Hi everyone,
I have run the rnaseq pipeline on a couple of datasets. Firstly, thank you for the work you have already put in. This pipeline is very well designed, and it has significantly simplified my workflow. I mainly ran it to support colleagues’ exploratory work. I’ve always found it a bit frustrating to reach the DESeq part, defining all the theoretical comparisons, only to wait for R to loop through everything. To address this, I’ve created a subworkflow that uses a metadata sheet to generate all comparisons and then runs them. I’d like to potentially integrate my subworkflow into the overall rnaseq pipeline and contribute a little to its development. But I saw that there’s already a closed PR request for something similar (
https://github.com/nf-core/rnaseq/issues/409), and the conclusion is that this wouldn’t be implemented directly in the rnaseq pipeline. May I ask if this is still the case?