Invention Grant
- Patent Title: Methods for detecting single nucleotide variants or indels by deep sequencing
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Application No.: US17507109Application Date: 2021-10-21
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Publication No.: US11359248B2Publication Date: 2022-06-14
- Inventor: Stefanie Ann Ward Mortimer , Amirali Talasaz , Darya Chudova , Helmy Eltoukhy
- Applicant: GUARDANT HEALTH, INC.
- Applicant Address: US CA Redwood City
- Assignee: GUARDANT HEALTH, INC.
- Current Assignee: GUARDANT HEALTH, INC.
- Current Assignee Address: US CA Redwood City
- Main IPC: C12Q1/6886
- IPC: C12Q1/6886 ; G01N33/574 ; G16B30/10 ; G16B20/20 ; C12Q1/6806 ; C12Q1/6869 ; C12M1/34 ; C12M1/00 ; G16H50/30 ; G16H50/20
Abstract:
Disclosed herein are methods for use in detection of single nucleotide variants (SNVs) or indels. The methods may comprise enriching cell-free DNA molecules for a panel of genomic regions and deep sequencing the enriched cfDNA to detect the SNVs or indels.
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