IP Library Granted Patent US 9,193,992
Granted Patent B2
US 9,193,992 · App. 13/894,886 · Granted Nov 24, 2015

Method for determining ploidy of a cell

Inventors: Bo U. Curry (Redwood City, CA); Jayati Ghosh (Cupertino, CA); Brian Jon Peter (Los Altos, CA); Arjun Vadapalli (Sunnyvale, CA)
Assignee: Agilent Technologies, Inc.
C12Q1/6827C12Q1/6883G06F19/18C12Q2600/158
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Quick Facts
Patent No.
US 9,193,992
App. No.
13/894,886
Granted
Nov 24, 2015
Kind
B2
Abstract

A method for determining the ploidy of a test genome is provided. In some embodiments, the method may comprises: a) obtaining a plurality of ratios for polymorphisms that are distributed throughout a test genome, wherein each of the ratios is a ratio of the measured copy number of uncut allele in a polymorphic site relative to the measured copy number of the uncut allele in the reference sample; b) taking the log of the ratios and plotting a distribution of the reference corrected log ratios of the SNP probes; and c) determining the ploidy of said the genome based on the number of peaks in that distribution.

Claims (36)

1. A method for determining the ploidy of a test genome, comprising:

a) obtaining a plurality of ratios for polymorphisms that are distributed throughout a test genome, wherein each of said ratios is a ratio of the measured copy number of one allele of a polymorphism relative to the measured copy number of said allele in a reference sample that has two copies of said allele;

b) plotting a distribution of the ratios to provide a distribution, wherein one axis of the distribution indicates a range of ratios and another axis of the distribution represents a number of ratios, wherein the distribution comprises a number of peaks; and

c) determining the ploidy of said test genome based on the number of peaks in said distribution.

2. The method of claim 1 , wherein said polymorphisms are single nucleotide polymorphisms (SNPs).

3. The method of claim 1 , wherein polymorphisms are on every chromosome in said genome.

4. The method of claim 1 , wherein said ratios are produced by comparing data obtained from microarray or NGS data.

5. The method of claim 1 , wherein said ratios are log 2 ratios.

6. The method of claim 1 , wherein a distribution of log 2 ratios comprising three peaks indicates that said test genome is diploid.

7. The method of claim 1 , wherein a distribution of log 2 ratios comprising four peaks indicates that said test genome is triploid.

8. The method of claim 1 , wherein said determining comprises determining the ploidy of said test genome based on said number of peaks and the intervals between the peaks.

9. The method of claim 8 , wherein a distribution of log 2 ratios comprising three peaks at intervals of approximately 1.00 and 0.58 indicate a triploid sample.

10. The method of claim 1 , wherein said determining comprises determining the ploidy of said test genome based on said number of peaks and the areas under the peaks.

11. The method of claim 10 , wherein a distribution of log 2 ratios that has four peaks, the second and third peaks of which having areas that are similar, indicates that said test genome is triploid.

12. The method of claim 1 , wherein said ratios are obtained by hybridizing said test and reference genome to an array comprising oligonucleotides that discriminate between different alleles of a SNP.

13. The method of claim 1 , wherein the ploidy of the test genome is determined automatically by analysis of said distribution by a computer.

14. The method of claim 1 , wherein said obtaining is done by subjecting a test genome to CGH and SNP analysis to obtain:

i. CGH data indicating which parts of said test genome are putatively diploid and which parts are putatively non-diploid; and

ii. SNP data comprising ratios indicating the allele-specific copy number of a plurality of SNPs that are present in putatively diploid regions of said test genome;

iii. SNP data comprising ratios for a plurality of SNPs that are present in putatively non-diploid region of said genome.

15. The method of claim 14 , wherein said method comprises adjusting said CGH data if said test genome is tetraploid or diploid.

16. The method of claim 1 , wherein said method comprises:

a) obtaining a plurality of ratios indicating which alleles of a plurality of single nucleotide polymorphisms (SNPs) are present in putatively diploid regions of a test genome and a reference genome;

b) plotting a distribution of the ratios to provide a distribution comprising four peaks; and

c) determining that said test sample is tetraploid or triploid because said distribution comprises four peaks;

d) calculating a plurality of probability distribution functions that fit said peaks; and

e) estimating the allele-specific copy number of a SNP of said test genome using said plurality of probability distribution functions.

17. The method claim 16 , comprising:

calculating a likelihood score for said allele-specific copy number of said SNP indicating the confidence that said allele-specific copy number has been correctly assigned, wherein said score are calculated using said plurality of probability distribution functions.

18. The method of claim 17 , further comprising removing allele-specific copy number from a dataset if its likelihood scores are below a threshold.

19. The method of claim 17 , wherein said calculating of step d), comprises:

calculating a first probability distribution function for SNP alleles in triploid regions of said test genome that have a copy number of 0 for SNP alleles that have a reference copy number of 1 or 2;

calculating a second probability distribution function for SNP alleles in triploid regions of said test genome that have a copy number of 1 for SNP alleles that have a reference copy number of 1 or 2;

calculating a third probability distribution function for SNP alleles in triploid regions of said test genome that have a copy number of 2 for SNP alleles that have a reference copy number of 1 or 2; and

calculating a third probability distribution function for SNP alleles in triploid regions of said test genome that have a copy number of 3 for SNP alleles that have a reference copy number of 1 or 2.

20. A tangible computer readable medium comprising instructions for performing the method of claim 1 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 7, 2013
From: CURRY, BO U.; PETER, BRIAN JON; GHOSH, JAYATI; VADAPALLI, ARJUN
To: AGILENT TECHNOLOGIES, INC.
Reel/Frame 030570/0605 →
Continuity (2)
Provisional Application 61655914 · Jun 5, 2012
Related Publication 20130323730A1 · Dec 5, 2013