The Prosigna Breast Cancer Prognostic Gene Signature Assay is indicated in female breast cancer patients who have undergone surgery in conjunction with locoregional treatment consistent with standard of care, either as:
CentoCancer - Our Comprehensive Oncogenetics Panel for Hereditary Mutations Hereditary pathogenic variants confer an increased risk of developing cancers during an individual’s lifetime. Early identification of pathogenic variants in genes which have a predisposition to cancer is a fundamental first step in the diagnosis, management and treatment of individuals and families with hereditary cancer syndromes..
InVisionFirst-Lung is a qualitative laboratory developed test that uses targeted advanced sequencing technology to detect single nucleotide variants (SNVs), copy number variants (CNVs), insertions and deletions (InDels) and structural variants in selected genes from DNA isolated from plasma samples from patients with non-small cell lung cancer (NSCLC). The test is intended to aid clinicians in treatment decisions for NSCLC patients
More about Invision First-lung
InVisionSeq is a qualitative laboratory developed test that uses targeted advanced sequencing technology to detect single nucleotide variants (SNVs), copy number variants (CNVs), insertions and deletions (InDels) in selected genes from DNA isolated from plasma samples from patients.