IP Library Granted Patent US 10,208,356
Granted Patent B1
US 10,208,356 · App. 16/161,981 · Granted Feb 19, 2019

Massively parallel single cell analysis

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Quick Facts
Patent No.
US 10,208,356
App. No.
16/161,981
Granted
Feb 19, 2019
Kind
B1
Abstract

The disclosure provides for methods, compositions, and kits for multiplex nucleic acid analysis of single cells. The methods, compositions and systems may be used for massively parallel single cell sequencing. The methods, compositions and systems may be used to analyze thousands of cells concurrently. The thousands of cells may comprise a mixed population of cells (e.g., cells of different types or subtypes, different sizes).

Claims (34)

1. A composition comprising:

a single bead, wherein the bead comprises a plurality of oligonucleotides,

wherein each of the plurality of oligonucleotides comprises a cellular label sequence, a molecular label sequence, and a target-binding region, wherein the cellular label sequence of each of the plurality of oligonucleotides is the same, wherein the cellular label sequence comprises 4-300 nucleotides, wherein the molecular label sequence comprises 4-300 nucleotides, and at least 100 of the plurality of oligonucleotides comprise different molecular label sequences.

2. The composition of claim 1 , further comprising a single cell, or a lysate of a single cell.

3. The composition of claim 2 , wherein said plurality of oligonucleotides is capable of labeling individual occurrences of target molecules associated with said single cell.

4. The composition of claim 3 , wherein said plurality of oligonucleotides is capable of labeling the individual occurrences of said target molecules associated with said single cell via hybridization of the individual occurrences of said target molecules to the target-binding regions of said plurality of oligonucleotides.

5. The composition of claim 3 , wherein said target molecules comprise nucleic acid molecules.

6. The composition of claim 5 , wherein said plurality of oligonucleotides is capable of labeling the individual occurrences of said target molecules associated with said single cell via a nucleic acid extension reaction.

7. The composition of claim 6 , wherein the nucleic acid extension reaction comprises a reverse transcription reaction.

8. The composition of claim 6 , wherein the nucleic acid extension reaction is performed using a reverse transcriptase, a DNA polymerase, or a combination thereof.

9. The composition of claim 3 , wherein a target molecule of said target molecules comprises a messenger ribonucleic acid (mRNA) molecule.

10. The composition of claim 3 , wherein a target molecule of said target molecules comprises a deoxyribonucleic acid (DNA) molecule.

11. The composition of claim 3 , wherein a target molecule of said target molecules comprises a sample tag oligonucleotide.

12. The composition of claim 11 , wherein the sample tag oligonucleotide is 25-300 nucleotides in length.

13. The composition of claim 1 , wherein the molecular label sequence is 4-30 nucleotides in length.

14. The composition of claim 1 , wherein the cellular label sequence is 4-30 nucleotides in length.

15. The composition of claim 1 , wherein at least 10,000 of said plurality of oligonucleotides comprise different molecular label sequences.

16. The composition of claim 1 , wherein about 1,000,000 of said plurality of oligonucleotides comprise different molecular label sequences.

17. The composition of claim 3 , wherein a target molecule of said target molecules is associated with said single cell via a peptide.

18. The composition of claim 17 , wherein the peptide comprises an antibody.

19. The composition of claim 18 , wherein the peptide is capable of binding to said single cell.

20. The composition of claim 1 , comprising a peptide.

21. The composition of claim 20 , wherein the peptide comprises an antibody.

22. The composition of claim 20 , wherein the peptide is associated with a sample tag oligonucleotide.

23. The composition of claim 22 , wherein the plurality of oligonucleotides is capable of labeling the sample tag oligonucleotide.

24. The composition of claim 1 , wherein said plurality of oligonucleotides comprises at least 700,000 oligonucleotide.

25. The composition of claim 1 , wherein said plurality of oligonucleotides comprises about 1,000,000 oligonucleotide.

26. The composition of claim 1 , wherein said target-binding region comprises a sequence selected from the group consisting of an oligo-dT sequence, a gene-specific sequence, a target-specific sequence, a multimer sequence, a random multimer sequence, and a complement thereof.

27. The composition of claim 1 , wherein said single bead comprises silica gel, Wang resin, Merrifield resin, polydimethylsiloxane (PDMS), polystyrene, glass, controlled pore glass, polypropylene, agarose, gelatin, hydrogel, a paramagnetic material, ceramic, plastic, glass, methylstyrene, acrylic polymer, titanium, latex, Sephadex, Sepharose, cellulose, nylon, silicone, or a combination thereof.

28. The composition of claim 1 , wherein said single bead is a hydrogel bead, a magnetic bead, or a combination thereof.

29. A partition comprising:

a. a composition of claim 1 ; and

b. a single cell, or a lysate of a single cell.

30. The partition of claim 29 , wherein the partition is a well or a droplet.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 28, 2018
From: FAN, CHRISTINA; FODOR, STEPHEN P.A.; FU, GLENN; FACER, GEOFFREY RICHARD; WILHELMY, JULIE
To: CELLULAR RESEARCH, INC.
Reel/Frame 047871/0783 →
MERGER Recorded Dec 28, 2018
From: TUCSON ACQUISITION CORP.
To: CELLULAR RESEARCH, INC.
Reel/Frame 047871/0786 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 28, 2018
From: CELLULAR RESEARCH, INC.
To: BECTON, DICKINSON AND COMPANY
Reel/Frame 047871/0821 →
Cited By (22)
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