docs part 2 - 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

18 stars 3 forks source link

docs part 2 #79

Closed mvheetve closed 5 months ago

mvheetve commented 5 months ago

Some changes were possibly not implemented with the last PR + added clarification to parameters.md about vcf_anno