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Just adding a note that @reichan1998 had asked how we want to designate an input as rnaseq -- I suggested using the library column (last column in samplesheet) e.g., with "rnaseq" for now, but I will check this doesn't conflict with any established practice we might have. (Also will check how these end up being designated in the metadata for our internal system)
Description of feature
Add subworkflow to align RNAseq data using STAR. Can be borrowed from nf-core/rnaseq.
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