I have HIV sequence data, where for three consecutive positions I have SNPS. These three all code for SNPS in the same codon.
predictcoding() returns the independently evaluated REFAA and VARAA, fine its expected behaviour. But a warning that "hey these variant amino acid mutations aren't true" would be nice!
I have HIV sequence data, where for three consecutive positions I have SNPS. These three all code for SNPS in the same codon. predictcoding() returns the independently evaluated REFAA and VARAA, fine its expected behaviour. But a warning that "hey these variant amino acid mutations aren't true" would be nice!