DK3260555T3 - Hidtil ukendt protokol til fremstilling af sekventeringsbiblioteker - Google Patents
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- DK3260555T3 DK3260555T3 DK17180803.3T DK17180803T DK3260555T3 DK 3260555 T3 DK3260555 T3 DK 3260555T3 DK 17180803 T DK17180803 T DK 17180803T DK 3260555 T3 DK3260555 T3 DK 3260555T3
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Claims (13)
1. Fremgangsmåde til fremstilling af et sekventeringsbibliotek fra en testprøve omfattende nukleinsyremolekyler, hvor fremgangsmåden omfatter på hinanden følgende trin af end-repairing, dA-tailing og adaptor-ligering af nukleinsyrerne, og hvor de på hinanden følgende trin undtager oprensning af de end-repaired produkter før dA-tailingtrinnet og undtager oprensning af dA-tailingprodukterne før adaptor-ligeringstrinnet.
2. Fremgangsmåde ifølge krav 1, hvor de på hinanden følgende trin udføres i fraværet af polyethylenglycol.
3. Fremgangsmåde ifølge krav 1 eller krav 2, hvor de på hinanden følgende trin udføres på mindre end 1 time.
4. Fremgangsmåde ifølge et hvilket som helst af de foregående krav, hvor nævnte nukleinsyrer er DNA-molekyler.
5. Fremgangsmåde ifølge et hvilket som helst af de foregående krav, hvor nævnte nukleinsyrer: (i) er genomiske DNA-molekyler; eller (ii) er humane genomiske DNA-molekyler.
6. Fremgangsmåde ifølge krav 5, hvor det nævnte genomiske DNA underkastes fragmentering inden de på hinanden følgende trin med end-repairing, dA-tailing og adaptor-ligering af nævnte nukleinsyrer.
7. Fremgangsmåde ifølge et hvilket som helst af kravene 1-5, hvor nævnte nukleinsyrer er cellefrie DNA- (cfDNA) molekyler og ikke underkastes fragmentering inden de på hinanden følgende trin med end-repairing, dA-tailing og adaptor-ligering af nævnte nukleinsyrer.
8. Anvendelse af et sekventeringsbibliotek fremstillet ifølge fremgangsmåden ifølge et hvilket som helst af kravene 1-7 i en nukleinsyresekventeringsmetode.
9. Anvendelse ifølge krav 8, hvor sekventeringsmetoden er en næste generation sekventerings- (NGS) metode.
10. Anvendelse ifølge krav 8, hvor nævnte sekventeringsmetode er en massiv parallel sekventeringsmetode, og hvor eventuelt: (i) nævnte sekventering er massiv parallel sekventering under anvendelse af sekventering-ved-syntese med reversible farve-terminatorer; eller (ii) nævnte sekventering er massiv parallel sekvensering under anvendelse af sekventering-ved-ligering.
11. Anvendelse ifølge krav 8, hvor nævnte sekventering omfatter en amplifikation.
12. Anvendelse ifølge krav 8, hvor nævnte sekventering er enkelt-molekyle sekventering.
13. Fremgangsmåde ifølge et hvilket som helst af kravene 1-7 eller anvendelse ifølge et hvilket som helst af kravene 8-12, hvor prøven: (a) er en plasmaprøve afledt fra perifert blod der omfatter en blanding af cfDNA afledt fra normale celler og kræftceller; (b) er afledt fra en blanding af kræft- og ikke-kræftceller fra en biologisk væske valgt fra serum, sved, tårer, sputum, urin, væske i øret, lymfevæske, spyt, rygmarvsvæske, udskylninger, knoglemarvssuspension, vaginaludskillelse, transcervikal udskylning, hjernevæske, bughulevæske, mælk, sekreter fra luftvejene, tarmkanalen og urogenitalen, og leukafereseprøver; eller (c) er valgt fra vævsbiopsier, podninger eller smear-prøver.
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