Product
An AI-powered platform for fast and precise
genetic variant interpretation in rare diseases
AI-powered variant interpretation platform for clinical decision support
Sample
Sequencing
Variant Call
Analysis
Report
Extensive
A wide range of variant types are supported, including SNV/INDEL, CNV, inversions, translocations, mobile element insertions, repeat expansions.
Reliable
Variants are automatically classified by EVIDENCE following modified ACMG guidelines, leveraging 3 modules, with interpretation accuracy of 99.4%.
Efficient
With AI variant prioritization tool, enable faster and more accurate diagnoses, raise your efficiency in diagnosis.
is the optimal solution for medical professionals
Streamlined Workflow
From sequencing data to final interpretation, all in one place.
Broad Variant Support
Analyze all variant types through an automated pipeline.
Trusted Annotations
Clinical insights backed by reliable databases.
AI-Powered Efficiency
Smart prioritization and advanced filtering for faster review.
What technology does it use?
3Cnet
AI-based pathogenicity prediction model trained on clinical, population, and evolutionary data. It improves variant classification accuracy by integrating data from ClinVar, gnomAD, and UniRef.
