A python framework to read in VCF files and a given Genbank genome and parse out the genes the SNPs occur in, and what if any changes in translation occur.
Goal 1: Read in genome from GenbankGoal 2: Find all CDS, and the sequence / translation.Goal 3: Find the position of each SNP in CDS.- Goal 4: Build replace the SNP base and get new translation.
- Goal 5: Identify what changes in amino acids occur if any.