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. 12, 2025

Filed:

Apr. 21, 2020
Applicant:

10x Genomics, Inc., Pleasanton, CA (US);

Inventors:

Michael Schnall-Levin, San Francisco, CA (US);

Alexander Wong, San Francisco, CA (US);

David Luther Alan Stafford, San Francisco, CA (US);

Assignee:

10X GENOMICS, INC., Pleasanton, CA (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
G16B 50/30 (2019.01); G16B 30/00 (2019.01); G16B 30/10 (2019.01); G16B 30/20 (2019.01); G16B 45/00 (2019.01); G16B 50/00 (2019.01); G16C 99/00 (2019.01);
U.S. Cl.
CPC ...
G16B 50/30 (2019.02); G16B 30/00 (2019.02); G16B 30/10 (2019.02); G16B 45/00 (2019.02); G16B 50/00 (2019.02); G16C 99/00 (2019.02); G16B 30/20 (2019.02);
Abstract

A system for providing structural variation or phasing information is provided. The system accesses a nucleic acid sequence dataset corresponding to a target nucleic acid in a sample. The dataset comprises a header, synopsis, and data section. The data section comprises a plurality of sequencing reads. Each sequencing read comprises a first portion corresponding to a subset of the target nucleic acid and a second portion that encodes an identifier for the sequencing read from a plurality of identifiers. One or more programs in the memory of the system use a microprocessor of the system to provide a haplotype visualization tool that receives a request for structural variation or phasing information from the dataset. The request is evaluated against the synopsis thereby identifying portions of the data section. Structural variation or phasing information is formatted for display in the haplotype visualization tool using the identified portions of the data section.


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