Biopharma Services
Laboratory services supporting drug development and clinical trials for biopharma partners
Company profile
Company profile
NeoGenomics is a leader in oncology diagnostics, specializing in precision medicine and genomics for cancer care. The company provides an extensive portfolio of over 500 tests covering all major testing modalities, including single-gene molecular testing, immunohistochemistry (IHC), flow cytometry, fluorescence in situ hybridization (FISH), DNA- and RNA-based next-generation sequencing (NGS), and comprehensive genomic profiling (CGP). NeoGenomics serves three primary markets: healthcare providers seeking precision oncology testing to support personalized patient care, biopharma partners developing cancer therapies and conducting clinical trials, and patients navigating their cancer treatment journey. The company's testing solutions span solid tumors and hematologic cancers, offering advanced tissue-based, liquid biopsy, and hematology tests. Key product lines include the PanTracer portfolio for comprehensive genomic profiling, RaDaR ST for minimal residual disease detection with sensitivity down to 1 part per million, and disease-specific panels for lung, breast, colorectal, gastric, gynecologic, and hematologic cancers. NeoGenomics maintains a database of over 2 million patient profiles from more than 40,000 unique providers across 4,000 healthcare organizations, providing oncology data solutions that deliver insights across the cancer care continuum. The company's mission centers on advancing personalized cancer care through scientific excellence, integrated solutions, and meaningful impact throughout the patient treatment journey.
Company description NeoGenomics official website
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01 · Operating footprint
Company-profile context for clinical focus, customers, deployment, integration, milestones, and partnerships.
Other deployment with recorded integration context.
Recorded integration context: EHR Integrations.
Company milestones
Unveiled new mission, vision, and tagline reflecting strengthened commitment to personalized cancer care. Launched RaDaR ST MRD detection technology. Introduced PanTracer Pro comprehensive testing solution combining CGP with IHC and ancillary testing.
Partnerships
No partners are currently listed.
02 · Flagship portfolio
Selected source-backed Company products and the available commercial context.
Laboratory services supporting drug development and clinical trials for biopharma partners
164-gene NGS assay for diagnostic evaluation and therapy guidance of myeloid neoplasms
Liquid biopsy NGS comprehensive genomic profile for advanced stage pan-solid tumors
One order for comprehensive genomic and biomarker insights for personalized therapy selection
Comprehensive tissue-based NGS genomic profile for pan-solid tumors
Comprehensive NGS genomic profile with HRD assessment for ovarian tumors
Real-world oncology data insights from over 2 million patient profiles
MRD detection technology for biopharma clinical trials and drug development
Personalized MRD detection using circulating tumor DNA to detect cancer recurrence before imaging
03 · Research intelligence
Publications, preprints, clinical validation, and regulatory records in Evidence Position order.
Publications, clinical validation, and regulatory records connected to this Company appear here.
Research
Nature genetics · Aug 4, 2026
MRI-based Response Assessment of Neoadjuvant Systemic Immunotherapy in Muscle-invasive Bladder Cancer: An Analysis of Inter-radiologist Variability and Diagnostic Accuracy in three Prospective Clinical Trials.European urology oncology · Jul 8, 2026
Identifying Patients With High-Risk Stage I NSCLC Using a Tumor-Informed Plasma ctDNA Assay.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · Jun 1, 2026
STAT6 mutational status and expression in primary mediastinal large B-cell lymphoma.Pathology · Jun 1, 2026
Clinicopathologic Analyses of 34 Cases of High-Grade Serous-Like Carcinoma (HG-SL-Ca) of the Breast.The American journal of surgical pathology · May 1, 2026
Pan-Cancer Pre-Treatment ctDNA Detection Using a Highly Sensitive Tumor-Informed Assay.International journal of molecular sciences · Apr 29, 2026
Clinical validation
No linked records are currently available.
Regulatory
No linked records are currently available.
04 · Company-reported outcomes
Company-reported outcomes and customer stories are distinct from linked Research Intelligence evidence.
RaDaR ST detection of distant metastatic recurrence before clinical detection in breast cancer patients
Detection of distant metastatic recurrences in 3.9-year study of 83 breast cancer patients
RaDaR ST analytical performance for MRD detection
RaDaR ST circulating tumor DNA detection capability
Early detection of breast cancer recurrence during 7-year surveillance when imaging showed no evidence of disease
RaDaR ST detected ctDNA 3 months before imaging found a single bone lesion, enabling early targeted treatment. Patient remains on therapy with no signs of progression 18 months later.
Recurrence monitoring for high-risk breast cancer patient 6 years after completing adjuvant therapy
RaDaR ST detected ctDNA 12 months before imaging confirmed cancer recurrence, providing a full year advance warning for intervention
Detection of distant metastatic recurrence in hormone receptor positive breast cancer patients
100% detection of distant metastatic recurrences with median lead time of 12.4 months before clinical detection in 3.9-year study
05 · Leadership
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No active leadership profiles are currently listed.
06 · Company updates
Recent articles published on NeoGenomics's official website.
No Company updates are currently listed.
07 · HAIC coverage
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08 · Official presence
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09 · Market pathway
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Market context
Companies using AI to analyze genomic, proteomic, metabolomic, or multi-omics data to provide personalized treatment recommendations, identify genetic risks, or develop targeted therapies. Includes genomic sequencing platforms with AI analysis, preventive medicine based on genetic risk assessment, and longevity care based on molecular and genetic data.
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