Next-generation sequencing
Providing clarity and actionable results
The diagnosis of bleeding and thrombosis disorders relies heavily on specialized coagulation assays, but genotype assays are increasing in utility and availability.
Created to meet the growing needs of our own clinical practice, we offer a comprehensive next-generation sequencing menu for patients who have bleeding and thrombosis disorders.
Next-generation sequencing Test menu
More information
NGS testing can provide useful information that assists physicians including:
- Confirming the diagnosis of bleeding and thrombosis disorders.
- Providing clarity and actionable results in situations where other testing methodologies provide inconclusive results for patients.
- Identifying mutations that could explain patients’ unusual hemostatic phenotype and laboratory results.
- Assays with single/small gene panels, focused panels, and comprehensive panels for bleeding/coagulation disorders, coagulation/angioedema, fibrinogen disorders, and thrombosis disorders.
Bleeding disorders single/small gene panels
Key testing
- GNF7 | Factor VII Deficiency, F7 Gene, Next-Generation Sequencing, Varies
- GNF11 | Hemophilia C (Factor XI Deficiency), F11 Gene, Next-Generation Sequencing, Varies
- GNF13 | Factor XIII Deficiency, F13A1 and F13B Genes, Next-Generation Sequencing, Varies
- GNFIB | Congenital Fibrinogen Disorders, FGA, FGB, and FGG Genes, Next-Generation Sequencing, Varies
- GNHMA | Hemophilia A, F8 Gene, Next-Generation Sequencing, Varies
- GNHMB | Hemophilia B, F9 Gene, Next-Generation Sequencing, Varies
Bleeding disorders focused panels
Key testing
- GNANG | Hereditary Angioedema Focused Gene Panel, Next-Generation Sequencing, Varies
- GNBLF | Bleeding Disorders, Focused Gene Panel, Next-Generation Sequencing, Varies
- GNVWD | von Willebrand Disease, VWF and GP1BA Genes, Next-Generation Sequencing, Varies
Bleeding disorders comprehensive panel
Key testing
Thrombosis disorders single/small gene panels
Key testing
- GNADM | Hereditary Thrombotic Thrombocytopenic Purpura, ADAMTS13 Gene, Next-Generation Sequencing, Varies
- GNANT | Antithrombin Deficiency, SERPINC1 Gene, Next-Generation Sequencing, Varies
- GNPRC | Protein C Deficiency, PROC Gene, Next-Generation Sequencing, Varies
- GNPRS | Protein S Deficiency, PROS1 Gene, Next-Generation Sequencing, Varies
Thrombosis disorders comprehensive panel
Key testing
Platelet disorders single/small gene panels
Key testing
Platelet disorders focused panels
Key testing
- GNMTC | Macro/Microthrombocytopenia Gene Panel, Next-Generation Sequencing, Varies
- GNHTC | Hereditary Thrombocytopenia Gene Panel, Next-Generation Sequencing, Varies
- GNPFD | Platelet Function Defect Gene Panel, Next-Generation Sequencing, Varies
- GNSPD | Platelet Storage Pool Deficiency Gene Panel, Next-Generation Sequencing, Varies
- GNVWD | von Willebrand Disease, VWF and GP1BA Genes, Next-Generation Sequencing, Varies
Platelet disorders comprehensive panel
Key testing