGTAACATTCCGAA 1918 95 GCTACCTAGATTCTTCAACTCATCGCTACC 1919 96 CAGTGTTAGAATGGCGGTGTGTAGCCGCTA 1920 [Table 21-1] Table 21. Random primer list (35-nucleotide) No. Primer sequence SEQ ID NO: 1 GCTTATAGACTACAGCTGCGAGGTATAAGGTCACT 1921 2 CGCTCAGCAGGATGCTATCCTAAGTTAATGTGGTG 1922 3 GAACTGAGCGGACATCAGCTAGGCCTACAATACAT 1923 4 TCGTGAACTTCTGCGTTGGTCTCTACCAAGGCGGT 1924 TAAGTCAGGTATCTTATCAGTGGTACACGGTACGA 1925 6 TAATAATGTTGCGCGTGACCGAGGAGGAATCCACT 1926 7 CTAGGAGTTCTCGTAAGCTGGAGTACCGTAACGTG 1927 8 GGACTCTCCTCAGAGGATCCTTCTTGCGCAGGCAT 1928 9 GCTAGAGGCCTGAGTACACCTTCTCGCATCAGGAT 1929 ATATCGCGAGCACTAACGTCGTTGTCGTTCTAGGA 1930 11 AGCGGTTACTATACCTGGCGGCTGACGTTGTTAGT 1931 12 GAGCTAGGTAGATCTCCAAGTGTAGCTAAGAAGAG 1932 13 GGAGTCGCTGGTGACGTATGCCGAGGATGAGCTTC 1933 14 CGCCGACCTCCTGTTCACGAAGCCGCCTGATGTAA 1934 AGTAGGCACTTAGTTATCGATTACGTTAGTTAGTC 1935 16 GGATGACGTCTCAGTCTACCTCGCAGTGTCGTCTA 1936 17 CTGGTTCGCGTTAGCAATACTAAGGCAGTCAGGAG 1937 18 ATATGGTCATATTGGCCTCTTCGAACACAGACTGT 1938 19 TATCAGAGGATAGCAGGTCTGAGTTGCAAGGCTAA 1939 GGTGGTCTGACCATAGCTGTTCTTCTCACAGAGAC 1940 21 GCAATACCAACGAGATGAGTATTCGTTGAAGCTCT 1941 22 CCAAGTCGACGCTGCATGAATGAGCGCTATTCACT 1942 23 CCATTAGATCGCTTCGAGACAATTAGGAGACATGA 1943 24 GATGACTGTACCTCCTATCATTGAGTGTGGACCAA 1944 ATATCTGGATGAATAGTGGTTAGGTAAGCAAGTAA 1945 26 ACCGACTATGTTAATTCGTGTCTGGATGGCAGAAT 1946 27 GTGGCAGTCTTGCTAGTATCTTAGACCATCACCAA 1947 28 CGCTATCTTAGTCGAGCACAATGTCTTCGTATAGG 1948 29 ATTAGTACGGCACGAACCGGCCATTCATGGCAGCT 1949 AGTACGACTATCAAGACTCCAGCGCTCTCCTTGGA 1950 31 ATGAGCCTCGGAGCGAACGTTATCGATCAGGCTGT 1951 32 TTGCGTGCAGTAGCACCGATACACAGCGCTTGTAT 1952 [Table 21-2] No. Primer sequence SEQ ID NO: 33 AACGGCTGCATCACCTACACTATACTCAACATCTA 1953 34 GTCGCTATGCGAGAAGTGGCGTGGAATGCTATGGT 1954 CATGGATACCTACTGACTTGACTTCTAGAGGACCG 1955 36 GAGTGACGCAGACACCGTAACGTCGAATCTTCTAG 1956 37 AGTACCGTCTGTGTGAATATTGTTCCTACGTTACA 1957 38 GGCTAATCGATAGTGACGAGTTCTGCACGCCTGAA 1958 39 GGCGAGCGCTCGTGGTTCTGAGTCGCTGTTAGATG 1959 40 TATCTCCAGCGTTATAAGCTACTGGAGCCGCTCGG 1960 41 CCTTCTGCGCAAGTCAAGGATTCGCTTAGATGGAC 1961 42 GTTGCTGACAGCCGTTGCGTACTTGCCTTAAGAAC 1962 43 GTGGCCTAATCACTCGCGCTTCATAGGCCGATAGG 1963 44 TGCATCTAGCCTACATCGGACCTTGTTATGGTAAT 1964 45 GGACAGCTACTGGACACCACCGAACTGGTAGTGTC 1965 46 AACTGGCGATGGACGGCCGCTCTTCCGCTACATAG 1966 47 GGAGCAGTTAGCTATGGAGCAGGCCGATAACCTGA 1967 48 ACTCTACGGTGCACCTCAGCCTTCATGCAATAGGC 1968 49 CTTGTAGCACAATACATTACTCTCCACGTGATAGC 1969 50 GGACGCTATCGATACCGTTATTCCTACTCTGTCGG 1970 51 GGATGATCGTCAACGATCAACTGACAGTTAGTCGA 1971 52 TGACAGTAGCAATGTCTCACGTCTGCACAACGGAA 1972 53 GTCGCAGGACCTCACGGATAGTAGTGCGAGGTCTA 1973 54 ATATCGGCGGACGCAATGACAGTTGTTGGCTGATG 1974 55 AAGCACCAAGGAGGTATGTTCCATCGAGGCGCTCG 1975 56 GACCGCACCTTATAGCTATATCCTGGTCTAGTACT 1976 57 TCTCAGAGGAAGGTTGAGCGTCTGACCAGGTTGGC 1977 58 TGGACCTAGAGACCTAGCTCGTCTCTTCGCGATCG 1978 59 CGGAGTGGTTCCACGCGACCTCGCAACTAATCCTT 1979 60 GGAGCCGCGCGCAGACTGACCTTGCTTGATCTACT 1980 61 ACTCTAAGTATATGCGCAGTTAGTATACTGAACCA 1981 62 GAGCATTGCTTCGCTTCGATGTCTATTCTGATCAG 1982 63 GCTTGTATTGCCACTCGAGTAGGTCGTGGCAGTAG 1983 64 ATCTGGACATTGCATTCGGTGTGTATACAGAAGGC 1984 [Table 21-3] No. Primer sequence SEQ ID NO: 65 GGTTGCGATCAGCTTGATAGCAGGTCATATCCTCA 1985 66 GCAGGTACTAACCTGAGATGCGTAGCTAACACAGG 1986 67 ATCTGCAAGGACGTAACGTCCTCGGAAGGTGAGGT 1987 68 ATAATCTTACGAGCCTCCAGTGAATAATGCAAGCA 1988 69 CAATCTCCGCACAGTCTTGTTCAGGTACAGACTTA 1989 70 ATGTGCGCAATTCAGCGTAAGTGCCTATTCATAAT 1990 71 TCGGACGCACACATCCTGTTGTCGAGAAGAGGAAG 1991 72 TCGGAAGCATCACATGAGCATCAGGAGTTCATTGC 1992 73 ATCTGGTTGTGGACTTCTATACAGTACCAGAGTGG 1993 74 CGTCTGAATATAGTTAGCTAGTAGTGTAATCCAGG 1994 75 TAATATCTGATCCGACCTATTATCTAGGACTACTC 1995 76 TATGCGGCCGTCCGTACCTCGTCTGCTTCAGTTGG 1996 77 TGGCTCAAGTTCCATATTGCCAAGACGACCTGGAG 1997 78 GCAGTTCTGCTAGGCGGTCCGAGGCAATTGAAGAG 1998 79 CATGGCACAGACGAAGTATGCACCACGCTCATTAA 1999 80 GGAGCGTACTACGACCATTCAACCGAATATGTTAC 2000 81 GCGTAGATCTCGCGACAGAGACAAGGTGCGAATGG 2001 82 TGGACTGAGGTTCTCCGGTCTATACTCCTGTAGGA 2002 83 TGGCTATAGCAACGGCTTCTTGTGATCGCATTGCA 2003 84 GGCGAAGAATCATGCGAGACGGAGTAGACGGACGT 2004 85 GAGCATTGCGAGTTGCACACGTGATATCAGACTGT 2005 86 CTGTTGACCTATGCCAGAATCAATACCTCAGATTA 2006 87 GTTAACAAGTAGATGCCAAGATACAACGAGAGACC 2007 88 GAGCAAGATTATAGTTAGGAAGATAGTTAACTCGC 2008 89 TCCGGAGTCGAGCATATGTGACCAACTCTCAACGC 2009 90 GGAGCTGCGATGCCGTTACCGACGTCATCTTCAAG 2010 91 GCTCTATCTTACACATTGGCGTACTGGACTCGCGA 2011 92 TTCTACATATTCATCGCCTACCGAGTTGCGCGAAG 2012 93 TGGACGTCTGACCTGTGTCTACATCGGTGGTGCTA 2013 94 GGCAGGACAGCTCCGTGTTCTACTCGAACCGCACT 2014 95 TGACAACCTCATGTCTCCGACCGCAGGCATACAAT 2015 96 GCAGGCCTAACAAGTGGTCACGAGGAGTCCTTATT 2016 3.1.2 Standard PCR To the genomic DNA described in 2. above (30 ng, NiF8-derived genomic DNA), random primers (final concentration: 0.6 µM; 10-nucleotide primer A), a 0.2mM dNTP mixture, 1.0 mM MgCl , and 1.25 units of DNA polymerase (PrimeSTAR, TAKARA) were added, and a reaction solution was prepared while adjusting the final reaction level to 50 µl.

