c96fee477c
-- Call sets with indels > 50 bp in length are tagged as CNVs in the tag (following the 1000 Genomes convention) and were unconditionally checking whether the CNV is already known, by looking at the known cnvs file, which is optional. Fixed. Has the annoying side effect that indels > 50bp in size are not counted as indels, and so are substrated from both the novel and known counts for indels. C'est la vie -- Added integration test to check for this case, using Mauricio's most recent VCF file for NA12878 which has many large indels. Using this more recent and representative file probably a good idea for more future tests in VE and other tools. File is NA12878.HiSeq.WGS.b37_decoy.indel.recalibrated.vcf in Validation_Data |
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| .. | ||
| CNV | ||
| annotator | ||
| beagle | ||
| coverage | ||
| diffengine | ||
| fasta | ||
| filters | ||
| genotyper | ||
| indels | ||
| phasing | ||
| qc | ||
| recalibration | ||
| validation | ||
| varianteval | ||
| variantrecalibration | ||
| variantutils | ||
| BAQIntegrationTest.java | ||
| ClipReadsWalkersIntegrationTest.java | ||
| PileupWalkerIntegrationTest.java | ||
| PrintReadsIntegrationTest.java | ||
| PrintReadsWalkerUnitTest.java | ||