Identify synonymous versus non synonymous variants
Hi, after a poolseq analysis, I have identified some genomic variants. I just want to check whether these variants change the amino acid (for those that fall in coding regions). I have a gff file, the genome in fasta and a table with candidates coordinates.
I'm not sure what would be the easiest way to do so.
Can anyone share experience on that? Thank you, Best regards, Julien
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