Automatic identification of subcellular phenotypes on human cell arrays

被引:152
作者
Conrad, C
Erfle, H
Warnat, P
Daigle, N
Lörch, T
Ellenberg, J
Pepperkok, R
Eils, R [1 ]
机构
[1] German Canc Res Ctr, DKFZ, D-69120 Heidelberg, Germany
[2] MetaSyst GmbH, D-68804 Altlusshiem, Germany
[3] European Mol Biol Lab, Gene Express Programme, D-69117 Heidelberg, Germany
[4] European Mol Biol Lab, Cell Biol Biophys Programme, D-69117 Heidelberg, Germany
关键词
D O I
10.1101/gr.2383804
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
Light microscopic analysis of cell morphology provides a high-content readout of cell function and protein localization. Cell arrays and microwell transfection assays on cultured cells have made cell phenotype analysis accessible to high-through put experiments. Both the localization of each protein in the proteome and the effect of RNAi knock-down of individual genes on cell morphology can be assayed by manual inspection of microscopic images. However, the use of morphological readouts for functional genomics requires fast and automatic identification of complex cellular phenotypes. Here, we present a fully automated platform for high-throughput cell phenotype screening combining human live cell arrays, screening microscopy, and machine-learning-based classification methods. Efficiency of this platform is demonstrated by classification of eleven subcellular patterns marked by GFP-tagged proteins. Our classification method can be adapted to virtually any microscopic assay based on cell morphology, opening a wide range of applications including large-scale RNAi screening in human cells.
引用
收藏
页码:1130 / 1136
页数:7
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