About
Long-read sequencing technologies have emerged as powerful players in genomics over the last few years.
These new technologies have proven their ability to resolve some of the most challenging regions of genomes, leading to, among other things, the discovery of novel mechanisms of disease. The workshop’s five-day program includes three days of plenary sessions featuring renowned speakers, expert users, and technology developers who will share their experiences applying long-read sequencing in basic and translational genomic science and also explore the commonalities and differences in the current technologies. The workshop also offers one day of hands-on wet-lab tutorial and an additional day of sessions covering computational approaches for effectively analyzing long-read sequencing data with state-of-the-art tools.
Throughout the event, participants will have the opportunity to network with genomics experts and industry leaders.
Research reported in this publication was supported by the National Human Genome Research Institute under award number R25HG010611. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
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