What we do

Your TrustedPartner forDiagnostics &Clinical Research

Providing advanced genomic testing solutions for clinicians, researchers, and patients with cutting-edge technology and expert analysis.

About Us

Neuberg Center For Genomic Medicine

Neuberg Center for Genomic Medicine (NCGM), based in Apex, North Carolina, is a one-stop solution for diagnostic and research-based genomic services, delivering best-in-class molecular diagnostics.

What we offer

1

An amalgamation of a team of experts, committed to quality, defines our strength. Assisted by the latest advanced technology and supported by an experienced bioinformatics team, we believe in working together with the health care service providers and researchers to try to solve the Genomic conundrum.

2

To facilitate the integration of Genomics into mainstream diagnostics, we provide a comprehensive range of genetic testing solutions along with the flexibility to customize testing for specific indications.

3

The Neuberg Center for Genomic Medicine follows strict quality control measures and is accredited with various prestigious International certifications.

Certified & Accredited

Accreditations

CAP Accreditation

9007683

CLIA Accreditation

34D2205781

What We Do

Our Services

Inherited Genetic Disorders

Comprehensive testing for hereditary conditions across all age groups using next-generation sequencing panels.

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Reproductive Genetics

Carrier screening, prenatal testing, and preimplantation genetic testing for family planning.

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Oncology — PlasmaSeq

Liquid biopsy and tumor profiling using advanced next-generation sequencing for cancer diagnosis.

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Pharmacogenomics

Personalized medicine through genetic-guided drug therapy optimization for improved outcomes.

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Research Services

Custom genomic research support for academic institutions and commercial partners.

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Custom
Need a Custom Genomic Solution?

Our research team works with you to design tailored genomic studies and testing panels.

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Science & Technology

What is
Genetic Testing?

Genetic testing is a diagnostic test that can analyse human DNA, RNA, chromosomes, proteins, or metabolites in order to detect alterations related to a heritable disorder. This in turn can confirm or rule out a suspected genetic condition or can also help determine a person's future chance of developing or passing on a genetic disorder.

NGS Sequencing
Next-generation platforms
PlasmaSeq
Liquid biopsy technology