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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

Make the workflow pluggable #91

Closed nvnieuwk closed 3 months ago

nvnieuwk commented 4 months ago

This PR makes the workflow pluggable + updates all modules (to make sure all tests run fully)

nvnieuwk commented 4 months ago

Sorry for the big PR, but most is just module updates. Can you please check the pluggable feature?