Hi everyone!
Recently, I got a RNA-seq data of species X. As far as i know, original annotation of species X was generated by Ensembl pipeline. After i ran "tophat->cufflinks->cuffcompare", i found many novel features from assembled transcripts. For example, novel transcripts and novel 5'/3' UTR were found.
My question is, how can i improve the original annotation file(GFF3) by drawing knowledge from RNA-seq data ? Is there any software can do this?
Thanks a lot!!
Recently, I got a RNA-seq data of species X. As far as i know, original annotation of species X was generated by Ensembl pipeline. After i ran "tophat->cufflinks->cuffcompare", i found many novel features from assembled transcripts. For example, novel transcripts and novel 5'/3' UTR were found.
My question is, how can i improve the original annotation file(GFF3) by drawing knowledge from RNA-seq data ? Is there any software can do this?
Thanks a lot!!
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