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

Bug/sex determination #97

Closed nvnieuwk closed 1 month ago

nvnieuwk commented 1 month ago

PR checklist

nvnieuwk commented 1 month ago

Fixes #95