Closed DarioS closed 2 years ago
Shouldn't all BAM files be recalibrated? It looks like a bad copy and paste from the germline variant pipeline.
# Collect sample IDs from samples.config # Only collect IDs for germline variant calling (labids ending in -B or -N) while read -r sampleid labid seq_center library; do if [[ ! ${sampleid} =~ ^#.*$ && ! ${labid} =~ -T.*$ && ! ${labid} =~ -P.*$ && ! ${labid} =~ -M.*$ ]]; then
Therefore, the nested tumour code segement will never be executed because any disease samples were previously excluded.
else samples_t+=("${labid}") group_input=${t_input} fi
Thanks for pointing out this Dario, all fixed now.
Shouldn't all BAM files be recalibrated? It looks like a bad copy and paste from the germline variant pipeline.
Therefore, the nested tumour code segement will never be executed because any disease samples were previously excluded.