TSO 500 for Pharma Partners

Pan‑tumor CGP solutions across tissue and liquid biopsy, providing enhanced coverage and sensitivity

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TSO 500 solution

Powering Precision Oncology

CGP powered by TruSight™ Oncology 500 ctDNA v2 and TruSight™ Oncology 500 High-Throughput

TSO 500 HT and TSO 500 ctDNA v2

Unlock the complexities of every tumor

TSO 500 HT and TSO 500 ctDNA v2 provide enhanced coverage, sensitivity, and speed, supporting biopharma partners in confident, data-driven decision making. From biomarker discovery and target validation to resistance detection, clinical trial enrollment, longitudinal monitoring, and patient stratification – TSO 500 delivers the molecular clarity needed to advance precision oncology.

Our clinically and analytically validated CGP tests – spanning both tissue and liquid biopsy – work seamlessly to uncover comprehensive molecular insights across pan-solid tumor indications.

TSO 500 HT

Maximize insights. Minimize tissue. One comprehensive panel

TSO 500 HT streamlines solid tumor profiling by combining DNA and RNA sequencing into a single, comprehensive assay. This approach enables biomarker identification, target validation, and patient stratification, helping to accelerate precision oncology development.

  • 517 cancer-relevant genes
    • DNA: SNVs, InDels and CNVs – 517 genes
    • RNA: Fusions & splice variants – 55 genes
    • IO gene signatures - MSI and TMB
  • High performance DNA + RNA sequencing for optimized fusion detection
Variant ClassAnalytical SensitivitySpecificityAccuracy
SNVs95.2%>99.9%99.9%
InDels92.4%>99.9%99.9%
CNVs100%99.6%99.7%
Fusions94.4%99.9%99.7%
LOD5% VAF for small variants
CNV reporting cutoff is 2.2X fold-change
  

Discover how our CGP solutions can support you—get in touch.

TSO 500 ctDNA v2

Simple blood sample. Deep insights. One comprehensive panel

A comprehensive, noninvasive liquid biopsy (ctDNA) lab developed test for solid tumors - enabling biomarker discovery, clinical trial enrollment, and longitudinal monitoring - empowering data-driven decisions even when tumor tissue is limited or unavailable.

  • 514 cancer-relevant genes
    • SNVs and InDels – 514 genes
    • CNVs – 58 genes
    • Fusions – 23 genes
    • IO gene signatures (MSI-H status; bTMB score)
  • High performance ctDNA assay
Variant ClassAnalytical SensitivitySpecificityAccuracyLOD*
SNVs/InDels92.01%99.80%99.65%0.23%
CNVs95%99.86%99.82%1.20 fold
Fusions100%100%100%0.5%

*LOD90 at 30ng input

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Get on touch

Explore how partnering with NeoGenomics Pharma Services can support you. ContactPharma@neogenomics.com