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Classification of Subcellular Phenotype Images by Decision Templates for Classifier Ensemble

机译:分类模板对分类模板的亚细胞表型图像分类

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Subcellular localization is a key functional characteristic of proteins. An automatic, reliable and efficient prediction system for protein subcellular localization is needed for large-scale genome analysis. The automated cell phenotype image classification problem is an interesting "bioimage informatics" application. It can be used for establishing knowledge of the spatial distribution of proteins within living cells and permits to screen systems for drug discovery or for early diagnosis of a disease. In this paper, three well-known texture feature extraction methods including local binary patterns (LBP), Gabor filtering and Gray Level Coocurrence Matrix (GLCM) have been applied to cell phenotype images and the multiple layer perceptron (MLP) method has been used to classify cell phenotype image. After classification of the extracted features, decision-templates ensemble algorithm (DT) is used to combine base classifiers built on the different feature sets. Different texture feature sets can provide sufficient diversity among base classifiers, which is known as a necessary condition for improvement in ensemble performance. For the HeLa cells, the human classification error rate on this task is of 17% as reported in previous publications. We obtain with our method an error rate of 4.8%.
机译:亚细胞定位是蛋白质的关键官能特征。大规模基因组分析需要自动,可靠和高效的蛋白质亚细胞定位预测系统。自动细胞表型图像分类问题是一个有趣的“BioImage信息学”应用程序。它可用于建立生物细胞内蛋白质的空间分布的知识,并允许筛选药物发现或用于早期诊断疾病的系统。在本文中,已经施加了三种众所周知的纹理特征提取方法,包括局部二进制图案(LBP),Gabor滤波和灰级Coocurrence矩阵(GLCM),已经应用于细胞表型图像,并且已经使用了多层Perceptron(MLP)方法分类细胞表型图像。在提取的特征分类之后,决策模板集合算法(DT)用于组合在不同特征集上构建的基本分类器。不同的纹理特征集可以在基本分类器之间提供足够的多样性,这被称为改进集合性能的必要条件。对于HeLa细胞,此任务的人类分类错误率为17%,如先前的出版物中报告。我们通过我们的方法获得4.8%的错误率。

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