v2.9.0

What's Changed

• Fix linting issues by @apriha in #179
• Parse Sano DTC format by @apriha in #180
• Add support to detect plink generated 23andme files by @teepean in #176
• Add PLINK test by @apriha in #181
• Parse PLINK by @apriha in #182
• Fix DtypeWarning by @apriha in #183
• Enhance VCF output by @apriha in #184

New Contributors

• @teepean made their first contribution in #176

Full Changelog: v2.8.2...v2.9.0

v2.8.2

What's Changed

• Lint and format with Ruff by @apriha in #175
• Fix OverflowError by @apriha in #178

Full Changelog: v2.8.1...v2.8.2

v2.8.1

What's Changed

• CI updates by @apriha in #172
• Fix GenomePrep resources by @apriha in #174

Full Changelog: v2.8.0...v2.8.1

v2.8.0

What's Changed

• Fix CI issues by @apriha in #169
• Support modern Python versions by @apriha in #170
• Update ezancestry, works local by @arvkevi in #171

Full Changelog: v2.7.2...v2.8.0

v2.7.2

Updated

• Fix CI builds

v2.7.1

Updated

• Fix CI builds

v2.7.0

Added

• Detect deduced chip array and chip version based on chip clusters
• Identify and filter low quality SNPs based on chip clusters
• Add various VCF output options related to low quality SNPs (drop and/or populate FILTER column)
• Add helper output functions (to_csv, to_tsv, to_vcf)
• Add ability to prefix chromosomes in VCF output

Updated

• Deprecate reading/writing class methods
• Deprecate save method

Fixed

• Write output file with no additional blank lines (Windows)

v2.6.0

Added

• Add support for CircleDNA
• Enable specification of unavailable VCF ALT allele

Updated

• More robust parsing of AncestryDNA and 23andMe files

v2.5.0

Added

• Add support for Python 3.10

v2.4.4

Updated

• Fix CI builds