Extru-seq: a method for predicting genome-wide Cas9 off-target sites with advantages of both cell-based and in vitro approaches

被引:0
作者
Jeonghun Kwon
Minyoung Kim
Woochang Hwang
Anna Jo
Gue-Ho Hwang
Minhee Jung
Un Gi Kim
Gang Cui
Heonseok Kim
Joon-Ho Eom
Junho K. Hur
Junwon Lee
Youngho Kim
Jin-soo Kim
Sangsu Bae
Jungjoon K. Lee
机构
[1] Toolgen,Department of Pre
[2] Hanyang University,Medicine, College of Medicine
[3] Hanyang University,Hanyang Institute of Bioscience and Biotechnology
[4] Hanyang University,Department of Chemistry
[5] Yonsei University College of Medicine,Department of Ophthalmology
[6] Stanford University,Department of Medicine, Division of Oncology
[7] National Institute of Food and Drug Safety Evaluation,Department of Genetics, College of Medicine
[8] Hanyang University,Department of Biochemistry and Molecular Biology
[9] Center for Genome Engineering,undefined
[10] Institute for Basic Science (IBS),undefined
[11] Seoul National University College of Medicine,undefined
来源
Genome Biology | / 24卷
关键词
CRISPR; Genome-wide; Off-target; Cell-based; In vitro;
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摘要
We present a novel genome-wide off-target prediction method named Extru-seq and compare it with cell-based (GUIDE-seq), in vitro (Digenome-seq), and in silico methods using promiscuous guide RNAs with large numbers of valid off-target sites. Extru-seq demonstrates a high validation rate and retention of information about the intracellular environment, both beneficial characteristics of cell-based methods. Extru-seq also shows a low miss rate and could easily be performed in clinically relevant cell types with little optimization, which are major positive features of the in vitro methods. In summary, Extru-seq shows beneficial features of cell-based and in vitro methods.
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