CellCognition: time-resolved phenotype annotation in high-throughput live cell imaging

被引:253
作者
Held, Michael [1 ,2 ]
Schmitz, Michael H. A. [1 ,2 ]
Fischer, Bernd [3 ]
Walter, Thomas [4 ]
Neumann, Beate [5 ]
Olma, Michael H. [1 ]
Peter, Matthias [1 ]
Ellenberg, Jan [4 ]
Gerlich, Daniel W. [1 ,2 ]
机构
[1] Swiss Fed Inst Technol, Inst Biochem, Zurich, Switzerland
[2] Marine Biol Lab, Woods Hole, MA 02543 USA
[3] European Mol Biol Lab, Genome Biol Unit, Heidelberg, Germany
[4] European Mol Biol Lab, Cell Biol & Biophys Unit, Heidelberg, Germany
[5] European Mol Biol Lab, Adv Light Microscopy Facil, Heidelberg, Germany
关键词
PHASE IDENTIFICATION; SPINDLE CHECKPOINT; SEGMENTATION; MICROSCOPY; CLASSIFICATION; REVEALS; NETWORK; NUCLEI; GENOME; CDC20;
D O I
10.1038/nmeth.1486
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Fluorescence time-lapse imaging has become a powerful tool to investigate complex dynamic processes such as cell division or intracellular trafficking. Automated microscopes generate time-resolved imaging data at high throughput, yet tools for quantification of large-scale movie data are largely missing. Here we present CellCognition, a computational framework to annotate complex cellular dynamics. We developed a machine-learning method that combines state-of-the-art classification with hidden Markov modeling for annotation of the progression through morphologically distinct biological states. Incorporation of time information into the annotation scheme was essential to suppress classification noise at state transitions and confusion between different functional states with similar morphology. We demonstrate generic applicability in different assays and perturbation conditions, including a candidate-based RNRNA interference screen for regulators of mitotic exit in human cells. CellCognition is published as open source software, enabling live-cell imaging-based screening with assays that directly score cellular dynamics.
引用
收藏
页码:747 / U118
页数:10
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