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:
Mar. 05, 2024

Filed:

Jun. 19, 2017
Applicant:

Sophia Genetics S.a., Saint-Sulpice, CH;

Inventors:

Lin Song, Saint-Sulpice, CH;

Tamara Steijger, Saint-Sulpice, CH;

Jonas Behr, Saint-Sulpice, CH;

Adam Novak, Saint-Sulpice, CH;

David Hernandez, Saint-Sulpice, CH;

Zhenyu Xu, Commugny, CH;

Assignee:

SOPHIA GENETICS S.A., Saint-Sulpice, CH;

Attorneys:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
G16B 50/20 (2019.01); G16B 20/20 (2019.01); G16B 30/00 (2019.01); G16B 30/10 (2019.01); G16B 50/00 (2019.01); G16B 20/00 (2019.01); G16B 50/40 (2019.01); G16B 50/50 (2019.01);
U.S. Cl.
CPC ...
G16B 50/20 (2019.02); G16B 20/20 (2019.02); G16B 30/00 (2019.02); G16B 30/10 (2019.02); G16B 50/00 (2019.02); G16B 20/00 (2019.02); G16B 50/40 (2019.02); G16B 50/50 (2019.02);
Abstract

A genomic data analyzer system method to analyze next generation sequencing genomic data from a sourcing laboratory. The method includes receiving, with a processor, a next generation sequencing analysis request from a sourcing laboratory, the next generation sequencing request comprising at least a raw next generation sequencing data file and the sourcing laboratory identification; identifying, with a processor, a first set of characteristics associated with the next generation sequencing analysis request, the first set of characteristics comprising at least a target enrichment technology identifier, a sequencing technology identifier, and a genomic context identifier; configuring, with a processor, a data alignment module to align the input raw sequencing data file in accordance with at least one characteristic of said first set of characteristics; and aligning, with the data alignment module processor, the input sequencing data to a genomic sequence.


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