2.6.0

• 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