On-Demand Webinars

Watch our webinars to discover how our solutions advance data-driven medicine, improving health outcomes. To view our upcoming live webinars please visit our events page here.
Area of Interest

All On-Demand Webinars

 Upcoming Events & Webinars
Event
Genomic advances in hereditary cancer: Optimizing variant detection and interpretation workflows

Hereditary cancer risk assessment is a rapidly advancing field, driven by the need for comprehensive variant detection, streamlined genomic workflows, and alignment with evolving guidelines. In the UK, testing is delivered through the NHS Genomic Laboratory Hub network, with each lab supporting a broad range of clinical indications under the National Genomic Test Directory. This […]

Areas of Interest:

Hereditary Cancers, Inherited Disorders, Rare Disorders
Event
AI in genomics: enhancing germline workflows to tackle the biggest research challenges

As the global healthcare research landscape evolves at lightning speed, we need to change the way we approach healthcare data by breaking down silos, fostering knowledge sharing, and democratizing access to anonymized real-world health insights. And as the volume and complexity of healthcare data continue to grow, the integration of next-generation data analytics and artificial […]

Areas of Interest:

Inherited Disorders, Platform, Rare Disorders
Event
Maximizing Efficiency: Implementing an Enhanced Exome Solution Across Multiple Indications

Watch on-demand the webinar “Maximizing Efficiency: Implementing an Enhanced Exome Solution Across Multiple Indications”, where Dr. Eirikur Briem, Head of Department of Genetics and Molecular Medicine at the Landspitali University Hospital in Ireland presents his institute’s experience in implementing the SOPHiA DDM™ Enhanced Exome Solutions.

Areas of Interest:

Inherited Disorders, Platform, Rare Disorders
Event
Harnessing AI & Big Data: The Next Frontier in Biotech and Healthcare

Filmed as part of the Swiss Biotech Day on May 5th 2025.An engaging panel discussion on the transformative role of AI-powered technology in building scalable, high-performance healthcare solutions. Discover how collaboration drives innovation and advances precision medicine. Discussion summary:Artificial intelligence and big data are revolutionizing biotech and healthcare, driving breakthroughs in precision medicine, clinical decision-making, […]

Areas of Interest:

Platform
Event
Evaluating Next-Generation Sequencing Solutions for Real-World Clinical Needs in Myeloid Malignancy

The diagnostic, prognostic, and treatment landscape of myeloid malignancies is evolving rapidly, with genomic biomarkers increasingly defining disease diagnosis and classification. Given the continuous discovery and refinement of genomic testing requirements in the context of changing (targeted) therapies and reimbursement recommendations, there is an increasing need for genomic solutions that keep pace with clinical and […]

Areas of Interest:

Blood Cancers
Event
Insights with Impact: Empowering Laboratories with a Decentralized MSK Solution for CGP

Comprehensive genomic profiling (CGP) using a matched tumor-normal approach can help improve somatic detection rate and streamline interpretation.

Areas of Interest:

Solid Tumors
Event
Advancing Precision Oncology with a Matched Tumor-Normal Approach: Insights From the Clinic

This webinar presents an in-depth look at how Memorial Sloan Kettering Cancer Center (MSK) is routinely using its molecular assays — MSK-IMPACT and MSK-ACCESS — together to inform precision oncology approaches.

Areas of Interest:

Liquid Biopsy, Solid Tumors
Event
Enhancing MRD Detection in AML: Insights From ASST Papa Giovanni XXIII Hospital’s NGS-Based Approach

In this webinar, Silvia Salmoiraghi, biologist at ASST Papa Giovanni XXIII Hospital in Bergamo, Italy, discuss the performance of the SOPHiA DDM™ Residual Acute Myeloid (RAM) Solution.

Areas of Interest:

Blood Cancers
Event
Advancing precision oncology with MSK-ACCESS® powered with SOPHiA DDM™ - ELBS & SOPHiA GENETICS webinar (European Liquid Biopsy Society)

SOPHiA GENETICS (Nasdaq: SOPH), a cloud-native healthcare technology company and a global leader in data-driven medicine, recently joined the European Liquid Biopsy Society (ELBS), a prestigious network consisting of partners from academia and industry with the common goal of making liquid biopsy tests part of the routine standard of care. SOPHiA GENETICS offers a comprehensive […]

Areas of Interest:

Liquid Biopsy
Event
Enhancing variant interpretation: Obtaining answers from a vast universe of data

Pinpointing pathogenic mutations from large, complex datasets can be difficult, time-consuming, and somewhat overwhelming. So, how can you streamline your genomic analysis, to make it quicker, easier, and more efficient? In this webinar you will learn how Alamut™ Visual Plus enables clinical researchers to: ➡️ Resolve splice-site variants using splicing scores and exonic splicing enhancer […]

Areas of Interest:

Alamut, Rare Disorders

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.

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SOPHiA DDM™ for Radiomics
Unlock entirely novel insights from your radiology images
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SOPHiA DDM™ for Multimodal
Explore new frontiers in biology and disease through novel insights
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