Genome-wide detection and analysis of CRISPR-Cas off-targets

Prog Mol Biol Transl Sci. 2021:181:31-43. doi: 10.1016/bs.pmbts.2021.01.012. Epub 2021 Mar 4.

Abstract

The clustered, regularly interspersed, short palindromic repeats (CRISPR) technology is revolutionizing biological studies and holds tremendous promise for treating human diseases. However, a significant limitation of this technology is that modifications can occur on off-target sites lacking perfect complementarity to the single guide RNA (sgRNA) or canonical protospacer-adjacent motif (PAM) sequence. Several in vivo and in vitro genome-wide off-target profiling approaches have been developed to inform on the fidelity of gene editing. Of these, GUIDE-seq has become one of the most widely adopted and reproducible methods. To allow users to easily analyze GUIDE-seq data generated on any sequencing platform, we developed an open-source pipeline, GS-Preprocess, that takes standard base-call output in bcl format and generate all required input data for off-target identification using bioconductor package GUIDEseq for off-target identification. Furthermore, we created a Docker image with GS-Proprocess, GUIDE-seq, and all its R and system dependencies already installed. The bundled pipeline will empower end users to streamline the analysis of GUIDE-seq data and motivate their use of higher throughput sequencing with increased multiplexing for GUIDE-seq experiments.

Keywords: CRISPR; GUIDE-seq; Genome editing; Off-targets analysis; Software.

MeSH terms

  • CRISPR-Cas Systems* / genetics
  • Gene Editing
  • High-Throughput Nucleotide Sequencing
  • Humans
  • RNA, Guide, CRISPR-Cas Systems*

Substances

  • RNA, Guide, CRISPR-Cas Systems