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
Jul 31, 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 simple fastp-MultiQC nextflow pipeline
UNDER CONSTRUCTION: Hybrid genome assembly pipeline using a combination of long and short sequencing reads
A nextflow pipeline for calling and annotating small germline variants from short DNA reads for WES and WGS data
How to channel sequencing reads from multiple subdirectories into nextflow pipeline
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