PCR was carried out under thermal cycle conditions comprising 98°C for 2 minutes and 30 cycles of 98°C for 10 seconds, 50°C for 15 seconds, and 72°C for 20 seconds, followed by storage at 4°C. In this example, numerous nucleic acid fragments obtained via PCR using random primers, including the standard PCR described above, are referred to as a DNA library. 3.1.3 Purification of DNA library and electrophoresis The DNA library obtained in 3.1.2 above was purified with the use of the MinElute PCR Purification Kit (QIAGEN) and subjected to electrophoresis with the use of the Agilent 2100 bioanalyzer (Agilent Technologies) to obtain a fluorescence unit (FU). 3.1.4 Examination of annealing temperature To the genomic DNA described in 2. above (30 ng, NiF8-derived genomic DNA), random primers (final concentration: 0.6 µM, 10-nucleotide primer A), a 0.2 mM dNTP mixture, 1.0 mM MgCl , and 1.25 units of DNA polymerase (PrimeSTAR, TAKARA) were added, and a reaction solution was prepared while adjusting the final reaction level to 50 µl.

PCR was carried out under thermal cycle conditions comprising 98°C for 2 minutes and 30 cycles of 98°C for 10 seconds, different annealing temperatures for 15 seconds, and 72°C for 20 seconds, followed by storage at 4°C. In this Example, 37°C, 40°C, and 45°C were examined as annealing temperatures. The DNA library obtained in this experiment was subjected to purification and electrophoresis in the same manner as in 3.1.3. 3.1.5 Examination of enzyme amount To the genomic DNA described in 2. above (30 ng, NiF8-derived genomic DNA), random primers (final concentration: 0.6 µM, 10-nucleotide primer A), a 0.2 mM dNTP mixture, 1.0 mM MgCl , and 2.5 units or 12.5 units of DNA polymerase (PrimeSTAR, TAKARA) were added, and a reaction solution was prepared while adjusting the final reaction level to 50 µl. PCR was carried out under thermal cycle conditions comprising 98°C for 2 minutes and 30 cycles of 98°C for 10 seconds, 50°C for 15 seconds, and 72°C for 20 seconds, followed by storage at 4°C. The DNA library obtained in this experiment was subjected to purification and electrophoresis in the same manner as in 3.1.3. 3.1.6 Examination of MgCl concentration To the genomic DNA described in 2. above (30 ng, NiF8-derived genomic DNA), random primers (final concentration: 0.6 µM, 10-nucleotide primer A), a 0.2 mM dNTP mixture, MgCl at a given concentration, and 1.25 units of DNA polymerase (PrimeSTAR, TAKARA) were added, and a reaction solution was prepared while adjusting the final reaction level to 50 µl. PCR was carried out under thermal cycle conditions comprising 98°C for 2 minutes and 30 cycles of 98°C for 10 seconds, 50°C for 15 seconds, and 72°C for 20 seconds, followed by storage at 4°C. In this Example, two-, three- and four-fold concentrations of a usual concentration were examined as MgCl concentrations. The DNA library obtained in this experiment was subjected to purification and electrophoresis in the same manner as in 3.1.3. 3.1.7 Examination of nucleotide length of random primer To the genomic DNA described in 2. above (30 ng, NiF8-derived genomic DNA), random primers (final concentration: 0.6 µM), a 0.2 mM dNTP mixture, 1.0 mM MgCl , and 1.25 units of DNA polymerase (PrimeSTAR, TAKARA) were added, and a reaction solution was prepared while adjusting the final reaction level to 50 µl. PCR was carried out under thermal cycle conditions comprising 98°C for 2 minutes and 30 cycles of 98°C for 10 seconds, 50°C for 15 seconds, and 72°C for 20 seconds, followed by storage at 4°C. In this Example, primers having 8 nucleotides (Table 7), 9 nucleotides (Table 8), 11 nucleotides (Table 9), 12 nucleotides (Table 10), 14 nucleotides (Table 11), 16 nucleotides (Table 12), 18 nucleotides (Table 13), and 20 nucleotides (Table 14) were examined as random primers.

The DNA library obtained in this experiment was subjected to purification and electrophoresis in the same manner as in 3.1.3. 3.1.8 Examination of random primer concentration To the genomic DNA described in 2. above (30 ng, NiF8-derived genomic DNA), random primers at a given concentration (10-nucleotide primer A), a 0.2 mM dNTP mixture, 1.0 mM MgCl , and 1.25 units of DNA polymerase (PrimeSTAR, TAKARA) were added, and a reaction solution was prepared while adjusting the final reaction level to 50 µl. PCR was carried out under thermal cycle conditions comprising 98°C for 2 minutes and 30 cycles of 98°C for 10 seconds, 50°C for 15 seconds, and 72°C for 20 seconds, followed by storage at 4°C. In this Example, 2, 4, 6, 8, 10, 20, 40, 60, 100, 200, 300, 400, 500, 600. 700, 800, 900, and 1000 µM were examined as random concentrations. The DNA library obtained in this experiment was subjected to purification and electrophoresis in the same manner as in 3.1.3. Also, in this experiment, the reproducibility of the repeated data was evaluated on the basis of the Spearman’s rank correlation (ρ > 0.9). 3.2 Verification of reproducibility via MiSeq 3.2.1 Preparation of DNA library To the genomic DNA described in 2. above (30 ng, NiF8-derived genomic DNA), random primers (final concentration: 60 µM, 10-nucleotide primer A), a 0.2 mM dNTP mixture, 1.0 mM MgCl , and 1.25 units of DNA polymerase (PrimeSTAR, TAKARA) were added, and a reaction solution was prepared while adjusting the final reaction level to 50 µl.

