We research the genetic basis of rare human disease

We use computational approaches and large genomic datasets to uncover novel genetic variants that cause rare disease, and understand the mechanisms through which they do so.

The group is based at the Big Data Institute and Centre for Human Genetics at the University of Oxford.

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Research

Find out more about our research.

Join us

We are on the look out for talented individuals who would like to work with us. Please get in touch!