RRC ID 62306
著者 Canver MC, Haeussler M, Bauer DE, Orkin SH, Sanjana NE, Shalem O, Yuan GC, Zhang F, Concordet JP, Pinello L.
タイトル Integrated design, execution, and analysis of arrayed and pooled CRISPR genome-editing experiments.
ジャーナル Nat Protoc
Abstract CRISPR (clustered regularly interspaced short palindromic repeats) genome-editing experiments offer enormous potential for the evaluation of genomic loci using arrayed single guide RNAs (sgRNAs) or pooled sgRNA libraries. Numerous computational tools are available to help design sgRNAs with optimal on-target efficiency and minimal off-target potential. In addition, computational tools have been developed to analyze deep-sequencing data resulting from genome-editing experiments. However, these tools are typically developed in isolation and oftentimes are not readily translatable into laboratory-based experiments. Here, we present a protocol that describes in detail both the computational and benchtop implementation of an arrayed and/or pooled CRISPR genome-editing experiment. This protocol provides instructions for sgRNA design with CRISPOR (computational tool for the design, evaluation, and cloning of sgRNA sequences), experimental implementation, and analysis of the resulting high-throughput sequencing data with CRISPResso (computational tool for analysis of genome-editing outcomes from deep-sequencing data). This protocol allows for design and execution of arrayed and pooled CRISPR experiments in 4-5 weeks by non-experts, as well as computational data analysis that can be performed in 1-2 d by both computational and noncomputational biologists alike using web-based and/or command-line versions.
巻・号 13(5)
ページ 946-986
公開日 2018-5-1
DOI 10.1038/nprot.2018.005
PII nprot.2018.005
PMID 29651054
PMC PMC6182299
MeSH Clustered Regularly Interspaced Short Palindromic Repeats* Computational Biology / methods* Endonucleases / metabolism* Gene Editing / methods* RNA, Guide, Kinetoplastida / genetics*
IF 10.419
リソース情報
ヒト・動物細胞 HUDEP-2(RCB4557)