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NeoGenomics Laboratories

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Fort Myers, Florida, US

About NeoGenomics Laboratories

Founded: 2002 Type: Public Company Size: 201-500 employees

NeoGenomics Laboratories is a specialized oncology reference laboratory providing the latest testing technologies, global/tech-only options, and interactive education to the pathology community

NeoGenomics offers the complete spectrum of diagnostic services in immunohistochemistry, FISH, flow cytometry,... Show more »

NeoGenomics Laboratories is a specialized oncology reference laboratory providing the latest testing technologies, global/tech-only options, and interactive education to the pathology community

NeoGenomics offers the complete spectrum of diagnostic services in immunohistochemistry, FISH, flow cytometry, cytogenetics, and molecular testing through our nationwide network of laboratories. We are dedicated to providing superior service, faster turn-around times, and complete attention to the needs of our clients and their patients.

Expertise

  • Staffed with Board-certified pathologists and specialty-trained cancer genetic professionals
  • Comprehensive oncology testing menu
  • Professional staff available for consultation

Service

  • Industry-leading turn-around times
  • Partnership programs designed for the community pathologist
  • Knowledgeable field and customer care team

Quality

  • Fully licensed technical and professional staff
  • CAP-accredited, CLIA licenses, and state licensed facilities
  • Dedicated logistics staff to manage ground and air specimen transportation

Company Awards

Business Expansion Award – September 2010
Presented by: Fort Myers Economic Development Organization

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Certifications & Qualifications

CLIA/CAP

Our Services (39)


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Clinical Biomarkers

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Gene Expression Analysis

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H&E Staining

Hematoxylin and eosin staining
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Companion Diagnostic Development

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CDx development and commercialization

CDx development and commercialization

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NanoString nCounter Analysis

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Immunophenotyping

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Biomarker Analysis

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Next Generation Sequencing (NGS)

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Full services on DNA, RNA. RNAseq, CHiP seq, whole exome sequencing, gene panels, mitochondrial sequencing

Full services on DNA, RNA. RNAseq, CHiP seq, whole exome sequencing, gene panels, mitochondrial sequencing

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Immunohistochemistry (IHC)

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Clinical IHC/FISH

Clinical IHC/FISH

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Myeloperoxidase Testing

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Fluorescence in situ Hybridization (FISH)

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Clinical IHC/FISH

Fluorescence in-situ Hybridization (FISH) is a branch of cancer genetics that focuses on detecting and locating the presence or absence of specific DNA sequences on chromosomes. FISH is also referred to as Molecular Cytogenetics.

To perform FISH, cells are fixed onto the surface of a slide, and then the... Show more »

Clinical IHC/FISH

Fluorescence in-situ Hybridization (FISH) is a branch of cancer genetics that focuses on detecting and locating the presence or absence of specific DNA sequences on chromosomes. FISH is also referred to as Molecular Cytogenetics.

To perform FISH, cells are fixed onto the surface of a slide, and then the slide is treated so that the chromosomal DNA is denatured into single strands.

Then, special fluorescently labeled DNA probes are applied onto the slide. The DNA probes are small pieces of single stranded DNA with a sequence from the gene of interest. Probes are only able to hybridize with their complimentary sequence, which is the gene or locus of interest on a particular chromosome. The DNA probes are allowed to hybridize with the denatured chromosomal DNA, and any excess probes are washed away.

After the excess probes are washed away, the slide is then viewed under a fluorescence microscope. The fluorescently labeled molecules reveal the physical location of the gene or locus of interest. Pathologists will then use specified cut off values to assess the results of the FISH test.

Frequently Ordered Test(s):

  • Hematologic Disease
    • AML
    • MDS
    • CLL
    • NHL
    • MM/MGUS
    • High Risk MM
  • Solid Tumor
    • Breast
    • HER2 (Non-breast)
    • Bladder
    • MelanoSITE™
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Cytogenetics

Price on request

Cytogenetics is the specialized area of laboratory medicine involving the study of normal and abnormal chromosomes and their relationship to disease. Cytogenetic studies are often ordered to answer diagnostic, prognostic and predictive questions in the treatment of hematologic malignancies and solid tumors.

We offer... Show more »

Cytogenetics is the specialized area of laboratory medicine involving the study of normal and abnormal chromosomes and their relationship to disease. Cytogenetic studies are often ordered to answer diagnostic, prognostic and predictive questions in the treatment of hematologic malignancies and solid tumors.

We offer traditional G-banding for metaphase analysis which includes the detection of chromosomal translocations, insertions, inversions, deletions and duplications. Additionally, proprietary wet lab processes increase the length of chromosomes and improve resolution, allowing our team members to ensure the highest quality karotype is performed.

Services Detail

  • 3-5 day Turn-around Time (14-21 days for Lymph Node/Tissue Biopsy)
  • Culture success rates of over 97%
  • Minimum of 20 cells analyzed (when applicable) and minimum target resolution of 400 bands
  • Analysis by two independent Cytogenetic Technologists and an additional quality control check for each case
  • Automation of metaphase identification high through-put services
  • Cases signed out by a board certified Cytogeneticist

Specimen Requirements:

  • Bone Marrow Aspirate: 1-2mL Sodium Heparin tube
  • Peripheral Blood: 2-5mL Sodium Heparin tube
  • Lymph Node/Tissue Biopsy: 2 pieces minimum; 0.2cm3
  • Fresh Tissue: Place in RPMI
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Flow Cytometry

Price on request

NeoGenomics uses 10-color flow cytometry for improved efficiency and reliability in evaluation and diagnosis of hematopoietic diseases. Some of the advantages of our 10-color flow cytometry service over those detecting fewer fluorochromes are:

  • More precise characterization of various cell populations
  • Improved detection of... Show more »

NeoGenomics uses 10-color flow cytometry for improved efficiency and reliability in evaluation and diagnosis of hematopoietic diseases. Some of the advantages of our 10-color flow cytometry service over those detecting fewer fluorochromes are:

  • More precise characterization of various cell populations
  • Improved detection of low-frequency abnormalities
  • Higher information content per tube conserves small specimens and minimizes chance of incomplete analyses
  • Reduced redundancy in use of antibodies, which helps control costs
  • Faster signal acquisition for better turnaround time
  • Simpler analysis of the data generated, with shorter reports
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In vitro Diagnostic Development

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Multiplex Immunohistochemistry (mIHC)

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MultiOmyxTM

MultiOmyxTM

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Protein Services

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Medical Devices & Diagnostics

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Clinical Laboratory Services

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Clinical Research

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Equipment

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Antibody/Antigen Detection Based Testing

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Histological Staining

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Genotyping and Gene Expression Assays

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DNA Hybridization

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DNA Services

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Pharmacology & Toxicology

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Biomarkers

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Nucleic Acid Services

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Biochemistry & Molecular Biology

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Biology

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DNA Sequencing

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Common Histochemical Stains

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Bioanalysis

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Cytometry

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Cells and Tissues

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Clinical and Anatomic Pathology

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Protein Expression Visualization

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Clinical Chemistry

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Immunostaining

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Ashi Malekafzali

Senior Director Pharma Services
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Robert Mata

Pharma Services Contract Analyst
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Jeff Owen

Marketing Manager, Research and Pharma Services

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