A more involved (controversial?) one, I've reworked the MultiQC handling in #CE8SSJV3N: https://github.com/nf-core/rnaseq/pull/1793 • Allow _1, _2 etc sample IDs without confusing the notation with read-endedness. Seemed to be something folks wanted to do, but it required some tinkering to make it work! • Moved all the MultiQC complexity rnaseq had accumulated in its main workflow out to a subworkflow to make the main workflow more readable.