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.