Analyzes hundreds of cancer-related genes to identify mutations, fusions, and amplifications from tumor or blood samples.
Tests like FoundationOne CDx are FDA-approved for guiding therapy decisions in various cancers, ensuring regulatory compliance and clinical validity.
Offers non-invasive testing via blood samples (e.g., FoundationOne Liquid CDx) for monitoring treatment response and detecting resistance mutations.
Delivers detailed reports with actionable insights, including therapy matches, clinical trial options, and prognostic information.
Seamlessly integrates reports into electronic health records (EHR) for easy access by healthcare providers.
Collaborates with laboratories and institutions worldwide to offer testing services and support research initiatives.
Helps oncologists select EGFR, ALK, or other targeted inhibitors based on specific genomic alterations in non-small cell lung cancer.
Assesses PD-L1 expression, tumor mutational burden, and microsatellite instability to determine eligibility for checkpoint inhibitors.
Identifies biomarkers that qualify patients for experimental therapies, accelerating enrollment in oncology trials.
Uses blood-based tests to track genomic changes during therapy, detecting resistance early and adjusting treatment plans.
Analyzes HER2, BRCA, and other mutations to predict outcomes and inform adjuvant or neoadjuvant strategies.
Identifies KRAS, NRAS, or BRAF alterations that indicate resistance to anti-EGFR therapies, guiding alternative options.
Provides genomic insights for hard-to-diagnose cancers, aiding in classification and personalized management.
Reveals multiple actionable targets to design synergistic drug combinations for advanced cancers.
Supports pharmaceutical companies by identifying biomarkers for new drug targets and validating therapies in trials.
Detects germline mutations in genes like BRCA1/2 to assess familial cancer risks and guide preventive measures.
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