共 40 条
CHOPCHOP: a CRISPR/Cas9 and TALEN web tool for genome editing
被引:827
作者:

Montague, Tessa G.
论文数: 0 引用数: 0
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机构:
Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA

Cruz, Jose M.
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h-index: 0
机构:
Harvard Univ, Sch Engn & Appl Sci, Cambridge, MA 02138 USA
Harvard Univ, Wyss Inst Biol Inspired Engn, Cambridge, MA 02138 USA Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA

Gagnon, James A.
论文数: 0 引用数: 0
h-index: 0
机构:
Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA

Church, George M.
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h-index: 0
机构:
Harvard Univ, Wyss Inst Biol Inspired Engn, Cambridge, MA 02138 USA
Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA

Valen, Eivind
论文数: 0 引用数: 0
h-index: 0
机构:
Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
机构:
[1] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
[2] Harvard Univ, Sch Engn & Appl Sci, Cambridge, MA 02138 USA
[3] Harvard Univ, Wyss Inst Biol Inspired Engn, Cambridge, MA 02138 USA
[4] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
关键词:
HUMAN-CELLS;
CRISPR-CAS9;
SYSTEM;
XENOPUS-TROPICALIS;
CAS9;
NUCLEASE;
DESIGN TOOL;
SPECIFICITY;
MUTAGENESIS;
DROSOPHILA;
EFFECTORS;
GENES;
D O I:
10.1093/nar/gku410
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Major advances in genome editing have recently been made possible with the development of the TALEN and CRISPR/Cas9 methods. The speed and ease of implementing these technologies has led to an explosion of mutant and transgenic organisms. A rate-limiting step in efficiently applying TALEN and CRISPR/Cas9 methods is the selection and design of targeting constructs. We have developed an online tool, CHOPCHOP (https://chopchop.rc.fas.harvard.edu), to expedite the design process. CHOPCHOP accepts a wide range of inputs (gene identifiers, genomic regions or pasted sequences) and provides an array of advanced options for target selection. It uses efficient sequence alignment algorithms to minimize search times, and rigorously predicts off-target binding of single-guide RNAs (sgRNAs) and TALENs. Each query produces an interactive visualization of the gene with candidate target sites displayed at their genomic positions and color-coded according to quality scores. In addition, for each possible target site, restriction sites and primer candidates are visualized, facilitating a streamlined pipeline of mutant generation and validation. The ease-of-use and speed of CHOPCHOP make it a valuable tool for genome engineering.
引用
收藏
页码:W401 / W407
页数:7
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