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Bridging the gap between genetic research and actionable clinical outcomes for lifelong genetic diagnosis under patient control

Our knowledge of the human genome is growing exponentially, yet medical professionals struggle to incorporate it into their decision making. Important research findings are neglected for a lack of simple, reliable and fast genetic analysis. We are a pioneering genetic analysis company that aims to unlock the true potential of Next Generation Sequencing (NGS), bridging the gap between genetic research and healthcare with a standardized analysis workflow and data management system to ensure that valuable insights from genetic research can be effectively applied in patient care.

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