Cas9-chromatin binding information enables more accurate CRISPR off-target prediction

被引:169
作者
Singh, Ritambhara [1 ,2 ]
Kuscu, Cem [1 ]
Quinlan, Aaron [1 ,3 ,4 ]
Qi, Yanjun [2 ]
Adli, Mazhar [1 ]
机构
[1] Univ Virginia, Sch Med, Dept Biochem & Mol Genet, Charlottesville, VA 22903 USA
[2] Univ Virginia, Dept Comp Sci, Charlottesville, VA 22903 USA
[3] Univ Virginia, Ctr Publ Hlth Genom, Charlottesville, VA 22903 USA
[4] Univ Virginia, Dept Publ Hlth Sci, Charlottesville, VA 22903 USA
关键词
RNA-GUIDED ENDONUCLEASES; HUMAN-CELLS; HUMAN GENOME; CAS NUCLEASES; SYSTEM; SITES; TOOL; IDENTIFICATION; SPECIFICITY; ACTIVATION;
D O I
10.1093/nar/gkv575
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The CRISPR system has become a powerful biological tool with a wide range of applications. However, improving targeting specificity and accurately predicting potential off-targets remains a significant goal. Here, we introduce a web-based CRISPR/Cas9 Off-target Prediction and Identification Tool (CROP-IT) that performs improved off-target binding and cleavage site predictions. Unlike existing prediction programs that solely use DNA sequence information; CROP-IT integrates whole genome level biological information from existing Cas9 binding and cleavage data sets. Utilizing whole-genome chromatin state information from 125 human cell types further enhances its computational prediction power. Comparative analyses on experimentally validated datasets show that CROP-IT outperforms existing computational algorithms in predicting both Cas9 binding as well as cleavage sites. With a user-friendly web-interface, CROP-IT outputs scored and ranked list of potential off-targets that enables improved guide RNA design and more accurate prediction of Cas9 binding or cleavage sites.
引用
收藏
页数:8
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