Clinical Interpretation Services
NHS-trained genomic experts for variant analysis and clinical reporting
Company profile
The UK's Most Trusted Genomic Interpretation Partner
Company profile
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.
Claim this profile to manage Company information and connect with the Health AI Central audience.
01 · Operating footprint
Company-profile context for clinical focus, customers, deployment, integration, milestones, and partnerships.
Cloud Saas · Other deployment with recorded integration context.
Company milestones
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
02 · Flagship portfolio
Selected source-backed Company products and the available commercial context.
NHS-trained genomic experts for variant analysis and clinical reporting
AI-powered variant prioritization and interpretation with explainable results
Automated variant re-analysis for unsolved cases
CGH array analysis and interpretation platform
AI-powered genomic analysis platform for rare disease, oncology, and infectious diseases
CLL prognostics with IGHV mutational status analysis
In-house HRD testing solution for ovarian cancer
Comprehensive liquid biopsy analysis for oncology
Epigenetic signature analysis for liquid biopsy
03 · Research intelligence
Publications, preprints, clinical validation, and regulatory records in Evidence Position order.
Publications, clinical validation, and regulatory records connected to this Company appear here.
Research
BMC medical genomics · Jan 5, 2026
Combined RNA Splicing and Patch-Clamp Analysis Reveal Pathogenicity of Splice-Altering Variants in KCNH2-Related LQTS.Circulation. Genomic and precision medicine · Apr 1, 2025
The incremental yield of prenatal exome sequencing over chromosome microarray for congenital heart abnormalities: A systematic review and meta-analysis.Prenatal diagnosis · Jun 1, 2024
Somatic variants as a cause of drug-resistant epilepsy including mesial temporal lobe epilepsy with hippocampal sclerosis.Epilepsia · May 1, 2024
Influence of autozygosity on common disease risk across the phenotypic spectrum.Cell · Oct 12, 2023
Assessing the Pathogenicity of In-Frame CACNA1F Indel Variants Using Structural Modeling.The Journal of molecular diagnostics : JMD · Dec 1, 2022
Clinical validation
No linked records are currently available.
Regulatory
No linked records are currently available.
04 · Company-reported outcomes
Company-reported outcomes and customer stories are distinct from linked Research Intelligence evidence.
DiagAI automatically identifies diagnostic variants
SmartPick variant suggestion accuracy
Variant prioritization performance
Platform capacity and scale
Making HRD testing routine clinical workflow using shallow WGS
Cut complexity and costs, proving reliable precision oncology testing achievable for regional labs
Building unified, future-proof genomics lab infrastructure
Revolutionized clinical diagnostics with comprehensive genomics capabilities
Overcoming NGS data bottlenecks with AI-powered bioinformatics
Scaled personalized medicine and redefined NGS analysis workflows
Advanced genomic analysis for transforming patient care
Empowered with advanced genomic analysis capabilities
Automated exome analysis at scale
Achieved precision medicine at scale with automated exome analysis success
Validation and implementation of in-house HRD testing
Successfully validated and implemented in-house HRD testing with SomaHRD
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
Embedding genomic interpretation into routine clinical care across multiple GLHs
Platform embedded into routine clinical care across multiple NHS Genomic Laboratory Hubs
National-scale genomic medicine program analysis
Established as cornerstone of UK genomic medicine, supporting national genomic medicine service
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
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 profiles and professional links from the current Company record.
No active leadership profiles are currently listed.
06 · Company updates
Recent articles published on Congenica's official website.
07 · HAIC coverage
Health AI Central reporting that mentions this Company.
No HAIC coverage is currently linked to this Company.
08 · Official presence
Curated official destinations from the active Company record.
09 · Market pathway
Other active Companies in the same market, selected alphabetically from the HAIC directory.
Market context
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 market10 · Pro research
Expanded Company research is in development.
Health AI Central Pro · Coming Soon
Pro Research will introduce expanded technical context, linked evidence analysis, and comparative Company research.
Linked research, clinical, and regulatory source pathways.
Expanded product, deployment, integration, and partnership research.
Record-level provenance and review context.