PCR was carried out under thermal cycle conditions comprising 98°C for 2 minutes and 30 cycles of 98°C for 10 seconds, 50°C for 15 seconds, and 72°C for 20 seconds, followed by storage at 4°C. The DNA library obtained in this experiment was subjected to purification and electrophoresis in the same manner as in 3.1.3. 3.2.2 Preparation of sequence library From the DNA library obtained in 3.2.1, a sequence library for MiSeq analysis was prepared using the KAPA Library Preparation Kit (Roche). 3.2.3 MiSeq analysis With the use of the MiSeq Reagent Kit V2 500 Cycle (Illumina), the sequence library for MiSeq analysis obtained in 3.2.2 was analyzed via 100 base paired-end sequencing. 3.2.4 Read data analysis Random primer sequence information was deleted from the read data obtained in 3.2.3, and the read patterns were identified. The number of reads was counted for each read pattern, the number of reads of the repeated analyses, and the reproducibility was evaluated using the correlational coefficient. 3.3 Analysis of rice variety Nipponbare 3.3.1 Preparation of DNA library To the genomic DNA described in 2. above (30 ng, Nipponbare-derived genomic DNA), random primers (final concentration: 60 µM, 10-nucleotide primer A), a 0.2 mM dNTP mixture, 1.0 mM MgCl , and 1.25 units of DNA polymerase (PrimeSTAR, TAKARA) were added, and a reaction solution was prepared while adjusting the final reaction level to 50 µl. PCR was carried out under thermal cycle conditions comprising 98°C for 2 minutes and 30 cycles of 98°C for 10 seconds, 50°C for 15 seconds, and 72°C for 20 seconds, followed by storage at 4°C. The DNA library obtained in this experiment was subjected to purification and electrophoresis in the same manner as in 3.1.3. 3.3.2 Preparation of sequence library, MiSeq analysis, and read data analysis Preparation of a sequence library using the DNA library prepared from Nipponbare-derived genomic DNA, MiSeq analysis, and analysis of the read data were performed in accordance with the methods described in 3.2.2, 3.2.3, and 3.2.4, respectively. 3.3.3 Evaluation of genomic homogeneity The read patterns obtained in 3.3.2 were mapped to the genomic information of Nipponbare (NC_008394 to NC_008405) using bowtie2, and the genomic positions of the read patterns were identified. 3.3.4 Non-specific amplification On the basis of the positional information of the read patterns identified in 3.3.3, the sequences of random primers were compared with the genome sequences to which such random primers would anneal, and the number of mismatches was determined. 3.4 Detection of polymorphism and identification of genotype 3.4.1 Preparation of DNA library To the genomic DNA described in 2. above (30 ng, NiF8-derived genomic DNA, Ni9-derived genomic DNA, hybrid progeny-derived genomic DNA, or Nipponbare-derived genomic DNA), random primers (final concentration: 60 µM, 10-nucleotide primer A), a 0.2 mM dNTP mixture, 1.0 mM MgCl , and 1.25 units of DNA polymerase (PrimeSTAR, TAKARA) were added, and a reaction solution was prepared while adjusting the final reaction level to 50 µl. PCR was carried out under thermal cycle conditions comprising 98°C for 2 minutes and 30 cycles of 98°C for 10 seconds, 50°C for 15 seconds, and 72°C for 20 seconds, followed by storage at 4°C. The DNA library obtained in this experiment was subjected to purification and electrophoresis in the same manner as in 3.1.3. 3.4.2 HiSeq analysis Analysis of the DNA libraries prepared in 3.4.1 was consigned to TakaraBio under conditions in which the number of samples was 16 per lane via 100 base paired-end sequencing, and the read data were obtained. 3.4.3 Read data analysis Random primer sequence information was deleted from the read data obtained in 3.4.2, and the read patterns were identified. The number of reads was counted for each read pattern. 3.4.4 Detection of polymorphism and identification of genotype On the basis of the read patterns and the number of reads obtained as a results of analysis conducted in 3.4.3, polymorphisms peculiar to NiF8 and Ni9 were detected, and the read patterns thereof were designated as markers. On the basis of the number of reads, the genotypes of the 22 hybrid progeny lines were identified. The accuracy for genotype identification was evaluated on the basis of the reproducibility attained by the repeated data concerning the 22 hybrid progeny lines. 3.5 Experiment for confirmation with PCR marker 3.5.1 Primer designing Primers were designed for a total of 6 markers (i.e., 3 NiF8 markers and 3 Ni9 markers) among the markers identified in 3.4.4 based on the marker sequence information obtained via paired-end sequencing (Table 22).

[Table 22] 3.5.2 PCR and electrophoresis With the use of the TaKaRa Multiplex PCR Assay Kit Ver.2 (TAKARA) and the genomic DNA described in 2. above (15 ng, NiF8-derived genomic DNA, Ni9-derived genomic DNA, or hybrid progeny-derived genomic DNA) as a template, 1.25 µl of Multiplex PCR enzyme mix, 12.5 µl of 2x Multiplex PCR buffer, and the 0.4 µM primer designed in 3.5.1 were added, and a reaction solution was prepared while adjusting the final reaction level to 25 µl. PCR was carried out under thermal cycle conditions comprising 94°C for 1 minute, 30 cycles of 94°C for 30 seconds, 60°C for 30 seconds, and 72°C for 30 seconds, and retention at 72°C for 10 minutes, followed by storage at 4°C. The amplified DNA fragment was subjected to electrophoresis with the use of TapeStation (Agilent Technologies). 3.5.3 Comparison of genotype data On the basis of the results of electrophoresis obtained in 3.5.2, the genotype of the marker was identified on the basis of the presence or absence of a band, and the results were compared with the number of reads of the marker. 3.6 Correlation between random primer density and length 3.6.1 Influence of random primer length at high concentration To the genomic DNA described in 2. above (30 ng, NiF8-derived genomic DNA), random primers having given lengths (final concentration: 10 µM), a 0.2 mM dNTP mixture, 1.0 mM MgCl , and 1.25 units of DNA polymerase (PrimeSTAR, TAKARA) were added, and a reaction solution was prepared while adjusting the final reaction level to 50 µl. In this experiment, 9 nucleotides (Table 8), 10 nucleotides (Table 1, 10-nucleotide primer A), 11 nucleotides (Table 9), 12 nucleotides (Table 10), 14 nucleotides (Table 11), 16 nucleotides (Table 12), 18 nucleotides (Table 13), and 20 nucleotides (Table 14) were examined as random primer lengths. PCR was carried out under thermal cycling conditions comprising 98°C for 2 minutes and 30 cycles of 98°C for 10 seconds, 50°C for 15 seconds, and 72°C for 20 seconds, followed by storage at 4°C. In the reaction system using random primers each comprising 10 or more nucleotides, PCR was carried out under thermal cycle conditions comprising 98°C for 2 minutes and 30 cycles of 98°C for 10 seconds, 50°C for seconds, and 72°C for 20 seconds, followed by storage at 4°C. The DNA library obtained in this experiment was subjected to purification and electrophoresis in the same manner as in 3.1.3. 3.6.2 Correlation between random primer density and length To the genomic DNA described in 2. above (30 ng, NiF8-derived genomic DNA), random primers of a given length were added to a given concentration therein, a 0.2 mM dNTP mixture, 1.0 mM MgCl , and 1.25 units of DNA polymerase (PrimeSTAR, TAKARA) were added thereto, and a reaction solution was prepared while adjusting the final reaction level to 50 µl. In this experiment, random primers comprising 8 to 35 nucleotides shown in Tables 1 to 21 were examined, and the random primer concentration from 0.6 to 300 µM was examined.

In the reaction system using random primers comprising 8 nucleotides and 9 nucleotides, PCR was carried out under thermal cycle conditions comprising 98°C for 2 minutes and 30 cycles of 98°C for 10 seconds, 37°C for 15 seconds, and 72°C for 20 seconds, followed by storage at 4°C. In the reaction system using a random primer of 10 or more nucleotides, PCR was carried out under thermal cycle conditions comprising 98°C for 2 minutes and 30 cycles of 98°C for 10 seconds, 50°C for 15 seconds, and 72°C for 20 seconds, followed by storage at 4°C. The DNA library obtained in this experiment was subjected to purification and electrophoresis in the same manner as in 3.1.3. Also, the reproducibility of the repeated data was evaluated on the basis of the Spearman's rank correlation (ρ > 0.9). 3.7 Number of random primers To the genomic DNA described in 2. above (30 ng, NiF8-derived genomic DNA), 1, 2, 3, 12, 24,or 48 types of random primers selected from the 96 types of random primers comprising 10 nucleotides (10-nucleotide primer A) shown in Table 1 were added to the final concentration of 60 µM therein, a 0.2 mM dNTP mixture, 1.0 mM MgCl , and 1.25 units of DNA polymerase (PrimeSTAR, TAKARA) were added thereto, and a reaction solution was prepared while adjusting the final reaction level to 50 µl. In this experiment, as the 1, 2, 3, 12, 24, or 48 types of random primers, random primers were selected successively from No. 1 shown in Table 1, and the selected primers were then examined.

PCR was carried out under thermal cycle conditions comprising 98°C for 2 minutes and 30 cycles of 98°C for 10 seconds, 50°C for 15 seconds, and 72°C for 20 seconds, followed by storage at 4°C. The DNA library obtained in this experiment was subjected to purification and electrophoresis in the same manner as in 3.1.3. Also, the reproducibility of the repeated data was evaluated on the basis of the Spearman’s rank correlation (ρ > 0.9). 3.8 Random primer sequence To the genomic DNA described in 2. above (30 ng, NiF8-derived genomic DNA), a set of primers selected from the 5 sets of random primers shown in Tables 2 to 6 was added to the final concentration of 60 µM therein, a 0.2 mM dNTP mixture, 1.0 mM MgCl , and 1.25 units of DNA polymerase (PrimeSTAR, TAKARA) were added thereto, and a reaction solution was prepared while adjusting the final reaction level to 50 µl. PCR was carried out under thermal cycle conditions comprising 98°C for 2 minutes and 30 cycles of 98°C for 10 seconds, 50°C for 15 seconds, and 72°C for 20 seconds, followed by storage at 4°C. The DNA library obtained in this experiment was subjected to purification and electrophoresis in the same manner as in 3.1.3. Also, the reproducibility of the repeated data was evaluated on the basis of the Spearman’s rank correlation (ρ > 0.9). 3.9 DNA library using human-derived genomic DNA To the genomic DNA described in 2. above (30 ng, human-derived genomic DNA), random primers (final concentration: 60 µM, 10-nucleotide primer A), a 0.2 mM dNTP mixture, 1.0 mM MgCl , and 1.25 units of DNA polymerase (PrimeSTAR, TAKARA) were added, and a reaction solution was prepared while adjusting the final reaction level to 50 µl.

