Please cite the paper below for the GUIDEseq package.
Lihua Julie Zhu, Michael Lawrence, Ankit Gupta, Herve Pages, Alper Kucukural, Manuel Garber and Scot A. Wolfe. GUIDEseq: a bioconductor package to analyze GUIDE-Seq datasets for CRISPR-Cas nucleases. BMC Genomics. 2017. 18(1):379
Corresponding BibTeX entry:
@Article{,
title = {GUIDEseq: a bioconductor package to analyze GUIDE-Seq
datasets for CRISPR-Cas nucleases},
author = {Lihua Julie Zhu and Michael Lawrence and Ankit Gupta and
Herve Pages and Alper Kucukural and Manuel Garber and Scot A.
Wolfe},
journal = {BMC Genomics},
volume = {18},
year = {2017},
number = {1},
url =
{http://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-017-3746-y},
pubmedid = {PMC5433024},
abstract = {Genome editing technologies developed around the
CRISPR-Cas9 nuclease system have facilitated the investigation of
a broad range of biological questions. These nucleases also hold
tremendous promise for treating a variety of genetic disorders.
In the context of their therapeutic application, it is important
to identify the spectrum of genomic sequences that are cleaved by
a candidate nuclease when programmed with a particular guide RNA,
as well as the cleavage efficiency of these sites. Powerful new
experimental approaches, such as GUIDE-seq, facilitate the
sensitive, unbiased genome-wide detection of nuclease cleavage
sites within the genome. Flexible bioinformatics analysis tools
for processing GUIDE-seq data are needed. Here, we describe an
open source, open development software suite, GUIDEseq, for
GUIDE-seq data analysis and annotation as a Bioconductor package
in R. The GUIDEseq package provides a flexible platform with more
than 60 adjustable parameters for the analysis of datasets
associated with custom nuclease applications. These parameters
allow data analysis to be tailored to different nuclease
platforms with different length and complexity in their guide and
PAM recognition sequences or their DNA cleavage position. They
also enable users to customize sequence aggregation criteria, and
vary peak calling thresholds that can influence the number of
potential off-target sites recovered. GUIDEseq also annotates
potential off-target sites that overlap with genes based on
genome annotation information, as these may be the most important
off-target sites for further characterization. In addition,
GUIDEseq enables the comparison and visualization of off-target
site overlap between different datasets for a rapid comparison of
different nuclease configurations or experimental conditions. For
each identified off-target, the GUIDEseq package outputs mapped
GUIDE-Seq read count as well as cleavage score from a user
specified off-target cleavage score prediction algorithm
permitting the identification of genomic sequences with
unexpected cleavage activity. The GUIDEseq package enables
analysis of GUIDE-data from various nuclease platforms for any
species with a defined genomic sequence. This software package
has been used successfully to analyze several GUIDE-seq datasets.
The software, source code and documentation are freely available
at
http://www.bioconductor.org/packages/release/bioc/html/GUIDEseq.html.},
}