Kidd et al., 2010 - Google Patents
Characterization of missing human genome sequences and copy-number polymorphic insertionsKidd et al., 2010
View HTML- Document ID
- 1940596077788763158
- Author
- Kidd J
- Sampas N
- Antonacci F
- Graves T
- Fulton R
- Hayden H
- Alkan C
- Malig M
- Ventura M
- Giannuzzi G
- Kallicki J
- Anderson P
- Tsalenko A
- Yamada N
- Tsang P
- Kaul R
- Wilson R
- Bruhn L
- Eichler E
- Publication year
- Publication venue
- Nature methods
External Links
Snippet
The extent of human genomic structural variation suggests that there must be portions of the genome yet to be discovered, annotated and characterized at the sequence level. We present a resource and analysis of 2,363 new insertion sequences corresponding to 720 …
- 238000003780 insertion 0 title abstract description 68
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- G06F19/18—Bioinformatics, i.e. methods or systems for genetic or protein-related data processing in computational molecular biology for functional genomics or proteomics, e.g. genotype-phenotype associations, linkage disequilibrium, population genetics, binding site identification, mutagenesis, genotyping or genome annotation, protein-protein interactions or protein-nucleic acid interactions
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- G06F19/22—Bioinformatics, i.e. methods or systems for genetic or protein-related data processing in computational molecular biology for sequence comparison involving nucleotides or amino acids, e.g. homology search, motif or SNP [Single-Nucleotide Polymorphism] discovery or sequence alignment
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