IP Library Granted Patent US 10,494,672
Granted Patent B2
US 10,494,672 · App. 16/283,544 · Granted Dec 3, 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 10,494,672
App. No.
16/283,544
Granted
Dec 3, 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 (20)

1. A system for nucleic acid sequencing, comprising:

a chip comprising a flow cell, an array in fluidic communication with said flow cell, a plurality of optical sensors in optical communication with said array, and circuitry operatively coupled to said plurality of optical sensors, wherein said array is configured to retain a plurality of nucleic acid molecules having sequences that are substantially identical to a nucleic acid sequence of a template nucleic acid molecule in a manner such that said plurality of nucleic acid molecules is in optical communication with an optical sensor of said plurality of optical sensors,

wherein said circuitry is configured to couple to one or more computer processors external to said chip, which one or more computer processors are configured to (i) bring said plurality of nucleic acid molecules in contact with nucleic acid bases in presence of polymerizing enzymes under conditions sufficient to incorporate at least a subset of said nucleic acid bases into growing strands complementary to said plurality of nucleic acid molecules, (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 at least said subset of 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 system further comprises said one or more computer processors.

3. The system of claim 1 , wherein said circuitry is electrically coupled to said plurality of optical sensors.

4. The system of claim 1 , wherein said array is configured to retain said plurality of nucleic acid molecules within a Debye length of a surface of said array or a surface of a feature immobilized on said array during sequencing.

5. The system of claim 1 , wherein said feature is a well.

6. The system of claim 1 , wherein said plurality of optical sensors is configured for reduced cross-talk between said plurality of optical sensors.

7. The system of claim 1 , wherein said array comprises a surface coating.

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

9. The system of claim 1 , wherein said plurality of optical sensors comprise charge-coupled device (CCD) sensors.

10. The system of claim 1 , wherein said flow cell is configured to direct said nucleic acid bases to said array.

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

12. The system of claim 1 , further comprising a fluidics interface configured to provide said nucleic acid bases to said flow cell.

13. The system of claim 12 , wherein said fluidics interface and said one or more computer processors are integrated within said system.

14. The system of claim 1 , wherein said one or more computer processors are programmed to monitor for phase error.

15. The system of claim 1 , wherein said one or more computer processors are programmed to correct for phase error.

16. The system of claim 1 , wherein said one or more computer processors are programmed to direct more than one type of nucleic acid base to said flow cell in a given nucleic acid sequencing cycle.

17. The system of claim 1 , wherein said one or more computer processors are programmed to direct four types of nucleic acid bases to said flow cell in a given nucleic acid sequencing cycle.

18. The system of claim 1 , wherein said one or more computer processors are programmed to direct more than one type of nucleic acid base to said flow cell in sequential nucleic acid sequencing cycles.

Assignments (6)
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 4, 2019
From: OLDHAM, MARK F.
To: GENAPSYS, INC.
Reel/Frame 050631/0915 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 18, 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 049789/0320 →
Continuity (9)
Continuation 16007969 · Jun 13, 2018
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 20190177791A1 · Jun 13, 2019