Talk Title: Analysis of Large-Scale Exome Sequence Data: Leveraging Variant Annotation to Clarify Genetic Contributions to Common Health-Related Phenotypes
Professor David Curtis has an an extensive background in psychiatric and statistical genetics, he brings decades of expertise from Cambridge, UCL, and Barts & The London School of Medicine. He is currently working on methods for detecting genetic variants affecting risk of complex diseases using large exome-sequenced datasets such as UK Biobank.
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Family friendly
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