Clinical assets

Thank you for your interest in learning more about the testing solutions we offer.  Feel free to browse the brochures below.

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The PanTracer Portfolio

PanTracer Pro

PanTracer™ Pro

Simplifies case management and enables a path to personalized treatment, providing comprehensive insights in a single order.

PanTracer Tissue tech sheet

PanTracer™ Tissue

Broad tissue-based CGP covering 517 genes with DNA + RNA sequencing for optimized fusion detection. Aligns with clinical guidelines and requires minimal tissue, enabling personalized therapy selection and trial matching.

PanTracer LBx

PanTracer™ LBx

Liquid biopsy CGP analyzing 514 genes from a simple blood draw. Provides high-sensitivity ctDNA insights for real-time decisions when tissue is limited, inadequate, or not feasible.

RaDaR® ST

RaDaR ST for breast cancer

RaDaR® ST for breast cancer

Address HR+/HER2- breast cancer long-term recurrence risk months before conventional methods. RaDaR ST provides over a year's advance warning of distant metastasis, opening the door to life-changing interventions.

RaDaR ST for head & neck cancer

RaDaR® ST for head & neck cancer

RaDaR ST delivers unprecedented sensitivity in detecting HPV-negative HNSCC recurrence, achieving 100% detection of relapsed patients by identifying ctDNA at ultra-low levels of 5ppm—ensuring no patient with recurrent disease goes undetected during the critical surveillance window.

Hematology solutions

Compass services

Compass®

Compass Hematopathology Services is a streamlined and personalized lab workup to help inform effective patient care management by providing diagnostic clarity to complex hematologic malignancies and prognostic and predictive information.

Neo Comp heme

Neo Comprehensive® - Heme Cancers

The Neo Comprehensive – Heme Cancers assay analyzes 433 genes using next‑generation sequencing (NGS) to detect DNA and RNA alterations for diagnostic evaluation, prognosis, risk stratification, and therapy guidance in hematologic malignancies.

Neo Comp myeloid

Neo Comprehensive® - Myeloid Disorders

Comprehensive genomic profiling (CGP) plays a pivotal role in differentiating disease subtypes and resolving complex diagnostic challenges with greater clarity and confidence than traditional diagnostic testing.

Clinical assets | NeoGenomics Laboratories