Program: Scientific Program
Session: Genome Therapies for Hemoglobinopathies
Session: Genome Therapies for Hemoglobinopathies
Saturday, December 5, 2015, 2:00 PM-3:30 PM
Hall D, Level 2
(Orange County Convention Center)
Sunday, December 6, 2015, 9:30 AM-11:00 AM
Valencia A (W415A), Level 4
(Orange County Convention Center)
RNA-guided Cas9 nucleases based on the prokaryotic CRISPR-Cas systems provide an unprecedented ease in being able to edit the genomes of diverse organisms. As a single unifying factor capable of co-localizing RNA, DNA, and protein, I believe tools and techniques based on Cas9 will grant exquisite control over cellular organization, regulation, and behavior. Here I will describe work on development of the CRISPR-Cas9 targeting methodology, and detail current and prospective genome-engineering methodologies.
Disclosures: No relevant conflicts of interest to declare.
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