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Hello there
It's not really a feature request, more a "help required"
I'm using derfinder to reannotate the Rat genome using RNA-seq data. I'm running fullcoverage() and regionmatrix() to id all the genomic region corresponding to transcript. However, fixing a unique cutoff value is problematic:
For weakly expressed genes, I lose the regions
For highly expressed genes, pre-transcript reads are not filtered enough and are identified as new regions.
I would like to know if there is a way to identify only region with a burst or a drop in reads according to surrounding background ?
Best
David
The text was updated successfully, but these errors were encountered:
Dalhte
changed the title
[Feature Request] A short description of the feature
[Help required] setting cutoff
Dec 4, 2023
Hello there
It's not really a feature request, more a "help required"
I'm using derfinder to reannotate the Rat genome using RNA-seq data. I'm running fullcoverage() and regionmatrix() to id all the genomic region corresponding to transcript. However, fixing a unique cutoff value is problematic:
For weakly expressed genes, I lose the regions
For highly expressed genes, pre-transcript reads are not filtered enough and are identified as new regions.
I would like to know if there is a way to identify only region with a burst or a drop in reads according to surrounding background ?
Best
David
The text was updated successfully, but these errors were encountered: