Open SarahNadeau opened 1 year ago
I forgot that ParSNP requires the core genome to be present in ALL strains, so I can't concatenate alignments to the same reference like I thought. New strains will change the alignment length.
Use a different alignment method, or call SNPs from SRA data instead?
It's expensive to re-make the NCBI database and re-generate the core genome alignment every time a build is updated.