PCR was carried out under thermal cycle conditions comprising 98°C for 2 minutes and 30 cycles of 98°C for 10 seconds, 50°C for 15 seconds, and 72°C for 20 seconds, followed by storage at 4°C. The DNA library obtained in this experiment was subjected to purification and electrophoresis in the same manner as in 3.1.3. Also, the reproducibility of the repeated data was evaluated on the basis of the Spearman’s rank correlation (ρ > 0.9). 4. Results and examination 4.1 Correlation between PCR conditions and DNA library size When PCR was conducted with the use of random primers in accordance with conventional PCR conditions (3.1.2 described above), the amplified DNA library size was as large as 2 kbp or more, but amplification of the DNA library of a target size (i.e., 100-bp to 500-bp) was not observed (Fig. 2). A DNA library of 100 bp to 500 bp could not be obtained because it was highly unlikely that a random primer would function as a primer in a region of 500 bp or smaller. In order to prepare a DNA library of the target size (i.e., 100 bp to 500 bp), it was considered necessary to induce non-specific amplification with high reproducibility.

The correlation between the annealing temperature (3.1.4 above), the enzyme amount (3.1.5 above), the MgCl concentration (3.1.6 above), the primer length (3.1.7 above), and the primer concentration (3.18 above), which are considered to affect PCR specificity, and the DNA library size were examined.

Fig. 3 shows the results of the experiment described in 3.1.4 attained at an annealing temperature of 45°C, Fig. 4 shows the results attained at an annealing temperature of 40°C, and Fig. 5 shows the results attained at an annealing temperature of 37°C. By reducing the annealing temperature from 45°C, 40°C, to 37°C, as shown in Figs. 3 to 5, the amounts of high-molecular-weight DNA library amplified increased, although amplification of low-molecular-weight DNA library was not observed.

Fig. 6 shows the results of the experiment described in 3.1.5 attained when the enzyme amount is increased by 2 times, and Fig. 7 shows the results attained when the enzyme amount is increased by 10 times the original amount. By increasing the enzyme amount by 2 times or 10 times a common amount, as shown in Figs. 6 and 7, the amounts of high-molecular-weight DNA library amplified increased, although amplification of low- molecular-weight DNA library was not observed.

Fig. 8 shows the results of the experiment described in 3.1.6 attained when the MgCl concentration is increased by 2 times a common amount, Fig. 9 shows the results attained when the MgCl concentration is increased by 3 times, and Fig. 10 shows the results attained when the MgCl concentration is increased by 4 times. By increasing the MgCl concentration by 2 times, 3 times, and 4 times the common amount, as shown in Figs. 8 to 10, the amounts of high-molecular-weight DNA library amplified varied, although amplification of a low-molecular-weight DNA library was not observed.

Figs. 11 to 18 show the results of the experiment described in 3.1.7 attained at the random primer lengths of 8 nucleotides, 9 nucleotides, 11 nucleotides, 12 nucleotides, 14 nucleotides, 16 nucleotides, 18 nucleotides, and 20nucleotides, respectively. Regardless of the length of a random primer, as shown in Figs. 11 to 18, no significant change was observed in comparison with the results shown in Fig. 2 (a random primer comprising 10 nucleotides).

The results of experiment described in 3.1.8 are summarized in Table 23.

[Table 23] Concentration Correlation Repeat Figure (m M) coefficient (r ) 2 - Fig. 19 Fig. 20 - 1st Fig. 21 6 0.889 2nd Fig. 22 1st Fig. 23 8 0.961 2nd Fig. 24 1st Fig. 25 0.979 2nd Fig. 26 1st Fig. 27 0.950 2nd Fig. 28 1st Fig. 29 40 0.975 2nd Fig. 30 1st Fig. 31 60 0.959 2nd Fig. 32 1st Fig. 33 100 0.983 2nd Fig. 34 1st Fig. 35 200 0.991 2nd Fig. 36 1st Fig. 37 300 0.995 2nd Fig. 38 1st Fig. 39 400 0.988 2nd Fig. 40 1st Fig. 41 500 0.971 2nd Fig. 42 600 - Fig. 43 Fig. 44 Fig. 45 Fig. 46 Fig. 47 - With the use of random primers comprising 10 nucleotides, as shown in Figs. 19 to 47, amplification was observed in a 1-kbp DNA fragment at the random primer concentration of 6 µM. As the concentration increased, the molecular weight of a DNA fragment decreased. Reproducibility at the random primer concentration of 6 to 500 µM was examined. As a result, a relatively low ρ value of 0.889 was attained at the concentration of 6 µM, which is 10 times higher than the usual level. At the concentration of 8 µM, which is equivalent to 13.3 times higher than the usual level, and at 500 µM, which is 833.3 times higher than the usual level, a high ρ value of 0.9 or more was attained.

The results demonstrate that a DNA fragment of 1 kbp or smaller can be amplified while achieving high reproducibility by elevating the random primer concentration to a level significantly higher than the concentration employed under general PCR conditions. When the random primer concentration is excessively higher than 500 µM, amplification of a DNA fragment of a desired size cannot be observed. In order to amplify a low-molecular- weight DNA fragment with excellent reproducibility, accordingly, it was found that the random primer concentration should fall within an optimal range, which is higher than the concentration employed in a general PCR procedure and equivalent to or lower than a given level. 4.2 Confirmation of reproducibility via MiSeq In order to confirm the reproducibility for DNA library production, as described in 3.2 above, the DNA library amplified with the use of the genomic DNA extracted from NiF8 as a template and random primers was analyzed with the use of a next-generation sequencer (MiSeq), and the results are shown in Fig. 48. As a result of 3.2.4 above, 47,484 read patterns were obtained. As a result of comparison of the number of reads obtained through repeated measurements, a high correlation (i.e., a correlational coefficient "r" of 0.991) was obtained, as with the results of electrophoresis. Accordingly, it was considered that a DNA library could be produced with satisfactory reproducibility with the use of random primers. 4.3 Analysis of rice variety Nipponbare As described in 3.3 above, a DNA library was prepared with the use of genomic DNA extracted from the rice variety Nipponbare, the genomic information of which has been disclosed, as a template, and random primers and subjected to electrophoresis, and the results are shown in Figs. 49 and 50. On the basis of the results shown in Figs. 49 and 50, the ρ value was found to be as high as 0.979. Also, Fig. 51 shows the results of analysis of the read data with the use of MiSeq. On the basis of the results shown in Fig. 51, the correlational coefficient "r" was found to be as high as 0.992. These results demonstrate that a DNA library of rice could be produced with very high reproducibility with the use of random primers.

As described in 3.3.3, the obtained read pattern was mapped to the genomic information of Nipponbare. As a result, DNA fragments were found to be evenly amplified throughout the genome at intervals of 6.2 kbp (Fig. 52). As a result of comparison of the sequence and genome information of random primers, 3.6 mismatches were found on average, and one or more mismatches were observed in 99.0% of primer pairs (Fig. 53).

The results demonstrate that a DNA library involving the use of random primers is produced with satisfactory reproducibility via non-specific amplification evenly throughout the genome. 4.4 Detection of polymorphism and genotype identification of sugarcane As described in 3.4, DNA libraries of the sugarcane varieties NiF8 and Ni9 and 22 hybrid progeny lines were produced with the use of random primers, the resulting DNA libraries were analyzed with the next-generation sequencer (HiSeq), the polymorphisms of the parent varieties were detected, and the genotypes of the hybrid progenies were identified on the basis of the read data. Table 24 shows the results.

