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We would like to thank the students from the Department of Communication, Lauren Archibald '18, Brian Lloyd '18 and Daniel Valentino '17, along with their professor John Kilker, III for the production of this video

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Using an established assay for CRISPR-based knock-in of sequences at the CLTA N-terminus (a highly expressed gene in HEK293T cells [Leonetti 2016] , neither our original split-wrmScarlet 11 sequence nor its mutant library enabled detectable complementation (Figure S10B, left panels)

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