Company profile

Cancer Genetics

Precision Medicine & Genomics

Company profile

About Cancer Genetics

SOPHiA GENETICS is a health technology company that has built SOPHiA DDM™, an AI-driven platform for precision medicine that analyzes complex health data to provide actionable clinical insights. The platform serves healthcare providers, biopharma companies, and patients globally, focusing primarily on oncology and rare genetic disorders. SOPHiA DDM™ processes genomic, radiomic, and multimodal data through advanced AI algorithms that achieve 98-99% accuracy across multiple applications. The company's technology supports end-to-end workflows for solid tumors, blood cancers, hereditary cancers, liquid biopsy, and inherited disorders. With a network of over 990 healthcare institutions across 75+ countries, SOPHiA GENETICS has analyzed more than 2.5 million genomic profiles. The platform is designed to be accurate, rapid, and scalable, adhering to strict regulatory standards including HIPAA and GDPR. The company's diverse team from 28 countries includes significant scientific expertise, with 30% holding PhDs. SOPHiA GENETICS operates on a philosophy of 'data for good,' connecting institutions globally while ensuring customers retain full control of their data. The platform offers specialized solutions including SOPHiA DDM™ for Genomics, Radiomics, and Multimodal analysis, along with add-on modules like Alamut Visual Plus and OncoPortal Plus.

Company description Cancer Genetics official website

Primary marketPrecision Medicine & Genomics
Commercial modelCommercial information available on request
Company presenceOfficial website
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01 · Operating footprint

Where the Company operates

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

Clinical focus

  • Blood cancers
  • Chronic Lymphoblastic Leukemia
  • Hereditary cancers
  • Inherited disorders
  • Kidney cancer
  • Liquid biopsy applications
  • Myeloproliferative conditions
  • Ovarian cancer
  • Rare disorders
  • Solid tumors

Who it serves

  • Bioinformaticians
  • BioPharma companies
  • Clinical laboratories
  • Geneticists
  • Healthcare institutions
  • Hospitals
  • Lab technicians
  • Oncologists
  • Pathologists
  • Radiologists

Deployment & integration

Deployment information is currently being developed.

Geographic context

MarketsGlobal presence across 75+ countries
Company sourceOfficial website

Company milestones

Platform expansion

Partnership with Jessa Ziekenhuis announced at European Congress of Pathology. Laboratorio Barnafi-Krause went live on SOPHiA DDM™. Published collaboration results with UroCCR. Reached 2 million genomic profiles analyzed milestone. Launched SOPHiA DDM™ Enhanced Exome Solutions. Presented at ASCO 2024 and BiotechX USA 2025.

Partnerships

Recorded partners

  • French Kidney Cancer Research Network (UroCCR)
  • Jessa Ziekenhuis
  • Laboratorio Barnafi-Krause
  • Memorial Sloan Kettering (MSK-ACCESS®)
  • The Royal Marsden NHS Foundation Trust
  • TomaLab Advanced Biomedical Assays

02 · Flagship portfolio

Products, workflows, and platform capabilities

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

No source-backed Company products are currently listed.

03 · Research intelligence

Research Intelligence evidence

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

Evidence position

Publications, clinical validation, and regulatory records connected to this Company appear here.

Research

Publications & preprints

BRCA1-mutant thymoma and the role of PARP inhibitors: a case report.

Pathology · Oct 1, 2026

Unacknowledged Burdens and Clinical Assets of BIPOC Genetic Counseling Students: Qualitative Evidence to Inform Supervision.

Journal of genetic counseling · Oct 1, 2026

Understanding Barriers and Motivators of Familial Hypercholesterolemia Genetic Testing: Insights From the Singapore Public.

Journal of genetic counseling · Oct 1, 2026

Recent Incidence Trends for Cutaneous T-Cell Lymphoma in the United States: A Surveillance, Epidemiology, and End Results (SEER) Database Analysis, 2000-2022.

Journal of the American Academy of Dermatology · Sep 2, 2026

Oxygen-dependent subcellular redistribution of PHD3 links the hypoxic microenvironment to mitochondrial metabolic reprogramming in ccRCC.

Experimental & molecular medicine · Sep 2, 2026

Diffusion MRI radiomics in meningiomas: imaging correlates of tumor grade and intraoperative consistency.

Neurosurgical focus · Sep 1, 2026

Clinical validation

Clinical-trial records

Genetic Counseling Patient Preference Intervention Versus Conventional Genetic Counseling for Women at Elevated Risk for Breast Cancer

NCT05325151 · Mentioned · ACTIVE NOT RECRUITING

Testing an Enhanced Digital Delivery Model for Inherited Cancer Genetic Testing in Young Adults With Cancer

NCT07091617 · Mentioned · RECRUITING

Genetic Risk Assessment for Cancer Education and Empowerment (GRACE) Project

NCT03326713 · Mentioned · COMPLETED

Molecular Basis of Langerhans and Non-Langerhans Cell Histiocytic Neoplasms and Castleman Disease

NCT05028621 · Mentioned · SUSPENDED

Mainstreaming Genetics: Evaluation of a Digital Application to Scale and Spread Oncologist-initiated Genetic Testing

NCT07387263 · Mentioned · RECRUITING

Chatbot to Maximize Hereditary Cancer Genetic Risk Assessment

NCT05562778 · Mentioned · RECRUITING

Regulatory

Regulatory records

Tissue of Origin Test Kit-FFPE

K173839 · 510k · Mar 15, 2018

04 · Company-reported outcomes

Outcomes and case studies

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

98-99% accuracy

AI algorithm accuracy across multiple health data applications

2.5M+ genomic profiles analyzed

Total genomic profiles processed through platform

Shortened turnaround time

End-to-end workflows for oncology and inherited disorders

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 Cancer Genetics

Recent articles published on Cancer Genetics'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.

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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