[Table 24] Table 24. Number of markers and genotyping accuracy of sugarcane varieties NiF8 and Ni9 Number F1_01 F1_02 Total Consistency Reproducibility Consistency Reproducibility Consistency Reproducibility markers NiF8 8,683 8,680 99.97% 8,682 99.99% 17,362 99.98% type 11,655 11,650 99.96% 11,651 99.97% 23,301 99.96% type Total 20,338 20,330 99.96% 20,333 99.98% 40,663 99.97% As shown in Table 24, 8,683 markers for NiF8 and 11,655 markers for Ni9; that is, a total of 20,338 markers, were produced. In addition, reproducibility for genotype identification of hybrid progeny lines was as high as 99.97%. This indicates that the accuracy for genotype identification is very high. In particular, sugarcane is polyploid (8x+n), the number of chromosomes is as large as 100 to 130, and the genome size is as large as 10 Gbp, which is at least 3 times greater than that of humans. Accordingly, it is very difficult to identify the genotype throughout the genomic DNA. As described above, numerous markers can be produced with the use of random primers, and the sugarcane genotype can thus be identified with high accuracy. 4.5 Experiment for confirmation with PCR marker As described in 3.5 above, the sugarcane varieties NiF8 and Ni9 and 22 hybrid progeny lines were subjected to PCR with the use of the primers shown in Table 22, genotypes were identified via electrophoresis, and the results were compared with the number of reads. Figs. 54 and55 show the number of reads and the electrophoretic pattern of the NiF8 marker N80521152, respectively. Figs. 56 and 57 show the number of reads and the electrophoretic pattern of the NiF8 marker N80997192, respectively. Figs. 58 and 59 show the number of reads and the electrophoretic pattern of the NiF8 marker N80533142, respectively. Figs. 60 and 61 show the number of reads and the electrophoretic pattern of the Ni9 marker N91552391, respectively. Figs. 62 and 63 show the number of reads and the electrophoretic pattern of the Ni9 marker N91653962, respectively. Figs. 64 and 65 show the number of reads and the electrophoretic pattern of the Ni9 marker N91124801, respectively.

As shown in Figs. 54 to 65, the results for all the PCR markers designed in 3.5 above were consistent with the results of analysis with the use of a next-generation sequencer. It was thus considered that genotype identification with the use of a next- generation sequencer would be applicable as a marker technique. 4.6 Correlation between random primer density and length As described in 3.6.1, the results of DNA library production with the use of random primers comprising 9 nucleotides (Table 8), 10 nucleotides (Table 1, 10-nucleotide primer A), 11 nucleotides (Table 9), 12 nucleotides (Table 10), 14 nucleotides (Table 11), 16 nucleotides (Table 12), 18 nucleotides (Table 13), and 20 nucleotides (Table 14) are shown in Figs. 66 to 81. The results are summarized in Table 25.

[Table 25] Correlation Random primer Repeat Figure length coefficient (r ) 1st Fig. 66 9 0.981 2nd Fig. 67 1st Fig. 68 0.979 2nd Fig. 69 1st Fig. 70 11 0.914 2nd Fig. 71 1st Fig. 72 12 0.957 2nd Fig. 73 1st Fig. 74 14 0.984 2nd Fig. 75 1st Fig. 76 16 0.989 2nd Fig. 77 1st Fig. 78 18 0.995 2nd Fig. 79 1st Fig. 80 0.999 2nd Fig. 81 When random primers were used at a high concentration of 10.0 µM, which is 13.3 times greater than the usual level, as shown in Figs. 66 to 81, it was found that a low- molecular-weight DNA fragment could be amplified with the use of random primers comprising 9 to 20 nucleotides while achieving very high reproducibility. As the nucleotide length of a random primer increased (12 nucleotides or more, in particular), the molecular weight of the amplified fragment was likely to be decreased. When random primers comprising 9 nucleotides were used, the amount of the DNA fragment amplified was increased by setting the annealing temperature at 37°C.

In order to elucidate the correlation between the density and the length of random primers, as described in 3.6.2 above, PCR was carried out with the use of random primers comprising 8 to 35 nucleotides at the concentration of 0.6 to 300 µM, so as to produce a DNA library. The results are shown in Table 26.

[Table 26] Table 26 The correlation between the concentration and the length of random primer for DNA library Primer Concentration Primer length M Factor relative 8 9 10 11 12 14 16 18 20 22 24 26 28 29 30 35 to reference 0.6 Reference × × × × × × × × × × × × × × × × 2 3.3-fold × × × × × × × × × × × × × × × × 4 6.7-fold × × × × × ○ ○ ○ ○ ○ ○ ○ ○ × × × 6 10.0-fold × × × × × ○ ○ ○ ○ ○ ○ ○ ○ ○ ○ × 8 13.3-fold × × × × ○ ○ ○ ○ ○ ○ ○ ○ ○ ○ × × 16.7-fold × × × × ○ ○ ○ ○ ○ ○ ○ ○ ○ ○ × × 33.3-fold × × × ○ ○ ○ ○ ○ ○ ○ ○ × × × × × 40 66.7-fold × ○ ○ ○ ○ ○ ○ ○ ○ × × × × × × × 60 100.0-fold × ○ ○ ○ ○ ○ ○ ○ ○ × × × × × × × 100 166.7-fold - × ○ ○ ○ ○ ○ ○ × - - - - - - - 200 333.3-fold - × ○ ○ × × × × × - - - - - - - 300 500.0-fold - × × × × × × × × - - - - - - - ○: DNA library covering 100 to 500 nucleotides could be amplified assuredly with high reproducibility ( ρ>0.9) ×: DNA library did not cover 100 to 500 nucleotides, or the reproducibility was low ( ρ<=0.9) -: Not carried out As shown in Table 26, it was found that a low-molecular-weight (100 to 500 nucleotides) DNA fragment could be amplified with high reproducibility with the use of random primers comprising 9 to 30 nucleotides at 4.0 to 200 μM. In particular, it was confirmed that low- molecular-weight (100 to 500 nucleotides) DNA fragments could be amplified assuredly with high reproducibility with the use of random primers comprising 9 to 30 nucleotides at 4.0 to 100 The results shown in Table 26 are examined in greater detail. As a result, the correlation between the length and the concentration of random primers is found to be preferably within a range surrounded by a frame as shown in Fig. 82. More specifically, the random primer concentration is preferably 40 to 60 μM when the random primers comprise 9 to 10 nucleotides.

It is preferable that a random primer concentration satisfy the condition represented by an -6.974 inequation: y > 3E + 08x , provided that the nucleotide length of the random primer is represented by x and the random primer concentration is represented by y, and 100 µM or lower, when the random primer comprises 10 to 14 nucleotides. The random primer concentration is preferably 4 to 100 mM when the random primer comprises 14 to 18 nucleotides. When a random primer comprises 18 to 28 nucleotides, the random primer concentration is preferably 4 µM or higher, and it satisfies the condition represented -5.533 by an inequation: y < 8E + 08x . When a random primer comprises 28 to 29 nucleotides, the random primer concentration is preferably 4 to 10 µM. The inequations y > 3E + 08x 6.974 -5.533 and y < 8E + 08x are determined on the basis of the Microsoft Excel power approximation.

By prescribing the number of nucleotides and the concentration of random primers within given ranges as described above, it was found that low-molecular-weight (100 to 500 nucleotides) DNA fragments could be amplified with high reproducibility. For example, the accuracy of the data obtained via analysis of high-molecular-weight DNA fragments with the use of a next-generation sequencer is known to deteriorate to a significant extent.

As described in this Example, the number of nucleotides and the concentration of random primers may be prescribed within given ranges, so that a DNA library with a molecular size suitable for analysis with a next-generation sequencer can be produced with satisfactory reproducibility, and such DNA library can be suitable for marker analysis with the use of a next-generation sequencer. 4.7 Number of random primers As described in 3.7 above, 1, 2, 3, 12, 24, or 48 types of random primers (concentration: 60µM) were used to produce a DNA library, and the results are shown in Figs. 83 to 94. The results are summarized in Table 27.

