Hi team, I’d like to help reduce common support requests by adding a "Troubleshooting & Common Errors" guide to the

nf-core/rnaseq

docs. The goal is to provide a quick "pre-flight" checklist for frequent issues like samplesheet formatting, genome/GTF mismatches, and container errors. I'm happy to draft a PR—does this align with your current documentation goals, or is there a preferred format you'd like me to follow?

Nice idea!

HEhehe, @Chris Hakkaart;)

This came up recently somewhere else as well 😅

The original pipeline to add the subpages that I know of was #C03PADVJ8RL , where you make a directory called 'usage/' where you add the subpages, and then link to that from the root

usage.md

.

#C09H9L3R614 recruitment! 😅