Explore a groundbreaking webinar on sequencing single-strand mismatch and damage patterns using long-read sequencing technology. Learn about a novel single-molecule method that achieves high fidelity for detecting single-base substitutions in either one or both DNA strands, as well as single-strand cytosine deamination events. Discover how this approach enables new studies of mutation origins in healthy tissues and cancer by detecting initiating single-strand events at single-molecule resolution. Presented by Dr. Gilad Evrony, a renowned physician-scientist from NYU Grossman School of Medicine, this 26-minute talk delves into the potential of this innovative genomics technology to revolutionize our understanding of somatic mutations and their role in genetic diseases and cancer development.
Sequencing Single-Strand Mismatch and Damage Patterns by Long-Read Sequencing
Overview
Syllabus
Sequencing Single-Strand Mismatch and Damage Patterns by Long-Read Sequencing
Taught by
Labroots
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