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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 validation #51

Open nvnieuwk opened 11 months ago

nvnieuwk commented 11 months ago

Description of feature

Add a way to perform validation in the pipeline instead of having to manually validate the output

nvnieuwk commented 11 months ago

https://github.com/acenglish/truvari/wiki/bench