Guardant Health, Inc.
GENETIC VARIANT DETECTION BASED ON MERGED AND UNMERGED READS

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Abstract:

Methods and systems for improving identification of nucleic acid variants by identifying genetic sequence reads having identical molecular barcodes and sequences among sequence reads from a nucleic acid sequencer, grouping the genetic reads into a family, and processing families comprising split reads to detect the variants in a sample of polynucleotide molecules.

Status:
Application
Type:

Utility

Filling date:

3 Sep 2019

Issue date:

5 Mar 2020