-- Previous version would count all alt alleles as present in a sample, even if only 1 were present, because of the way VariantEval subsetted VCs -- Updated code for subsetting VCs by sample to be clearer about how it handles rederiving alleles -- Update a few pieces of code to get previous correct behavior -- Updated a few MD5s as now ref calls at sites in dbSNP are counted as having a comp sites, and therefore show up in known sites when Novelty strat is on (which I think is correct) -- Walkers that used old subsetting function with true are now using clearer version that does rederive alleles by default |
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| .. | ||
| CNV | ||
| annotator | ||
| beagle | ||
| bqsr | ||
| coverage | ||
| diagnostics | ||
| diffengine | ||
| fasta | ||
| filters | ||
| genotyper | ||
| indels | ||
| phasing | ||
| qc | ||
| validation | ||
| varianteval | ||
| variantrecalibration | ||
| variantutils | ||
| BAQIntegrationTest.java | ||
| ClipReadsWalkersIntegrationTest.java | ||
| FlagStatIntegrationTest.java | ||
| PileupWalkerIntegrationTest.java | ||
| PrintReadsIntegrationTest.java | ||
| PrintReadsUnitTest.java | ||