#!/bin/bash -Ceuo pipefail
tabix -l HCC1395_tumor_vs_HCC1395_BL.tnseq.filtered.vcf.gz > HCC1395_tumor_vs_HCC1395_BL.chromosomes.txt

cat <<-END_VERSIONS > versions.yml
"NFCORE_SAREK:SAREK:BAM_VARIANT_CALLING_SOMATIC_ALL:EXTRACT_CHROMOSOMES_TNSEQ":
    bcftools: $(bcftools --version 2>&1 | head -n1 | sed 's/^.*bcftools //; s/ .*$//')
END_VERSIONS