History

0.1.0 (2019-07-08)

  • First release.

0.1.1 (2019-08-08)

  • Read and process multialignments from fasta and csv files (Python module only).

0.1.2 (2019-10-17)

  • Add tests with and without reference included in multialignments;

  • Add tests with real datasets (coming from haplogroup-specific multialignments).

0.1.3 (2019-10-18)

  • Add more detailed tests for real datasets;

  • Implement more efficient frequency calculation;

  • Add dunder methods and sanity checks;

  • Fix requirements and testing framework;

  • Clean code.

0.2.0 (2020-03-07)

  • Remove numpy and pandas from requirements as they are installed by scikit-bio;

  • Move tests module inside allfreqs;

  • Add ci module for internal management;

  • Clean code.

0.3.0 (2020-04-02)

  • Add option to allow ambiguous nucleotides shown separately.