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Timezone: Asia/Seoul
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Invited Talk
8:30 AM - 9:30 AM
Invited Talk
1:30 PM - 2:30 PM

Making effective medicines is challenging: more than 90 percent of drug candidates fail in pre-clinical research or clinical trials. A major contributor to this low success rate is the enormous space of biological and therapeutic possibilities. In the underlying biology of disease, there are thousands of different cell types and states, about 20,000 genes in our genome, more than 105 disease associated loci, and perhaps 1013 or more ways in which they could meaningfully combine. To make medicines targeting this biology, one could consider at least 1060 possible small molecules with medicine-like properties, approximately 2032 relevant antibodies to consider, billions of people, and about 10,000 different diseases. Now, however, we are at a major inflection point: we can collect large-scale data, at high-resolution, from human biology, and crucially, combine these large datasets with AI to be able to represent, reason and generate over these enormous spaces to yield testable predictions of missing or nonexistent information and iteratively improve our models. Although it is not possible to test every possibility in a lab, clinical trial, or even an entire population, with the scale of data it is currently possible to generate, we can use AI to bridge different layers of biology, determine the impact of combinations of genetic mutations or drug perturbations, predict disease progression, and generate therapeutic molecules de novo or through optimization. Key to the success of this approach is an integrated interplay between data and AI, or a “Lab in the Loop,” where experimental or clinical data are used to train models, the models are used to help predict and design the next set of experiments, and the process is iterated, at scale, both to yield key predictions in any specific project and improve the model for all projects. In this talk, I will describe how we built such a Lab in the Loop of experiments and AI in Genentech across our target discovery, drug discovery and drug development efforts to serve patients across therapeutic areas.

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Speaker Bio
Aviv Regev
Aviv Regev is a computational biologist and systems biologist and Executive Vice President and Head of Genentech Research and Early Development in Genentech/Roche. She is a core member at the Broad Institute of MIT and Harvard and professor at the Department of Biology of the Massachusetts Institute of Technology. In 2020, Regev became the Head and Executive Vice President of Genentech Research and Early Development, based in South San Francisco, and a member of the extended Corporate Executive Committee of Roche. Previously, she was a Core Institute Member (now on leave), Chair of the Faculty, Founding Director of the Klarman Cell Observatory and co-Director Cell Circuits Program at the Broad Institute of MIT and Harvard. She was also a professor in the Department of Biology at the Massachusetts Institute of Technology (now on leave), as well as an Investigator at the Howard Hughes Medical Institute. Regev's research includes work on gene expression (with Eran Segal and David Botstein), and the use of π-calculus to represent biochemical processes. Regev’s team has been a leading pioneer of single-cell genomics experimental and computational methods.
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Test Of Time
2:30 PM - 3:00 PM