Now in beta
Advanced literature review, automated variant analysis, and intelligent genetics workflows.

Features
Instantly find clinical and scientific evidence for genes or variants with AI.
Get StartedFind all papers associated with a variant and extract proband counts, segregation analyses, functional studies, and more
Answer specific genetics related questions, pulling in evidence from 20+ sources that you already trust
Gather information about many genes or variants within minutes
Extract evidence from 20+ sources that you already trust
Integrations
Seamlessly integrate with 20+ trusted databases and resources that your team relies on daily












Use Cases
Augment your existing workflows with trusted genomic intelligence.
Rapidly assess pathogenicity with comprehensive literature evidence, functional studies, and population data
Streamline ACMG/AMP classification with automated evidence gathering and standardized reporting
Build comprehensive gene profiles with disease associations, phenotypes, and molecular mechanisms
Prepare for MDT meetings with patient-specific evidence summaries and treatment recommendations
Analyze variant frequencies across diverse populations and identify ancestry-specific patterns
Speed up discovery with deep literature mining, hypothesis generation, and data synthesis
Pricing
Start free and scale as your team grows.
Perfect for getting started and exploring
$0
per month
Access to core platform
10 queries per month
Community support
Ideal for research and clinical teams
$100
per month
100 queries per month
Bulk analysis
Export to standard formats
Custom solutions for large organizations
Custom pricing
500+ queries per month
Team collaboration
Custom workflows