Automated analysis of time-lapse fluorescence microscopy images: From live cell images to intracellular foci
Motivation: Complete, accurate and reproducible analysis of intracellular foci from fluorescence microscopy image sequences of live cells requires full automation of all processing steps involved: cell segmentation and tracking followed by foci segmentation and pattern analysis. Integrated systems for this purpose are lacking. Results: Extending our previous work in cell segmentation and tracking, we developed a new system for performing fully automated analysis of fluorescent foci in single cells. The system was validated by applying it to two common tasks: intracellular foci counting (in DNA damage repair experiments) and cell-phase identification based on foci pattern analysis (in DNA replication experiments). Experimental results show that the system performs comparably to expert human observers. Thus, it may replace tedious manual analyses for the considered tasks, and enables high-content screening.
|Persistent URL||dx.doi.org/10.1093/bioinformatics/btq434, hdl.handle.net/1765/28411|
|Grant||This work was funded by the European Commission 7th Framework Programme; grant id fp7/201842 - European Network for Cell Imaging and Tracking Expertise (ENCITE)|
Dzyubachyk, O.M, Essers, J, van Cappellen, W.A, Baldeyron, C, Inagaki, A, Niessen, W.J, & Meijering, E. (2010). Automated analysis of time-lapse fluorescence microscopy images: From live cell images to intracellular foci. Bioinformatics, 26(19), 2424–2430. doi:10.1093/bioinformatics/btq434