COSMID: A Web-based Tool for Identifying and Validating CRISPR/Cas Off-target Sites

被引:279
作者
Cradick, Thomas J.
Qiu, Peng
Lee, Ciaran M.
Fine, Eli J.
Bao, Gang [1 ]
机构
[1] Georgia Inst Technol, Dept Biomed Engn, Atlanta, GA 30332 USA
来源
MOLECULAR THERAPY-NUCLEIC ACIDS | 2014年 / 3卷
基金
美国国家卫生研究院;
关键词
bioinformatics; bulges; off-target; program; RISPR; specificity; IMMUNE-SYSTEM; ADAPTIVE IMMUNITY; DNA CLEAVAGE; CAS9; SEARCHES; SPECIFICITY; NUCLEASES; DELETIONS; BACTERIA; DEFENSE;
D O I
10.1038/mtna.2014.64
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Precise genome editing using engineered nucleases can significantly facilitate biological studies and disease treatment. In particular, clustered regularly interspaced short palindromic repeats (CRISPR) with CRISPR-associated (Cas) proteins are a potentially powerful tool for modifying a genome by targeted cleavage of DNA sequences complementary to designed guide strand RNAs. Although CRISPR/Cas systems can have on-target cleavage rates close to the transfection rates, they may also have relatively high off-target cleavage at similar genomic sites that contain one or more base pair mismatches, and insertions or deletions relative to the guide strand. We have developed a bioinformatics-based tool, COSMID (CRISPR Off-target Sites with Mismatches, Insertions, and Deletions) that searches genomes for potential off-target sites (http://crispr.bme.gatech.edu). Based on the user-supplied guide strand and input parameters, COSMID identifies potential off-target sites with the specified number of mismatched bases and insertions or deletions when compared with the guide strand. For each site, amplification primers optimal for the chosen application are also given as output. This ranked-list of potential off-target sites assists the choice and evaluation of intended target sites, thus helping the design of CRISPR/Cas systems with minimal off-target effects, as well as the identification and quantification of CRISPR/Cas induced off-target cleavage in cells.
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页数:10
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