2021_06
June 2021 release:
- General: Improved GRCh38 support in several tools.
- General: Using BGZIP for compressed VCFs now to allow indexing them with tabix.
- VcfAnnotateFromBed: Made separator configurable; Added check for separator in source BED file; Fixed broken output VCF if input has no FORMAT column.
- VcfAnnotateFromVcf: Fixed crash in VCF header parser.
- NGSDExportSamples: Added ancestry column.
- SampleAncestry: Improved runtime and memory use.
- SampleGender: Improved runtime for algorithm 'hetx'.
- SomaticQC: Added support for mutect2.
- NGSD:
- Added disease status 'Unclear' to table 'sample'.
- Added table 'processed_sample_ancestry'.
- Added percent occupied to 'runqc_lane' (for Illumina NovaSeq).
Please do not use the auto-generated 'Source code' packages - they will not work!