首页> 外文会议>International symposium on multispectral image processing and pattern recognition;MIPPR 2009 >Segmentation-based Retrospective Shading Correction in Fluorescence Microscopy E. Coli Images for Quantitative Analysis
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Segmentation-based Retrospective Shading Correction in Fluorescence Microscopy E. Coli Images for Quantitative Analysis

机译:荧光定量大肠杆菌图像中基于分段的回顾性阴影校正,用于定量分析

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Due to the inherent imperfections in the imaging process, fluorescence microscopy images often suffer from spurious intensity variations, which is usually referred to as intensity inhomogeneity, intensity non uniformity, shading or bias field. In this paper, a retrospective shading correction method for fluorescence microscopy Escherichia coli (E. Coli) images is proposed based on segmentation result. Segmentation and shading correction are coupled together, so we iteratively correct, the shading effects based on segmentation result and refine the segmentation by segmenting the image after shading correction. A fluorescence microscopy E. Coli image can be segmented (based on its intensity value) into two classes: the background and the cells, where the intensity variation within each class is close to zero if there is no shading. Therefore, we make use of this characteristics to correct the shading in each iteration. Shading is mathematically modeled as a multiplicative component and an additive noise component. The additive component is removed by a denoising process, and the multiplicative component is estimated using a fast algorithm to minimize the intra-class intensity variation. We tested our method on synthetic images and real fluorescence E.coli images. It works well not only for visual inspection, but also for numerical evaluation. Our proposed method should be useful for further quantitative analysis especially for protein expression value; comparison.
机译:由于成像过程中的固有缺陷,荧光显微镜图像经常遭受杂散强度变化的影响,这通常被称为强度不均匀,强度不均匀,阴影或偏置场。提出了一种基于分割结果的荧光显微镜大肠杆菌图像回顾性阴影校正方法。分割和阴影校正是结合在一起的,因此我们根据分割结果迭代校正阴影效果,并通过对阴影校正后的图像进行分割来细化分割。可以将荧光显微镜大肠杆菌图像(基于其强度值)分为两类:背景和细胞,如果没有阴影,则每一类中的强度变化接近于零。因此,我们利用此特性来校正每次迭代中的阴影。阴影在数学上被建模为乘法分量和加性噪声分量。通过去噪处理去除加法分量,并使用快速算法估算可乘分量,以最大程度地减少类内强度变化。我们在合成图像和真实荧光大肠杆菌图像上测试了我们的方法。它不仅适用于外观检查,而且适用于数值评估。我们提出的方法应有助于进一步的定量分析,尤其是蛋白质表达值。比较。

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