- Fixed imports in our fork of pyvenn
- Fixed broken Pyvenn dependency
- Update PyVCF to PyVCF3
- Fix defect in narrow command wrongly printing ALT=. when GT=.
- Add the
count
command to count samples, positions, calls, snps, indels, other variants, filtered calls, missing calls, and filter reasons. - Add the
plot
command to plot calls along the length of the genome and show the location of filtered calls. - Change the text of the compare report to refer to "Calls", not "Sample snps".
- Drop support for Python 3.4, which is not supported by matplotlib.
- Add support for Python 3.7.
- Replace None with '.' when printing call data.
- Support VCF files with multiple alternate alleles per position.
- Support reading gzip compressed vcf files.
- First public release.