首页> 美国卫生研究院文献>PLoS Computational Biology >A benchmark of computational CRISPR-Cas9 guide design methods
【2h】

A benchmark of computational CRISPR-Cas9 guide design methods

机译:计算CRISPR-Cas9指南设计方法的基准

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The popularity of CRISPR-based gene editing has resulted in an abundance of tools to design CRISPR-Cas9 guides. This is also driven by the fact that designing highly specific and efficient guides is a crucial, but not trivial, task in using CRISPR for gene editing. Here, we thoroughly analyse the performance of 18 design tools. They are evaluated based on runtime performance, compute requirements, and guides generated. To achieve this, we implemented a method for auditing system resources while a given tool executes, and tested each tool on datasets of increasing size, derived from the mouse genome. We found that only five tools had a computational performance that would allow them to analyse an entire genome in a reasonable time, and without exhausting computing resources. There was wide variation in the guides identified, with some tools reporting every possible guide while others filtered for predicted efficiency. Some tools also failed to exclude guides that would target multiple positions in the genome. We also considered two collections with over a thousand guides each, for which experimental data is available. There is a lot of variation in performance between the datasets, but the relative order of the tools is partially conserved. Importantly, the most striking result is a lack of consensus between the tools. Our results show that CRISPR-Cas9 guide design tools need further work in order to achieve rapid whole-genome analysis and that improvements in guide design will likely require combining multiple approaches.
机译:基于CRISPR的基因编辑的流行导致产生了大量用于设计CRISPR-Cas9指南的工具。这也受到以下事实的驱动:在使用CRISPR进行基因编辑时,设计高度特异性和有效的指南是一项至关重要的任务,而不是琐碎的任务。在这里,我们彻底分析了18种设计工具的性能。根据运行时性能,计算要求和生成的指南对它们进行评估。为实现此目的,我们实现了一种在执行给定工具时审核系统资源的方法,并在源自鼠标基因组的大小递增的数据集上测试了每个工具。我们发现只有五个工具具有计算性能,这使它们可以在合理的时间内分析整个基因组,而不会耗尽计算资源。所确定的指南存在很大差异,一些工具报告了所有可能的指南,而其他工具则进行了过滤以提高预测效率。一些工具也未能排除针对基因组中多个位置的指导。我们还考虑了两个集合,每个集合都有一千多个指南,可提供实验数据。数据集之间的性能差异很大,但是工具的相对顺序是部分保留的。重要的是,最惊人的结果是工具之间缺乏共识。我们的结果表明,CRISPR-Cas9指南设计工具需要进一步的工作才能实现快速的全基因组分析,指南设计的改进可能需要结合多种方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号