Professional Services

Accelerate breakthroughs with our tailored enablement services

Improve efficiency, accuracy, and scalability of your workflows with professional services driven by skilled personnel, proven solutions, and steadfast dedication.

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OVERVIEW

Maximize the power of genomics data to drive global health equity

The emergence of precision medicine and the advances in AI and molecular techniques is transforming the way research in drug development is conducted. Genetic testing has become pivotal to accessing precision therapies however, there’s a gap in the accessibility and adoption of NGS-based testing across the globe.

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 DDM^TM Clinical Trial Assay and SOPHiA DMM^TM Follow-on Dx can be further validated to Companion Diagnostic (CDx) level

Streamline your daily work

Our suite of professional services enables you to focus on high-value work and make faster, more effective, and confident data-driven decisions.

Maximizing efficiency, caring for excellence

Implementing a genomics application is complex and time-consuming. The SOPHiA DDM™ MaxCare Program empowers labs achieving trusted high-quality results, while meeting stringent standards. Our experts provide on-site consultation, hands-on training, and performance assessments for seamless workflow implementation, enhancing your data’s statistical power.

With 550+ programs completed across 360+ institutions, we offer proven expertise in adopting diverse NGS-based applications, facilitating your lab self-validation and accreditation efforts.

Accelerated adoption

Expect ~120 days from onboarding to completion, with seamless implementation of genomics applications, tailored to your requirements.

Increased efficiency

Optimize your workflows with comprehensive training on genomics applications, adapted to your needs, throughout the full onboarding process.

Enhanced confidence

Obtain verification support to meet and exceed your standard and increase confidence in your results, while leveraging your samples and workflows.

Streamlining data integration for enhanced efficiency

Dealing with data from multiple, siloed sources is a manual, error prone, and non-scalable process. The SOPHiA DDM™ Platform automates data management and pipeline execution and increases productivity by eliminating the need to manually upload sequencer output files, enter Electronic Health Records (EHR), and input Laboratory Information Management Systems (LIMS) data.

Leverage our collaboration with external service providers to foster seamless, automated data flow between your instruments, EHR, LIMS and the SOPHiA DDM™ Platform.

Enhanced efficiency

Automate manual tasks to boost your productivity. Spend less time on redundant manual processes, and more time on high-value work.

Improved scalability

Streamline your workflows to rapidly and efficiently deliver comprehensive and integrated genomics analysis by automating data flows.

Increased accuracy

Reduce data entry errors by connecting SOPHiA DDM™ to various databases and systems to extract more insights from your data through downstream analysis.

Increase productivity with a standardized NGS workflow

Manual liquid handling presents challenges for lab technicians with heavy workloads, potentially leading to errors and variability, especially when working with small samples and complex library preparation protocols.

Maximize your efficiency by automating your library preparation. By combining SOPHiA GENETICS™ sample‑to‑report applications with automated liquid handling platforms, you can standardize your NGS workflow and minimize manual intervention.

Enhanced productivity

Minimize human intervention to increase productivity, while reducing errors and saving resources.

Standardized workflows

Obtain high-quality libraries with standardized protocols to ensure reliable analytical performance.

Expert support

Get the needed fit-for-purpose support from instrument pre-installation to long-term projects.

Empowering your internal validation efforts

One of the biggest blockers in validating a genomic application is the availability of tumor-normal clinical samples containing variants of interest. Not only is it critical to have a sufficient number of samples to ensure optimal coverage, but also of good quality to ensure robust results.

With an empower-forward network, SOPHiA GENETICS™ Sample Sourcing, we help you find high-quality samples to streamline your validation workflows in a simple manner and efficiently implement NGS-based workflows in your laboratory.

Accelerated adoption

Fasten your time-to-implementation and remove blockers during your validation process.

Tailored approach

Reach your verification and validation needs with the right sample strategy and our experts consultative approach.

Access to a global network

Connect with like-minded sites and benefit from mutual support during your validation journey.

“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 GENETICS was a natural choice when our RNA‑seq workflows faced unforeseen challenges. Their commitment to understanding our unique needs and seamlessly co‑creating a bespoke solution from the ground up ensured a swift return to normal operations. With SOPHiA GENETICS, efficient communication and tailored innovation aren’t just promises; they’re the foundation of our continued success.”
Medical Biologist
Reference Laboratory
France
“SOPHiA GENETICS and Clinisys impressed us with their meticulous approach, deep understanding of the subject matter, and their ability to foresee the big picture implications of their work. Their thoughtful commitment greatly reduced data entry errors and the need to rerun complex dataset analyses.”
J. Mark Tuthill, MD
Division Head, Pathology Informatics
Henry Ford Health, USA
“The combined drive for quality is, in my experience, mastered by the automation partnership between SOPHiA GENETICS and Hamilton. The SOPHiA GENETICS™ Applications with the Hamilton Clinical NGS STARlet provides the robustness and reproducibility we need in our daily NGS workflow.”
Hans Bruinsma
Pathologie
Zuid‑West Nederland – ETZ Tilburg