Short cycle methods for sequencing polynucleotides
View Patent ↗The invention provides methods for sequencing a polynucleotide comprising stopping an extension cycle in a sequence by synthesis reaction before the reaction has run to near or fill completion.
1. A method for sequencing a nucleic acid template, the method comprising:
conducting a sequencing-by-synthesis reaction on a template nucleic acid/primer duplex, wherein the reaction is controlled such that on average no more than three nucleotides are added to the primer per incorporation cycle; and
determining a sequence of the template based upon order of incorporation of the nucleotides to the primer over multiple incorporation cycles, wherein the nucleotides are not chain terminating nucleotides, and wherein the template/primer duplexes are individually optically resolvable.
2. The method of claim 1 , wherein the reaction conditions are controlled such that on average only one nucleotide is added to the primer.
3. The method of claim 1 , wherein the reaction is controlled by modifying polymerase activity.
4. The method of claim 1 , wherein the reaction is controlled by the addition of cofactors.
5. The method of claim 1 , wherein the reaction is controlled by a label on the nucleotide(s).
6. The method of claim 1 , wherein the sequencing reaction is conducted using a modified polymerase.
7. The method of claim 1 , wherein the reaction is controlled by temperature.
8. The method of claim 1 , wherein the determining comprises optically identifying the incorporated nucleotide(s).
9. The method of claim 8 , wherein the optically identifying employs fluorescence resonance energy transfer (FRET).
10. The method of claim 9 , wherein the FRET donor attaches to a polymerase used in the sequencing reaction.
11. The method of claim 9 , wherein a DNA-binding protein is used to allow FRET.
12. The method of claim 1 , wherein the nucleotide comprises an optically detectable label.
13. The method of claim 1 , wherein the nucleotide(s) are a natural or non-natural nucleotide chosen from a nucleotide analogue and a modified nucleotide.
14. The method of claim 1 , wherein the nucleotide comprises a label connected to the nucleotide through a linker, and the reaction is controlled by the length or type of linker connecting the nucleotide and the label.
15. The method of claim 1 , wherein nucleotide comprises an optical label and the optical label is a fluorescent label which is linked by a cleavable linker to the deoxyribose of the nucleotide(s).
16. The method according to claim 1 , wherein the reaction is controlled by exposure time of the nucleotide to the duplex.
17. The method according to claim 1 , wherein the nucleotide comprises a label and the reaction is controlled by the type of label or where the label is attached to the nucleotide.
18. The method according to claim 1 , wherein the nucleotide comprises a blocker and the reaction is controlled by the blocker.
19. The method according to claim 1 , wherein the duplexes are attached to a solid support.
20. A method for sequencing a nucleic acid template, the method comprising:
conducting a sequencing-by-synthesis reaction on a template nucleic acid/primer duplex, wherein the reaction is controlled such that on average no more than one nucleotide is added to the primer per incorporation cycle; and
determining a sequence of the template based upon order of incorporation of the nucleotides to the primer over multiple incorporation cycles, wherein the nucleotides are not chain terminating nucleotides, and wherein the template/primer duplexes are individually optically resolvable.