Nucleic acid analysis by joining barcoded polynucleotide probes

Patent metadata

Field	Value
Publication number	US-11118216-B2
Application number	US-201615758065-A
Country	US
Kind code	B2
Filing date	Nov 8, 2016
Priority date	Sep 8, 2015
Publication date	Sep 14, 2021
Grant date	Sep 14, 2021

Abstract

Disclosed are compositions, methods and kits for determining the presence, absence, amount, copy number, or other characteristics of one or more polynucleotide sequences in two or more samples and use thereof in genotyping, evaluation of copy number variation, expression analysis, determination of splice variants and fusion genes, and other genetic analyses.

First claim

The invention claimed is:

1. A method for analyzing one or more target polynucleotides in one or more samples, the method comprising the steps of:
(a) providing one or more samples, each sample comprising one or more target polynucleotides, each target polynucleotide comprising a first target sequence and a second target sequence;
(b) providing a plurality of first and second complementary probes comprising a first and second complementary probe for each target polynucleotide,
(i) each first complementary probe having two sequence portions that are complementary to a first target sequence of the target polynucleotide, and two sequence portions that are non-complementary to the first target sequence, wherein the non-complementary portions include an interrogation site bar code sequence and a universal sequence, and wherein a first complementary sequence portion is at 5′ of the interrogation site bar code and a second complementary sequence portion is at 3′ of the interrogation site bar code, wherein the universal sequence is 5′ to the first complementary sequence portion; and
(ii) each second complementary probe having a sequence portion that is complementary to a second target sequence of the target polynucleotide and an immediately adjacent sequence portion that is non-complementary to said second target sequence;

(c) incubating said plurality of first and second complementary probes with each sample under hybridization conditions such that first and second complementary probes hybridize to their complementary target polynucleotide in a sample to form a hybridization complex;
(d) joining first and second complementary probes that are hybridized to first and second target sequences of a target polynucleotide in a sample to form a product polynucleotide; and
(e) determining the presence, absence, amount or copy number of each target polynucleotide in said one or more samples by analyzing product polynucleotides or the complements thereof.

2. The method according to claim 1 , wherein the immediately adjacent sequence portion of said second complementary probe comprises a universal sequence.

3. The method according to claim 2 , wherein the universal sequence of said second complementary probe comprises a universal primer sequence that is complementary to a primer sequence which can be used to add one or more of (i) a sample index, (ii) an additional sequence, (iii) an additional sequence for sequence data generation or another form of detection, and (iv) another moiety.

4. The method according to claim 3 wherein the universal primer sequence includes a PCR primer sequence and/or a primer sequence to add an additional sequence for sequence data generation or another form of detection.

5. The method according to claim 3 , wherein the additional sequence for sequence data generation or another form of detection is an adapter for next generation sequencing.

6. The method according to claim 3 , wherein the additional sequence for sequence data generation or another form of detection is a capture sequence, optionally wherein the capture sequence is for capture on a solid support.

7. The method according to claim 1 , wherein the universal sequence of said first complementary probe comprises a universal primer sequence that is complementary to a priming sequence which can be used to add one or more of (i) a sample index, (ii) an additional sequence, (iii) an additional sequence for sequence data generation or another form of detection, and (iv) another moiety.

8. The method according to claim 7 wherein the universal primer sequence includes a PCR primer sequence and/or a primer sequence to add an additional sequence for sequence data generation or another form of detection.

9. The method according to claim 7 , wherein the additional sequence for sequence data generation or another form of detection is an adapter for next generation sequencing.

10. The method according to claim 7 , wherein the additional sequence for sequence data generation or another form of detection is a capture sequence, optionally wherein the capture sequence is for capture on a solid support.

11. The method according to claim 1 , wherein the method is solution-based.

12. The method according to claim 1 , wherein the 3′ end of the first complementary probe is complementary to one form of a single nucleotide polymorphism (SNP) or other genetic variation.

13. The method according to claim 1 , wherein the method is for use in genotyping, wherein the method comprises providing one or more variants of the first complementary probe, wherein the variants differ in the identity of the nucleotide or nucleotides at the 3′ end of the first complementary probe, and wherein said determining comprises quantifying the relative frequencies of product polynucleotides or complements thereof comprising the sequences of the one or more variants of the first complementary probe compared to the sequences of the other variants of said first complementary probe and correlating said frequencies with a genotype.

14. The method according to claim 1 , wherein the method is for use in determining the copy number variation of a target polynucleotide, and wherein said determining comprises comparing the amount of signal produced for a product polynucleotide or the complement thereof to a known reference or to the amount of signal produced by another product polynucleotide or the complement thereof.

15. The method according to claim 1 , wherein the method is for use in expression analysis in determining presence of a target polynucleotide, wherein the target polynucleotide is an RNA transcript, and wherein said determining comprises comparing the amount of signal produced for a product polynucleotide or the complement thereof to a known reference or to the amount of signal produced by another product polynucleotide or the complement thereof.

16. The method according to claim 1 further comprising pooling product polynucleotides formed from the samples.

17. The method according to claim 16 , further comprising enriching said product polynucleotides prior to the pooling step.

18. The method according to claim 17 , wherein said enriching comprises, (a) providing a set of PCR priming sequences comprising a first primer that is associated with a priming sequence on the first complementary probe, and a second primer that is complementary to a PCR priming sequence on the second complementary probe, and (b) amplifying the product polynucleotide.

19. The method according to claim 1 , wherein in (a) two or more samples are provided.

Assignees

• Affymetrix Inc

Inventors

• Koshinsky Heather
• Curry John D
• O'Callahan Robert
• Mccoy Adam
• Fitzpatrick Daniel
• Dickinson Philip H
• Schweitzer Anthony C

Classifications

• C12Q1/6827 Primary

  for detection of mutation or polymorphism · CPC title

• C12Q1/6862

  Ligase chain reaction [LCR] · CPC title

• C12Q1/686

  Polymerase chain reaction [PCR] · CPC title

• C12Q2525/161

  incorporating target specific and non-target specific sites · CPC title

• C12Q2525/204

  specific length of the oligonucleotides · CPC title