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:
Aug. 22, 2023

Filed:

Jan. 14, 2021
Applicant:

Ancestry.com Dna, Llc, Lehi, UT (US);

Inventors:

Ahna R. Girshick, Berkeley, CA (US);

Natalie Telis, Mountain View, CA (US);

Julie M. Granka, San Francisco, CA (US);

Asher Keith Haug Baltzell, Salt Lake City, UT (US);

Shiya Song, San Mateo, CA (US);

Genevieve Heather Linnea Roberts, Salt Lake City, UT (US);

Shannon Ries McCurdy, Berkeley, CA (US);

Jialiang Gu, Berkeley, CA (US);

Assignee:

Ancestry.com DNA, LLC, Lehi, UT (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
G16B 20/20 (2019.01); G16B 40/20 (2019.01); G16B 5/20 (2019.01); G16B 20/40 (2019.01); G16B 10/00 (2019.01); G16B 40/30 (2019.01);
U.S. Cl.
CPC ...
G16B 20/20 (2019.02); G16B 5/20 (2019.02); G16B 10/00 (2019.02); G16B 20/40 (2019.02); G16B 40/20 (2019.02); G16B 40/30 (2019.02);
Abstract

Disclosed are techniques for predicting a trait of an individual and identifying a set of enriched record collections of a genetic community. To predict a trait of an individual, DNA features and non-DNA features of the individual are accessed to generate a feature vector that is inputted into a machine learning model. The machine learning model generates a prediction of the trait. The prediction may be based on an inheritance prediction and/or a community prediction. To identify a set of enriched record collections, individuals belonging to a genetic community are identified and a set of candidate record collections are accessed. A community count and a background count is determined for each candidate record collection. The set of enriched record collections are identified based on a comparison of the community count and the background count. The genetic community may be annotated using the set of enriched record collections.


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