Teresa W Lo, Kevin J Cutler, H James Choi, Paul A Wiggins
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引用次数: 0
摘要
延时拍摄[-50mm][-4mm]请展开作者“H. James Choi”的名字。显微镜是研究细菌细胞生物学的有力工具。开发便于对这些数据集进行自动化分析的管道是该领域的长期目标。在本文中,我们描述了OmniSegger管道开发为一个开源,模块化和整体的算法套件,其输入是原始显微镜图像,其输出是广泛的定量细胞分析,包括动态细胞细胞术数据和细胞可视化。本文中描述的更新版本介绍了两个主要改进:(i)对细胞形态的鲁棒性和(ii)对一系列常见成像模式的支持。为了证明对细胞形态的稳健性,我们对大肠杆菌的增殖动力学进行了分析,分析了一种诱导成丝的药物。为了证明对新图像模式的扩展支持,我们分析了通过五种不同模式成像的细胞:相衬,两种明场模式,细胞质和膜荧光。总之,这条管道将大大增加细菌显微镜可处理分析的范围。
OmniSegger: A time-lapse image analysis pipeline for bacterial cells.
Time-lapse [-50mm][-4mm]Please expand the first name for author "H. James Choi".microscopy is a powerful tool to study the biology of bacterial cells. The development of pipelines that facilitate the automated analysis of these datasets is a long-standing goal of the field. In this paper, we describe the OmniSegger pipeline developed as an open-source, modular, and holistic suite of algorithms whose input is raw microscopy images and whose output is a wide range of quantitative cellular analyses, including dynamical cell cytometry data and cellular visualizations. The updated version described in this paper introduces two principal refinements: (i) robustness to cell morphologies and (ii) support for a range of common imaging modalities. To demonstrate robustness to cell morphology, we present an analysis of the proliferation dynamics of Escherchia coli treated with a drug that induces filamentation. To demonstrate extended support for new image modalities, we analyze cells imaged by five distinct modalities: phase-contrast, two brightfield modalities, and cytoplasmic and membrane fluorescence. Together, this pipeline should greatly increase the scope of tractable analyses for bacterial microscopists.
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