Hi all,
Would like to know if there is a minimum number of transcripts required in a GTF file in order for cufflinks to run properly?
I've also tried this with cuffdiff:-
1) full genome GTF
2) take 10 transcripts out of the full GTF
the FPKMs seem to pile on in the results from the smaller GTF file.
Am I doing something wrong? The reason I'm doing this is for screening some potentially novel transcripts / locations in the genome, and would likely be working with a much smaller set of GTF entries.
Advise is much welcomed!!!
Would like to know if there is a minimum number of transcripts required in a GTF file in order for cufflinks to run properly?
I've also tried this with cuffdiff:-
1) full genome GTF
2) take 10 transcripts out of the full GTF
the FPKMs seem to pile on in the results from the smaller GTF file.
Am I doing something wrong? The reason I'm doing this is for screening some potentially novel transcripts / locations in the genome, and would likely be working with a much smaller set of GTF entries.
Advise is much welcomed!!!
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