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How an NHS England genomics laboratory is streamlining hereditary cancer analysis with SOPHiA DDM™
Discover how precision genomics research at Hospital de Amor, Brazil, uncovered a rare gene fusion in a pediatric glioma, providing valuable insights to support a young patient's health journey.
Prof. Barbara Izzo and her team at CEINGE – Biotecnologie Avanzate opened the doors of their laboratory to discuss the growing importance of integrated molecular approaches in the diagnosis of acute myeloid leukemia (AML).
Hear Dr. Gilles Millat speak about the expansion of cardiogenetic testing and how the SOPHiA DDM™ Cardio Peer Network strengthens variant classification workflows.
Discover how a patient from São Paulo, Brazil, finally found answers after decades of uncertainty thanks to the dedicated efforts of the Bioma Genetics Laboratory.
See how Centre Léon Bérard scaled their cell-free DNA analysis with a tailor-made liquid biopsy solution for mutation detection across cancer types.
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, […]
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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