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681 Gateway Blvd
South San Francisco, CA 94080
Rewriting Cancer's Script: Insights from Saturation Genome Editing
Presented by
Dr. David J. Adams
Senior Group Leader and Interim Head of Cancer, Ageing and Somatic Mutation, Wellcome Sanger Institute
Covered in this Webinar
How NRF2 and KEAP1 variants reprogram cancer cells to resist therapy.
How saturation-seq couples SGE with single-cell transcriptomics to map variant effects at unprecedented resolution.
How functional and clinical data integration enables confident classification of gain-of-function mutations.
Every mutation tells a story — but most remain unread. Join Dr. David Adams from the Wellcome Sanger Institute to explore how cutting-edge functional genomics is transforming our understanding of cancer genetics.
In this live webinar, Dr. Adams will share how saturation genome editing (SGE) and single-cell transcriptomics can reveal which mutations drive tumor growth and treatment resistance — providing a new framework for functional variant classification across oncology.
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