[Table 27] Number of Correlation Repeat Figure random primers coefficient (r ) 1st Fig. 83 1 0.984 2nd Fig. 84 1st Fig. 85 2 0.968 2nd Fig. 86 1st Fig. 87 3 0.974 2nd Fig. 88 1st Fig. 89 12 0.993 2nd Fig. 90 1st Fig. 91 24 0.986 2nd Fig. 92 1st Fig. 93 48 0.978 2nd Fig. 94 As shown in Figs. 83 to 94, it was found that low-molecular-weight DNA fragments could be amplified with the use of any of 1, 2, 3, 12, 24, or 48 types of random primers while achieving very high reproducibility. In particular, it is understood that as the number of types of random primers increases, a peak in the electrophoretic pattern decreases, and a deviation is likely to disappear. 4.8 Random primer sequence As described in 3.8 above, DNA libraries were produced with the use of sets of random primers shown in Tables 2 to 6 (i.e., 10-nucleotide primer B, 10-nucleotide primer C, 10-nucleotide primer D, 10-nucleotide primer E, and 10-nucleotide primer F), and the results are shown in Figs. 95 to 104. The results are summarized in Table 28.

[Table 28] Correlation Random primer Repeat Figure set coefficient (r ) 1st Fig. 95 -nucleotide B 0.916 2nd Fig. 96 1st Fig. 97 -nucleotide C 0.965 2nd Fig. 98 1st Fig. 99 -nucleotide D 0.986 2nd Fig. 100 1st Fig. 101 -nucleotide E 0.983 2nd Fig. 102 1st Fig. 103 -nucleotide F 0.988 2nd Fig. 104 As shown in Figs. 95 to 104, it was found that low-molecular-weight DNA fragments could be amplified with the use of any sets of 10-nucleotide primer B, 10- nucleotide primer C, 10-nucleotide primer D, 10-nucleotide primer E, or 10-nucleotide primer F while achieving very high reproducibility. 4.9 Production of human DNA library As described in 3.9 above, a DNA library was produced with the use of human- derived genomic DNA and random primers at a final concentration of 60 µM (10-nucleotide primer A), and the results are shown in Figs. 105 and 106. Fig. 105 shows the results of the first repeated experiment, and Fig. 106 shows the results of the second repeated experiment.

As shown in Figs. 105 and 106, it was found that low-molecular-weight DNA fragments could be amplified while achieving very high reproducibility even if human-derived genomic DNA was used.

[Example 2] 1. Flowchart In this Example, first DNA fragments were prepared by PCR using genomic DNA as a template and random primers according to the schematic diagrams shown in Figs. 107 and 108. Subsequently, second DNA fragments were prepared by PCR using the first DNA fragments as templates and next-generation sequencer primers. The prepared second DNA fragments were used as a sequencer library for conducting sequence analysis using a so- called next generation sequencer. Genotype was analyzed based on the obtained read data. 2. Materials In this Example, genomic DNAs were extracted from the sugarcane variety NiF8 and the rice variety Nipponbare using the DNeasy Plant Mini Kit (QIAGEN), and the extracted genomic DNAs were purified. The purified genomic DNAs were used as NiF8- derived genomic DNA and Nipponbare-derived genomic DNA, respectively. 3. Method 3.1 Examination of sugarcane variety NiF8 3.1.1 Designing of random primers and next-generation sequencer primers In this Example, random primers were designed based on 3'-end 10 nucleotides of the next-generation sequencer adapter (Nextera adapter, Illumina, Inc.). Specifically, in this Example, GTTACACACG (SEQ ID NO: 2041, 10-nucleotide G) was used as a random primer. In addition, next-generation sequencer primers were designed based on the sequence information on the Nextera adapter of Illumina, Inc. in the above manner (Table 29).

[Table 29] No. Primer sequence SEQ ID NO: AATGATACGGCGACCACCGAGATCTACA 1 CCTCTCTATTCGTCGGCAGCGTCAGATG 2042 TGTATAAGAGACAG CAAGCAGAAGACGGCATACGAGATTAAG 2 GCGAGTCTCGTGGGCTCGGAGATGTGT 2043 ATAAGAGACAG 3.1.2 Preparation of DNA library A dNTP mixture at a final concentration of 0.2 mM, MgCl at a final concentration of 1.0 mM, and DNA Polymerase(TAKARA, PrimeSTAR) at a final concentration of 1.25 units, and a random primer (10-nucleotide G) at a final concentration of 60 µM were added to NiF8-derived genomic DNA(30 ng) described in 2. above. A DNA library (first DNA fragments) was prepared by PCR (treatment at 98°C for 2 minutes, reaction for 30 cycles of 98°C for 10 seconds, 50°C for 15 seconds, and 72°C for 20 seconds, and storage at 4°C) in a final reaction volume of 50 µl. 3.1.3 Purification and electrophoresis The DNA library obtained in 3.1.2 above was purified with the use of the MinElute PCR Purification Kit (QIAGEN) and subjected to electrophoresis with the use of the Agilent 2100 bioanalyzer( Technologies) to obtain a fluorescence unit (FU). Also, the reproducibility of the repeated data was evaluated on the basis of the Spearman’s rank correlation (ρ > 0.9). 3.1.4 Preparation of next-generation sequencer DNA library A dNTP mixture at a final concentration of 0.2 mM, MgCl at a final concentration of 1.0 mM, DNA Polymerase(TAKARA, PrimeSTAR) at a final concentration of 1.25 units, and a next-generation sequencer primer at a final concentration of 0.5 µM were added to the first DNA fragment (100 ng) purified in 3.1.3 above. A next-generation sequencer DNA library (second DNA fragments) was prepared by PCR (treatment at 95°C for 2 minutes, reaction for 25 cycles of 98°C for 15 seconds, 55°C for 15 seconds, 72°C for 20 seconds, treatment at 72°C for 1 minutes, and storage at 4°C) in a final reaction volume of 50 µl.

The DNA library for a next-generation sequencer was subjected to purification and electrophoresis in the same manner as in 3.1.3. 3.1.5 MiSeq analysis The next-generation sequencer DNA library (a second DNA fragment) in 3.1.4 above was analyzed by MiSeq via 100 base paired-end sequencing using MiSeq Reagent Kit V2 500 Cycle (Illumina). 3.1.6 Read data analysis The read patterns were identified from the read data obtained in 3.1.5. The number of reads was counted for each read pattern, the number of reads of the repeated analyses, and the reproducibility was evaluated using the correlational coefficient. 3.2 Examination of rice variety Nipponbare 3.2.1 Designing of random primers and next-generation sequencer primers In this Example, random primers were designed based on 10 nucleotides of the 3' end of the next-generation sequencer adapter Nextera adapter of Illumina, Inc. That is, in this Example, a sequence of 10 nucleotides positioned at the 3' end of the Nextera adapter and 16 types of nucleotide sequences prepared by adding an arbitrary nucleotide sequence of 2 nucleotides to the 3' end of the sequence of 10 nucleotides to results in a full length of 12 nucleotides were designed as random primers (Table 30, 12-nucleotide B).

