Is there any further filtering?

Issue #3 new
created an issue

I tried to reproduce your results obtained in sorghum by using the full-length RoIs from control and PEG treated that you uploaded ( So I parsed those reads with an identifiable 5', 3' and poly-A tail from both files and concatenated them. Then I ran TAPIS with the default parameters. However, when I compare these results with the transcripts inside the sorghum_isoseq.gtf file that you uploaded (, my output is much bigger. Even though I'm obtaining almost the same number genes that you did (I found 14,531 genes), my output had a much higher number of different transcripts: 48,261 versus those 23,667 transcripts that you found.

So my question is if you did any further filtering after the final output that returns . Should I modify any parameter to get better results?

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