Description
Create a subworkflow that prepares all genome files required as input for alignment and further downstream processes. This part is inspired by the nf-core/rnaseq/subworkflows/local/prepare_genome subworkflow.
Examples of output:
- Everything prepared in Step 1: Prepare Annotations of the old lncpipe pipeline (line 180)
- HISAT index (now required as input)
- STAR index (now required as input)