[Table 30] No. Primer sequence SEQ ID NO: 1 TAAGAGACAGAA 2044 2 TAAGAGACAGAT 2045 3 TAAGAGACAGAC 2046 4 TAAGAGACAGAG 2047 TAAGAGACAGTA 2048 6 TAAGAGACAGTT 2049 7 TAAGAGACAGTC 2050 8 TAAGAGACAGTG 2051 9 TAAGAGACAGCA 2052 TAAGAGACAGCT 2053 11 TAAGAGACAGCC 2054 12 TAAGAGACAGCG 2055 13 TAAGAGACAGGA 2056 14 TAAGAGACAGGT 2057 TAAGAGACAGGC 2058 16 TAAGAGACAGGG 2059 In addition, in this Example, a next-generation sequencer primer designed based on the sequence information on the Nextera adapter of Illumina, Inc. in the same manner as in 3.1.1. 3.2.2 Preparation of DNA library A dNTP mixture at a final concentration of 0.2 mM, MgCl at a final concentration of 1.0 mM, and DNA Polymerase(TAKARA, PrimeSTAR) at a final concentration of 1.25 units, and a random primer (12-nucleotide B) at a concentration of 40 µM were added to Nipponbare-derived genomic DNA(30 ng) described in 2. above. A DNA library (first DNA fragments) was prepared by PCR (treatment at 98°C for 2 minutes, reaction for 30 cycles of 98°C for 10 seconds, 50°C for 15 seconds, 72°C for 20 seconds, and storage at 4°C) in a final reaction volume of 50 µl. 3.2.3 Purification and electrophoresis The DNA library obtained in 3.2.2 above was purified with the use of the MinElute PCR Purification Kit (QIAGEN) and subjected to electrophoresis with the use of the Agilent 2100 bioanalyzer (Technologies) to obtain a fluorescence unit (FU). Also, the reproducibility of the repeated data was evaluated on the basis of the Spearman’s rank correlation (ρ > 0.9). 3.2.4 Preparation of next-generation sequencer DNA library A dNTP mixture at a final concentration of 0.2 mM, MgCl at a final concentration of 1.0 mM, DNA Polymerase(TAKARA, PrimeSTAR) at a final concentration of 1.25 units, and a next-generation sequencer primer at a concentration of 0.5 µM were added to the first DNA fragment (100ng) purified in 3.2.3 above. A next-generation sequencer DNA library (second DNA fragments) was prepared by PCR (treatment at 95°C for 2 minutes, reaction for 25 cycles of 98°C for 15 seconds, 55°C for 15 seconds, 72°C for 20 seconds, treatment at 72°C for 1 minutes, and storage at 4°C) in a final reaction volume of 50 µl. Purification of the DNA library for next-generation sequencers and electrophoresis were conducted in the same manner as in 3.1.3. 3.2.5 MiSeq analysis The next-generation sequencer DNA library (second DNA fragment) in 3.2.4 above was analyzed by MiSeq via 100 base paired-end sequencing using MiSeq Reagent Kit V2 500 Cycle (Illumina). 3.2.6 Read data analysis The read patterns in 3.2.5 were mapped to the genomic information of Nipponbare (NC_008394 to NC_008405) using bowtie2, the degree of consistency between the random primer sequence and genomic DNA was confirmed. The read patterns were identified from the read data obtained in 3.2.5. The number of reads was counted for each read pattern, the number of reads of the repeated analyses, and the reproducibility was evaluated using the correlational coefficient. 4. Results and Examination 4.1 Results of examination of the sugarcane variety NiF8 Figs. 109 and 110 show the results of electrophoresis after conducting PCR using a random primer consisting of 10 nucleotides (10-nucleotide G) of the 3' end of the next- generation sequencer adapter (Nextera adapter, Illumina, Inc.) at a high concentration of 60 µl. As shown in Figs. 109 and 110, amplification was observed in a wide region ranging from 100 bp to 500 bp (the first DNA fragment). It was considered that amplification could be observed in a wide region because amplification was observed also in a region other than the genomic DNA region corresponding to the random primer. In addition, since the rank correlation coefficient among the repeated data was 0.957 (> 0.9), reproducibility was confirmed in the amplification pattern.

Next, Figures 111 and 112 shows the results of electrophoresis after conducting PCR using the next-generation sequencer primer in the manner described in 3.1.4. That is, in order to prepare a DNA library (second DNA fragments) bound to a next-generation sequencer adapter (Nextera adapter), PCR was conducted using a next-generation sequencer primer comprising the sequence of the Nextera adapter of Illumina, Inc. and the first DNA fragment as a template. Accuracy of analysis with the use of the next-generation sequencer of Illumina, Inc. is significantly reduced in a case in which the DNA library includes may short fragments having lengths of 100 bp or less or long fragments having lengths of 1 kbp or more. Since the next-generation sequencer DNA library (second DNA fragments) prepared in this Example was distributed mainly in a range of 150 bp to 1 kbp with a peak around 500 bp as illustrated in Figs. 111 and 112, the DNA library was considered to be an appropriate next-generation sequencer DNA library. In addition, since the rank correlation coefficient among the repeated data was 0.989 (> 0.9), reproducibility was confirmed in the amplification pattern.

In addition, as a result of analysis of the DNA library (second DA fragment) by next-generation sequencer MiSeq, 3.5-Gbp read data and 3.6-Gbp read data were obtained.

The values indicating accuracy of MiSeq data (>= Q30) were 93.3% and 93.1%. Since the values recommended by the manufacturer were 3.0 Gbp or more for read data and 85.0% or more for >= Q30, the next-generation sequencer DNA library (second DNA fragments) prepared in this Example was considered to be applicable to next-generation sequencer analysis. In order to confirm reproducibility, the number of reads of the repeated analyses were compared for 34,613 read patterns obtained by MiSeq. Fig. 113 shows the results. As shown in Fig. 113, there was a high correlation of r = 0.996 in terms of the number of reads of the repeated analyses as with the results of electrophoresis.

As described above, a DNA library (first DNA fragments) was obtained by conducting PCR using random primer comprising 10 nucleotides at the 3' end of a next- generation sequencer adapter (Nextera Adaptor, Illumina, Inc.) at a high concentration, and then, PCR was conducted using a next-generation sequencer primer comprising the sequence of Nextera Adaptor. Accordingly, it was possible to conveniently produce a next- generation sequencer DNA library (second DNA fragments) comprising many fragments with favorable reproducibility. 4.2 Results of examination of rice variety Nipponbare Figs. 114 and 115 show the results of electrophoresis after conducting PCR using nucleotides positioned at the 3' end of the next-generation sequencer adopter (Nextera adaptor, Illumina, Inc.) and 16 types of random primers (12-nucleotide B) having a full length of 12 nucleotides obtained by adding an arbitrary sequence of 2 nucleotides to the sequence of 10 nucleotides at the 3' end at a high concentration of 40 µl. As shown in Figs. 114 and 115, amplification was observed in a wide region ranging from 100 bp to 500 bp(the first DNA fragment). It was considered that amplification could be observed in a wide region because amplification was observed also in a region other than the genomic DNA region corresponding to the random primer as in the case of 4.1. In addition, since the rank correlation coefficient was 0.950 (> 0.9), reproducibility was confirmed in the amplification pattern.

Next, Figures 116 and 117 shows the results of electrophoresis after conducting PCR using the next-generation sequencer primer in the manner described in 3.2.4. That is, in order to prepare a DNA library (second DNA fragments) bound to a next-generation sequencer adapter (Nextera adapter), PCR was conducted using a next-generation sequencer primer comprising the sequence of the Nextera adapter of Illumina, Inc. and the first DNA fragment as a template. As a result, since the next-generation sequencer DNA library (the second DNA fragment) prepared in this Example was distributed mainly in a range of 150 bp to 1 kbp with a peak around 300 bp as illustrated in Figs. 116 and 117, the DNA library was considered to be an appropriate next-generation sequencer DNA library. In addition, since the rank correlation coefficient among the repeated data was 0.992 (> 0.9), reproducibility was confirmed in the amplification pattern.

In addition, as a result of analysis of the obtained DNA library (second DNA fragments) by next-generation sequencer MiSeq, 4.0-Gbp read data and 3.8-Gbp read data were obtained. The values indicating accuracy of MiSeq data (>= Q30) were 94.0% and 95.3%. As in the case of 4.1.1, in view of the above results, the next-generation sequencer DNA library (second DNA fragments) prepared in this Example was considered to be applicable to next-generation sequencer analysis. Fig. 118 shows the results obtained by comparing random primer sequences and the reference sequence of rice variety Nipponbare in order to evaluate the degree of consistency between the random primer sequences of 19,849 read patterns obtained by MiSeq and the genome. As shown in Fig. 118, the average degree of consistency between the random primer sequences and the reference sequence of rice variety Nipponbare was 34.5%. In particular, since there was no identical read pattern between the random primer sequences and the reference sequence of rice variety Nipponbare, it was considered that any read pattern indicated that a random primer was bound to a sequence not corresponding to the random primer, and the resulting sequence was amplified. The above results were considered to correspond to the results obtained by the bioanalyzer. In order to confirm read pattern reproducibility, the number of reads of the repeated analyses were compared. Fig. 119 shows the results. As shown in Fig. 119, there was a high correlation of r=0.999 in terms of the number of reads of the repeated analyses as with the results of electrophoresis.

As described above, a DNA library (first DNA fragments) was obtained by conducting PCR using 16 types of random primers having a full length of 12 nucleotides obtained by adding an arbitrary sequence of 2 nucleotides to the 3' end of 10 nucleotides at high concentrations, where the 10 nucleotides position at the 3' end of a next-generation sequencer adapter (Nextera Adaptor, Illumina, Inc.) and then, PCR was conducted using a primer comprising the sequence of Nextera Adaptor. Accordingly, it was possible to conveniently produce a next-generation sequencer DNA library (second DNA fragments) comprising many fragments with favorable reproducibility.

