Closed jdreyf closed 3 years ago
Hi @jdreyf , sorry for the slow response. By default, we did not include PE capabilities with the riboseq
module as more often then not, ribosome profiling is performed using SE sequencing due to the small size of the RPFs. If you have PE total RNA, I would process these samples separate from the RPF samples using the peRNAseq
module, but I would have some hesitancy combining SE RPF and PE RNA reads in the same analysis, unless you were to include this distinction as a factor during differential expression analysis. I may be missing the point, but as far as I am aware, I have not seen any PE RPF library generation methods (or at least, none that are used widely).
@j-berg: It appears that paired end input libraries are accommodated with
peRNAseq
, but I don't see any mention of paired ends in theriboseq
documentation at https://xpresspipe.readthedocs.io/en/latest/content/riboseq.html.We have paired end input and RPF libraries, so we would like xpresspipe to handle this case.
Thanks for your continued help.