Oncomine™ Comprehensive Assay Plus – Complete CGP test, now on the Genexus™ system

Clinically validated accuracy

  • SNVs: sensitivity ~98–99 %, specificity ~99 %
  • Indels and fusions: ~98 % each
  • CNV gain (≥8 copies): sensitivity ~99.6 %, specificity ~99.9 %
  • MSI: >99 % concordance
  • TMB: correlation r² ≈ 0.945 compared to exome-based standards

Fast and automated workflow

  • Only 20 minutes hands-on time, with two operator touchpoints

  • Complete sample-to-report workflow using two instruments:

  • Reports generated in under 5 minutes
  • Total duration: approx. 5h for extraction + 26h for sequencing, with up to 4 runs/week (16 samples)
  • Requires just 20–30 ng DNA and 20 ng RNA (e.g., one FFPE slide), even from the first sample

All-in-one solution from a single provider

  • Instruments, consumables, analytics software (Oncomine Reporter), and support
  • Suitable for both translational medicine applications and preclinical cancer research

Why implement it?

  • Speed – “Next-day” CGP results, enabling maximum flexibility and rapid decisions
  • Validated reliability – ~94 % success rate on FFPE samples, with high sensitivity and specificity
  • Comprehensive insights – from point mutations to gene fusions, actionable biomarkers, and genomic instability markers
  • Operational efficiency – JAVA-like automated workflow, saving both time and costs

Regardless of your level of NGS experience, the Genexus™ system simplifies the implementation of in-house CGP with consistent performance and enhanced operational efficiency.