Analysis of nucleic acids

Patent metadata

Field	Value
Publication number	US-11499181-B2
Application number	US-201816235996-A
Country	US
Kind code	B2
Filing date	Dec 28, 2018
Priority date	Feb 9, 2011
Publication date	Nov 15, 2022
Grant date	Nov 15, 2022

Abstract

Method of haplotype analysis. In an exemplary method, an aqueous phase containing nucleic acid may be partitioned into a plurality of discrete volumes. At least one allele sequence may be amplified in the volumes from each of a first polymorphic locus and a second polymorphic locus that exhibit sequence variation in the nucleic acid. At least one measure of co-amplification of allele sequences from both loci in the same volumes may be determined. A haplotype of the first and second loci may be selected based on the at least one measure of co-amplification.

First claim

We claim:

1. A method of haplotype analysis, the method comprising:
partitioning an aqueous phase containing nucleic acid into a plurality of discrete volumes;
amplifying in the volumes at least one allele sequence from each of a first polymorphic locus and a second polymorphic locus that exhibit sequence variation in the nucleic acid;
determining at least one measure of co-amplification of allele sequences from both loci in the same volumes; and
selecting a haplotype of the first and second loci based on the at least one measure of co-amplification; and
wherein determining at least one measure includes determining a number of volumes that exhibit co-amplification of a particular allele sequence of the first locus and a particular allele sequence of the second locus, and wherein selecting a haplotype is based on the number of volumes.

2. The method of claim 1 , wherein the first and second loci are contained in a target region of the nucleic acid, and wherein the step of partitioning results in an average concentration of less than about five copies of the target region per volume.

3. The method of claim 1 , wherein the step of determining at least one measure includes a step of determining at least one correlation coefficient for allele-specific amplification data of the first locus correlated with allele-specific amplification data of the second locus from the same volumes.

4. The method of claim 1 , wherein the step of determining at least one measure includes a step of determining a first correlation coefficient and a second correlation coefficient for allele-specific amplification data of a first allele sequence and a second allele sequence of the first locus correlated respectively with allele-specific amplification data of the second locus from the same volumes, and wherein the step of selecting a haplotype is based on a step of comparing the first and second correlation coefficients with each other.

5. The method of claim 1 wherein the step of determining a number of volumes includes a step of determining a first number of volumes and a second number of volumes that exhibit respective co-amplification of a first allele sequence or a second allele sequence of the first locus with a particular allele sequence of the second locus, and wherein the step of selecting a haplotype is based on first and second numbers of volumes.

6. The method of claim 1 , wherein the step of partitioning includes a step of forming an emulsion in which the volumes are droplets.

7. A method of haplotype analysis, the method comprising:
partitioning an aqueous phase containing nucleic acid into a plurality of discrete volumes;
amplifying in the volumes at least one allele sequence from each of a first polymorphic locus and a second polymorphic locus contained in a target region of the nucleic acid;
collecting allele-specific amplification data for each of the loci from individual volumes;
correlating allele-specific amplification data for the first locus with allele-specific amplification data for the second locus from the same volumes, wherein correlating includes determining a number of volumes exhibiting co-amplification of a particular allele sequence from both loci; and
selecting a haplotype of the target region for the first and second loci based on the step of correlating.

8. The method of claim 7 , wherein the step of partitioning includes a step of forming an emulsion, and wherein the step of collecting includes a step of collecting data from individual droplets of the emulsion.

9. The method of claim 8 , wherein the step of forming an emulsion includes a step of passing the aqueous phase through an orifice such that monodisperse droplets of the aqueous phase are generated.

10. The method of claim 7 , wherein the step of partitioning disposes an average of less than about one genome equivalent of the nucleic acid in each volume.

11. The method of claim 7 , wherein the step of partitioning includes a step of forming at least about 1000 volumes.

12. The method of claim 7 , wherein the step of partitioning includes a step of forming droplets that are about 10 to 1000 micrometers in diameter.

13. The method of claim 7 , wherein the step of partitioning includes a step of partitioning an aqueous phase including optically distinguishable fluorescent probes capable of hybridizing specifically to each allele sequence amplified.

14. The method of claim 7 , wherein the step of amplifying includes a step of amplifying a pair of different allele sequences from the first locus, and wherein the step of collecting data includes a step of collecting data that distinguishes amplification of each allele sequence of the pair in individual droplets.

15. The method of claim 7 , wherein the step of correlating includes a step of separately correlating allele-specific amplification data for each allele sequence of the first locus with allele-specific amplification data for the allele sequence of the second locus.

16. The method of claim 7 , wherein the step of selecting a haplotype is based on which allele-specific amplification data for the first locus exhibits a higher correlation with such allele-specific amplification data for the second locus.

17. The method of claim 7 , further comprising a step of applying a threshold to the allele-specific amplification data to convert it to binary form, wherein the step of correlating is performed with the binary form of the data.

18. A method of haplotype analysis, the method comprising:
partitioning an aqueous phase including nucleic acid into a plurality of discrete volumes, wherein partitioning includes forming an emulsion, and wherein forming an emulsion includes passing the aqueous phase through an orifice such that monodisperse droplets of the aqueous phase are generated;
amplifying in the volumes an allele sequence from each of a first polymorphic locus and a second polymorphic locus in the nucleic acid;
collecting allele-specific amplification data for each allele sequence from individual droplets of the emulsion; and
selecting a haplotype of the nucleic acid based at least in part on whether the amplification data indicates a negative or a positive correlation for amplification of the allele sequences in the same volumes.

Assignees

• Bio Rad Laboratories Inc

Inventors

• Regan John F
• Saxonov Serge
• Lucero Michael Y
• Hindson Benjamin J
• Belgrader Phillip
• Dube Simant
• So Austin P
• Mellen Jeffrey C
• Heredia Nicholas J
• Ness Kevin D
• Colston Jr Billy W

Classifications

• C12Q1/683

  involving restriction enzymes, e.g. restriction fragment length polymorphism [RFLP] · CPC title

• C12Q1/6858 Primary

  Allele-specific amplification · CPC title

• C12Q1/6806

  Preparing nucleic acids for analysis, e.g. for polymerase chain reaction [PCR] assay (C12Q1/6804 takes precedence) · CPC title

• C12Q1/6883

  for diseases caused by alterations of genetic material · CPC title

• C12Q2535/125

  Allele specific primer extension · CPC title