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