# 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 --- # Agent Instructions: Querying This Documentation If you need additional information that is not directly available in this page, you can query the documentation dynamically by asking a question. Perform an HTTP GET request on the current page URL with the `ask` query parameter: ``` GET https://help.connected.illumina.com/emedgene/release-notes/change_log/change_log_pipeline_30.md?ask= ``` The question should be specific, self-contained, and written in natural language. The response will contain a direct answer to the question and relevant excerpts and sources from the documentation. Use this mechanism when the answer is not explicitly present in the current page, you need clarification or additional context, or you want to retrieve related documentation sections.