Multiplex nucleic acid detection methods and systems

• US 10,280,469 B2
• Filed: 10/18/2016
• Issued: 05/07/2019
• Est. Priority Date: 04/03/2009
• Status: Active Grant

• Current Assignee: LifeOS Genomics Corporation
• Original Assignee: LifeOS Genomics Corporation
• Inventors: Liu, Timothy Z.
• Primary Examiner(s): Whisenant, Ethan C
• Application Number:
  US15/296,059
• Publication Number:
  US 20170101687A1
• Time in Patent Office: 931 Days
• CPC Class Codes: C12Q 1/6844 Nucleic acid amplification reactions
• CPC Class Codes: C12Q 1/6886 for cancer immunoassay for cancer G01N33/574
• CPC Class Codes: C12Q 2527/125 Specific component of sample, medium or buffer
• CPC Class Codes: C12Q 2527/153 Viscosity
• CPC Class Codes: C12Q 2565/537 characterised by the capture oligonucleotide acting as a primer
• CPC Class Codes: C12Q 2600/154 Methylation markers
• CPC Class Codes: C12Q 2600/156 Polymorphic or mutational markers

Abstract

A method of quantifying multiple target nucleic acid sequences in a sample includes generating from a sample at least a plurality of first template molecules and at least a plurality of second template molecules. At least part of said first and at least part of said second template molecules are randomly distributed into individual reaction sites. A cluster of nucleic acid amplicons of said first template molecule and at least a cluster of nucleic acid amplicons of said second template molecule are generated by clonal amplification or replication. The ID codes of all said nucleic acid amplicon clusters are identified. The quantity of at least said first and second target nucleic acid sequences in said sample is quantified by statistical analysis of respective positive numbers of identified unique ID codes of first and second target nucleic acid sequences.

Claims

1. A method of quantifying multiple target nucleic acid sequences in a sample, containing at least a first target nucleic acid sequence and a second target nucleic acid sequence, the method comprising:

(a) generating from a sample at least a plurality of first template molecules and at least a plurality of second template molecules, wherein said first template molecules comprise a sequence of a first target nucleic acid sequence and a first identity sequence (IS) tag, and said second template molecules comprise a sequence of a second target nucleic acid sequence and a second IS tag, and wherein said first IS tag comprises a first identification (ID) code and said second IS tag comprises a second ID code;

(b) randomly distribute at least part of said first and at least part of said second template molecules generated from step (a) into individual reaction sites on a surface, wherein the total number of said individual reaction sites and reaction volume are known, and the average number of said template molecules in each said individual reaction site is less than one;

(c) generating at least one cluster of nucleic acid amplicons of said first template molecule and at least one cluster of nucleic acid amplicons of said second template molecules in spatially isolated said individual reaction sites on said surface;

(d) simultaneously identifying said ID codes of all said nucleic acid amplicon clusters on said surface, wherein a unique ID code from any said nucleic acid amplicon cluster represents a positive identification of a target nucleic acid sequence in said sample, wherein said ID codes of said IS tags on said nucleic acid amplicons is determined by comparing base composition to designated ID codes through a probe hybridization, wherein 10^n (or 10ⁿ) kinds of the base compositions are distinguished in n times of a paired-probe ligation during the probe hybridization; and

(e) determining the quantity of at least said first and second target nucleic acid sequences in said sample by statistical analysis of respective positive numbers of identified unique ID codes of said first and second target nucleic acid sequences among said known number of individual reaction sites and said known reaction volumes on said surface.

2. The method of claim 1, wherein said sample comprises at least one endogenous or exogenous reference nucleic acid sequence of known amount, and said reference nucleic acid sequence is encoded to a pre-specified ID code during template molecule preparation.

3. The method of claim 1, wherein said individual reaction sites comprise a space on said surface, and each said individual reaction site is isolated from surrounding individual reaction sites by physical barriers, immiscible liquid barriers, surface tension, or a combination thereof.

4. The method of claim 1, wherein said individual reaction sites on said surface comprise known different features and known different reaction volumes.

5. The method of claim 1, wherein all said individual reaction sites on said surface comprise known identical features and known identical reaction volume.

6. The method of claim 1, wherein said individual reaction sites are concavities with fixed volume formed on said surface and are further isolated by a water immiscible fluid during said enzymatic amplification or replication on said surface.

