Add family support - Githubissues

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

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Add family support #57

Closed nvnieuwk closed 9 months ago

nvnieuwk commented 10 months ago

Description of feature

Add some way to merge single-sample VCFs into multi-sample VCFs (possible with bcftools merge)

nvnieuwk commented 9 months ago

Added in #61