Ability to genotype candidate variants from input vcf is retained and can be turned on by command line argument but is disabled by default. Code, by default, will build a consensus of the most common indel event at a pileup. If that consensus allele has a count bigger than N (=5 by default), we proceed to genotype by computing probabilistic realigmment, AF distribution etc. and possibly emmiting a call. Needed for this, also added ability to build haplotypes from list of alleles instead of from a variant context. git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@4893 348d0f76-0448-11de-a6fe-93d51630548a |
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