Machine Learning Improves the Precision and Robustness of High-Content Screens: Using Nonlinear Multiparametric Methods to Analyze Screening Results

被引:47
作者
Horvath, Peter [1 ]
Wild, Thomas [2 ,3 ]
Kutay, Ulrike [4 ]
Csucs, Gabor [1 ]
机构
[1] ETH, Light Microscopy Ctr, CH-8093 Zurich, Switzerland
[2] Univ Munich, Gene Ctr, Munich, Germany
[3] Univ Munich, Dept Biochem, Munich, Germany
[4] ETH, Inst Biochem, CH-8093 Zurich, Switzerland
关键词
machine learning; siRNA screening; Advanced Cell Classifier; multiparametric methods; CELLCLASSIFIER;
D O I
10.1177/1087057111414878
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Imaging-based high-content screens often rely on single cell-based evaluation of phenotypes in large data sets of microscopic images. Traditionally, these screens are analyzed by extracting a few image-related parameters and use their ratios (linear single or multiparametric separation) to classify the cells into various phenotypic classes. In this study, the authors show how machine learning-based classification of individual cells outperforms those classical ratio-based techniques. Using fluorescent intensity and morphological and texture features, they evaluated how the performance of data analysis increases with increasing feature numbers. Their findings are based on a case study involving an siRNA screen monitoring nucleoplasmic and nucleolar accumulation of a fluorescently tagged reporter protein. For the analysis, they developed a complete analysis workflow incorporating image segmentation, feature extraction, cell classification, hit detection, and visualization of the results. For the classification task, the authors have established a new graphical framework, the Advanced Cell Classifier, which provides a very accurate high-content screen analysis with minimal user interaction, offering access to a variety of advanced machine learning methods. (Journal of Biomolecular Screening 2011;16:1059-1067)
引用
收藏
页码:1059 / 1067
页数:9
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