🗂️ Navigation
🔧 Congenica

Congenica

The Clinical Decision Support Platform for Genomics.

Visit Website →

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)

Diagnosis of rare and inherited diseases Pediatric genetics Prenatal testing National genomics programs Translational research

✅ 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

Fabric Genomics SOPHiA GENETICS PierianDx

Strong partnerships with national genomics initiatives.

💻 Platforms

Web API

🔌 Integrations

LIMS/EHR integration via API Integration with various annotation databases

🛟 Support Options

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

🔒 Compliance & Security

✓ HIPAA ✓ BAA Available ✓ GDPR ✓ ISO 27001 ✓ SSO ✓ ISO 27001 ✓ ISO 13485 ✓ CE-IVD

💰 Pricing

Contact for pricing

✓ 14-day free trial

Visit Congenica Website →