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 VCF to BEDPE conversion #49

Open nvnieuwk opened 11 months ago

nvnieuwk commented 11 months ago

Description of feature

https://github.com/ctsa/svtools

nvnieuwk commented 6 months ago

This is needed for visualization in Chromoscope