Long-read sequencing technologies reveal mutations lurking in the “camouflaged” genome
- Published on: October 28 2019
Dr. Mark T.W. Ebbert is Assistant Professor of Neuroscience at the Mayo Clinic, USA with a background in computational biology, bioinformatics and genomic studies. His research focuses on characterising the structural mutations associated with Alzheimer’s disease, amyotrophic lateral sclerosis (ALS), and frontotemporal dementia.
During this webinar, Mark shares his experience in using nanopore sequencing to reveal mutations lurking in the “camouflaged” genome.
