| Intuitive Variant Analysis Workflow |
- Table Filters that can be pre-set at an institution level or an individual user level to standardize analysis workflow
- Integrated with third-party databases, such as Clinvar, gnomAD, OMIM, Cosmic to provide all of the information in one view
- Functionality for multi-sample comparisons, such as tumor-normal and exome trio analysis
- Integrated Genome browser shows the dynamic view of the case, and provides real-time access to BAM file from the browser
- Patient and order-level information including clinical history accessible in the same window during analysis
- AI based Genosity engine built in to learn as your data grows to facilitate faster analysis
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| User-Friendly Report Generation Interface |
- Single click to switch from analysis to report mode
- Flexible report layout templates allow branding as well as white labeling
- Content templates allow save and reuse of approved variant results to save time in future
- ACMG and AMP classification system supported for germline and somatic tests respectively
- Ability to add clinical trial recommendations and secondary/incidental findings
- Variant reclassification and report amendments with version control supported
- Case Assignment functionality for primary, secondary, and director approval
- PIN security for electronic signature sign out
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| Genosity Knowledgebase and Interpretation Services |
- >100,000 and growing pre-loaded variant classifications and interpretations in Genosity Knowledgebase to reduce curation burden and expedite review process
- Approval process configured for saving variant classification and interpretation for later use
- Share variant interpretations with partner institutions by choice
- Our highly experienced clinical team of board-certified geneticist and genetic counselors available to assist in variant review, interpretation and drafting reports if needed
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