v0.1.1

Added

• Updated code to handle records with multiple alts (#97).

Changed

• Genomic Source Class to a required parameter (#97).
• GitHub Action workflow to install dependencies from requirements.txt (#103).

Fixed

• Variant Inner-End calculation (#98).
• Installation error due to PyVCF by switching to PyVCF3 (#103).

v0.1.0

This is our first minor version release with support for structural variant conversion and incorporation of clinical annotations. For more details follow Readme. We would love to hear your feedback! If you find any issue please open an Issue.

Added

• Support for Structural Variants (#86).
• Support for Clinical Annotations (#89).

v0.0.17

Added

• Exposed a new parameter to configure ratio for determining Homoplasmic vs Heteroplasmic (#19).

Changed

• Build process to PEP 517 (#18).

Fixed

• Excluded records with incorrect CHROM values in vcf file (#19).
• Removed 'Human reference sequence assembly version' component from variant observation (#36).
• Case where conversion region is not studied (#66).
• FHIR validation errors and warnings (#77).