slim_vcf2fasta_chrom.py currently requires the Chlamydomonas annotation table (as well as the ANT parser) to generate reference sequence.
This could be removed by adding a separate script that generates that reference sequence as a FASTA file, after which this script would just read in that FASTA and immediately get to assigning alternate alleles based on variants in the SLiM output.
slim_vcf2fasta_chrom.py
currently requires the Chlamydomonas annotation table (as well as theANT
parser) to generate reference sequence.This could be removed by adding a separate script that generates that reference sequence as a FASTA file, after which this script would just read in that FASTA and immediately get to assigning alternate alleles based on variants in the SLiM output.