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nf-cmgg / structural

A bioinformatics best-practice analysis pipeline for calling structural variants (SVs), copy number variants (CNVs) and repeat region expansions (RREs) from short DNA reads
https://nf-cmgg.github.io/structural/
MIT License
19 stars 2 forks source link

Add FilterBatch subworkflow #15

Closed nvnieuwk closed 1 year ago

nvnieuwk commented 2 years ago

GATK-SV: FilterBatch.wdl