[Example 3] 1. Materials and Method 1.1 Materials In this Example, genomic DNA was extracted from the rice variety Nipponbare using the DNeasy Plant Mini kit (QIAGEN), and the extracted genomic DNAs were purified. The purified genomic DNA was used as Nipponbare-derived genomic DNA. 1.2 Preparation of DNA library To the genomic DNA described in 1.1 above (30 ng, Nipponbare-derived genomic DNA), random primers (final concentration: 60 µM, 10-nucleotide primer A), a 0.2 mM dNTP mixture, 1.0 mM MgCl , and 1.25 units of DNA polymerase (PrimeSTAR, TAKARA) were added, and a reaction solution was prepared while adjusting the final reaction level to 50 µl. PCR was carried out under thermal cycle conditions comprising 98°C for 2 minutes and 30 cycles of 98°C for 10 seconds, 50°C for 15 seconds, and 72°C for 20 seconds, followed by storage at 4°C. The DNA library obtained in this experiment was purified by the MinElute PCR Purification Kit (QIAGEN). 1.3 Preparation of sequence library From the DNA library obtained in 1.2, a sequence library for MiSeq analysis was prepared using the KAPA Library Preparation Kit (Roche). 1.4 MiSeq analysis With the use of the MiSeq Reagent Kit V2 500 Cycle (Illumina), the sequence library for MiSeq analysis obtained in 1.3 was analyzed via 100 base paired-end sequencing. 1.5 Analysis of nucleotide sequence information Random primer sequence information was deleted from the read data obtained in 1.4, and nucleotide sequence information of each read was identified. Mapping of nucleotide sequence information of each read on genomic information of rice Kasalath (kasalath_genome) was conducted by bowtie2, and single nucleotide polymorphism (SNP) and insertion or deletion mutation (InDel) were identified as markers for each chromosome. 2. Results and examination Table 31 shows the results of mapping of nucleotide sequence information of the DNA library prepared using random primers based on the genomic DNA from the rice variety Nipponbare on the genomic information of rice Kasalath.

[Table 31] Chromosome SNP InDel Total 1 5,579 523 6,102 2 4,611 466 5,077 3 4,916 569 5,485 4 3,859 364 4,223 4,055 373 4,428 6 4,058 375 4,433 7 3,848 286 4,134 8 3,303 294 3,597 9 2,694 227 2,921 2,825 229 3,054 11 3,250 246 3,496 12 2,753 239 2,992 Total 45,751 4,191 49,942 As shown in Table 31, it was possible to identify 2,694 to 5,579 SNPs (3,812.6 SNPs on average, 45,751 SNPs in total) for each chromosome. As shown in Table 31, it was also possible to identify insertion/deletion (InDel) of 227 to 569 SNPs (349.3 SNPs on average, 4,191 SNPs in total) for each chromosome. The above results revealed that it is possible to identify a DNA marker as a characteristic nucleotide sequence present in the genome of a test organism by comparing nucleotide sequence information on a DNA library prepared using random primers and known nucleotide sequence information in the manner shown in this Example.

All publications, patents and patent applications cited in the present description are incorporated herein by reference in their entirety.

Claims (13)

1. A method for analyzing genomic DNA, comprising steps of: preparing a DNA library, which is produced by the method comprising conducting a nucleic acid amplification reaction in a reaction solution containing genomic DNA and a random primer comprising 9 to 30 nucleotides using genomic DNA as a template to obtain DNA fragments by the nucleic acid amplification reaction, wherein when the random primer contains 9 to 10 nucleotides, the concentration of the random primer is set to 40 to 60 μM; when the random primer contains 10 to 14 nucleotides, the concentration of the random primer is set to 100 μM or less, and said concentration is defined by the formula -6.974 y > 3E + 08x , provided that the nucleotide length of the random primer is represented by "x" and the concentration of the random primer is represented by "y"; when the random primer contains 14 to 18 nucleotides, the concentration of the random primer is set to 4 to 100 μM; when the random primer contains 18 to 28 nucleotides, the concentration of the random primer is set to 4 μM or more, and said concentration is defined by the formula y -5.533 < 8E + 08x ; when the random primer contains 28 to 29 nucleotides, the concentration of the random primer is set to 6 to 10 μM; and when the random primer contains 30 nucleotides, the concentration of the random primer is set to 6 μM; determining the nucleotide sequence of DNA fragments contained in the DNA library produced; and confirming the presence or absence of specific DNA fragments based on the nucleotide sequence.

2. The method for analyzing genomic DNA according to claim 1, wherein the presence or absence of the specific DNA fragments is confirmed based on the number of reads of the nucleotide sequence of the specific DNA fragments.

3. The method for analyzing genomic DNA according to claim 1, wherein the nucleotide sequence of DNA fragments contained in the DNA library is compared with known sequence information or with the nucleotide sequence of DNA fragments contained in a DNA library produced using genomic DNA from a different organism or tissue, and the presence or absence of the specific DNA fragments is confirmed based on differences in the nucleotide sequences.

4. The method for analyzing genomic DNA according to claim 1, further comprising steps preparing a pair of primers for specifically amplifying the specific DNA fragments ; conducting a nucleic acid amplification reaction using genomic DNA extracted from a target organism as a template and the pair of primers; and confirming the presence or absence of the specific DNA fragments in the genomic DNA based on the results of the nucleic acid amplification reaction.

5. The method for analyzing genomic DNA according to claim 1, wherein the DNA fragments each comprise 100 to 500 nucleotides.

6. A method for analyzing genomic DNA, comprising steps of: conducting a nucleic acid amplification reaction in a first reaction solution comprising genomic DNA and a random primer comprising 9 to 30 nucleotides at a high concentration to obtain first DNA fragments by the nucleic acid amplification reaction using the genomic DNA as a template, wherein when the random primer contains 9 to 10 nucleotides, the concentration of the random primer is set to 40 to 60 μM; when the random primer contains 10 to 14 nucleotides, the concentration of the random primer is set to 100 μM or less, and said concentration is defined by the formula -6.974 y > 3E + 08x , provided that the nucleotide length of the random primer is represented by "x" and the concentration of the random primer is represented by "y"; when the random primer contains 14 to 18 nucleotides, the concentration of the random primer is set to 4 to 100 μM; when the random primer contains 18 to 28 nucleotides, the concentration of the random primer is set to 4 μM or more, and said concentration is defined by the formula y -5.533 < 8E + 08x ; when the random primer contains 28 to 29 nucleotides, the concentration of the random primer is set to 6 to 10 μM; and when the random primer contains 30 nucleotides, the concentration of the random primer is set to 6 μM; conducting a nucleic acid amplification reaction in a second reaction solution comprising the obtained first DNA fragments and a primer, which has a 3'-end nucleotide sequence capable of hybridizing to a 5'-end nucleotide sequence of the first DNA fragments to obtain second DNA fragments; preparing a DNA library with the second DNA fragments or DNA fragments obtained by a nucleic acid amplification reaction using the second DNA fragments as templates or a nucleic acid amplification reaction to be conducted repeatedly; determining the nucleotide sequence of DNA fragments contained in the DNA library prepared; and confirming the presence or absence of specific DNA fragments based on the nucleotide sequence.

7. The method for analyzing genomic DNA according to claim 6, wherein the primer for amplifying the second DNA fragments comprises a region used for a nucleotide sequencing reaction, or the primer used for a nucleic acid amplification reaction using the second DNA fragments as templates or a nucleic acid amplification reaction to be conducted repeatedly comprises a region used for a nucleotide sequencing reaction.

8. The method for analyzing genomic DNA according to claim 6, wherein the presence or absence of specific DNA fragments is confirmed based on the number of reads of the nucleotide sequence of the specific DNA fragments.

9. The method for analyzing genomic DNA according to claim 6, wherein the nucleotide sequence of DNA fragments contained in the DNA library is compared with known sequence information or with the nucleotide sequence of DNA fragments contained in a DNA library produced using genomic DNA from a different organism or tissue, and the presence or absence of the specific DNA fragments is confirmed based on differences in the nucleotide sequences.

10. The method for analyzing genomic DNA according to claim 6, which further comprises steps of: preparing a pair of primers for specifically amplifying the specific DNA fragments; conducting a nucleic acid amplification reaction using genomic DNA extracted from a target organism as a template and the pair of primers; and confirming the presence or absence of the specific DNA fragments in the genomic DNA based on the results of the nucleic acid amplification reaction.

11. The method for analyzing genomic DNA according to claim 6, wherein the first DNA fragments each comprise 100 to 500 nucleotides.

12. The method according to any one of claims 1 to 5, substantially as herein described with reference to any one or more of the examples but excluding comparative examples.

13. The method according to any one of claims 6 to 11, substantially as herein described with reference to any one or more of the examples but excluding comparative examples.