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Semiautomatic quality determination of 3D confocal microscope scans of neuronal cells denoised by 3D wavelet shrinkage

机译:通过3D小波收缩对神经元细胞进行3D共聚焦显微镜扫描的半自动质量测定

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Abstract: The main goal of this work is to denoise 3D confocal microscope scans of neuronal cells taken at high resolution such that neuronal structures of size smaller than 1 $mu@m become visible. Although scanning confocal microscopes give much clearer images than ordinary light microscopes do, the images are still noisy and blurred. Our goal is to filter out the noise in these images without disturbing the smallest neuronal structures which have the same signal amplitude and geometric size as the noise. In order to obtain a good scale-space representation of the analyzed image, we use the 3D-wavelet transformation. We extend the denoising method of Donoho for 3D data and obtain several ways of computing thresholds and noise variances. Finally we develop a quality measure, for images with tree like structures, to determine the denoising method and wavelet form best suited for a particular confocal scan.!11
机译:摘要:这项工作的主要目的是对高分辨率采集的神经元细胞进行3D共聚焦显微镜扫描去噪,以使小于1μm的神经元结构可见。尽管扫描共聚焦显微镜可以提供比普通光学显微镜更清晰的图像,但是图像仍然嘈杂且模糊。我们的目标是在不干扰最小神经元结构的情况下滤除这些图像中的噪声,这些神经元结构具有与噪声相同的信号幅度和几何尺寸。为了获得所分析图像的良好比例空间表示,我们使用3D小波变换。我们扩展了3D数据的Donoho去噪方法,并获得了几种计算阈值和噪声方差的方法。最后,我们针对具有树状结构的图像开发一种质量度量,以确定最适合特定共焦扫描的去噪方法和小波形式。11

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