Previously, if a SNP occurred in sample A at a position that was in the middle of a deletion for sample B, sample B would be genotyped as homozygous reference there (but it's NOT reference - there's a deletion). Now, sample B is genotyped as having a symbolic DEL allele. Minor cleanup added. Note that I also removed Laura's previous fix for this problem. Existing integration tests change because I've added a new header line to the VCF being output. I also added several tests for the new functionality showing: 1. genotyping from separate and already combined gvcfs give the same output 2. genotyping over multiple spanning deletions works 3. combining works too Existing unit tests also cover this case. |
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| gatk-tools-protected | ||
| pom.xml | ||