v0.24

• Fixing problem with self-test on gnomAD genomes with chrY (#51)
• Suppress writing out *Carriers information in INFO column for SVs (#53)

v0.23

IMPORTANT COMPATIBILITY NOTE:
For annotating SVs, the output of this version is not compatible with varfish-server v1.2 (Anthenea) and early versions of the v2 (Bollonaster) development branch.
You can generate compatible files by adding the --opt-out=chrom2-columns,dbcounts-columns as arguments to annotate-svs.

• Adding chrom2/count columns to output of annotate-sv (#41)
• Writing out BND mates for Delly (#45)

v0.22

• Adding db-stats command (#25)
• Adding issue templates (#28)
• Adding continuous integration with GitHub Actions (#28)
• Adding unit tests for annotate command (#31)
• Adding unit tests for annotate-sv command (#33)
• Writing out gzip-ed files if output file name ends in .gz (#11)
• Do not write out asterisk alleles (#18)
• Adding tests for GRCh38 (#22)
• Adding self-tests for annotation (#27)
• Allow properly counting hemizygous variants when pedigree file is given (#36)

v0.21

v0.21

• Bumping jannovar-core dependency for fixes in chrMT annotation.

v0.20

• Further bumping of jannovar-core against log4shell.
• Fixing problem with missing SVMETHOD annotation of SV VCFs.

v0.19

• Bumping jannovar-core dependencies against log4shell vulnerability.

v0.18

• Fixing problems with querying in GRCh38.

v0.17

• Adding support for GRCh38 release.

v0.16

• Fixing import of ExAC r1 VCF.
• Prevent import of REF and ALT alleles with sizes above 1000bp (field lengths in database).

v0.15

• Properly removing "chr" prefix for data aligned to hg19.
• Checking whether the supported release GRCh37/hg19 was used.
  Will only allow processing of such genomes and block variants from GRCh38/hg38 which would lead to incorrect results.