Hi Chris. I'm seeking to use the roadmap RNA-Seq data to identify and analyze splice sites active in each cell type. Is there some way to get these from the PASH output? Perhaps something analogous to the BowTie/TopHat Junction files? Right now I only seem to have access to PASH .bed outputs and am not familiar with the interpretation of columns 4-6 (e.g.)
chr1 22336244 22336343 HAL:1220:C0NTJACXX:3:1112:2443:33889 1 +
chr1 22336249 22336348 HAL:1220:C0NTJACXX:3:1112:3363:36331 1 -
Thanks!
I don't know with any certainty (thus this is a comment), but I'd guess that Pash being able to handle normal and bisulfite treated read alignment played a role. Then at least there's just one single tool that can used for everything. I wouldn't have chosen that, but that's at least an argument in favor of Pash.