Company profile

Congenica

The UK's Most Trusted Genomic Interpretation Partner

Precision Medicine & Genomics

Company profile

About Congenica

Congenica is a clinical genomics company that transforms raw sequencing data into actionable clinical insights for precision medicine. Founded at the Wellcome Sanger Institute in 2012, Congenica has been at the heart of the UK's genomic medicine journey for over a decade, from the 100,000 Genomes Project to today's NHS Genomic Laboratory Hubs (GLHs). In 2025, Congenica joined SeqOne to create a global leader in AI-powered genomic medicine. The company's platform provides advanced NGS analysis across rare diseases, oncology, and infectious diseases, combining AI-driven variant prioritization with clinical-grade accuracy. Their DiagAI technology automatically identifies 96% of diagnostic variants with 92% specificity, ranking 90% of causal variants in the top 3 positions. The platform includes comprehensive capabilities for panels, whole exome sequencing (WES), and whole genome sequencing (WGS), with multi-caller architecture, CNV/SV detection, mitochondrial analysis, and automated ACMG classification. Congenica serves health systems, diagnostic laboratories, and genomic medicine services worldwide, with particular strength in the UK's NHS where they support multiple Genomic Laboratory Hubs. The company also provides Clinical Interpretation Services through NHS-trained genomic experts who deliver variant analysis and clinical reporting. As part of the SeqOne family, Congenica now operates with a 125+ person team across Cambridge, Paris, and Montpellier, backed by €20M in recent funding and serving 190+ laboratories in 35+ countries.

Company description Congenica official website

Mission. Genomic Medicine for Everyone. We believe every patient deserves the benefit of genomic medicine, regardless of geography or healthcare system.

Primary marketPrecision Medicine & Genomics
Commercial modelCommercial information available on request
Company presenceOfficial website
Work at Congenica?

Claim this profile to manage Company information and connect with the Health AI Central audience.

Claim this listing

01 · Operating footprint

Where the Company operates

Company-profile context for clinical focus, customers, deployment, integration, milestones, and partnerships.

Clinical focus

  • Antimicrobial resistance
  • Bacterial infections
  • Chronic lymphocytic leukemia (CLL)
  • Hematological cancers
  • Hereditary cancers
  • Inherited disorders
  • Ovarian cancer (HRD testing)
  • Rare diseases
  • Solid tumors
  • Viral diseases

Who it serves

  • Clinical genetics services
  • Diagnostic laboratories
  • Genomic Laboratory Hubs
  • National genomics programs
  • University hospitals

Deployment & integration

Cloud Saas · Other deployment with recorded integration context.

Geographic context

Markets35+ countries globally · Africa · Americas · Europe · Hong Kong · Middle East · United Kingdom
Company sourceOfficial website

Company milestones

Platform expansion

September 2025: Acquired by SeqOne to create global leader in AI-powered genomic medicine. November 2024: Achieved IVDR certification. 2023: Named exclusive tertiary analysis partner for Hong Kong Genome Project. November 2025: Launched SomaLBx and SomaMethyl for liquid biopsy analysis. May 2025: SeqOne raised €20M in growth funding.

Partnerships

Recorded partners

  • Agilent Technologies
  • Genomics England (100,000 Genomes Project)
  • Hong Kong Genome Project
  • MGI Tech
  • NHS Genomic Laboratory Hubs
  • Oxford Nanopore Technologies
  • SeqOne (parent company)
  • Wellcome Sanger Institute

02 · Flagship portfolio

Products, workflows, and platform capabilities

Selected source-backed Company products and the available commercial context.

Clinical Interpretation Services

NHS-trained genomic experts for variant analysis and clinical reporting

Service · OtherCompany source

DiagAI

AI-powered variant prioritization and interpretation with explainable results

Software · Cloud SaaSCompany source

GenomeAlert

Automated variant re-analysis for unsolved cases

Software · Cloud SaaSCompany source

SeqOne CGH Array Interpretation

CGH array analysis and interpretation platform

Software · Cloud SaaSCompany source

SeqOne Platform (Congenica)

AI-powered genomic analysis platform for rare disease, oncology, and infectious diseases

Platform · Cloud SaaSCompany source

SomaHemato

CLL prognostics with IGHV mutational status analysis

Software · Cloud SaaSCompany source

SomaHRD

In-house HRD testing solution for ovarian cancer

Software · Cloud SaaSCompany source

SomaLBx

Comprehensive liquid biopsy analysis for oncology

Software · Cloud SaaSCompany source

SomaMethyl

Epigenetic signature analysis for liquid biopsy

Software · Cloud SaaSCompany source

03 · Research intelligence

Research Intelligence evidence

Publications, preprints, clinical validation, and regulatory records in Evidence Position order.

