Closed KyleEwart closed 2 years ago
Thanks for the question. The program is ideally for noncoding elements. Currently PhyloAcc doesn't support protein sequences as input. You could give CDS sequence a try, but PhyloAcc won't distinguish between synonymous and nonsynonymous substitutions.
Thanks for the question. The program is ideally for noncoding elements. Currently PhyloAcc doesn't support protein sequences as input. You could give CDS sequence a try, but PhyloAcc won't distinguish between synonymous and nonsynonymous substitutions.
Many thanks for your reply. Regards, Kyle
Hi @ xyz111131, Can PhyloAcc be used to investigate accelerated evolution of a set of candidate genes (i.e. can the set of conserved elements be ‘coding’ genes)? Or is the program only suitable for conserved noncoding elements?
I was hoping to use PhyloAcc investigate rate changes for thousands of single-copy Orthologue protein sequences from ~10 species. If this is possible, could the input fasta file be an amino acid alignment, or would you suggest using the corresponding cds sequence alignments?
Many thanks in advance, Kyle