Classification of subcellular location patterns in fluorescence microscope images based on modified threshold adjacency statistics

F. Kheirkhah, S. Haghipour
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引用次数: 2

Abstract

The ongoing biotechnology revolution promises a complete understanding of the mechanisms by which cells and tissues carry out their functions. As proteins are integral components of cell function, it is critical to understand their properties such as structure and localization. The study of protein subcellular localization (PSL) is important for elucidating protein functions involved in various cellular processes. The subcellular location of proteins is most often determined by visual interpretation of fluorescence microscope images, but in recent years, to perform high-resolution, high-throughput analysis of ten thousands of expressed proteins for the many cell types and cellular conditions under which they may be found creates, automated methods that are needed. In this review, we use a novel method that determines an improved features set, that distinguish subcellular patterns with high accuracy and high speed. This method based on modified threshold adjacency statistics (MTAS), the essence which is to threshold the images. Previous work that uses threshold adjacency statistics (TAS), introduces a simple set of Subcellular Location Features (SLF) which are computed by counting the number of threshold pixels adjacent.
基于改进阈值邻接统计的荧光显微镜图像亚细胞定位模式分类
正在进行的生物技术革命保证了对细胞和组织执行其功能的机制的全面理解。由于蛋白质是细胞功能不可或缺的组成部分,因此了解其结构和定位等特性至关重要。蛋白质亚细胞定位(PSL)的研究对于阐明参与各种细胞过程的蛋白质功能具有重要意义。蛋白质的亚细胞位置通常是通过荧光显微镜图像的视觉解释来确定的,但近年来,为了对许多细胞类型和细胞条件下可能发现的成千上万的表达蛋白质进行高分辨率,高通量分析,需要创建自动化方法。在这篇综述中,我们使用一种新的方法来确定改进的特征集,以高精度和高速区分亚细胞模式。该方法基于改进阈值邻接统计(MTAS),其实质是对图像进行阈值处理。先前的工作使用阈值邻接统计(TAS),引入了一组简单的亚细胞定位特征(SLF),通过计算阈值相邻像素的数量来计算。
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