v0.1.1

1. Fixed duplicated DP and AF in somatic mode.
2. Added DP and AF in germline output VCF.

v0.1.0

1. Added somatic variant representation unification workflow. User can enable by using the --somatic_mode option. The somatic mode prioritizes only low-VAF sites (default 0.08, configurable using --max_af_for_somatic_unification) during processing and optimized alignment scanning for computational efficiency. A configurable edit distance thresholds (maximum 0 for SNV and 4 for Indel) is used. This allows for gaps between VCF haplotypes and alignment haplotypes for more potential matches into manual consideration.

v0.0.1

Initial release.