COMPOSITIONS AND METHODS FOR REPRESENTATIONAL SELECTION OF NUCLEIC ACIDS FROM COMPLEX MIXTURES USING HYBRIDIZATION

• US 20150065387A1
• Filed: 11/07/2014
• Published: 03/05/2015
• Est. Priority Date: 10/10/2006
• Status: Active Grant

• Current Assignee: Illumina Incorporated
• Original Assignee: Illumina Incorporated
• Inventors: Stuelpnagel, John R., Barker, David L., Velarde, Jorge Jr., Barnard, Steven M., Graige, Michael
• Granted Patent: US 9,139,826 B2
• Time in Patent Office: Days
• US Class Current: 506/9
• CPC Class Codes: C12N 15/1072 Differential gene expression library synthesis, e.g. subtracted libraries, differential screening
• CPC Class Codes: C12Q 1/6837 using probe arrays or probe chips C12Q1/6874 takes precedence
• CPC Class Codes: C12Q 2565/515 characterised by the interaction between or sequential use of two or more arrays

Abstract

The invention provides a method of selecting a representational sample of nucleic acid sequences from a complex mixture. The method includes: (a) contacting a complex mixture of nucleic acids under conditions sufficient for hybridization with a population of capture probes complementary to one or more nucleic acids comprising a predetermined portion of the sequence collectively present in the complex mixture to form hybridization complexes of the one or more nucleic acids with the population of probes, the population of capture probes being attached to a solid support, and (b) removing unhybridized nucleic acids to select a representational sample of nucleic acids having a complexity of less than 10% but more than 0.001% of the complex mixture, wherein the representational sample comprises a nucleic acid copy having a proportion of each sequence in the copy relative to all other sequences in the copy substantially the same as the proportions of the sequences in the predetermined portion of one or more nucleic acids within the complex mixture. A method of selecting a representational sample of genomic sequences from a complete genome also is provided. The invention further provides a nucleic acid population that includes a representational sample having a complexity of less than 10% but more than 0.001% of a complex mixture, the representational sample comprising a nucleic acid copy having a proportion of each sequence in the copy relative to all other sequences in the copy substantially the same as the proportions of sequences in a predetermined portion of a sequence collectively present in one or more nucleic acids within the complex mixture.

Claims

1-17. -17. (canceled)

18. A method of selecting a representational sample of nucleic acid sequences from a mixture of nucleic acids, comprising:

(a) providing a mixture of nucleic acids;

(b) providing a population of solid support-attached capture probes, said population comprising nucleic acids complementary to nucleic acids comprising a predetermined portion of the nucleic acid sequences collectively present in said mixture of nucleic acids;

(c) contacting said mixture of nucleic acids with said population of solid support-attached capture probes under conditions sufficient for hybridization of said nucleic acids with said capture probes, wherein the capture probes are randomly located on the solid support;

(d) removing unhybridized nucleic acids from the solid support to separate desired sequences from undesired sequences within the mixture;

thereby selecting a representational sample of nucleic acids, wherein the proportion of each sequence in said representational sample relative to all other sequences in said representational sample is substantially the same as the proportions of the sequences in said mixture;

(e) amplifying the nucleic acids in the representational sample on the solid support to generate an amplified representational sample; and

(f) performing a sequence analysis of the amplified representational sample.

19. The method of claim 18, wherein the mixture of nucleic acids comprises genomic DNA sequence having a complexity of at least 1.7 Gbp.

20. The method of claim 18, wherein the mixture of nucleic acids comprises amplified DNA sequence.

21. The method of claim 18, wherein a representational sample has a complexity of at least 0.001% and at most 49% of said mixture.

22. The method of claim 18, wherein step (e) comprises maintaining separation of sequences by attachment to identifiable locations on the solid support.

23. The method of claim 18, wherein performing a sequence analysis comprises SBS.

24. The method of claim 18, wherein performing a sequence analysis comprises sequencing by ligation.

25. The method of claim 18, wherein performing a sequence analysis comprises pyrosequencing.

26. The method of claim 18, wherein performing a sequence analysis comprises hybridizing a primer to a nucleic acid in the amplified representational sample and monitoring the extension of the primer by a polymerase.

27. The method of claim 18, wherein said solid support comprises microspheres.

28. The method of claim 18, wherein said solid support comprises a planar surface.

30. The method of claim 18, wherein said population of capture probes comprise an amount in molar excess compared to complementary sequences within said predetermined portion of nucleic acids.

31. The method of claim 19, wherein said population of capture probes comprise sequences having complementarity to both strands of said genomic DNA.

32. A method of analyzing a mixture of nucleic acids comprising:

(a) providing a mixture of nucleic acids comprising amplified DNA sequence;

(b) providing a population of solid support-attached capture probes, said population comprising nucleic acids complementary to nucleic acids comprising a predetermined portion of the nucleic acid sequences collectively present in said mixture;

(c) contacting said mixture of nucleic acids with said population of solid support-attached capture probes under conditions sufficient for hybridization of said nucleic acids with said capture probes, wherein the capture probes are randomly located on the solid support,

(d) removing unhybridized nucleic acids from the solid support to separate desired sequences from undesired sequences within the mixture;

thereby selecting a representational sample of nucleic acids, wherein the proportion of each sequence in said representational sample relative to all other sequences in said representational sample is substantially the same as the proportions of the sequences in said mixture;

(e) amplifying the nucleic acids in the representational sample on the solid support to generate an amplified representational sample; and

(f) detecting individual nucleic acids in said amplified representational sample to determine a sequence characteristic of said predetermined portion of the nucleic acid sequences collectively present in said mixture.

33. The method of claim 32, wherein said sequence characteristic comprises the nucleotide sequence for said predetermined portion of the nucleic acid sequences collectively present in said mixture.

34. The method of claim 32, wherein said sequence characteristic comprises the copy number for sequences in said predetermined portion of the nucleic acid sequences collectively present in said mixture.

35. The method of claim 32, wherein said sequence characteristic comprises loss of heterozygosity in said predetermined portion of the nucleic acid sequences collectively present in said mixture.

36. The method of claim 32, wherein said sequence characteristic comprises the genotype of said predetermined portion of the nucleic acid sequences collectively present in said mixture.

37. The method of claim 32, wherein said sequence characteristic comprises the methylation status of said predetermined portion of the nucleic acid sequences collectively present in said mixture.