Automated analysis of high-content microscopy data with deep learning

被引:180
作者
Kraus, Oren Z. [1 ,2 ]
Grys, Ben T. [2 ,3 ]
Ba, Jimmy [1 ]
Chong, Yolanda [4 ]
Frey, Brendan J. [1 ,2 ,5 ,6 ]
Boone, Charles [2 ,3 ,5 ]
Andrews, Brenda J. [2 ,3 ,5 ]
机构
[1] Univ Toronto, Dept Elect & Comp Engn, Toronto, ON, Canada
[2] Univ Toronto, Donnelly Ctr Cellular & Biomol Res, Toronto, ON, Canada
[3] Univ Toronto, Dept Mol Genet, Toronto, ON, Canada
[4] Johnson & Johnson, Janssen Pharmaceut Companies, Cellular Pharmacol, Discovery Sci, Beerse, Belgium
[5] Canadian Inst Adv Res, Program Genet Networks, Toronto, ON, Canada
[6] Canadian Inst Adv Res, Program Learning Machines & Brains, Toronto, ON, Canada
基金
美国国家卫生研究院;
关键词
deep learning; high-content screening; image analysis; machine learning; Saccharomyces cerevisiae; SINGLE-CELL; PROTEIN LOCALIZATION; SACCHAROMYCES-CEREVISIAE; CLASSIFICATION; ABUNDANCE; CIRCUITRY; PATHWAYS; PATTERNS; GENES;
D O I
10.15252/msb.20177551
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
Existing computational pipelines for quantitative analysis of high-content microscopy data rely on traditional machine learning approaches that fail to accurately classify more than a single dataset without substantial tuning and training, requiring extensive analysis. Here, we demonstrate that the application of deep learning to biological image data can overcome the pitfalls associated with conventional machine learning classifiers. Using a deep convolutional neural network (DeepLoc) to analyze yeast cell images, we show improved performance over traditional approaches in the automated classification of protein subcellular localization. We also demonstrate the ability of DeepLoc to classify highly divergent image sets, including images of pheromone-arrested cells with abnormal cellular morphology, as well as images generated in different genetic backgrounds and in different laboratories. We offer an open-source implementation that enables updating DeepLoc on new microscopy datasets. This study highlights deep learning as an important tool for the expedited analysis of high-content microscopy data.
引用
收藏
页数:15
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