Procedure: 1. Sites that are likely homozygous-variant but are called as heterozygous are identified. 2. For each site and read group, we compute the proportion of bases in the pileup supporting an alternate allele. 3. A one-sample, left-tailed t-test is performed with the null hypothesis being that the alternate allele distribution has a mean of 0.95 and the alternate hypothesis being that the true mean is statistically significantly less than expected (pValue < 1e-9). git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@1989 348d0f76-0448-11de-a6fe-93d51630548a |
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