Hi, I'm using whole-exome sequencing (WES) for somatic variant calling. During the process, I tried to follow the approach described here: https://pubmed.ncbi.nlm.nih.gov/28420412/ **Basically my workflow …
I have read this post: https://www.biostars.org/p/136937 to further understand the output generated by bcftools isec. I'm trying to find variants that are common by location …
**Note1 - Previous version: https://www.biostars.org/p/271694/** **Note2 - this data is for hg19 / GRCh37** **Note3 - GRCh38 data is available [HERE][1]** ------------------------------- The tutorial has …
<p>Is there an easy way to extract the allele (monomorphic or polymorphic wrt the reference) for a sample across all reads at specific locations, given …
Can you try running
which bcftoolsfollowed by justbcftoolsand paste both outputs here? This might be a version mismatch.Also, just to eliminate a possibility, you're not typing the
$as part of the command, right?