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🔧 Nostos Genomics

Nostos Genomics

AI-powered variant interpretation for rare diseases.

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Overview

Nostos Genomics provides AION, a platform that automates the interpretation of genetic variants for Mendelian diseases. It uses a 'digital twin' approach to model the molecular effect of variants, providing a transparent and evidence-based assessment to help clinicians make diagnoses faster and more accurately.

✨ Key Features

  • AI-powered variant interpretation (AION)
  • Focus on rare and Mendelian diseases
  • Explainable AI (XAI) provides evidence for predictions
  • Automated ACMG classification
  • VCF and phenotype (HPO) input

🎯 Key Differentiators

  • Focus on explainable AI (XAI) to build trust
  • Novel 'digital twin' approach to variant effect prediction
  • Specialization in automating interpretation for Mendelian diseases

Unique Value: Provides a transparent, AI-driven interpretation of genetic variants that not only gives an answer but also shows the evidence behind it, increasing confidence and speed in rare disease diagnosis.

🎯 Use Cases (4)

Rare disease diagnosis Variant of Uncertain Significance (VUS) resolution Clinical genetics research Accelerating trio analysis

✅ Best For

  • Demonstrated to reduce interpretation time and identify causal variants missed by other methods

💡 Check With Vendor

Verify these considerations match your specific requirements:

  • Somatic cancer analysis
  • Labs not focused on rare Mendelian diseases

🏆 Alternatives

Fabric Genomics (GEM) Congenica Varsome

Unlike 'black box' AI models, its focus on explainability allows clinicians to understand and verify the AI's reasoning, which is critical for clinical adoption.

💻 Platforms

Web API

🔌 Integrations

API for integration into existing workflows

🛟 Support Options

  • ✓ Email Support
  • ✓ Dedicated Support (Varies tier)

🔒 Compliance & Security

✓ HIPAA ✓ BAA Available ✓ GDPR ✓ CE-IVD

💰 Pricing

Contact for pricing

✓ 14-day free trial

Visit Nostos Genomics Website →