Advancing the Toolchain for Interpreting Human Genetic Variation Using Deep Learning and Single-Cell Genomics

Explore cutting-edge approaches to interpreting human genetic variation in this workshop presentation by Oliver Stegle from the European Molecular Biology Laboratory and German Cancer Research Center (DKFZ). Delve into the integration of deep learning techniques with single-cell genomics to advance the toolchain for genetic analysis. Learn about the latest developments in multimodal data integration and their applications in understanding human genetics. Gain insights into the work being conducted at the Novo Nordisk Foundation Center (NNFC) at the Broad Institute and its implications for genetic research.

NNFC Workshop: Oliver Stegle