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Ensemble Approach for Predicting Genetic Disease through Case-Control Study

机译:通过病例对照研究预测遗传病的综合方法

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摘要

The origin of many diseases can be revealed by knowing the gene regulation. Genetic disease an abnormality in individual's genome. These abnormalities can be occurred due to mutation in single base in DNA or due to the involvement in the addition or subtraction of entire chromosomes. To measure the expression levels of bulk of genes simultaneously, DNA microarrays are used. Microarray data is set of DNA sequences representing the entire set of genes of an organism, arranged in a grid pattern so that the expression of thousands of genes can be detected at the same time. In this paper we propose an approach for diagnosing genetic disease, to accomplish this goal we need to select the most informative ones that can accurately distinguish one class of genes from another. For that the genes with high significance are iteratively extracted. The goal of this paper is to develop method, which increases the classification accuracy, for identifying significant differentially expressed clusters of genes using Recursive Cluster Elimination (RCE) that is based on an ensemble clustering approach.
机译:通过了解基因调控可以揭示许多疾病的起源。遗传病是个体基因组中的异常。这些异常可能是由于DNA中单个碱基的突变或由于涉及整个染色体的添加或扣除而发生的。为了同时测量大量基因的表达水平,使用了DNA微阵列。微阵列数据是一组DNA序列,它们代表一个有机体的全部基因,并以网格模式排列,因此可以同时检测成千上万个基因的表达。在本文中,我们提出了一种诊断遗传疾病的方法,要实现此目标,我们需要选择最能提供信息的方法,以准确区分一类基因和另一类基因。为此,具有重要意义的基因被反复提取。本文的目的是开发一种方法,该方法可以提高分类精度,从而可以使用基于整体聚类方法的递归聚类消除(RCE)来识别重要的差异表达基因簇。

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