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cfDNApipe: A comprehensive quality control and analysis pipeline for cell-free DNA high-throughput sequencing data
Explore and filter structural variant calls from Lumpy and Delly VCF files
A tool to extract ATGC/Indel read counts at user specific loci from BAM files
Pipeline for variant imputation in low depth sequencing data using GLIMPSE
My lab book for current project: Identifying structural variation in WGS data
Script and data for Hill, Leitch & Gaya (2021) doi: 10.1016/j.fbr.2021.03.003