Attma is a new way to do self-serve genomic analytics. Anyone can ask questions in plain language and get detailed, trustworthy answers.

Experience the power of conversational AI built specifically for clinical genomics and bioinformatics workflows
Simply ask "Show me pathogenic BRCA1 variants" and get instant, accurate results. No complex syntax required.
AttmaAI delivers clinical variant interpretation with industry-leading 92% accuracy, surpassing competitors at 85-88%.
From VCF upload to comprehensive clinical report in 60 seconds. GPU-accelerated analysis for real-time results.
Real-time multi-user discussions, shared analyses, and collaborative case reviews with your clinical team.
Automated 5-tier clinical interpretation following ACMG/AMP guidelines with comprehensive evidence scoring.
Pre-built genomics analyses for BRCA, Lynch syndrome, and more. Load templates and get insights instantly.
Experience the power of AI-driven insights that understand your questions and deliver clinical-grade results
Type a question in plain language and get detailed, trustworthy answers. Our AI assistant understands genomics terminology and delivers accurate insights backed by clinical evidence.

AttmaAI goes beyond surface-level analysis. Our AI can explore multiple lines of inquiry, fix its own errors, and provide comprehensive clinical interpretation with 92% accuracy.

Get started in 60 seconds with our pre-built genomics templates. Load BRCA analysis, Lynch syndrome screening, or custom workflows and customize them for your specific needs.

AttmaAI combines cutting-edge machine learning with clinical genomics expertise to deliver accurate, actionable insights
92% accuracy clinical variant interpretation. Our AI understands genomics terminology and delivers evidence-based insights.
Context-aware discussions that remember previous queries. Ask follow-up questions and refine your analysis naturally.
Automated 5-tier clinical interpretation following ACMG/AMP guidelines with comprehensive evidence scoring.
Automatic inheritance pattern detection and family risk assessment with interactive pedigree visualization.
AI-powered comprehensive patient reports generated in seconds. Export-ready with clinical recommendations.
Real-time multi-user analysis sessions. Share insights, discuss cases, and collaborate with your clinical team.
Choose the perfect plan with full AttmaAI access and conversational analysis capabilities
Perfect for small research teams getting started
Ideal for growing clinical genomics teams
For large healthcare organizations
Have questions about pricing? View our FAQ or contact us