What can you detect?
Comprehensive Biomarker Detection
The Oncomine™ Comprehensive Assay Plus enables detection of a wide range of genomic alterations critical for cancer diagnosis and treatment planning:
- Single Nucleotide Variants (SNVs) & Indels – Small insertions and deletions across 517 genes
- Copy Number Variations (CNVs) – Gene amplifications and deletions
- Gene Fusions – Structural rearrangements including ALK, ROS1, RET, and NTRK fusions
- Microsatellite Instability (MSI) – Comprehensive MSI status determination
- Tumor Mutational Burden (TMB) – Assessment of overall mutation load
- Loss of Heterozygosity (LOH) – Detection of allelic imbalance
Clinical Accuracy
- 99.26% Positive Percent Agreement (PPA) for SNVs
- 97.03% PPA for Indels
- 99.59% Overall accuracy across variant types
Fast, Automated Workflow
Running on the Genexus™ Integrated Sequencer, the entire workflow—from library preparation to variant reporting—is automated, reducing hands-on time to approximately 5 minutes per sample. Results are available in as little as one business day, enabling rapid clinical decision-making.