IP Library Patent Application 13127669
Patent Application
App. No. 13/127,669

METHODS OF SAMPLE ENCODING FOR MULTIPLEX ANALYSIS OF SAMPLES BY SINGLE MOLECULE SEQUENCING

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Quick Facts
Patent No.
US None
App. No.
13/127,669
Abstract

The invention generally relates to methods for sequencing a plurality of nucleic acids from different samples. In certain embodiments, methods of the invention provide contacting a nucleic acid duplex including a primer nucleic acid hybridized to a template nucleic acid with a polymerase enzyme in the presence of a first detectably labeled nucleotide under conditions that permit the polymerase to add nucleotides to the primer in a template-dependent manner, in which a unique oligonucleotide sequence is attached to the template nucleic acid so that the template nucleic acid may be differentiated from other template nucleic acid molecules, detecting a signal from the incorporated labeled nucleotide, and sequentially repeating the contacting and detecting steps at least once, wherein sequential detection of incorporated labeled nucleotide determines the sequence of the nucleic acid.

Claims (37)

1 . A method for sequencing a nucleic acid, the method comprising:

contacting a nucleic acid duplex comprising a primer nucleic acid hybridized to a template nucleic acid with a polymerase enzyme in the presence of a first detectably labeled nucleotide under conditions that permit the polymerase to add nucleotides to the primer in a template-dependent manner, wherein a unique oligonucleotide sequence is attached to the template nucleic acid so that the template nucleic acid may be differentiated from other template nucleic acid molecules;

detecting a signal from the incorporated labeled nucleotide; and

sequentially repeating the contacting and detecting steps at least once, wherein sequential detection of incorporated labeled nucleotide determines the sequence of the nucleic acid.

2 . The method according to claim 1 , wherein prior to the contacting step, the method further comprises ligating the oligonucleotide sequence to the template molecule.

3 . The method according to claim 1 , wherein the oligonucleotide sequence further comprises a primer sequence.

4 . The method according to claim 1 , wherein the primer sequence is a polyA tail.

5 . The method according to claim 3 , wherein the oligonucleotide sequence comprises from about 5 nucleotides to about 15 nucleotides excluding the primer sequence.

6 . The method according to claim 1 , wherein the oligonucleotide sequence excludes a terminal thymine on both the 5′ and the 3′ end of the oligonucleotide.

7 . The method according to claim 1 , wherein the oligonucleotide sequence excludes any homopolymer region.

8 . The method according to claim 1 , wherein the oligonucleotide sequence further comprises at least one locked nucleic acid.

9 . The method according to claim 1 , wherein the duplex is attached to a substrate.

10 . The method according to claim 9 , wherein at least a portion of the duplexes are individually optically resolvable.

11 . The method according to claim 9 , wherein the duplex is directly attached to the substrate.

12 . The method according to claim 9 , wherein the duplex is indirectly attached to the substrate.

13 . The method according to claim 1 , wherein the detectable label is an optically detectable label.

14 . The method according to claim 13 , wherein the optically detectable label is a fluorescent label.

15 . A method for sequencing a plurality of nucleic acids from different samples, the method comprising:

contacting a plurality of nucleic acid duplexes comprising a primer nucleic acid hybridized to a template nucleic acid with a polymerase enzyme in the presence of a first detectably labeled nucleotide under conditions that permit the polymerase to add nucleotides to the primer in a template-dependent manner, wherein the template nucleic acids are provided from a plurality of samples, and a unique oligonucleotide sequence is attached to the template nucleic acids from each sample so that the template nucleic acids from the different samples may be differentiated from each other;

detecting a signal from the incorporated labeled nucleotide; and

sequentially repeating the contacting and detecting steps at least once, wherein sequential detection of incorporated labeled nucleotide determines the sequence of the plurality of nucleic acids.

16 . The method according to claim 15 , wherein the samples are obtained from different tissues or body fluids in a single subject.

17 . The method according to claim 15 , wherein the samples are obtained from different subjects.

18 . The method according to claim 15 , wherein the duplexes are attached to a substrate.

19 . The method according to claim 18 , wherein at least a portion of the duplexes are individually optically resolvable.

20 . A method for sequencing a plurality of nucleic acids from different samples, the method comprising:

obtaining template nucleic acids from a plurality of samples;

ligating the template nucleic acids from each sample with a unique oligonucleotide sequence so that the template nucleic acids from the different samples may be differentiated from each other;

pooling the template nucleic acid molecules from the plurality of samples;

hybridizing the pooled template nucleic acid molecules with a plurality of primers to form duplexes comprising a primer nucleic acid hybridized to a template nucleic acid;

contacting the plurality of nucleic acid duplexes with a polymerase enzyme in the presence of a first detectably labeled nucleotide under conditions that permit the polymerase to add nucleotides to the primer in a template-dependent manner;

detecting a signal from the incorporated labeled nucleotide; and

sequentially repeating the contacting and detecting steps at least once, wherein sequential detection of incorporated labeled nucleotide determines the sequence of the plurality of nucleic acids.

21 . The method according to claim 20 , wherein prior to the contacting step, the method further comprises attaching the duplexes to a substrate.

22 . The method according to claim 21 , wherein at least a portion of the duplexes are individually optically resolvable.

23 . The method according to claim 20 , wherein the samples are obtained from different tissues or body fluids in a single subject.

24 . The method according to claim 20 , wherein the samples are obtained from different subjects.

Assignments (8)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 10, 2016
From: CAUSEY, MARIE; STEINMANN, KATHLEEN
To: HELICOS BIOSCIENCES CORPORATION
Reel/Frame 040281/0221 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 28, 2013
From: HELICOS BIOSCIENCES CORPORATION
To: FLUIDIGM CORPORATION
Reel/Frame 030714/0546 →
LICENSE Recorded Jun 28, 2013
From: FLUIDIGM CORPORATION
To: PACIFIC BIOSCIENCES OF CALIFORNIA, INC.
Reel/Frame 030714/0598 →
LICENSE Recorded Jun 28, 2013
From: FLUIDIGM CORPORATION
To: SEQLL, LLC
Reel/Frame 030714/0633 →
LICENSE Recorded Jun 28, 2013
From: FLUIDIGM CORPORATION
To: ILLUMINA, INC.
Reel/Frame 030714/0783 →
LICENSE Recorded Jun 28, 2013
From: FLUIDIGM CORPORATION
To: COMPLETE GENOMICS, INC.
Reel/Frame 030714/0686 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 2, 2011
From: JOSEPH, ELAINE
To: HELICOS BIOSCIENCES CORPORATION
Reel/Frame 027319/0126 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 1, 2011
From: THOMPSON, JOHN F.
To: HELICOS BIOSCIENCES CORPORATION
Reel/Frame 027307/0094 →