• 28th March 2022

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  • 29th March 2022

We are pleased to announce the 16th in our series of meetings on rare diseases, which will present an exciting blend of genomic science and clinical medicine. This meeting will explore how cutting-edge genomic research translates into clinical care and informs our understanding of the biology of rare disease. This year’s meeting will discuss how the use of diverse genomes can help drive precision medicine and more equitable healthcare benefits. We will also focus on non-Mendelian forms of rare disease and new approaches to treat rare disease. We will also discuss how high-throughput functional assays can improve the interpretation of variants and discuss the ongoing challenges and opportunities in implementing genomics in mainstream healthcare systems across the world.