| Literature DB >> 28835906 |
Jijun Cheng1,2, Wen Pan1,2, Jun Lu1,2,3,4.
Abstract
Genetic screens using single-guide-RNA (sgRNA) libraries and CRISPR technology have been powerful to identify genetic regulators for both coding and noncoding regions of the genome. Interrogating functional elements in noncoding regions requires sgRNA libraries that are densely covering, and ideally inexpensive, easy to implement and flexible for customization. We present a Molecular Chipper protocol for generating dense sgRNA libraries from genomic regions of interest. This approach utilizes a combination of random fragmentation and a Type III restriction enzyme to derive a dense coverage of sgRNA library from input DNA.Entities:
Keywords: CRISPR-Cas9; Molecular chipper; Non-coding genome; Reporter screen; sgRNA library
Year: 2017 PMID: 28835906 PMCID: PMC5564686 DOI: 10.21769/BioProtoc.2373
Source DB: PubMed Journal: Bio Protoc ISSN: 2331-8325