Make data speak
in rare childhood epilepsies
We want to understand how to better identify and treat childhood brain disorders. Gene discovery has already transformed the way we understand rare neurological disorders in children. However, while genetic studies can be performed at scale, the analysis of clinical data often needs to be performed manually. Our goal is to expand the data science approaches established for analyzing genomic data and clinical information so that we can leverage large-scale data to better understand natural histories and treatment responses.