7. The method of claim 1, wherein said number of individual reaction sites on said surface is larger than 10,000.

8. The method of claim 1, wherein said clusters of nucleic acid amplicons are directly attached to said surface, or through an intermediate substrate on said surface.

9. The method of claim 1, wherein the position of each cluster of nucleic acid amplicons is fixed relative to other nucleic acid amplicon clusters on said surface during said the analysis process.

10. The method of claim 1, further comprising:

determining the sequence variations of said target nucleic acid sequences by analyzing the sequence variations of said nucleic acid amplicons on said surface.

22. The method of claim 1, wherein said at least one cluster of nucleic acid amplicons of said first template molecule and at least one cluster of nucleic acid amplicons of said second template molecules were generated by clonal amplification or replication.

11. A method of quantifying multiple target nucleic acid sequences in a sample, containing at least a first target nucleic acid sequence and a second target nucleic acid sequence, the method comprising:

(a) generating from a sample at least a plurality of first template molecules and at least a plurality of second template molecules, wherein said first template molecules comprise a sequence of a first target nucleic acid sequence and a first identity sequence (IS) tag, and said second template molecules comprise a sequence of a second target nucleic acid sequence and a second IS tag, and said first IS tag comprises a first identification (ID) code and said second IS tag comprises a second ID code in a homogenous amplification;

(b) randomly distributing at least part of said first and at least part of said second template molecules generated from step (a) into individual reaction sites on a surface in a flow cell, wherein the number of said individual reaction sites and reaction volume are known, and the average number of said template molecules in each said individual reaction site is less than one;

(c) generating at least one cluster of nucleic acid amplicons of said first template molecule and at least one cluster of nucleic acid amplicons of said second template molecules in said individual reaction sites on said surface in said flow cell;

(d) simultaneously identifying said ID codes of all said nucleic acid amplicon clusters on said surface in said flow cell, wherein a unique ID code from any said nucleic acid amplicon cluster represents a positive identification of a target nucleic acid sequence in said sample, wherein said ID codes of said IS tags on said nucleic acid amplicons is determined by comparing base composition to designated ID codes through a probe hybridization, wherein 10^n (or 10ⁿ) kinds of the base compositions are distinguished in n times of a paired-probe ligation during the probe hybridization; and

(e) determining the quantity of at least said first and second target nucleic acid sequences in said sample by statistical analysis of respective positive numbers of identified unique ID codes of said first and second target nucleic acid sequences among said known number of individual reaction sites and said reaction volumes on said surface in said flow cell.

12. The method of claim 11, further comprising:

quantifying the nucleic acid of said template molecules after step (a) of homogenous gene specific pre-amplification reaction.

13. The method of claim 11, wherein said sample comprises at least one endogenous or exogenous reference nucleic acid sequence of known amount, and said reference nucleic acid sequence is encoded to a pre-specified ID code during said homogenous gene specific pre-amplification.

14. The method of claim 11, wherein said individual reaction sites comprise a space on said surface, and each said individual reaction site is isolated from surrounding individual reaction sites by physical barriers, immiscible liquid barriers, surface tension, or a combination thereof.

15. The method of claim 11, wherein said individual reaction sites on said surface comprise known different features and known different reaction volumes.

16. The method of claim 11, wherein all said individual reaction sites on said surface comprise known identical features and known identical reaction volume.

17. The method of claim 11, wherein said individual reaction sites are concavities with fixed volume formed on said surface and are further isolated by a water immiscible fluid during said enzymatic amplification or replication on said surface in said flow cell.

18. The method of claim 11, wherein said number of individual reaction sites on said surface in said flow cell is larger than 10,000.

19. The method of claim 11, wherein said clusters of nucleic acid amplicons are directly attached to said surface or through an intermediate substrate on said surface in said flow cell.

20. The method of claim 11, wherein the position of each cluster of nucleic acid amplicons is fixed relative to other nucleic acid amplicon clusters on said surface in said flow cell during said the analysis process.

21. The method of claim 11, further comprising:

determining the sequence variations of said target nucleic acid sequences by analyzing the sequence variations of said nucleic acid amplicons on said surface in said flow cell.

23. The method of claim 11, wherein said at least one cluster of nucleic acid amplicons of said first template molecule and at least one cluster of nucleic acid amplicons of said second template molecules were generated by clonal amplification or replication.