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

Add Svync standardization + other fixes #72

Closed nvnieuwk closed 6 months ago

nvnieuwk commented 6 months ago

PR checklist

nvnieuwk commented 6 months ago

Thanks! Gotta fix those tests first and then I'll merge, after this I'll do a template update and rebranding to the new repository name and after that I'll keep on digging for the join error