Let’s Make Diagnoses for Rare Disease Common

How is WGS used as the driving force behind precision medicine to provide diagnosis to rare disease patients? Case studies demonstrating the value of precision medicine and the downstream benefits to the population health will be provided

Preparing for the Tsunami of Genomic Data

NGS has triggered a tidal wave of genomic data, whose footprint has rapidly expanded beyond the capacity of our existing storage. In partnership with data optimisation and compression experts Geneformics, we will explore the challenges and opportunities of these giant datasets

A genome journey

Elena Flowers of the UCSF School of Nursing is out to get her genome sequenced, to help her students prepare for the clincal future of genomics