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Confocal fluorescence microscopy and force-volume imaging in atomic force microscopy: A signal processing perspective

机译:原子力显微镜中的共焦荧光显微镜和力体积成像:信号处理的观点

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This lecture deals with signal processing methods dedicated to hyperspectral data recorded in confocal fluorescence microscopy and atomic force microscopy (AFM), with applications to biological imaging. We first address two typical inverse problems arising in confocal microscopy, namely hyperspectral image restoration (or deconvolution) and hyperspectral unmixing. The second part of the lecture is dedicated to the analysis of force curves and force-volume images recorded in AFM. Their interpretation is done using physico-chemical models, e.g., electrostatic and mechanical models. The quantitative estimation of parameters from experimental force curves is based on fully automated tools. This leads us to reconstruct a set of images at the nanoscale, each corresponding to a specific physico-chemical parameter.
机译:本讲座介绍专用于共聚焦荧光显微镜和原子力显微镜(AFM)中记录的高光谱数据的信号处理方法,并将其应用于生物成像。我们首先解决共聚焦显微镜中出现的两个典型的逆问题,即高光谱图像恢复(或反卷积)和高光谱分解。讲座的第二部分致力于分析AFM中记录的力曲线和力-体积图像。它们的解释是使用物理化学模型(例如静电和机械模型)完成的。根据实验力曲线对参数进行定量估计是基于全自动工具。这使我们重建了一组纳米级的图像,每个图像都对应于特定的物理化学参数。

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