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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.
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页数:8
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