Genomics of Rare Disease: Beyond the Exome 2016

The meeting features the latest findings related to the genomic basis of rare diseases, which can provide powerful insights into human biology. As we move beyond exome sequencing to whole genome sequencing, the opportunities and challenges that arise for human genome analysis and clinical practice will also be explored. This year's meeting will focus on the links between monogenic and polygenic disorders and will explore the various modifiers of rare disease.