CRISPR Genome Editing Made Easy Through the CHOPCHOP Website

Research output: Contribution to journalResearch articleInvitedpeer-review

Contributors

  • Kornel Labun - , University of Bergen (Author)
  • Maximilian Krause - , Norwegian Research Centre, University of Bergen (Author)
  • Yamila Torres Cleuren - , University of Bergen (Author)
  • Eivind Valen - , University of Bergen (Author)

Abstract

The design of optimal guide RNA (gRNA) sequences for CRISPR systems is challenged by the need to achieve highly efficient editing at the desired location (on-target editing) with minimal editing at unintended locations (off-target editing). Although laboratory validation should ideally be used to detect off-target activity, computational predictions are almost always preferred in practice due to their speed and low cost. Several studies have therefore explored gRNA-DNA interactions in order to understand how CRISPR complexes select their genomic targets. CHOPCHOP (https://chopchop.cbu.uib.no/) leverages these developments to build a user-friendly web interface that helps users design optimal gRNAs. CHOPCHOP supports a wide range of CRISPR applications, including gene knock-out, sequence knock-in, and RNA knock-down. Furthermore, CHOPCHOP offers visualization that enables an informed choice of gRNAs and supports experimental validation. In these protocols, we describe the best practices for gRNA design using CHOPCHOP.

Details

Original languageEnglish
Article numbere46
JournalCurrent protocols
Volume1
Issue number4
Publication statusPublished - Apr 2021
Peer-reviewedYes
Externally publishedYes

External IDs

PubMed 33905612
ORCID /0000-0002-7715-1160/work/142255285

Keywords

Keywords

  • Cas9, CRISPR, CRISPRi/a, gene knock-out, genome editing, guide design, knock-down, knock-in, nickase, RNA targeting