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:
Jan. 05, 2021

Filed:

Oct. 21, 2015
Applicant:

Baylor College of Medicine, Houston, TX (US);

Inventors:

Olivier Lichtarge, Bellaire, TX (US);

Teng-Kuei Hsu, Houston, TX (US);

Panagiotis Katsonis, Pearland, TX (US);

Amanda Michele Koire, Houston, TX (US);

Assignee:

Baylor College of Medicine, Houston, TX (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
G16B 20/00 (2019.01); G16B 10/00 (2019.01); G16B 35/00 (2019.01); G16C 20/60 (2019.01); G06F 17/13 (2006.01);
U.S. Cl.
CPC ...
G16B 20/00 (2019.02); G06F 17/13 (2013.01); G16B 10/00 (2019.02); G16B 35/00 (2019.02); G16C 20/60 (2019.02);
Abstract

A method and computer system for identifying genes associated with a phenotype includes obtaining data representing mutations in a cohort of subjects exhibiting a phenotype. An evolutionary action (EA) score is calculated for each mutation using the data obtained. For each gene in the cohort, respective distributions of the calculated EA scores are determined for mutations found in the gene. The determined distributions of EA scores are quantitatively compared within the cohort and with random distributions to establish comparison data. Based on the comparison data, distributions of EA scores are identified that are non-random, and linkage of each gene in the cohort to the phenotype is assessed based on the identified non-random distributions to identify genes associated with the phenotype. The phenotype can be a disease, such as cancer, and linkage of each gene in the cohort to the disease can be assessed to identify disease causing genes.


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