A bioinformatics best-practice analysis pipeline for calling structural variants (SVs), copy number variants (CNVs) and repeat region expansions (RREs) from short DNA reads
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Updated
Jun 5, 2024 - Nextflow
A bioinformatics best-practice analysis pipeline for calling structural variants (SVs), copy number variants (CNVs) and repeat region expansions (RREs) from short DNA reads
A nextflow pipeline for calling and annotating small germline variants from short DNA reads for WES and WGS data
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