* with option --gvcf CLP will now put extra checks that a gvcf must adhere to (existance of <NON_REF> allele at every variant, and that the variants in total cover the entire requested intervals, or the whole genome if no intervals have been specified) * works on gvcf produced by HC when using either GVCF or BP_RESOLUTION mode * added positive and negative tests |
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| intellij_example.tar.bz2 | ||
| pom.xml | ||