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Image processing tools dedicated to quantification in 3-D fluorescence microscopy

机译:图像处理工具专用于3-D荧光显微镜中的定量

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3-D optical fluorescent microscopy now becomes an efficient tool for the volume investigation of living biological samples. Developments in instrumentation have permitted to beat off the conventional Abbe limit. In any case the recorded image can be described by the convolution equation between the original object and the Point Spread Function (PSF) of the acquisition system. Due to the finite resolution of the instrument, the original object is recorded with distortions and blurring, and contaminated by noise. This induces that relevant biological information cannot be extracted directly from raw data stacks. If the goal is 3-D quantitative analysis, then to assess optimal performance of the instrument and to ensure the data acquisition reproducibility, the system characterization is mandatory. The PSF represents the properties of the image acquisition system; we have proposed the use of statistical tools and Zernike moments to describe a 3-D PSF system and to quantify the variation of the PSF. This first step toward standardization is helpful to define an acquisition protocol optimizing exploitation of the microscope depending on the studied biological sample. Before the extraction of geometrical information and/or intensities quantification, the data restoration is mandatory. Reduction of out-of-focus light is carried out computationally by deconvolution process. But other phenomena occur during acquisition, like fluorescence photo degradation named "bleaching", inducing an alteration of information needed for restoration. Therefore, we have developed a protocol to pre-process data before the application of deconvolution algorithms. A large number of deconvolution methods have been described and are now available in commercial package. One major difficulty to use this software is the introduction by the user of the "best" regularization parameters. We have pointed out that automating the choice of the regularization level; also greatly improves the reliability of the measurements although it facilitates the use. Furthermore, to increase the quality and the repeatability of quantitative measurements a pre-filtering of images improves the stability of deconvolution process. In the same way, the PSF pre-filtering stabilizes the deconvolution process. We have shown that Zemike polynomials can be used to reconstruct experimental PSF, preserving system characteristics and removing the noise contained in the PSF.
机译:3-D光学荧光显微镜现在成为生物样品体积调查的有效工具。仪器的发展允许击败传统的ABBE极限。在任何情况下,记录的图像可以通过采集系统的原始对象和点扩展功能(PSF)之间的卷积方程来描述。由于仪器的有限分辨率,原始物体被扭曲和模糊,并被噪声污染。这引起了无法直接从原始数据堆栈提取相关的生物信息。如果目标是3-D定量分析,则评估仪器的最佳性能并确保数据采集再现性,系统表征是强制性的。 PSF表示图像采集系统的属性;我们提出使用统计工具和Zernike时刻来描述3-D PSF系统并量化PSF的变化。标准化的第一步是有助于定义根据所研究的生物样品优化显微镜的利用的采集协议。在提取几何信息和/或强度定量之前,数据恢复是强制性的。通过去卷积过程计算减少焦点光。但是其他现象发生在采集期间发生,如荧光照片降解命名为“漂白”,诱导恢复所需信息的改变。因此,我们在应用解压缩算法之前开发了一个关于预处理数据的协议。已经描述了大量的解卷积方法,现在可以使用商业包装。使用此软件的一个主要困难是用户的“最佳”正则化参数的介绍。我们已经指出,自动化正则化水平的选择;尽管它有助于使用,但大大提高了测量的可靠性。此外,为了提高定量测量的质量和可重复性,图像的预滤波改善了去卷积过程的稳定性。以相同的方式,PSF预过滤稳定了解卷积过程。我们已经表明,Zemike多项式可用于重建实验性PSF,保留系统特征并去除PSF中包含的噪声。

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