Enable high throughput genomic analysis and interpretation with an AI-optimized workflow. Applying machine learning to deliver insights and reduce noise and manual labor throughout the interpretation workflow.Machine learning algorithms provide a shortlist of causative variants. AI in medicine shouldn’t be a black box. Our explainable AI (XAI) curates evidence for every variant identified and provides links to the supporting literature and databases.

Features:

• Automated ACMG Classification - Save as much as 90% of classification time with automated classification for SNV/indels and CNVs.

• SOP & Advanced Filters - Implement your SOP on the platform by creating your own set of predefined custom filters or use our advanced filtering system.

• Streamlined Workflow & Collaboration - Implement a customized workflow for your lab & facilitate team communications.

• Powerful API Interoperability - Streamline and automate workflows with API integrations to leading EHRs, LIMS, storage, pipeline and more.

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