Over the past decade, advances in high-throughput genome sequencing together with dramatic cost reductions have transformed basic research and clinical medicine. Exome- and whole-genome analysis are becoming routine aspects of medical care, advancing the diagnosis and treatment of rare genetic disorders and a variety of cancers. Genome sequencing and analysis is having a profound impact on newborn care, both in helping solve diagnostic odysseys of newborns in intensive care and in monitoring the long-term benefits of genomic medicine.
In this inaugural Clinical OMICs Keynote webinar, we are proud to host two renowned leaders in the field of genomic medicine, Drs Stephen Kingsmore and Robert Green, who will discuss their pioneering work in the field of newborn genome sequencing and analysis:
Following the presentations, there will be a live Q&A on the future of newborn screening and genomic medicine with both presenters.