Single nucleotide variants (SNVs) shape cellular phenotypes and disease susceptibility in cancer. To investigate the functional consequences of SNVs, scientists use single nucleotide CRISPR base editors to make precise genetic changes.
In this Technique Talk, Francisco J. Sánchez-Rivera will discuss how to develop base editor sensor libraries for the high-throughput analysis of causative variants in preclinical cancer models.
Learning Objectives
How to engineer and manipulate single nucleotide bases with precision in cells and organisms
How single nucleotide changes influence cancer initiation and progression
Monday, June 20, 2022
10:00 – 11:00 AM Eastern Time
This webinar will also be available on-demand.
Instructor
Francisco J. Sánchez-Rivera, PhD Assistant Professor Department of Biology Koch Institute for Integrative Cancer Research MIT
TS_WEBINARSIGNUP_TSU_Technique Talk: CRISPR for Genome Engineering in Drosophila December 14 2021
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