v2.29.0

This version adds the sample-genome feature added by @ozemsbg .
This feature enables a user to create a simulated VCF from an original VCF carrying AF values or by assuming a fixed AF value and applying that to the variants carried in a VCF.

v2.23.0

This is the version of the code used to generate the data and analysis presented in the aligner paper.

Please see release notes for a summary of what has been added.