IP Library Granted Patent US 10,266,892
Granted Patent B2
US 10,266,892 · App. 16/007,969 · Granted Apr 23, 2019

Systems and methods for genetic and biological analysis

Inventors: Hesaam Esfandyarpour (Redwood City, CA); Kosar Baghbani Parizi (Redwood City, CA); Mark F. Oldham (Emerald Hills, CA); Eric S. Nordman (Palo Alto, CA); Richard T. Reel (Hayward, CA); Susanne Baumhueter (Redwood City, CA); Cheryl Heiner (La Honda, CA); Frank Lee (Irvine, CA)
Assignee: GENAPSYS, INC.
C12Q1/6874G01N27/327G01N33/5438G01N33/54313
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Quick Facts
Patent No.
US 10,266,892
App. No.
16/007,969
Granted
Apr 23, 2019
Kind
B2
Abstract

The invention relate to systems and methods for sequencing polynucleotides, as well as detecting reactions and binding events involving other biological molecules. The systems and methods may employ chamber-free devices and nanosensors to detect or characterize such reactions in high-throughput. Because the system in many embodiments is reusable, the system can be subject to more sophisticated and improved engineering, as compared to single use devices.

Claims (35)

1. A system for nucleic acid sequencing, comprising:

an array comprising a plurality of features in optical communication with a plurality of optical sensors, wherein said array is integrated with said plurality of optical sensors, wherein, during use, a feature of said plurality of features retains or immobilizes a plurality of nucleic acid molecules having sequences that are substantially identical to a nucleic acid sequence of a template nucleic acid molecule, and wherein an optical sensor of said plurality of optical sensors is in optical communication with said feature; and

one or more computer processors operatively coupled to said array, wherein said one or more computer processors are programmed to (i) bring said plurality of nucleic acid molecules in contact with nucleic acid bases in the presence of polymerizing enzymes under conditions sufficient to incorporate said nucleic acid bases into growing strands complementary to said plurality of nucleic acid molecules, wherein said plurality of nucleic acid molecules is brought in contact with said nucleic acid bases without applying an electric field to confine or isolate said nucleic acid bases within said feature, (ii) use said optical sensor to detect one or more signals indicative of said nucleic acid bases incorporated into said growing strands, and (iii) use said one or more signals detected in (ii) to identify said nucleic acid bases, to thereby generate a sequence corresponding to said nucleic acid sequence of said template nucleic acid molecule.

2. The system of claim 1 , wherein said plurality of features is a plurality of wells.

3. The system of claim 1 , wherein said plurality of optical sensors are complementary metal-oxide semiconductor (CMOS) sensors.

4. The system of claim 1 , wherein said feature comprises a polymer that is configured to reduce a migration rate of said nucleic acid bases or said plurality of nucleic acid molecules.

5. The system of claim 1 , wherein said plurality of features is in fluid communication with a flow cell, which flow cell is configured to direct said nucleic acid bases to said feature comprising said plurality of nucleic acid molecules.

6. The system claim 1 , wherein, during use, at least a portion of said plurality of nucleic acid molecules is within a Debye layer of a surface of said feature.

7. The system of claim 6 , wherein during use, said one or more signals are indicative of a change in charge or conductivity within said Debye layer.

8. The system of claim 1 , wherein said array and said plurality of optical sensors are part of a chip.

9. The system of claim 1 , wherein said plurality of features is configured to retain said plurality of nucleic acid molecules.

10. The system of claim 1 , wherein said plurality of features includes capture sequences that are configured to immobilize said plurality of nucleic acid molecules.

11. A system for nucleic acid sequencing, comprising:

an array comprising a plurality of features in optical communication with a plurality of optical sensors, wherein said array is integrated with said plurality of optical sensors, wherein during use said plurality of features retains or immobilizes a plurality of nucleic acid molecules, wherein a feature of said plurality of features is configured to contain a nucleic acid molecule of said plurality of nucleic acid molecules, and wherein an optical sensor of said plurality of optical sensors is in optical communication with said feature; and

one or more computer processors operatively coupled to said array, wherein said one or more computer processors are programmed to (i) bring said nucleic acid molecule in contact with nucleic acid bases in the presence of a polymerizing enzyme under conditions sufficient to incorporate at least one of said nucleic acid bases into a growing strand complementary to said nucleic acid molecule, (ii) use said optical sensor to detect one or more signals indicative of said at least one of said nucleic acid bases incorporated into said growing strand, (iii) use said one or more signals detected in (ii) to identify said at least one of said nucleic acid bases, and (iv) monitor and correct for phase error introduced during incorporation of said at least one of said nucleic acid bases into said growing strand, to thereby generate a sequence of said nucleic acid molecule.

