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Dr Owen Siggs
An early-career clinician-scientist with a career focus on the clinical impact of germline and somatic genetic variation.
Doctor Owen Siggs is an early-career clinician-scientist and an inaugural Snow Fellow, with a career focus on the clinical impact of germline and somatic genetic variation.
Owen trained in science and clinical medicine in Adelaide, in immunology and genomics at the John Curtin School of Medical Research with Professor Chris Goodnow, as a General Sir John Monash Scholar at The Scripps Research Institute in California with Nobel Laureate Professor Bruce Beutler, and at the University of Oxford with the Nuffield Professor of Medicine Richard Cornall. He was then a Sir Henry Wellcome Postdoctoral Fellow at The Wellcome Trust Sanger Institute and a Junior Research Fellow at the University of Cambridge, and a Visiting Fellow at the Broad Institute of MIT and Harvard.
His research career has spanned the use of large-scale genome-wide mutagenesis to discover the function of genes essential for immunity, to the use of exome and genome sequencing to diagnose severe inherited diseases. His current interests include the use of large-scale population and single cell genomics to understand the clinical impact of germline and somatic genetic variation, and the application of this information in clinical practice.
Doctor Owen Siggs is an early-career clinician-scientist and an inaugural Snow Fellow, with a career focus on the clinical impact of germline and somatic genetic variation.
Owen trained in science and clinical medicine in Adelaide, in immunology and genomics at the John Curtin School of Medical Research with Professor Chris Goodnow, as a General Sir John Monash Scholar at The Scripps Research Institute in California with Nobel Laureate Professor Bruce Beutler, and at the University of Oxford with the Nuffield Professor of Medicine Richard Cornall. He was then a Sir Henry Wellcome Postdoctoral Fellow at The Wellcome Trust Sanger Institute and a Junior Research Fellow at the University of Cambridge, and a Visiting Fellow at the Broad Institute of MIT and Harvard.
His research career has spanned the use of large-scale genome-wide mutagenesis to discover the function of genes essential for immunity, to the use of exome and genome sequencing to diagnose severe inherited diseases. His current interests include the use of large-scale population and single cell genomics to understand the clinical impact of germline and somatic genetic variation, and the application of this information in clinical practice.