 My name is Professor Matthew loose. I'm from the University of Nottingham, where I run the sequencing facility and run a research group. So at the moment my research activity is focused on developing tools and methods to exploit Nanopore sequencing to best understand human disease and human disorders, as well as develop methods for faster genome assembly and faster sequence analysis. Ynd yn credu eto a fydd Follow Up yma presupydytoedd jameil ei eddych leirwyr ac mae'r adroddoriaeth nawr hefyd ac ei wneud beth leirwyr i gysylltu carton a yn cael Feyddr felínig typod bullying ac y ffordd region, mae'n cael dim gyd, erhawn lle shade ac mae'r adroddoriaeth newydd yma, interesting and useful. I think single molecule techniques for people studying the human genome are incredibly interesting. There are regions of the human genome that we just find difficult to see with short reads and so long reads can help bridge those gaps. It also brings sequencing closer to the patient or closer to the sample, closer to the individual and anyone can use it in their own laboratory.