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The user-friendly interface provides at-a-glance visualization of bespoke, clinically-relevant insights for streamlined variant interpretation.
Actionable biomarker identification
Variant tier classification
Rich interpretive information
Clinical trial matching
Comprehensive reporting
>13,000 ongoing clinical trials around the globe are matched with detected variants and individual parameters such as country and disease.
Key variant information, actionable insights, and personalized annotations and interpretations can be added to your report in just a few clicks.
The OncoPortal™ Knowledge Base launches with a single click, automatically matching molecular profiles to relevant clinical associations. Selected clinical evidence can be seamlessly added to your report for fast, simplified interpretation.
The OncoPortal™ oncology knowledgebase is curated by experts to compile all relevant clinical insights in one place. It is powered by the Genomenon Cancer Knowledgebase (CKB) and is manually expanded with curations and user contributions.
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 at [email protected] to obtain the appropriate product information for your country of residence.
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