Fabric Genomics
The new standard for clinical genomics.
Overview
Fabric Genomics provides a comprehensive bioinformatics and clinical interpretation platform designed for healthcare providers. It leverages advanced AI algorithms to analyze genomic data, identify disease-causing variants, and generate clinical reports. The platform supports a range of applications, including rare disease diagnosis, carrier screening, and somatic cancer analysis, aiming to make clinical genomics more accurate, efficient, and scalable.
✨ Key Features
- AI-powered variant interpretation (Fabric GEM)
- Scalable secondary and tertiary analysis
- Support for WGS, WES, and gene panels
- Somatic and germline variant analysis
- Customizable clinical reporting
- Integrated knowledge bases (e.g., ClinVar, OMIM)
🎯 Key Differentiators
- Proprietary AI (GEM) for rapid and accurate variant interpretation
- Proven ability to scale to whole-genome analysis
- Strong focus on clinical utility and diagnostic yield
Unique Value: Accelerates the time to diagnosis for genetic diseases by using AI to rapidly and accurately interpret complex genomic data, providing clinicians with actionable insights.
🎯 Use Cases (4)
✅ Best For
- Powering diagnostics at leading children's hospitals
- Interpreting whole genomes for undiagnosed disease programs
- Clinical reporting for commercial genetic testing labs
💡 Check With Vendor
Verify these considerations match your specific requirements:
- Basic academic research not focused on clinical interpretation
- Drug discovery research
🏆 Alternatives
Offers a more advanced, AI-driven interpretation engine that goes beyond simple filtering, improving diagnostic yield and reducing the need for manual curation compared to other clinical interpretation platforms.
💻 Platforms
🔌 Integrations
🛟 Support Options
- ✓ Email Support
- ✓ Phone Support
- ✓ Dedicated Support (Enterprise tier)
🔒 Compliance & Security
💰 Pricing
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