| Literature DB >> 27261176 |
Abstract
Genome editing technologies such as clustered regularly interspaced short palindromic repeats (CRISPR) systems have ushered in a new era of targeted DNA manipulation. The easy programmability of CRISPR using short oligonucleotides enables rapid synthesis of large-scale libraries for functional genetic screens. Here we present fundamental concepts and methods for pooled CRISPR screens and review biological results from recent genome-scale loss-of-function and gain-of-function screens. We also discuss new frontiers in pooled screens, including novel effector domains for functional screens and applications in the noncoding genome.Entities:
Keywords: CRISPR; Cancer; Cas9; Genetic screens; Genome engineering; Noncoding
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Year: 2016 PMID: 27261176 PMCID: PMC5133192 DOI: 10.1016/j.ab.2016.05.014
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365