[ENH] Be able to switch between ref b37 and b38

KCCG / ClinSV

Robust detection of clinically relevant structural and copy number variation from whole genome sequencing data

Other

65 stars 8 forks source link

[ENH] Be able to switch between ref b37 and b38 #28

Closed J-Bradlee closed 2 years ago

J-Bradlee commented 2 years ago

As part as the feature implementations for version 1.1. See #27

This is a dedicated issue to the backwards capability feature request (task 1 for version 1.1).

We essentially want one version to be able to handle both supported reference genomes, rather than having to switch between the two if we want to use one or the other.

J-Bradlee commented 2 years ago

results.zip Just finished a run through, after a bit of debugging on my end. The results looks good after fixing that wig line count bug. We should be able to switch ref 37 and 38 quite readily.