Cytognomix, Inc.

Personalized genomic diagnostic products

Diagnostic results from a patient with acute myelogenous leukemia

About Us

Phone: 519-858-5050

Fax: 519-858-5142

E-mail: info@cytognomix.com

Cytognomix’s Single Copy (sc) technology brings precise, sensitive, informative and proprietary genetic disease management tools to advanced clinical laboratories for detection of chromosome anomalies related to genetic disease. Cytognomix designs and produces molecular cytogenetic tests using fluorescent in-situ hybridization scFISH probes. In addition, microarray-based comparative genomic hybridization (aCGH) can use SC technology for increased reproducibility. A key component is our semantic genome browser that simplifies the selection of appropriate single copy products for nearly any gene-mapped disease. Most importantly, use of Cytognomix’s scFISH probes will assure correct diagnosis and make possible more personalized treatment than conventional approaches.

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Probes detecting inversion 16 in acute myelogenous leukemia

Cytognomix.com                                                      19-Dec-09