PUBLICATION

CRISPR-DO for genome-wide CRISPR design and optimization

Authors
Ma, J., Köster, J., Qin, Q., Hu, S., Li, W., Chen, C., Cao, Q., Wang, J., Mei, S., Liu, Q., Xu, H., Liu, X.S.
ID
ZDB-PUB-160713-5
Date
2016
Source
Bioinformatics (Oxford, England)   32(21): 3336-3338 (Journal)
Registered Authors
Li, Wei
Keywords
none
MeSH Terms
  • Animals
  • Clustered Regularly Interspaced Short Palindromic Repeats*
  • Computational Biology*
  • DNA
  • Exons
  • Gene Editing*
  • Genome*
  • Humans
  • Mice
  • RNA, Guide, Kinetoplastida
PubMed
27402906 Full text @ Bioinformatics
Abstract
Despite the growing popularity in using CRISPR/Cas9 technology for genome editing and gene knockout, its performance still relies on well designed single guide RNAs (sgRNA). In this study, we propose a web application for the Design and Optimization (CRISPR-DO) of guide sequences that target both coding and non-coding regions in spCas9 CRISPR system across human, mouse, zebrafish, fly and worm genomes. CRISPR-DO uses a computational sequence model to predict sgRNA efficiency, and employs a specificity scoring function to evaluate the potential of off-target effect. It also provides information on functional conservation of target sequences, as well as the overlaps with exons, putative regulatory sequences and single nucleotide polymorphisms (SNP). The web application has a user-friendly genome-browser interface to facilitate the selection of the best target DNA sequences for experimental design.
CRISPR-DO is available at http://cistrome.org/crispr/ CONTACT: qiliu@tongji.edu.cn, hanxu@jimmy.harvard.edu, xsliu@jimmy.harvard.edu.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping