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We sat down with Prof. Jacques Cadranel, International Coordinator of the DEEP-Lung-IV study and Head of the Pneumology Department at the Hospital Group University Hospitals of Eastern Paris, who shared his experience in this collaboration with SOPHiA GENETICS, and the importance of the integration of multimodal data in clinical practice to advance personalized medicine in lung cancer.
Discover how Bioma Genetics used SOPHiA DDM™ exome solutions to uncover hereditary breast cancer risk and impact early family management.
Discover how A.C. Camargo Cancer Center uses SOPHiA DDM™ to support genetic analysis in hereditary cancer, leading to personalized patient care strategies.
We met with Dr. Sébastien Couraud, DEEP-Lung-IV Scientific Committee member and Head of the Pulmonology and Thoracic Oncology Department at Hospices Civils de Lyon, to talk about his participation in SOPHiA GENETICS’s DEEP-Lung-IV study and reflect on the benefits of multimodal approaches to transform precision medicine and improve patient outcomes. Watch the spotlight: Hello Sébastien, […]
Discover expert insights on the evolving role of exome and genome sequencing in clinical diagnostics. Learn how virtual panels, reimbursement trends, and technical advancements are shaping genomic medicine.
We sat down with Prof. Jean-Christophe Bernhard, UroCCR Coordinator, and Dr. Gaëlle Margue, Urology Fellow, at University Hospital Bordeaux, to discuss the collaboration between UroCCR – the French Kidney Cancer Research Network - and SOPHiA GENETICS, and get their insights on the use of AI-powered multimodal approaches to improve patient care.
We’re excited to shine a spotlight on Elexandra Barboza-Arguedas, who delivered an insightful presentation during our ACMG exhibit theatre session this year. In this interview, she shares deeper insights into her work at the Molecular Diagnostics Laboratory and how the SOPHiA DDM™ Platform is helping her team streamline workflows and uncover critical insights tailored to the unique genetic landscape of the Costa Rican population.
Discover how adding radiomic features with SOPHiA DDM™ for Radiomics, to clinical and dosimetric data enhances the prediction of acute lung toxicity in patients receiving radiotherapy for lung cancer.
We were glad to host Dr. Davide Martorana, Senior Molecular Geneticist at the Medical Genetic Lab of the University-Hospital of Parma in Italy, who shared with us his institute’s experience with the adoption of the New Generation SOPHiA DDM™ Platform. Read the spotlight:
More than six people die every hour in the US from a blood cancer. Solutions can’t come fast enough for those who suffer with these cancers all around the world. Fortunately, researchers studying blood diseases have experienced rapid advances in their capabilities to develop and test effective therapies with some extremely significant advancements.
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.
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