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Expanding equitable access to precision medicine worldwide
We enable the deployment of high-quality genomics applications at scale, helping deliver innovative therapies to diverse patient populations, advancing precision medicine globally.
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Enhance access to AI-driven genomics solutions

Genomic information is key for matching patients to the right clinical trials and treatments, but global genomic testing adoption has been slow and disparate.

Our unique approach to next-generation sequencing (NGS) assay deployment in laboratories across the world facilitates increased patient access to diagnostic testing for precision medicine, closing critical gaps in oncology care.

Leverage our expertise in developing and deploying genomics applications and the data generated within the SOPHiA GENETICS network to enhance patient and market access to relevant genomic information, and match patients to the right clinical trials and treatments.
*SOPHiA DDMTM Clinical Trial Assay and SOPHiA DMMTM Follow-on Dx can be further validated to Companion Diagnostic (CDx) level

Maximizing post-market success with global deployment

Broaden your impact by driving global testing adoption

Accelerate adoption of advanced genomic testing with decentralized deployment of NGS assays, and dedicated support programs, designed to empower laboratories worldwide.

Our approach equips labs with streamlined workflows, expert guidance, and robust quality standards, widening adoption of high-quality, and standardized genomic testing worldwide.
Expert-led support
Benefit from the SOPHiA DDM™ MaxCare Program to help labs obtain robust results and confidently adopt NGS tests with expert on-site consultation.
Tailored solutions
Leverage existing NGS-based applications that can be further customized and validated to CTA or CDx level.
Global network
Scale the adoption of genomics testing, even in underserved regions, by leveraging the vast SOPHiA DDM™ decentralized network.

Boost patient access with sponsored NGS testing

Maximize patient access to your newly launched precision therapy by sponsoring the routine use of high-quality NGS-based assays across priority markets.

Through a decentralized and scalable platform, labs gain accurate, and timely genomic testing, reducing healthcare system burdens, and improving patient outcomes, while demonstrating cost-effectiveness of your product.
Accurate analysis
Harness best-in-class NGS assays and AI-powered algorithms to obtain accurate, standardized data worldwide, driving confidence in routine results.
Global network
Tap into a decentralized ecosystem to accelerate local adoption of genomic tests for broader reach and improve patient access.
Valuable routine insights
Turn routine testing into strategic intelligence, with clear insights into disease trends and market dynamics through SOPHiA DDM™.

Drive launch success with education and awareness

Empower medical professionals with education, evidence, and proof points that build trust and confidence in precision diagnostics.

By leveraging a global connected network, standardized real-world data, evidence from test early adopters, and deep genomics expertise, we accelerate the adoption of robust NGS assays, and reduce time to diagnosis, thus broadening global access to biomarker-driven therapies.
Robust real-world data
Gain actionable insights from real-world data to identify testing patterns across regions and strengthen your medical education strategy.
Post-commercial support
Leverage expertise to uncover gaps in care and promote the adoption of new diagnostic solutions among your priority markets.
Enhanced confidence
Harness evidence and experience from test early adopters to foster peer-driven trust and confidence in new precision medicine strategies.

“Through this collaboration, we aim to enable the widespread application of precision medicine in oncology across Africa, and thus contributing to the improvement of patient outcomes across the African continent.

“Our collaboration with SOPHiA GENETICS has the potential to uncover genomic mutations that correlate with clinical response to ADCT-402. We have observed significant single-agent clinical activity in our pivotal Phase II trial of ADCT-402 in a broad population of patients with relapsed or refractory diffuse large B-cell lymphoma. The insights from this collaboration will allow us to better identify and understand the characteristics of patients who respond best to treatment. We look forward for the results of this research enabled by SOPHiA’s unique platform”
Patrick van Berkel
Sr VP of Research and Development, ADC Therapeutics

SOPHiA DDM™ MaxCare Program

Comprehensive support from sample to report, for accelerated in-house adoption of NGS workflows.

Our Partner Testimonials

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 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
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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
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