Hi Yan,
I suspected that this was what you were originally asking, but then
reconsidered when I read the subject line again. This is because one of
the functions of Cufflinks is to do what you are asking - it brings
together mapped RNA-seq data to produce transcript/genes based on either
read
Hi Jen,
Thanks for your reply! I know this workflow. I am just wondering if there
is a tool in Galaxy to combine the reads that mapped to the same gene with
different positions before running cufflinks.
Thanks again,
Yan
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发件人: Jennifer Jackson [mailto:j...@bx.psu.edu]
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