Compositions and methods for nucleic acid sequencing
Compositions and methods for nucleic acid sequencing include template constructs that comprise double stranded portions in a partially or completely contiguous constructs, to provide for redundant sequence determination through one or both of sequencing sense and antisense strands, and iteratively sequencing the entire construct multiple times. Additional sequence components are also optionally included within such template constructs. Methods are also provided for the use and preparation of these constructs as well as sequencing compositions for their application.
1. A method of determining a sequence of a double-stranded nucleic acid sample, comprising:
(a) locking the forward strand and the reverse strand of the nucleic acid sample together thereby forming a single-stranded circular pair-locked molecule, wherein the forward strand and the reverse strand are complementary to each other and both ends of the forward strand and both ends of the reverse strand are joined by linking oligonucleotides;
(b) performing single molecule sequencing of the circular pair-locked molecule thereby obtaining sequence data of the circular pair-locked molecule, wherein sequence data comprises sequences of the forward strand and the reverse strand of the circular pair-locked molecule; and
(c) determining the sequence of the double-stranded nucleic acid sample by comparing the sequences of the forward strand and the reverse strand of the circular pair-locked molecule.
2. The method of claim 1 , wherein said locking the forward strand and the reverse strand of the nucleic acid sample together comprises joining 5′ end of the forward strand to 3′ end of the reverse strand and joining 3′ end of the forward strand to 5′ end of the reverse strand by said linking oligonucleotides, and wherein said linking oligonucleotides are two hairpin adaptors.
3. The method of claim 2 , wherein said obtaining sequence data comprises annealing a primer complementary to at least part of at least one of the hairpin adaptors and extending the primer.
4. The method of claim 1 , wherein said single molecule sequencing comprises sequencing by synthesis technology.
5. The method of claim 1 , wherein said single molecule sequencing is performed in the presence of an electrochemical system comprising a nanopore sensor.
6. A method of determining a sequence of a double-stranded nucleic acid sample, comprising:
(a) linking the forward strand and the reverse strand of the nucleic acid sample together thereby forming a single-stranded circular template molecule, wherein the forward strand and the reverse strand are complementary to each other and both ends of the forward strand and both ends of the reverse strand are joined by linking oligonucleotides;
(b) performing a single molecule sequencing of the circular template molecule thereby obtaining sequence data of the circular template molecule, wherein sequence data comprises sequences of the forward strand and the reverse strand of the circular template molecule; and
(c) determining the sequence of the double-stranded nucleic acid sample by comparing the sequences of the forward strand and the reverse strand of the circular template molecule.
7. The method of claim 6 , wherein the linking oligonucleotides are two hairpin adaptors and said linking the forward strand and the reverse strand of the nucleic acid sample together comprises joining 5′ end of the forward strand to 3′ end of the reverse strand and joining 3′ end of the forward strand to 5′ end of the reverse strand by said two hairpin adaptors.
8. The method of claim 7 , wherein said obtaining sequence data comprises annealing a primer complementary to at least part of at least one of the hairpin adaptors and extending the primer.
9. The method of claim 6 , wherein said single molecule sequencing comprises sequencing by synthesis technology.
10. The method of claim 6 , wherein said single molecule sequencing is performed in the presence of an electrochemical system comprising a nanopore sensor.