Ed is a Data Manager in the Rare Disease Analysis team, working at the intersection of genomic data management, software engineering, and analysis. His primary focus is coordinating the transfer, ingestion, and processing of genomic data from external collaborators into the organization's cloud infrastructure. Ed also contributes to the development of data visualization tools, data transfer solutions, and improvements to the production pipelines. With a diverse skill set, he supports the team in their mission to diagnose rare diseases through large-scale genomic data analysis.
The Centre for Population Genomics is a joint national initiative of Garvan Institute of Medical Research and the Murdoch Children’s Research Institute. The Institutes are national leaders in genomic research, with complementary strengths spanning large-scale genomics, data science, population health, and clinical impact.
The Centre for Population Genomics values diversity in our team and our work. We believe that including all human diversity in genomic research will empower medical care that benefits everyone.
We pay our respect to all Aboriginal and Torres Strait Islander cultures and to their Elders past and present. We gratefully accept the invitation in the Uluru Statement from the Heart “to walk with us in a movement of the Australian people for a better future”.
