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
18 stars 3 forks source link

New series of fixes and features #21

Closed nvnieuwk closed 1 year ago

nvnieuwk commented 1 year ago

PR checklist

nvnieuwk commented 1 year ago

Thanks!