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

Template v2.13.1 sync + update all modules #73

Closed nvnieuwk closed 6 months ago

nvnieuwk commented 6 months ago

PR checklist

nvnieuwk commented 6 months ago

Thanks! I'll try and fix it all now :p