# Change log pipeline 30

## Features

* Feature | New XAI for CNVs and compound heterozygous SNV-CNV variants
* Feature | New and more accurate phenotypic match model, Phenomeld
* Feature | Support for DRAGEN 4.0 with ML for customers running their own DRAGEN and through Emedgene
* Feature | Lab Page | Gene Coverage - Region coverage statistics will now be calculated based on the case’s kit associated BED file
* Feature | Default BED files for coding regions, clinical regions (used for exome) and genomes were updated with latest RefSeq Curated and Gencode versions.
* Feature | Re-including Polyphen annotation, and update to consider most severe value
* Feature | Support for DRAGEN Force Genotyping caller

## Bug Fixes

* Bug Fix | Quality metrics for duplications when CN > 3