hg38 and long read sequencing

[ryan-moreno]

Hello,

Thank you for sharing InfoGenomeR. Do you have an estimate on when the integration with hg38 will be complete? What about the --additional_svs flag? I have been trying to rework the code to implement these things for my own use case but have run into many issues. I would be happy to help with the development of these features if I can get some questions answered about the origins of some of the reference files.