Entering edit mode
10.8 years ago
samsara
▴
630
I have been using HTSeq to count number of reads per feature for RNA-Seq. I am just wondering, Is it possible to get counts through Tophat by providing GTF file without using HTSeq?
Did you compare htseq and featureCounts in term of DE genes (using DESeq or edgeR) ?
No, because the difference in counting is usually very minor. The count differences are almost entirely due to an off-by-one difference in interpretation of GTF/GFF file coordinates.