For Patients

Better care starts with better information. With SOPHiA GENETICS, physicians understand cancers and rare disorders on a deeper level.
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Why we look at health data

Cancers and rare diseases are complex conditions driven by multiple factors. To understand each case, healthcare professionals must pinpoint the specific causes of the disease, often requiring the integration and analysis of different data types. Historically, this process has been time-consuming and challenging, hindering personalized treatment decisions.
That’s why we developed the SOPHiA DDM™ Platform: where others see data, we see answers. Our platform empowers healthcare professionals with accurate insights by integrating and the analyzing diverse health data, complementing their knowledge and experience. This enables them to focus on what truly matters: delivering the best care for every case.
Fast, accurate analysis

Artificial Intelligence-driven analysis for faster, more accurate answers.

Connected with leading healthcare providers

A global network of data supporting past, current, and future patients.

Promoting better decisions

Automatic identification of genetic signatures related to approved treatments.

Keeping data secure

Patient-specific information is secured and de-identified.

Our vision to change the healthcare landscape

Powered by artificial intelligence (AI), the SOPHiA DDM™ Platform generates precise, actionable insights from data. The data stays securely at its source, while anonymized insights are shared globally, enabling secure collaboration among healthcare institutions and researchers.

We designed the platform to build one of the most connected healthcare networks, ensuring users worldwide can access the same level of knowledge and insights, enabling precision medicine approaches.
Together, we can redefine how cancer and rare inherited disorders are diagnosed and treated, driving innovation in healthcare.
About Us

SOPHiA GENETICS products are for Research Use Only and not for use in diagnostic procedures unless specified otherwise.

SOPHiA DDM™ Dx Hereditary Cancer Solution, SOPHiA DDM™ Dx RNAtarget Oncology Solution and SOPHiA DDM™ Dx Homologous Recombination Deficiency Solution are available as CE-IVD products for In Vitro Diagnostic Use in the European Economic Area (EEA), the United Kingdom and Switzerland. SOPHiA DDM™ Dx Myeloid Solution and SOPHiA DDM™ Dx Solid Tumor Solution are available as CE-IVD products for In Vitro Diagnostic Use in the EEA, the United Kingdom, Switzerland, and Israel. Information about products that may or may not be available in different countries and if applicable, may or may not have received approval or market clearance by a governmental regulatory body for different indications for use. Please contact us at [email protected] to obtain the appropriate product information for your country of residence.

All third-party trademarks listed by SOPHiA GENETICS remain the property of their respective owners. Unless specifically identified as such, SOPHiA GENETICS’ use of third-party trademarks does not indicate any relationship, sponsorship, or endorsement between SOPHiA GENETICS and the owners of these trademarks. Any references by SOPHiA GENETICS to third-party trademarks is to identify the corresponding third-party goods and/or services and shall be considered nominative fair use under the trademark law.

SOPHiA DDM™ Overview
Unlocking Insights, Transforming Healthcare
Learn About SOPHiA DDM™ 
SOPHiA DDM™ for Genomics

Oncology 

Rare and Inherited Disorders

Add-On Modules

SOPHiA DDM™ for Radiomics
Unlock entirely novel insights from your radiology images
Learn About SOPHiA DDM™ for Radiomics 
SOPHiA DDM™ for Multimodal
Explore new frontiers in biology and disease through novel insights
Learn About SOPHiA DDM™ for Multimodal
Professional Services
Accelerate breakthroughs with our tailored enablement services
Learn About our Professional Services