Our mission is to leverage our proprietary OrbiSeq™ technology platform for early disease detection, treatment and prevention of complex diseases.
Our game-changing OrbiSeq™ technology platform analyzes repetitive DNA which uniquely reflects both inherited and acquired disease risk.
Since the first sequencing of the human genome in 2003, tremendous gains have been made in understanding hereditary cancer syndromes, with over 50 having been identified. Genetic tests to assess a person’s inherited risk of developing certain cancers are abundant. However, the tests are not clinically actionable for most healthy people. Genetic mutations measure population risk, not individual risk. Genetic mutations (SNPs) identify increased disease risk, but their presence doesn’t guarantee disease will occur, and their absence doesn’t guarantee disease will not occur. Complex diseases are caused by a combination of genetic mutations and environmental factors, including lifestyle. Orbit Genomics’ proprietary OrbiSeq technology platform analyzes a different part of your DNA that uniquely reflects both inherited predisposition to disease and the risk you’ve acquired from from living. We analyze your DNA’s early warning system.
Science & Technology
Accelerating precision medicine by developing clinically actionable tests.
Improving lung cancer diagnosis.
Founded as a collaboration between Dr. Harold “Skip” Garner and Ventac Partners.