Tandem sequencing top and bottom strands of double stranded nucleic acid using arrays configured for single molecule detection

• US 9,605,311 B2
• Filed: 07/10/2014
• Issued: 03/28/2017
• Est. Priority Date: 10/22/2008
• Status: Active Grant

• Current Assignee: Illumina Incorporated
• Original Assignee: Illumina Incorporated
• Inventors: Kester, Henri A.
• Primary Examiner(s): Wilder, Cynthia B
• Application Number:
  US14/327,892
• Publication Number:
  US 20150011408A1
• Time in Patent Office: 992 Days
• Field of Search: 435/91.2
• US Class Current: 1/1
• CPC Class Codes: C12Q 1/6855 Ligating adaptors
• CPC Class Codes: C12Q 1/6858 Allele-specific amplification
• 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 2523/125 Bisulfite(s)
• CPC Class Codes: C12Q 2525/117 incorporating modified base
• CPC Class Codes: C12Q 2525/125 incorporating agents resulting in resistance to degradation
• CPC Class Codes: C12Q 2525/191 incorporating an adaptor
• CPC Class Codes: C12Q 2525/301 Hairpin oligonucleotides
• CPC Class Codes: C12Q 2535/119 Double strand sequencing
• CPC Class Codes: C12Q 2600/156 Polymorphic or mutational markers

Abstract

The present invention relates to compositions, methods and systems for analyzing the methylation state of nucleic acids. Some embodiments relate to a compositions, methods and systems for analyzing the methylation state of DNA with a gene array.

Claims

1. A method of determining the sequence of a plurality of nucleic acid pairs, said method comprising:

a) providing a sample comprising a plurality of double-stranded template nucleic acids having a template strand and a complementary strand;

b) providing a solid support having a plurality of sites configured for single-molecule detection;

c) for each of a plurality of template nucleic acids, linking the template strand and complementary strand by ligating a looped oligonucleotide to the double-stranded template nucleic acid to form a plurality of nucleic acid pairs comprising a looped structure that forms a physical tether between the template strand and the complementary strand, each nucleic acid pair comprising a free 3′

end and a free 5′

end;

d) coupling the different nucleic acid pairs to the sites of the solid support, thereby spatially resolving the different pairs from each other; and

e) determining the nucleotide sequence of the nucleic acid pairs on the solid support, wherein single molecules are detected individually, and wherein the template strand and the complementary strand remain physically tethered by the looped structure.

2. The method of claim 1, wherein step e) comprises a sequencing technique wherein bases are removed from a strand on the solid support.

3. The method of claim 1, wherein step e) comprises a sequencing technique wherein bases are successively added to a free 3′

hydroxyl group.

4. The method of claim 1, wherein step e) begins from the 3′

end of the nucleic acid pair.

5. The method of claim 1, wherein the solid support comprises a material selected from the group consisting of:

plastic, ceramic, glass, polystyrene, methylstyrene, acrylic polymers, paramagnetic materials, thoria sol, carbon graphite, titanium dioxide, sepharose, cellulose, nylon, cross-linked micelles and teflon.

6. The method of claim 1, wherein the sequence of the nucleic acid pair forms an imperfect inverted repeat.

7. The method of claim 1, wherein the free 3′

end comprises a 3′

adapter sequence.

8. The method of claim 1, wherein the free 5′

end comprises a 5′

adapter sequence.

9. The method of claim 7, wherein the 3′

adapter sequence comprises a sequence complementary to a capture probe.

10. The method of claim 8, wherein the 5′

adapter sequence comprises a sequence complementary to a capture probe.

11. The method of claim 1, wherein the physical tether is a covalent linkage between the template strand and the complementary strand.