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:
Jul. 05, 2022

Filed:

May. 13, 2020
Applicant:

The Regents of the University of California, Oakland, CA (US);

Inventors:

Charles Chiu, San Francisco, CA (US);

Samia Naccache, San Francisco, CA (US);

Scot Federman, Portola Valley, CA (US);

Doug Stryke, Albany, CA (US);

Steve Miller, San Mateo, CA (US);

Erik Samayoa, San Francisco, CA (US);

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

Embodiments are directed to systems and methods for pathogen detection using next-generation sequencing (NGS) analysis of a sample. Embodiments may apply alignment algorithms (e.g., SNAP and/or RAPSearch alignment algorithms) to align individual sequence reads from a sample in a next-generation sequencing (NGS) dataset against reference genome entries in a classified reference genome database. Embodiments of the present invention may include classifying, filtering, and displaying results to a clinician that can then quickly and easily obtain the results of the sequencing to identify a pathogen or other genetic material in a sample that is being tested. A negative sample and a corresponding database can be used to remove contaminants from a list of candidate pathogens. Thus, embodiments are directed to a system that is configured to filter the results of a sequencing alignment and classify a sample quickly.


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