Entering edit mode
6 months ago
RUBEM
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0
Hi everyone, I have data from a variant call in rna-seq and I wanted to check if some of the variants are linked to the rna editing effect, I already researched it and didn't find a satisfactory answer.
abs.
As in you found workflows but disagree with the logic? Please provide more information as we don't know what answers you've found unsatisfactory, or why.
In fact, I found more talking about the RNA editing process than tools that can perform this analysis. My question is how I could do it, whether I use bam aligned or the vcf file and which tool I can use. Sorry, I'm not that experienced in bioinformatics.