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EuPaGDT: a web tool tailored to design CRISPR guide RNAs for eukaryotic pathogens

机译:EuPaGDT:一个为设计用于真核病原体的CRISPR指导RNA设计的网络工具

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摘要

Recent development of CRISPR-Cas9 genome editing has enabled highly efficient and versatile manipulation of a variety of organisms and adaptation of the CRISPR-Cas9 system to eukaryotic pathogens has opened new avenues for studying these otherwise hard to manipulate organisms. Here we describe a webtool, Eukaryotic Pathogen gRNA Design Tool (EuPaGDT; available at ), which identifies guide RNA (gRNA) in input gene(s) to guide users in arriving at well-informed and appropriate gRNA design for many eukaryotic pathogens. Flexibility in gRNA design, accommodating unique eukaryotic pathogen (gene and genome) attributes and high-throughput gRNA design are the main features that distinguish EuPaGDT from other gRNA design tools. In addition to employing an array of known principles to score and rank gRNAs, EuPaGDT implements an effective on-target search algorithm to identify gRNA targeting multi-gene families, which are highly represented in these pathogens and play important roles in host–pathogen interactions. EuPaGDT also identifies and scores microhomology sequences flanking each gRNA targeted cut-site; these sites are often essential for the microhomology-mediated end joining process used for double-stranded break repair in these organisms. EuPaGDT also assists users in designing single-stranded oligonucleotides for homology directed repair. In batch processing mode, EuPaGDT is able to process genome-scale sequences, enabling preparation of gRNA libraries for large-scale screening projects.
机译:CRISPR-Cas9基因组编辑的最新发展已实现了对多种生物的高效和多功能操纵,而CRISPR-Cas9系统对真核病原体的适应性为研究这些原本难以操纵的生物开辟了新途径。在这里,我们描述了一个网络工具,即真核病原体gRNA设计工具(EuPaGDT;可在处获得),该工具可识别输入基因中的引导RNA(gRNA),以指导用户为许多真核生物病原体提供知情且适当的gRNA设计。 gRNA设计的灵活性,适应独特的真核病原体(基因和基因组)属性以及高通量gRNA设计是EuPaGDT与其他gRNA设计工具不同的主要特征。除采用一系列已知原理对gRNA进行评分和排名外,EuPaGDT还实施了一种有效的针对目标的搜索算法,以识别靶向多基因家族的gRNA,这些家族在这些病原体中具有很高的代表性,并在宿主与病原体的相互作用中发挥重要作用。 EuPaGDT还可以识别和评分每个靶向gRNA的切割位点两侧的微同源序列;这些位点对于这些生物中用于双链断裂修复的微同源性介导的末端连接过程通常是必不可少的。 EuPaGDT还可以帮助用户设计用于同源性定向修复的单链寡核苷酸。在批处理模式下,EuPaGDT能够处理基因组规模的序列,从而能够为大型筛选项目准备gRNA库。

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