Dear all,
Can tophat or cufflinks be used to simply assign a sequence read to a gene based on genome position? Or can another program do that with SAM output or anything else (e.g. PSL)?
Cufflinks reports FPKM for genes and transcripts based on the number of reads most likely mapping to them. I think it would be cool if you had something like a --read_to_gene option that reports which reads most likely belonged to which gene/transcript.
Can this be done with Tophat/cufflinks or another program?
Thanks for any advice.
J.
Update: I just found something and this thread solves it;
Actually, it would still be good if TopHat/Cufflinks could optionally output reads to transcript assignments as it takes into account paired end data for isoform assignment. Any fresh views still very much appreciated.
Can tophat or cufflinks be used to simply assign a sequence read to a gene based on genome position? Or can another program do that with SAM output or anything else (e.g. PSL)?
Cufflinks reports FPKM for genes and transcripts based on the number of reads most likely mapping to them. I think it would be cool if you had something like a --read_to_gene option that reports which reads most likely belonged to which gene/transcript.
Can this be done with Tophat/cufflinks or another program?
Thanks for any advice.
J.
Update: I just found something and this thread solves it;
Actually, it would still be good if TopHat/Cufflinks could optionally output reads to transcript assignments as it takes into account paired end data for isoform assignment. Any fresh views still very much appreciated.
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