Overview

Clinically curated DNA+RNA panel covering 52 actionable genes for rapid routine oncology diagnostics.

Why this Test Matters

Precision oncology depends on identifying clinically actionable genomic alterations. This assay helps clinicians select targeted therapies, evaluate immunotherapy eligibility, identify prognostic biomarkers, detect resistance mechanisms, and match patients to suitable clinical trials while minimizing sequential testing.

Who Should Consider this Test?

● Newly diagnosed solid tumors
● Lung, colorectal, breast and thyroid cancers
● Patients requiring rapid actionable biomarkers

Applicable Cancer Types

Most solid tumors

What is Covered?

  • 52 genes
  • SNVs
  • InDels
  • CNVs
  • RNA fusions

Clinical Utility​

  • Treatment selection
  • Prognostic and predictive biomarkers
  • Clinical trial matching
  • Identification of actionable alterations
  • Comprehensive clinical interpretation

Technology

Integrated DNA+RNA workflow

key Features

Parameter Details
Sample Type
FFPE tissue
Samples
1 sample
Turnaround Time
10–14 working days
Report Includes
Variant interpretation, therapy associations, clinically actionable biomarkers
Quality
High-depth NGS with rigorous QC