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Combined mRMR filter and sparse Bayesian classifier for analysis of gene expression data

机译:组合MRMR过滤器和稀疏贝叶斯分类器,用于分析基因表达数据

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Many disorders can be diagnosed by analysis of gene expression microarrays and this can save lots of lives. However, as gene expression data have high dimensions, establishing a method to identify the genes related to the target disease still remains a challenge, because it should provide a well-grounded prediction about the disease status. To this end, the best subset of genes should be distinguished for the classification task. In this paper, we have introduced a new framework for the analysis of gene expression data. Our proposed algorithm tries to find the best feature subset, in two main stages. First, an information theoretic forward feature selection algorithm called mRMR (minimum redundancy, maximum-relevancy) is used to find a candidate set for best features. In the next stage, the RVM (Relevance Vector Machine) classifier which is well suited for gene data analysis is utilized. The RVM has frequent privileges over other classifiers, namely, it can return a membership probability for each class that can be very vital for diagnosis of dramatic diseases, and it can also lead to a more sparse approach to fit a model over the training data which will help to avoid overfitting, etc. The Experimental results showed that the proposed algorithm outperforms the previous works in both classification accuracy and sparsity of the model.
机译:可以通过分析基因表达微阵列来诊断许多疾病,这可以节省大量的生命。然而,随着基因表达数据具有高尺寸,建立一种鉴定与目标疾病相关的基因的方法仍然是一个挑战,因为它应该提供对疾病状态的良好接地的预测。为此,应为分类任务区分最佳基因子集。在本文中,我们介绍了一种用于分析基因表达数据的新框架。我们所提出的算法尝试在两个主要阶段中找到最佳特征子集。首先,使用称为MRMR(最小冗余,最大相关性)的信息理论前向特征选择算法用于找到最佳功能的候选集。在下一阶段,利用适用于基因数据分析的RVM(相关矢量机)分类器。 RVM在其他分类器中具有频繁的权限,即它可以返回对诊断戏剧性疾病非常重要的每个类的隶属概率,并且它也可能导致更稀疏的方法来适应培训数据的模型将有助于避免过度拟合等。实验结果表明,该算法在模型的分类精度和稀疏性方面优于先前的工作。

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