IP Library Granted Patent US 10,240,197
Granted Patent B1
US 10,240,197 · App. 16/194,047 · Granted Mar 26, 2019

Methods for analyzing nucleic acids from single cells

Inventors: Sydney Brenner (Ely, GB); Gi Mikawa (Great Shelford, GB); Robert Osborne (Great Chesterford, GB); Andrew Slatter (London, GB)
Assignee: 10X GENOMICS, INC.
C12Q1/6874C12N15/1065C12Q1/686C12Q1/6806C12Q1/6855
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,240,197
App. No.
16/194,047
Granted
Mar 26, 2019
Kind
B1
Abstract

Aspects of the present invention include analyzing nucleic acids from single cells using methods that include using tagged polynucleotides containing multiplex identifier sequences.

Claims (33)

1. A method of counting nucleic acids in a sample, the method comprising:

(a) providing a sample comprising a plurality of cells, wherein a cell of the plurality of cells comprises a plurality of sample polynucleotides;

(b) generating a plurality of tagged polynucleotides from the plurality of sample polynucleotides of said cell and a plurality of oligonucleotide tags, wherein a tagged polynucleotide of the plurality of tagged polynucleotides comprises:

(i) a sample sequence from a sample polynucleotide of the plurality of sample polynucleotides;

(ii) a first tag sequence distinguishing said sample polynucleotide from sample polynucleotides from other cells; and

(iii) a second tag sequence distinguishing said sample polynucleotide from other sample polynucleotides from said cell;

(c) sequencing the tagged polynucleotide to determine the sample sequence, the first tag sequence, and the second tag sequence; and

(d) using the first tag sequence and the second tag sequence to count a number of sample polynucleotides in said plurality of sample polynucleotides of said cell.

2. The method of claim 1 , wherein the method further comprises amplifying the plurality of tagged polynucleotides prior to the sequencing step (c).

3. The method of claim 1 , wherein the plurality of sample polynucleotides is selected from DNA and RNA.

4. The method of claim 1 , wherein the plurality of sample polynucleotides comprises mRNA.

5. The method of claim 1 , wherein the plurality of tagged polynucleotides is generated through at least one ligation reaction.

6. The method of claim 1 , wherein an oligonucleotide tag of said plurality of oligonucleotide tags comprises said first tag sequence and said second tag sequence.

7. The method of claim 1 , wherein an oligonucleotide tag of said plurality of oligonucleotide tags comprises a sequence that is configured to hybridize to said sample polynucleotide.

8. The method of claim 1 , wherein the plurality of tagged polynucleotides is generated by (i) hybridizing an oligonucleotide tag of said plurality of oligonucleotide tags to said sample polynucleotide and (ii) extending said oligonucleotide tag or said sample polynucleotide or both.

9. The method of claim 1 , wherein the plurality of tagged polynucleotides is generated through at least one linear amplification reaction.

10. The method of claim 1 , wherein the plurality of tagged polynucleotides is generated through at least one reverse transcription reaction.

11. The method of claim 1 , wherein the plurality of tagged polynucleotides is generated through at least one polymerase chain reaction (PCR).

12. The method of claim 1 , wherein substantially every sample polynucleotide of said plurality of sample polynucleotides is associated with the same first tag sequence.

13. The method of claim 1 , wherein at least 90 percent of said plurality of sample polynucleotides is associated with a unique second tag sequence.

14. The method of claim 1 , wherein at least 95 percent of said plurality of sample polynucleotides is associated with a unique second tag sequence.

15. The method of claim 1 , wherein at least 99 percent of said plurality of sample polynucleotides is associated with a unique second tag sequence.

16. The method of claim 1 , wherein substantially every sample polynucleotide of said plurality of sample polynucleotides is associated with a unique second tag sequence.

17. The method of claim 1 , wherein the number of different second tag sequences is larger than the number of sample polynucleotides.

18. The method of claim 17 , wherein the number of different second tag sequences is at least ten times the number of sample polynucleotides.

19. The method of claim 18 , wherein the number of different second tag sequences is at least one hundred times the number of sample polynucleotides.

20. The method of claim 1 , wherein said plurality of sample polynucleotides are randomly associated with said plurality of oligonucleotide tags to generate said plurality of tagged polynucleotides.

21. The method of claim 1 , wherein step (c) comprises hybridizing said tagged polynucleotide to a solid support.

22. The method of claim 20 , wherein said solid support is a bead.

23. The method of claim 1 , wherein step (d) comprises using said first tag sequence to distinguish (i) the number of sample polynucleotides having said sample sequence from said cell from (ii) the number of sample polynucleotides having said sample sequence from other cells.

24. The method of claim 1 , wherein step (d) comprises determining the number of different second tag sequences associated with said sample sequence, thereby estimating the number of sample polynucleotides having said sample sequence from said cell.

25. The method of claim 1 , wherein said plurality of sample polynucleotides comprises substantially all mRNA molecules of said cell.

26. The method of claim 1 , wherein said plurality of sample polynucleotides comprises a subset of polynucleotides of said cell having the same sequence.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 26, 2018
From: BRENNER, SYDNEY; MIKAWA, GI; OSBORNE, ROBERT; SLATTER, ANDREW
To: POPULATION GENETICS TECHNOLOGIES LTD.
Reel/Frame 047579/0304 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 26, 2018
From: POPULATION GENETICS TECHNOLOGIES LTD.
To: 10X GENOMICS, INC.
Reel/Frame 047579/0515 →
Continuity (9)
Continuation 15677957 · Aug 15, 2017
Continuation 14792094 · Jul 6, 2015
Continuation 14172694 · Feb 4, 2014
Continuation 14021790 · Sep 9, 2013
Continuation 13859450 · Apr 9, 2013
Continuation 13622872 · Sep 19, 2012
Continuation 13387343
Provisional Application 61288792 · Dec 21, 2009
Provisional Application 61235595 · Aug 20, 2009
Cited By (28)
US 12,195,786 US 12,227,793 US 12,234,501 US 12,241,059 US 12,247,247 US 12,247,248 US 12,252,730 US 12,252,731 US 12,252,733 US 12,252,734 US 12,252,735 US 12,252,736 US 12,252,737 US 12,305,219 US 12,305,220 US 12,305,221 US 12,371,733 US 12,371,734 US 12,428,671 US 12,428,685 US 12,467,076 US 12,480,115 US 12,534,721 US 12,612,666 US 12,655,471 US 12,663,345 US 12,680,138 US 12,691,452