Dear all,
Thank you very much for providing this incredible tool.
I have a question related to the in-house RNA-seq processing pipeline.
I was wondering how the internal data processing pipeline handles reads mapping to multiple genes/regions (multi-mapper)?
The GDC pipeline is removing all reads that map to more than one gene, which makes it impossible to study genes with orthologues in the genome. Thus, I was wondering if your in-house processing handle this differently. Unfortunately, I couldn´t find this information in the original publication or the github page.
I look much forward to
hearing from you.
All the best,
Vladimir