Oncomine Precision Assay (OPA)

R21 750

An NGS-based tumour profiling assay detecting 78 variants – including mutations, copy number variants, and fusions – across 50 key oncogenes. Supports treatment selection across multiple solid tumour types


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Comprehensive tumour profiling NGS panel

A next-generation sequencing (NGS) assay that profiles tumour DNA and RNA to direct treatment to the specific tumour type. The panel analyses 78 variants — including mutations, copy number variants (CNVs), and fusion variants — across 50 key cancer genes, including EGFR, ALK, BRAF, NTRK, ROS1, RET, KRAS, PIK3CA, and ERBB2. Results are delivered as a diagnostic and treatment interpretation, giving a thorough molecular profile to guide clinical decision-making.

  • Tumour sample, collected by a surgeon or pathologist
  • Supports both FFPE tissue and liquid biopsy samples
  • 78 variants analysed: 45 mutations, 14 CNVs, 19 fusion variants
  • 50-gene panel covering key oncology targets (EGFR, ALK, BRAF, NTRK, ROS1, RET, KRAS, PIK3CA, ERBB2, and more)
  • Diagnostic and treatment-directing interpretation
  • Supports treatment selection across multiple solid tumour types

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