Hi everyone,
I have a question in the case of, codons and regions in the whole DNA.
I wanted to design a pair of primers that include 167, 198 and 200 codons.
But I couldn't find them in the whole genes. I started from ATG(start codon) and continue to count and reach 167. but something is wrong. To get the right ORF, if I encountered the stop codon, should I continue the counting number of codons, or i should stop and start again from the next ATG?
https://www.ncbi.nlm.nih.gov/nuccore/DQ459314.1?feature=CDS
This link is related to the whole sequence.
Thanks