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

Only save the last dev docs #81

Closed nvnieuwk closed 5 months ago

nvnieuwk commented 5 months ago

Description of feature

Only the last dev documentation should be built as dev version. This documentation should also never be set as the latest

nvnieuwk commented 5 months ago

Fixed in the dev branch