Detecting and visualizing cell phenotype differences from microscopy images using transportbased morphometry

被引:57
作者
Basu, Saurav [1 ]
Kolouri, Soheil [1 ]
Rohde, Gustavo K. [1 ,2 ]
机构
[1] Carnegie Mellon Univ, Dept Biomed Engn, Ctr Bioimage Informat, Pittsburgh, PA 15213 USA
[2] Carnegie Mellon Univ, Dept Elect & Comp Engn, Lane Ctr Computat Biol, Pittsburgh, PA 15213 USA
基金
美国国家卫生研究院;
关键词
optimal transport; cell morphometry; high content screening; NUCLEAR-STRUCTURE; HISTOPATHOLOGY; SETS;
D O I
10.1073/pnas.1319779111
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Modern microscopic imaging devices are able to extract more information regarding the subcellular organization of different molecules and proteins than can be obtained by visual inspection. Predetermined numerical features (descriptors) often used to quantify cells extracted from these images have long been shown useful for discriminating cell populations (e. g., normal vs. diseased). Direct visual or biological interpretation of results obtained, however, is often not a trivial task. We describe an approach for detecting and visualizing phenotypic differences between classes of cells based on the theory of optimal mass transport. The method is completely automated, does not require the use of predefined numerical features, and at the same time allows for easily interpretable visualizations of the most significant differences. Using this method, we demonstrate that the distribution pattern of peripheral chromatin in the nuclei of cells extracted from liver and thyroid specimens is associated with malignancy. We also show the method can correctly recover biologically interpretable and statistically significant differences in translocation imaging assays in a completely automated fashion.
引用
收藏
页码:3448 / 3453
页数:6
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