清脆的
可药性
药物发现
基因组编辑
Cas9
计算生物学
计算机科学
生物
生物信息学
遗传学
基因
作者
Françis Robert,Sidong Huang,Jerry Pelletier
标识
DOI:10.2174/1566523217666171121164615
摘要
The ability of most laboratories to easily access CRISPR/Cas9 engineering tools has caused a revolution in biology. One of the areas that will continue to be impacted by genome editing is the drug discovery process.CRISPR/Cas9 will not only serve to accelerate the drug discovery pipeline, but also streamline line it by identifying high-value targets, facilitating the validation of drug: target interactions and mechanisms of action, and stimulating the development of phenotype-based high throughput screens as alternatives to target-based assays.We review the literature and hurdles that have been overcome to develop the current generation of tools being used to enrich the drug discovery paradigm.
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