Methods and compositions for efficient base calling in sequencing reactions

• US 8,617,811 B2
• Filed: 01/28/2009
• Issued: 12/31/2013
• Est. Priority Date: 01/28/2008
• Status: Active Grant

• Current Assignee: Complete Genomics Incorporated (BGI Genomics Co., Ltd.)
• Original Assignee: Complete Genomics Incorporated (BGI Genomics Co., Ltd.)
• Inventors: Drmanac, Radoje
• Primary Examiner(s): Lu, Frank
• Application Number:
  US12/361,507
• Publication Number:
  US 20090263802A1
• Time in Patent Office: 1,798 Days
• Field of Search: 435/6, 435/91.1, 435/91.2, 435/91.51, 435/183, 435/283.1, 435/287.1, 435/287.2, 436/94, 436/501, 536/23.1, 536/24.3, 536/24.33, 536/25.3, 536/25.32
• US Class Current: 435/6.1
• CPC Class Codes: C12Q 1/68 involving nucleic acids
• CPC Class Codes: C12Q 1/686 Polymerase chain reaction [PCR]
• CPC Class Codes: C12Q 1/6869 Methods for sequencing
• CPC Class Codes: C12Q 1/6874 involving nucleic acid arrays, e.g. sequencing by hybridisation
• CPC Class Codes: C12Q 1/6876 Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
• CPC Class Codes: C12Q 2565/102 Multiple non-interacting labels
• CPC Class Codes: C12Q 2565/1025 labels being on the same oligonucleotide
• CPC Class Codes: C12Q 2565/518 characterised by the immobilisation of the nucleic acid sample or target

Abstract

The present invention is directed to methods and compositions for acquiring nucleotide sequence information of target sequences. In particular, the present invention provides methods and compositions for improving the efficiency of sequencing reactions by using fewer labels to distinguish between nucleotides and by detecting nucleotides at multiple detection positions in a target sequence.

Claims

1. A method of identifying a first nucleotide at a first detection position of a target sequence of at least some of a plurality of immobilized polynucleotides, comprising:

a) providing a surface comprising said plurality of immobilized polynucleotides, each of said polynucleotides comprising one or more monomers, each of said one or more monomers comprising;

i) a first target domain of said target sequence;

ii) a first detection position in said first target domain;

iii) a first adapter adjacent to said first target domain, wherein said first adapter comprises a first anchor site and each of said plurality of immobilized polynucleotides comprises the same first anchor site;

b) providing a first sequencing set comprising first, second, third, and fourth probe sets;

wherein each of said probe sets comprises a pool of probes, wherein the probes in each of said pool of probes comprises a probe domain having a specific nucleotide at a first interrogation position of said probe domain, and degenerate or universal nucleotides at other positions of said probe domain,

and wherein;

i) the probes in the first probe set comprise

a first unique label;

ii) the probes in the second probe set comprise a second unique label;

iii) the probes in the third probe set comprise said first unique label and said second unique label or

some probes in the third probe set comprise said first unique label and some probes in the third probe set comprise said second unique label;

iv) the probes in the fourth probe set comprise no label or a third unique label, wherein said first unique label, said second unique label and said third unique label are different labels and are distinguishable;

c) hybridizing first anchor probes to said first anchor site of said plurality of immobilized polynucleotides, thereby producing hybridized first anchor probes;

d) applying said first, second, third, and fourth probe sets to said surface under a condition which favors probe hybridization only if perfect complementarity exists between said probe domain and said target sequence so that, for said at least some of said plurality of immobilized polynucleotides, a probe of the first, second, third or the fourth probe set hybridizes to said first target domain, and said specific nucleotide at said first interrogation position of said probe of the first, second, third or fourth probe set hybridizes to the first nucleotide of said first detection position of said first target domain, and one or more first hybridized probes are produced;

e) ligating said one or more first hybridized probes to one or more of said hybridized first anchor probes which are adjacent to said one or more first hybridized probes, thereby forming first ligation products;

f) identifying said first nucleotide at said first detection position of said target sequence of said at least some of said plurality of immobilized polynucleotides by detecting the presence or absence of said first unique label and/or said second unique label in the first ligation products.

2. The method according to claim 1 wherein the first unique label and the second unique label comprise different fluorophores.

3. The method according to claim 1, wherein said first unique label comprises a first fluorophore, and said second unique label comprises a second fluorophore.

4. The method according to claim 3, wherein said third probe set comprises a plurality of third probes with said first fluorophore and a plurality of said third probes with said second fluorophore.

5. The method according to claim 1 wherein said first unique label associated with the probes in the first probe set comprises a first fluorophore at a first intensity, said second unique label associated with the probes in the second probe set comprises said first fluorophore at a second intensity, and said first intensity and said second intensity are different and are distinguishable.

6. The method according to claim 5 wherein said probes in the fourth probe set comprise a third unique label, said third unique label comprises said first fluorophore at a third intensity, and said first intensity, said second intensity, and said third intensity are different and are distinguishable.

