see tools/frq/wrapper.sh. series of scripts to extract allele freq and gene names from vcf files. additional script to visualize results.
requires:
single sample per input vcf
next steps:
will require reformatting to nextflow, currently written as a wrapper script
update figure script to accept list of single_sample and loop through "per sample plots" for each sample, currently the "all sample plots" are redundant
see
tools/frq/wrapper.sh. series of scripts to extract allele freq and gene names from vcf files. additional script to visualize results.requires:
next steps: