Empire Genomics - Enabling Personalized Medicine

New Products & Services

Empire Genomics (EG) is a molecular diagnostics company that develops and offers a comprehensive menu of assay services for use in diagnosing and guiding precise therapeutic treatments for patients. The EG services are designed to specifically meet the needs of pathologists, oncologists and researchers. Our mission is to address the problem the medical community faces with the rapid pace of molecular technology innovations, and the need for the delivery of clinically relevant, cost effective patient decision support tools. Ultimately, through our continued growth customers will be able to realize: faster and more effective drug development, lower healthcare costs, and better clinical outcomes for patients. Empire is uniquely positioned to bring this innovative service to the medical community through its highly qualified team, state of the art facilities and key strategic partnerships with leaders in the global research community. We are a resource to make personalized medicine a reality for you.

FISH Probes

Custom FISH probes, solid tumor probes, loci specific probes, and control probes.

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BAC Clones

Empire Genomics offers its customers access to over one million BAC clones as either bacterial stabs or purified DNA.

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Custom Services

Empire Genomics offers an assortment of custom services to meet your research or clinical needs.

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Genotyping

SNP analysis services let you measure genetic variations.


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Array CGH Services

Receive high-resolution evaluations of DNA copy number alterations associated with chromosome aberrations.

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Circulating Tumor Cells

Easily count CTCs to determine the prognosis of patients with metastatic breast, colorectal or prostate cancer.

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FISH Probes Manufactured

Scientific Citations

Recent News

Characterization of HPV and host genome interactions in primary head and neck cancers

A significant proportion of head and neck cancer is driven by human papillomavirus (HPV) infection, and the expression of viral oncogenes is involved ...

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Identification of a Novel FN1-FGFR1 Genetic Fusion as a Frequent Event in Phosphaturic Mesenchymal Tumour

Phosphaturic mesenchymal tumours (PMT) are uncommon soft tissue and bone tumours that typically cause hypophosphataemia and tumour-induced osteomalaci...

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A novel insertion ins(18;5)(q21.1;q31.2q35.1) in acute myeloid leukemia associated with microdeletions at 5q31.2, 5q35.1q35.2 and 18q12.3q21.1 detected by oligobased array comparative genomic hybridization

Background: Nonrandom clonal chromosomal aberrations can be detected in approximately 55% of adult patients with acute myeloid leukemia (AML). ...

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