> For the complete documentation index, see [llms.txt](https://help.bioinsight.illumina.com/llms.txt). Markdown versions of documentation pages are available by appending `.md` to page URLs; this page is available as [Markdown](https://help.bioinsight.illumina.com/emedgene/release-notes/change_log/change_log_pipeline_30.md).

# 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


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