药物发现
高含量筛选
工作流程
计算机科学
知识抽取
计算生物学
功能(生物学)
鉴定(生物学)
数据科学
图像(数学)
表型筛选
药品
数据挖掘
人工智能
表型
生物信息学
生物
细胞
药理学
基因
进化生物学
数据库
植物
生物化学
遗传学
作者
Sean Lin,Kenji Schorpp,Ina Rothenaigner,Kamyar Hadian
标识
DOI:10.1016/j.drudis.2020.06.001
摘要
While target-based drug discovery strategies rely on the precise knowledge of the identity and function of the drug targets, phenotypic drug discovery (PDD) approaches allow the identification of novel drugs based on knowledge of a distinct phenotype. Image-based high-content screening (HCS) is a potent PDD strategy that characterizes small-molecule effects through the quantification of features that depict cellular changes among or within cell populations, thereby generating valuable data sets for subsequent data analysis. However, these data can be complex, making image analysis from large HCS campaigns challenging. Technological advances in image acquisition, processing, and analysis as well as machine-learning (ML) approaches for the analysis of multidimensional data sets have rendered HCS as a viable technology for small-molecule drug discovery. Here, we discuss HCS concepts, current workflows as well as opportunities and challenges of image-based phenotypic screening and data analysis.
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