- Filter vcf files on Genotype fields and variant call information such as zygosity, VAF, and read depth. Filters can include complex boolean logic, and can be used with annotation data.
- Directly annotate large, many-sample VCFs using `oc vcfanno`. A new vcf is created with `OC_XYZ` fields in the INFO column. Efficiently uses many threads to process genome-scale input.
- Python 3.12 compatibility
- View errors affecting specific variants from the jobs table in the GUI
- Fixes to checking for and installing annotator updates from the GUI
- Improved config file handling for converters