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Updated: Jul 11, 2025

Generation of Genomic Deletions in Mammalian Cell Lines via CRISPR/Cas9
Published on: January 3, 2015
CRISPR-mediated genome editing allows for efficient on demand creation of >200 kb deficiencies with precise
Meera Trivedi1, Lamine J Camara2, Hannes E Bülow1,2
1Dominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York, United States.
Abstract:
Deficiency mapping remains a useful tool in the process of identifying causative genetic lesions in C. elegans mutant strains isolated from forward genetic screens, in particular of non-coding mutants. However, there are significant areas across the genome with no deficiency coverage at all, and the boundaries of many deficiencies remain poorly defined. Here, we describe a simple methodology to generate balanced deficiency strains with up to 230 kb molecularly defined deletions (mini-deficiencies) using CRISPR/Cas9, thus providing a simple path for both precise and tailored deficiency mapping.
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