Sequencing Single-Strand Mismatch and Damage Patterns by Long-Read Sequencing

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