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Joint pre-processing framework for two-dimensional gel electrophoresis images based on nonlinear filtering background correction and normalization techniques

机译:基于非线性滤波背景校正和归一化技术的二维凝胶电泳图像的联合预处理框架

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摘要

A commonly used gel-based approach for proteomic analysis is two-dimensional gel electrophoresis (2-DGE), a technique that separates proteins in a sample based on both their isoelectric point and molecular weight [1]. This technique is often used in preliminary comparative proteomic analyses, as it is capable of resolving thousands of proteins in a single run. Once the proteins in the sample have been separated, the gel is then scanned and the imaged processed using computational tools. Often these 2-DGE images exhibit anomalies due to the technique itself or to the image scan and acquisition [2]. The purpose of 2-DGE image analysis is to detect the proteins (black spots) within the gel. However, a noisy background with variable intensity, diffuse or low-intensity spots, and over-saturated spots often hinder the detection of individual proteins. Therefore, a pre-processing step that minimizes these anomalies is an open issue in the literature, as an important phase prior to analysis of these kinds of images [3].
机译:常用的凝胶基方法是蛋白质组学分析的方法是二维凝胶电泳(2-DGE),一种基于其等电点和分子量的样品中分离蛋白质的技术[1]。该技术通常用于初步的比较蛋白质组学分析,因为它能够在一次运行中解析成千上万的蛋白质。一旦样品中的蛋白质已经分开,然后扫描凝胶并使用计算工具处理成像处理。由于技术本身或图像扫描和采集,这些2-DGE图像通常会表现出异常,或者图像扫描和采集[2]。 2-DGE图像分析的目的是检测凝胶内的蛋白质(黑点)。然而,具有可变强度,漫射或低强度点和过饱和点的嘈杂背景通常阻碍单个蛋白质的检测。因此,最小化这些异常的预处理步骤是文献中的开放问题,作为分析这些类型的图像之前的重要阶段[3]。

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