12. The system of claim 11 , wherein said plurality of features is a plurality of wells.

13. The system of claim 11 , wherein said plurality of optical sensors are complementary metal-oxide semiconductor (CMOS) sensors.

14. The system of claim 11 , wherein said feature comprises a polymer that is configured to reduce a migration rate of said nucleic acid bases or said nucleic acid molecule.

15. The system of claim 11 , wherein said plurality of features is in fluid communication with a flow cell, which flow cell is configured to direct said nucleic acid bases to said feature comprising said nucleic acid molecule.

16. The system of claim 11 , wherein, during use, said nucleic acid molecule is within a Debye layer of a surface of said feature.

17. The system of claim 16 , wherein, during use, said one or more signals are indicative of a change in charge or conductivity within said Debye layer.

18. The system of claim 11 , wherein said array and plurality of optical sensors are part of a chip.

19. The system of claim 11 , wherein said plurality of features is configured to retain said plurality of nucleic acid molecules.

20. The system of claim 11 , wherein said plurality of features includes capture sequences that are configured to immobilize said plurality of nucleic acid molecules.

21. The system of claim 1 , wherein said optical sensor detects said one or more signals from said nucleic acid bases incorporated into said growing strands.

22. The system of claim 11 , wherein said optical sensor detects said one or more signals from said nucleic acid bases incorporated into said growing strands.

23. The system of claim 1 , further comprising a fluidics interface configured to bring said nucleic acid molecule in contact with said nucleic acid bases.

24. The system of claim 11 , further comprising a fluidics interface configured to bring said nucleic acid molecule in contact with said nucleic acid bases.

25. The system of claim 23 , wherein said fluidics interface and said one or more computer processors are integrated within said system.

26. The system of claim 24 , wherein said fluidics interface and said one or more computer processors are integrated within said system.

27. The system of claim 11 , wherein said one or more computer processors are programmed to monitor and correct for phase error at a position along said growing strand during incorporation of said at least one of said nucleic acid bases into said growing strand.

28. The system of claim 1 , wherein said one or more computer processors are programmed to bring said nucleic acid molecule in contact with more than one type of nucleic acid base simultaneously.

29. The system of claim 1 , wherein said one or more computer processors are programmed to bring said nucleic acid molecule in contact with four types of nucleic acid bases simultaneously.

30. The system of claim 11 , wherein said one or more computer processors are programmed to bring said nucleic acid molecule in contact with more than one type of nucleic acid base simultaneously.

31. The system of claim 11 , wherein said one or more computer processors are programmed to bring said nucleic acid molecule in contact with four types of nucleic acid bases simultaneously.

Assignments (7)
SECURITY INTEREST Recorded Jun 30, 2023
From: SEQUENCING HEALTH, INC.
To: OXFORD FINANCE LLC, AS COLLATERAL AGENT
Reel/Frame 064180/0928 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 12, 2023
From: GENAPSYS, INC.
To: SEQUENCING HEALTH, INC.
Reel/Frame 062355/0443 →
RELEASE OF SECURITY INTEREST Recorded Jan 26, 2021
From: OXFORD FINANCE LLC, AS COLLATERAL AGENT
To: GENAPSYS, INC.
Reel/Frame 055107/0633 →
SECURITY INTEREST Recorded Jun 25, 2020
From: GENAPSYS, INC.
To: OXFORD FINANCE LLC
Reel/Frame 053053/0088 →
RELEASE OF SECURITY INTEREST Recorded Jul 17, 2019
From: OXFORD FINANCE LLC
To: GENAPSYS, INC.
Reel/Frame 049782/0910 →
SECURITY INTEREST Recorded Feb 6, 2019
From: GENAPSYS, INC.
To: OXFORD FINANCE LLC, AS COLLATERAL AGENT
Reel/Frame 048257/0131 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 10, 2019
From: ESFANDYARPOUR, HESAAM; PARIZI, KOSAR BAGHBANI; OLDHAM, MARK F.; NORDMAN, ERIC S.; REEL, RICHARD T.; BAUMHUETER, SUSANNE; HEINER, CHERYL; LEE, FRANK
To: GENAPSYS, INC.
Reel/Frame 047960/0165 →
Continuity (8)
Continuation 15896572 · Feb 14, 2018
Continuation 14119859
Continuation In Part 13397581 · Feb 15, 2012
Continuation In Part PCTUS2011054769 · Oct 4, 2011
Provisional Application 61491081 · May 27, 2011
Provisional Application 61565651 · Dec 1, 2011
Provisional Application 61620381 · Apr 4, 2012
Related Publication 20180282806A1 · Oct 4, 2018