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iSBatch: a batch-processing platform for data analysis and exploration of live-cell single-molecule microscopy images and other hierarchical datasets

机译:iSBatch:用于数据分析和探索活细胞单分子显微镜图像和其他分层数据集的批处理平台

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摘要

Recent technical advances have made it possible to visualize single molecules inside live cells. Microscopes with single-molecule sensitivity enable the imaging of low-abundance proteins, allowing for a quantitative characterization of molecular properties. Such data sets contain information on a wide spectrum of important molecular properties, with different aspects highlighted in different imaging strategies. The time-lapsed acquisition of images provides information on protein dynamics over long time scales, giving insight into expression dynamics and localization properties. Rapid burst imaging reveals properties of individual molecules in real-time, informing on their diffusion characteristics, binding dynamics and stoichiometries within complexes. This richness of information, however, adds significant complexity to analysis protocols. In general, large datasets of images must be collected and processed in order to produce statistically robust results and identify rare events. More importantly, as live-cell single-molecule measurements remain on the cutting edge of imaging, few protocols for analysis have been established and thus analysis strategies often need to be explored for each individual scenario. Existing analysis packages are geared towards either single-cell imaging data or in vitro single-molecule data and typically operate with highly specific algorithms developed for particular situations. Our tool, iSBatch, instead allows users to exploit the inherent flexibility of the popular open-source package ImageJ, providing a hierarchical framework in which existing plugins or custom macros may be executed over entire datasets or portions thereof. This strategy affords users freedom to explore new analysis protocols within large imaging datasets, while maintaining hierarchical relationships between experiments, samples, fields of view, cells, and individual molecules.
机译:最近的技术进步使得可视化活细胞内的单个分子成为可能。具有单分子敏感性的显微镜可以对低丰度蛋白质进行成像,从而可以定量表征分子特性。这些数据集包含有关重要分子特性的广泛信息,在不同的成像策略中突出显示了不同的方面。图像的延时采集可以长期提供有关蛋白质动力学的信息,从而深入了解表达动力学和定位特性。快速爆发成像可实时显示单个分子的性质,告知其在复合物中的扩散特性,结合动力学和化学计量。但是,信息的丰富性大大增加了分析协议的复杂性。通常,必须收集和处理大型图像数据集,以产生统计上可靠的结果并识别罕见事件。更重要的是,由于活细胞单分子测量仍处于成像的前沿,因此很少建立分析方案,因此对于每种情况,通常都需要探索分析策略。现有的分析软件包适用于单细胞成像数据或体外单分子数据,并且通常使用针对特定情况开发的高度特定的算法进行操作。相反,我们的工具iSBatch允许用户利用流行的开源软件包ImageJ的固有灵活性,从而提供了一个层次结构的框架,其中现有的插件或自定义宏可以在整个数据集或其一部分上执行。这种策略使用户可以自由地在大型成像数据集中探索新的分析方案,同时保持实验,样品,视野,细胞和单个分子之间的层次关系。

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  • 来源
    《Molecular BioSystems》 |2015年第10期|2699-2708|共10页
  • 作者单位

    Zernike Institute for Advanced Materials, Centre for Synthetic Biology, University of Groningen, The Netherlands;

    Zernike Institute for Advanced Materials, Centre for Synthetic Biology, University of Groningen, The Netherlands;

    Zernike Institute for Advanced Materials, Centre for Synthetic Biology, University of Groningen, The Netherlands;

    Zernike Institute for Advanced Materials, Centre for Synthetic Biology, University of Groningen, The Netherlands;

    Zernike Institute for Advanced Materials, Centre for Synthetic Biology, University of Groningen, The Netherlands,School of Chemistry, University of Wollongong, Wollongong, NSW 2522, Australia;

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