Congenica
The Clinical Decision Support Platform for Genomics.
Overview
Congenica provides a clinical decision support platform that enables rapid and accurate interpretation of complex genomic data. Originally developed at the Wellcome Sanger Institute, the platform is used globally to streamline workflows for rare disease diagnostics, helping clinicians to make confident decisions and improve patient outcomes.
✨ Key Features
- Rare and inherited disease analysis
- Automated variant prioritization
- Trio and family-based analysis
- Customizable clinical reporting
- Integration of phenotypic data (HPO terms)
- Somatic cancer analysis capabilities
🎯 Key Differentiators
- Exclusive clinical decision support partner for the NHS Genomic Medicine Service
- Strong expertise in rare disease diagnostics
Unique Value: Provides a clinically validated platform for the diagnosis of rare diseases and cancer.
🎯 Use Cases (5)
✅ Best For
- Key partner in the UK's 100,000 Genomes Project
- Demonstrated to increase diagnostic yield and reduce analysis time
💡 Check With Vendor
Verify these considerations match your specific requirements:
- Labs focused exclusively on radiomics or non-genomic data
🏆 Alternatives
Strong partnerships with national genomics initiatives.
💻 Platforms
🔌 Integrations
🛟 Support Options
- ✓ Email Support
- ✓ Phone Support
- ✓ Dedicated Support (Varies tier)
🔒 Compliance & Security
💰 Pricing
✓ 14-day free trial
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