04 · Company-reported outcomes

Outcomes and case studies

Company-reported outcomes and customer stories are distinct from linked Research Intelligence evidence.

96% diagnostic variant detection

DiagAI automatically identifies diagnostic variants

92% specificity

SmartPick variant suggestion accuracy

90% of causal variants ranked in top 3

Variant prioritization performance

200,000+ patient analyses annually

Platform capacity and scale

Genekor Medical

Making HRD testing routine clinical workflow using shallow WGS

Cut complexity and costs, proving reliable precision oncology testing achievable for regional labs

Uppsala University Hospital

Building unified, future-proof genomics lab infrastructure

Revolutionized clinical diagnostics with comprehensive genomics capabilities

Cerba Internacional

Overcoming NGS data bottlenecks with AI-powered bioinformatics

Scaled personalized medicine and redefined NGS analysis workflows

CHU de Reims

Advanced genomic analysis for transforming patient care

Empowered with advanced genomic analysis capabilities

AP-HM (Assistance Publique - Hôpitaux de Marseille)

Automated exome analysis at scale

Achieved precision medicine at scale with automated exome analysis success

North West GLH

Validation and implementation of in-house HRD testing

Successfully validated and implemented in-house HRD testing with SomaHRD

Hong Kong Genome Project

Exclusive tertiary analysis partner for 40,000-50,000 patient genome initiative

Named exclusive tertiary analysis partner for Hong Kong's first large-scale genome programme

NHS Genomic Medicine Service

Embedding genomic interpretation into routine clinical care across multiple GLHs

Platform embedded into routine clinical care across multiple NHS Genomic Laboratory Hubs

Genomics England (100,000 Genomes Project)

National-scale genomic medicine program analysis

Established as cornerstone of UK genomic medicine, supporting national genomic medicine service

Manchester North West GLH

HRD testing implementation with transparent genomic instability score calculation

High-resolution sample information with detailed genomic instability score calculation providing additional confidence in clinical reporting

St George's University Hospitals NHS Foundation Trust

Detection of low-level variants that could lead to missed diagnoses

Demonstrated diagnostic utility in cases where low variant levels could have led to missed diagnosis, providing reassurance to clinical team

05 · Leadership

Leadership team

Leadership profiles and professional links from the current Company record.

No active leadership profiles are currently listed.

06 · Company updates

Updates from Congenica

Recent articles published on Congenica's official website.

07 · HAIC coverage

Coverage and analysis

Health AI Central reporting that mentions this Company.

No HAIC coverage is currently linked to this Company.

08 · Official presence

Company sources and channels

Curated official destinations from the active Company record.

09 · Market pathway

Additional Companies in this Market

Other active Companies in the same market, selected alphabetically from the HAIC directory.

Market context

Precision Medicine & Genomics

Companies using AI to analyze genomic, proteomic, metabolomic, or multi-omics data to provide personalized treatment recommendations, identify genetic risks, or develop targeted therapies. Includes genomic sequencing platforms with AI analysis, preventive medicine based on genetic risk assessment, and longevity care based on molecular and genetic data.

Explore the full market directory or compare this Company with additional active profiles.

View all Companies in this market

10 · Pro research

Coming soon

Expanded Company research is in development.

Health AI Central Pro · Coming Soon

Deeper Company research is coming soon.

Pro Research will introduce expanded technical context, linked evidence analysis, and comparative Company research.

ResearchEvidence analysis

Linked research, clinical, and regulatory source pathways.

CompanyTechnical context

Expanded product, deployment, integration, and partnership research.

MethodSource & review record

Record-level provenance and review context.

Coming Soon