The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
May. 28, 2024

Filed:

Jan. 30, 2018
Applicant:

Myriad Women's Health, Inc., South San Francisco, CA (US);

Inventors:

Jared Robert Maguire, Oakland, CA (US);

Alexander D. Robertson, San Francisco, CA (US);

Eric Andrew Evans, Brisbane, CA (US);

Assignee:

Myriad Women's Health, Inc., South San Francisco, CA (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
G16B 20/10 (2019.01); C12Q 1/6858 (2018.01); C12Q 1/6869 (2018.01); G16B 30/10 (2019.01);
U.S. Cl.
CPC ...
C12Q 1/6858 (2013.01); C12Q 1/6869 (2013.01); G16B 20/10 (2019.02); G16B 30/10 (2019.02);
Abstract

A method of identifying and quantifying copy number variations in a gene of interest for a genomic DNA sample includes (i) fragmenting a genomic DNA sample to produce a plurality of polynucleotide fragments, (ii) isolating a plurality of target polynucleotide fragments, (iii) sequencing the plurality of target polynucleotide fragments, (iv) aligning fragment sequences to a reference sequence, (v) calculating read depths for base positions of the plurality of target polynucleotide fragments, (vi) calculating copy number likelihoods for each base position of the reference sequence, (vii) performing a breakpoint analysis on a set of fragment sequences to identify at least one sequence variation located between selected breakpoint regions of the target gene and calculate modified copy number likelihoods for base positions of the reference sequence based on the at least one sequence variation, and (viii) determining whether the target gene includes at least one copy number variation.


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