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:
Apr. 14, 2020

Filed:

Jan. 16, 2018
Applicant:

Helix Opco, Llc, San Carlos, CA (US);

Inventors:

James Lu, Redwood City, CA (US);

Jim Chou, San Francisco, CA (US);

William Lee, Mountain View, CA (US);

Chris Williams, San Francisco, CA (US);

James Warren, Redwood City, CA (US);

Ruomu Jiang, Menlo Park, CA (US);

Assignee:

Helix OpCo, LLC, San Carlos, CA (US);

Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
G06F 16/9535 (2019.01); G06F 16/951 (2019.01); G16B 30/00 (2019.01); G16B 40/00 (2019.01); G16B 50/00 (2019.01); G16B 50/30 (2019.01); G16B 30/10 (2019.01); G16B 20/20 (2019.01); G06F 9/54 (2006.01); G06Q 30/06 (2012.01); H04L 29/08 (2006.01);
U.S. Cl.
CPC ...
G16B 30/00 (2019.02); G06F 9/547 (2013.01); G06F 16/951 (2019.01); G06F 16/9535 (2019.01); G16B 20/20 (2019.02); G16B 30/10 (2019.02); G16B 40/00 (2019.02); G16B 50/00 (2019.02); G16B 50/30 (2019.02); G06Q 30/0601 (2013.01); H04L 67/10 (2013.01);
Abstract

Systems, platforms, methods and media for providing genomic services are disclosed. In one example, a genomic services platform comprises a network interface through which are received genomic sequence reads derived from a biological sample obtained from a user The platform also includes a bioinformatics processing pipeline including a read alignment module configured to generate observed sequence data by aligning the sequence reads relative to a reference sequence, a variant calling module operative to identify observed variants in the observed sequence data, and a variant refinement module for producing a set of refined variants associated with the user. A variant imputation module produces a set of imputed variants associated with the user, and a variant storage module disposed to receive a query from network infrastructure of a partner application provider and to provide selected ones of the refined or imputed variants in response to the query.


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