Hi everyone
Is there a tool to combine VCFs generated from different germline variant callers such as Lofreq, iVAR, Bcftools and haplotypecaller (maybe union or intersection) that chooses variants based on something like majority voting rule like if a variant is supported by atleast 3 or more variant callers it's gonna keep it.
I know there exists many ensembl method like SomaticCombiner for Somatic variant calling algorithms but I couldn't find anything on germline.
Hi David Langenberger
I have been using bcftools but I don't know how to get like a proportion value of how many variant callers support a particular variant (like 50% of variant callers support this particular variant).
Will definitely check out CombineVariants.
I couldn't find the JAMM, can you please share the link of paper/github?
I am afraid
CombineVariants
is not available anymore as per discussion thread here