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Predicting subcellular localization of multi-label proteins by incorporating the sequence features into Chou's PseAAC

机译:通过将序列特征掺入Chou的PSEAAC来预测多标签蛋白的亚细胞定位

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The emergence of numerous genome projects has made the experimental classification of the protein localization almost impossible due to the exponential increase in the number of protein samples. However, most of the applications are merely developed for single-plex and completely ignored the presence of one protein at two or more locations in a cell. In this regard, few attempts were carried out to target Multi-label protein localizations; consequently, undesirable accuracies are achieved. This paper presents a novel approach, in which a discrete feature extraction method is fused with physicochemical properties of amino acids by using Chou's general form of Pseudo Amino Acid Composition. The technique is tested on two benchmark datasets namely: Gpos-mploc and Virus-mPLoc. The empirical results demonstrated that the proposed method yields better results via two examined classifiers i.e. ML-KNN and Rank-SVM. It is established that the proposed model has improved values in all performance measures considered for the comparison.
机译:由于蛋白质样本数量的指数增加,许多基因组项目的出现几乎是不可能的蛋白质定位的实验分类。然而,大多数应用仅用于单吡克隆,并且完全忽略了细胞中的两个或更多个位置处的一种蛋白质的存在。在这方面,对靶向多标签蛋白质定位进行了几次尝试;因此,实现了不希望的准确性。本文提出了一种新的方法,其中通过使用Chou的伪氨基酸组合物的一般形式与氨基酸的物理化学性能融合。该技术在两个基准数据集上测试:GPOS-MPLOC和病毒-MPLOC。经验结果表明,该方法通过两种研究的分类剂即可产生更好的结果。ML-KNN和RANK-SVM。建立所提出的模型在考虑比较的所有性能措施中具有改善的值。

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