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The Oncomine Myelodysplastic Syndrome (MDS) Panel detects genetic mutations linked to MDS and blood cancers. Accurate, next-generation sequencing. Book your test today.
The Prothrombin Mutation Analysis is a genetic test designed to detect the G20210A mutation in the prothrombin (F2) gene, a key risk factor for inherited thrombophilia. This highly accurate, DNA-based assay identifies individuals with increased risk of abnormal blood clotting, aiding in the diagnosis and management of thrombotic disorders.
The Somatic HRR (Homologous Recombination Repair) Panel is a cutting-edge genomic test that analyzes tumor tissue for mutations in DNA repair genes — helping oncologists detect aggressive cancers early, assess treatment response, and recommend personalized therapies like PARP inhibitors.