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Classification of Scleroderma and Normal Biopsy Data and Identification of Possible Biomarkers of the Disease

机译:硬皮病和正常活检数据的分类以及疾病的可能生物标志物的鉴定

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Scleroderma is an autoimmune disease of the connective tissues, which thickens and hardens the affected areas. Recently, researchers have found evidence that genes are important factors for this disease, and there exist consistent differences in the patterns of gene expressions of skin biopsies from affected and non-affected individuals. In this paper, we apply genetic programming (GP) on the gene expression data of scleroderma and normal biopsies to evolve the classification rules that can differentiate between them. In these evolved rules, we have found six genes that have differential gene expression levels in scleroderma and normal biopsies and thus individually can classify all the samples correctly. In addition to these genes, we have also found some simple rules containing two or more genes that can classify all the samples perfectly.
机译:硬皮病是一种结缔组织的自身免疫性疾病,其增厚并强化受影响的区域。最近,研究人员发现了证据,即基因是这种疾病的重要因素,并且存在受影响和非受影响的个体的皮肤活组织检查的基因表达模式的一致差异。在本文中,我们将遗传编程(GP)应用于硬皮病和正常活组织检查的基因表达数据,以发展可以区分它们的分类规则。在这些演变的规则中,我们发现了六个基因,其在硬皮病和正常活组织检查中具有差异基因表达水平,因此单独地可以正确分类所有样品。除了这些基因外,还发现一些简单的规则,其中包含两个或更多个基因,可以完全分类所有样品。

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