Hi all,
I have sucessfully completed an RNAseq pipeline with the old version of Cufflinks and I'm now trying to run the same data through the new versions of Tophat and Cufflinks. Namely, I'm hoping to add on all the bells and whistles of the new Cufflinks (bias correction, multi-read correct, and RABT).
My problem seems to be in implementing the RABT portion of Cufflinks. I suspect it might be a problem with the format of my GFF3 annotation. Could anyone who has successfully run the new version of Cufflinks please post a few lines of their annotation file?
Also, for researchers working on "more" complete genomes, how did you handle the completed-ness of the genome annotation vs. the increase in false-positives as was mentioned in the Roberts et al paper describing RABT?
Any help would be GREATLY appreciated!!!
I have sucessfully completed an RNAseq pipeline with the old version of Cufflinks and I'm now trying to run the same data through the new versions of Tophat and Cufflinks. Namely, I'm hoping to add on all the bells and whistles of the new Cufflinks (bias correction, multi-read correct, and RABT).
My problem seems to be in implementing the RABT portion of Cufflinks. I suspect it might be a problem with the format of my GFF3 annotation. Could anyone who has successfully run the new version of Cufflinks please post a few lines of their annotation file?
Also, for researchers working on "more" complete genomes, how did you handle the completed-ness of the genome annotation vs. the increase in false-positives as was mentioned in the Roberts et al paper describing RABT?
Any help would be GREATLY appreciated!!!
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