IVDNGS™ Blood Cancer Panel (Somatic & Germline) – NGS

IVDNGS™ Blood Cancer Panel (Somatic & Germline) – NGS

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.

Key Features

  • 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

Clinical Applications

  • 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

Sample Requirements & Workflow

ParameterDetails
Sample TypePeripheral blood, bone marrow, FFPE
DNA Input≥10 ng
Turnaround Time7–10 working days
OutputClinical report with interpretation