4.8 Article

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

期刊

NUCLEIC ACIDS RESEARCH
卷 43, 期 18, 页码 -

出版社

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkv575

关键词

-

资金

  1. University of Virginia School of medicine
  2. Pilot project (Pediatric Center of Excellence in Nephrology grant) [NIH P50 DK096373]
  3. V Scholar award from V cancer research foundation
  4. V scholar Foundation

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据