Comprehensive Genomic Profiling for Hematologic Malignancies Using NGS Technology
The IVDNGS™ Blood Cancer Panel (Somatic & Germline) is an advanced, Next-Generation Sequencing (NGS)-based assay designed to detect clinically relevant genetic alterations associated with a broad spectrum of hematological malignancies. This dual-purpose panel allows for the identification of both somatic mutations (tumor-acquired) and germline variants (inherited), offering a complete genetic landscape for personalized diagnosis, prognosis, and therapy selection.
With high analytical sensitivity and coverage across a wide range of gene targets, this panel is ideal for leukemia, lymphoma, myeloma, and other blood cancers.
Covers 250+ genes relevant to hematologic malignancies
Detects SNVs, indels, CNVs, translocations, and gene fusions
Analyzes both somatic and germline mutations in a single workflow
Compatible with blood, bone marrow, and extracted DNA
Optimized for clinical relevance and decision-making
Includes actionable mutations, prognostic markers, and risk stratification
Developed under IVD compliance and ISO 13485 standards
Acute Myeloid Leukemia (AML)
Chronic Lymphocytic Leukemia (CLL)
Acute Lymphoblastic Leukemia (ALL)
Myelodysplastic Syndromes (MDS)
Non-Hodgkin & Hodgkin Lymphoma
Multiple Myeloma
Inherited blood cancer predisposition syndromes
Parameter | Details |
---|---|
Sample Type | Peripheral blood, bone marrow, FFPE |
DNA Input | ≥10 ng |
Turnaround Time | 7–10 working days |
Output | Clinical report with interpretation |
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