Cargando…
Tag-seq: a convenient and scalable method for genome-wide specificity assessment of CRISPR/Cas nucleases
Genome-wide identification of DNA double-strand breaks (DSBs) induced by CRISPR-associated protein (Cas) systems is vital for profiling the off-target events of Cas nucleases. However, current methods for off-target discovery are tedious and costly, restricting their widespread applications. Here we...
Autores principales: | Huang, Hongxin, Hu, Yongfei, Huang, Guanjie, Ma, Shufeng, Feng, Jianqi, Wang, Dong, Lin, Ying, Zhou, Jiajian, Rong, Zhili |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8253812/ https://www.ncbi.nlm.nih.gov/pubmed/34215845 http://dx.doi.org/10.1038/s42003-021-02351-3 |
Ejemplares similares
-
Engineered Cas12a-Plus nuclease enables gene editing with enhanced activity and specificity
por: Huang, Hongxin, et al.
Publicado: (2022) -
Genome-wide target specificities of CRISPR-Cas9 nucleases revealed by multiplex Digenome-seq
por: Kim, Daesik, et al.
Publicado: (2016) -
GUIDE-Seq enables genome-wide profiling of off-target cleavage by CRISPR-Cas nucleases
por: Tsai, Shengdar Q., et al.
Publicado: (2014) -
Engineered circular guide RNAs boost CRISPR/Cas12a- and CRISPR/Cas13d-based DNA and RNA editing
por: Zhang, Xin, et al.
Publicado: (2023) -
MiniCAFE, a CRISPR/Cas9-based compact and potent transcriptional activator, elicits gene expression in vivo
por: Zhang, Xin, et al.
Publicado: (2021)