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Prion Research at the University of Toronto. In vivo imaging of protein aggregation. The Watts lab is part of the Tanz Centre for Research in Neurodegenerative Diseases. At the University of Toronto.

Extracting useful information from large genomic datasets. The MacArthur lab uses cutting-edge genomic technologies at massive scale to understand the impact of human genetic variation, and to provide answers to families affected by rare genetic diseases. We lead an international consortium that has assembled ExAC. Is an intuitive online portal for exploring exome and whole-genome sequencing data from rare disease families.

The Raymond and Beverley Sackler Laboratory for Computational Biology at Harvard Medical School. What will we do when there are a million genomes? We develop computational approaches to make sense of genetic variation.

Rare disease genetics- UCL exomes consortium. Friday, 25 November 2016. Cryptic exons and TDP-43 in neurodegenerative diseases. I am delighted to see on BioRxiv. From my PhD student Jack Humphrey. Jack works in collaboration between the UCL Genetics Institute and the UCL Institute of Neurology.