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100,000 Genomes: the road to personalised genomic medicine
Tue 21 March 2017, 19:30 – 20:30 GMT
A technology breakthrough that started in Cambridge has brought us to where we are able to decode the entire DNA sequence of 100,000 genomes to determine mutations that cause rare genetic diseases and cancer. Dr David Bentley, Chief Scientist illumina and Professor Mark Caulfield, Chief Scientist Genomics England discuss how this project promises to revolutionise the way we practice medicine.