Releases: dnanexus-rnd/GLnexus
Releases · dnanexus-rnd/GLnexus
v1.1.4
v1.1.3
Experimental Strelka2 support
With --config Strelka2
GLnexus can merge Strelka2 gVCFs into pVCF. This is highly experimental right now (first attempt that produced well-formed output).
Bump a few dependency revisions
Fix two DeepVariant corner cases
- Don't call 0/0 from reference bands whose GT is not 0/0
- Fix obscure code path triggered by cluster of non-normalized gVCF alleles: monoallelic indel which some discovered allele didn't originally overlap, then got realigned and unified
The DeepVariant configuration remains experimental!
xAtlas calibration, QC squeezing
- Major improvements to xAtlas configuration including calibrated AQ filtering and genotype revision in the
xAtlas
configuration preset. There is also anxAtlas_unfiltered
preset with those features disabled. (#138) - Optional "squeezing" of output pVCF reduces pVCF size and runtime by reporting fewer QC details for most reference-identical genotypes. (#136)
- Currently opt-in with
--squeeze, -S
but planned to become the default - Further compression is possible by piping into spVCF for squeezing and/or sparse encoding.
- Currently opt-in with
- Minor:
- pVCF DP is filled in with gVCF MIN_DP instead of DP when both are present
- Accept rare HaplotypeCaller variant records with no AD or DP fields (considers all depths zero)
- Automatically test Getting Started examples
Fix performance regression
Memory and thread budget parameters introduced in #134 were not taking the desired defaults when not provided on the command-line.
v1.0.1
v1.0.0
test_travis_release
travis: deploy tagged revisions of glnexus_cli to GitHub releases