rnaseq
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Turn sample processing into a subworkflow
https://github.com/nf-core/rnaseq/blob/29f8b393fc979beff9a88a2b37fcb6cb1d4ee994/workflows/rnaseq.nf#L192-L235
I'd love if we could move this to a nf-core subworkflow, so I can just nf-core subworkflows update it in nascent...
I'd be happy to make it happen, just want to get buy-in first.
This is probably tiny enough that it doesn't warrant needing a subworkflow 😅 Having said that, have you seen this PR to nf-core/fetchngs? This might help here. Could imagine porting this to a nf_core_rnaseq_utils subworkflow that can be shared.
https://github.com/nf-core/fetchngs/pull/213/files