# Change log workbench 2.29

## **Features:**

* Support for interpreting SV insertions, including compound heterozygous
* STR enhancements - new pathogenicity filter, allele frequency added to visualization
* New visualization tracks for ClinVar, ClinVar SV and BigWig
* Emedgene Curate supports CNVs
  * Selectable overlap in related cases
  * Export from Analyze to Curate
* Workflow improvements
  * Gene-related disease card improvement
  * Edit interpretation summary
  * Variant page sidecar redesign
* Analysis table enhancement - when variant has conflicting classifications it will be displayed in black
* DRAGEN QC metrics available for download on lab page
* Input sample file errors exposed in the cases page
* Support for ACMG 78 genes in filter
* Admins can add tags in management page
* Header design change to match Illumina software

## **Enhancement:**

* Added organization setting activity log, viewable from dashboard page on all activity including by ILMN support teams on the backend
* Enable lossless compression on PDF reports (a support request)
* API | Ability to get detailed version information via API calls
* Analysis Tools | Preset Filters | Apply gene list on the fly - validate gene symbols with NCBI ID

## **Bug fixes:**

* mtDNA visualization on GRCh37 bug fixes
* Lab Page | Warning when mtDNA were called on wrong reference and no data is presented
* Curate | SNV variants include alt validation
* Curate | Support Indels and mtDNA
* Var Page | Visualization | Instability issues fixed
* Var Page | Remove related disease for genes of unknown significance
* Var Page | Fix broken OMIM links for genes associated with multiple diseases
* Var Page | STR | Allow selection of existing interpretation paragraph
* Analysis Tools | Fix zygosity other family members
* Analyze | Export to Curate | Fix disease export field