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Increasing the Accuracy of NEWFM using a Geometric Graph-Based Gene Selection Algorithm

机译:使用基于几何图的基因选择算法提高Newfm的准确性

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In a microarray dataset with thousands of genes, the majority of the genes are irrelevant to the occurrence of disease. One of the challenges in analyzing microarray datasets is selecting a suitable number of the most relevant genes with maximum classification accuracy. A neural network with weighted fuzzy membership functions (NEWFM) is a supervised neuro-fuzzy system that reduces the size of available data to improve classification accuracy and computational efficiency. This paper proposes a new gene selection algorithm based on a geometric graph using the bounded sum of weighted fuzzy membership functions (BSWFM) that improves the accuracy of NEWFM. The proposed gene selection algorithm reduces computational load and improves accuracy by removing irrelevant genes using the Euclidean distances of the centers of gravity multiplied by the non-overlap area between two BSWFMs. Further, the results of comparative experiments conducted using the colon cancer and the leukemia microarray problem datasets indicate that NEWFM with the proposed gene selection algorithm is more accurate than NEWFM without the proposed algorithm. More specifically, 2000 genes from the colon cancer dataset and 7129 genes from the leukemia dataset used as inputs to NEWFM without the proposed algorithm resulted in accuracies of 90.3% and 58.8%, respectively. In contrast, inputs of seven minimum genes from the colon cancer dataset and nine minimum genes from the leukemia dataset to NEWFM with the proposed algorithm resulted in accuracies of 96.8% and 100%, respectively.
机译:在具有成千上万基因的微阵列数据集中,大多数基因与疾病的发生无关。分析微阵列数据集的挑战之一是选择具有最大分类精度的合适数量的最相关的基因。具有加权模糊会员函数(NewFM)的神经网络是一个监督的神经模糊系统,可降低可用数据的大小,以提高分类准确性和计算效率。本文提出了一种基于几何图的新基因选择算法,该算法使用界限的加权模糊隶属函数(BSWFM)的界限,提高了Newfm的准确性。所提出的基因选择算法通过使用两种BSWFM之间的非重叠区域乘以非重叠区域来减少计算负荷并通过消除不相关的基因来降低无关基因。此外,使用结肠癌和白血病微阵列问题数据集进行的比较实验结果表明,具有所提出的基因选择算法的Newfm比没有所提出的算法更准确。更具体地说,来自结肠癌数据集的2000个基因和来自白血病数据集的7129基因,其用作没有所提出的算法的Newfm的输入,导致精度为90.3%和58.8%。相反,来自结肠癌数据集的七个最小基因的输入和来自白血病数据集的九个最小基因与所提出的算法的Newfm产生96.8%和100%的准确度。

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