7. The method according to claim 5 wherein the first unique label and the second unique label comprise different numbers of molecules of said first fluorophore, resulting in differences in said first intensity and said second intensity of said first fluorophore.

8. The method according to claim 5 wherein differences in said first intensity and said second intensity of said first fluorophore are created by changing the number of the probes within each of said first, second, and third probe sets.

9. The method according to claim 1, wherein said method further comprises identifying a second nucleotide at a second detection position of said target sequence of said at least some of said plurality of immobilized polynucleotides, wherein each of said one or more monomers further comprises:

i) a second target domain of said target sequence, wherein said first target domain and said second target domain are located on different parts of said target sequence;

ii) a second detection position in said second target domain;

iii) a second adapter adjacent to said second target domain, wherein said second adaptor is the first adaptor or is a different adaptor, wherein said second adapter comprises a second anchor site and each of said plurality of immobilized polynucleotides comprises the same second anchor site;

and wherein said method further comprises;

f) providing a second sequencing set comprising fifth, sixth, seventh, and eight probe sets each of which probe sets comprises a second pool of probes, the probes in each of said second pool of probes comprises a probe domain having a specific nucleotide at a second interrogation position of a probe domain, and degenerate or universal nucleotides at other positions of said probe domain,

and wherein

i) the probes in the fifth probe set comprise

a fourth unique label;

ii) the probes in the sixth probe set comprise

a fifth unique label;

iii) the probes in the seventh probe set comprise

said fourth unique label and said fifth unique label, or some probes in the seventh probe set comprise said fourth unique label and some probes in the seventh probe set comprise said fifth unique label;

iv) the probes in the eighth probe set comprise

no label or a sixth unique label, wherein said fourth unique label, said fifth unique label and said sixth unique label are different labels and are distinguishable;

g) hybridizing second anchor probes to said second anchor site of said plurality of immobilized polynucleotides, thereby producing hybridized second anchor probes;

h) applying said fifth, sixth, seventh or eighth probe sets to said surface under a condition which favors probe hybridization only if perfect complementarity exists between said probe domain and said target sequence so that, for said at least some of said plurality of immobilized polynucleotides, a probe of the fifth, sixth, seventh or the eighth probe set hybridizes to said second target domain and said specific nucleotide at said second interrogation position of said probe of the fifth, sixth, seventh or eighth probe set hybridizes to the second nucleotide of said second detection position of said second target domain, and one or more second hybridized probes are produced;

i) ligating said one or more second hybridized probes to one or more of said hybridized second anchor probes which are adjacent to said one or more second hybridized probes, thereby forming second ligation products;

f) identifying said second nucleotide at said second detection position of said target sequence of said at least some of said plurality of immobilized polynucleotides by detecting the presence or absence of said fourth unique label and/or fifth unique label in the second ligation products.

10. The method according to claim 9 wherein the second adapter adjacent to said second target domain is the first adaptor.

11. The method according to claim 10 wherein, for each of said one or more monomers, said second target domain and the first target domain are contiguous in the target sequence.

12. The method according to claim 9, wherein said fourth unique label comprises a third fluorophore, and said fifth unique label comprises a fourth fluorophore which is different from the third fluorophore.

13. The method according to claim 12, wherein said seventh probe set comprises a plurality of probes with said third fluorophore and a plurality of probes with said fourth fluorophore.

14. The method according to claim 9 wherein said fourth unique label comprises a fluorophore at a fourth intensity, said fifth unique label comprises said fluorophore at a fifth intensity, said sixth unique label comprises said fluorophore at a sixth intensity and said fourth intensity, said fifth intensity, and said sixth intensity are different.

15. The method according to claim 14 wherein differences in said fourth intensity and said fifth intensity of said fluorophore are created by changing the number of the probes within each of said fifth, sixth, and seventh probe sets.

16. The method according to claim 9 wherein said probes in the seventh probe set comprise said fourth unique label and said fifth unique label.

17. The method according to claim 9 wherein at least one of the fourth unique label and the fifth unique label is a dissociable label.

18. The method according to claim 17 further comprising detecting the presence or absence of said dissociable label in one or more of the second ligation products, dissociating said dissociable label from the second ligation products, and detecting the fourth unique label or the fifth unique label remaining in the second ligation products after the dissociation.

19. The method according to claim 9 wherein said second anchor probes and said second sequencing set are applied simultaneously.

20. The method according to claim 1 wherein said probes in the third probe set comprise said first unique label and said second unique label.

21. The method according to claim 1 wherein at least one of the first unique label and the second unique label is a dissociable label.

22. The method according to claim 21 further comprising detecting the presence or absence of said dissociable label in one or more of the first ligation products, dissociating said dissociable label from the first ligation products, and detecting the first unique label or the second unique label remaining in the first ligation products after the dissociation.

23. The method according to claim 1 wherein said first anchor probes and said first sequencing set are applied simultaneously.

24. The method according to claim 1 wherein the probes in said fourth probe set comprise a third unique label.

25. The method according to claim 1 wherein the probes in said fourth probe set comprise no label.

26. The method according to claims 1 and 9 wherein the immobilized polynucleotides are immobilized concatemers.