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Gene mining: a novel and powerful ensemble decision approach to hunting for disease genes using microarray expression profiling

机译:基因挖掘:使用微阵列表达谱寻找疾病基因的新颖而强大的整体决策方法

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摘要

Current applications of microarrays focus on precise classification or discovery of biological types, for example tumor versus normal phenotypes in cancer research. Several challenging scientific tasks in the post-genomic epoch, like hunting for the genes underlying complex diseases from genome-wide gene expression profiles and thereby building the corresponding gene networks, are largely overlooked because of the lack of an efficient analysis approach. We have thus developed an innovative ensemble decision approach, which can efficiently perform multiple gene mining tasks. An application of this approach to analyze two publicly available data sets (colon data and leukemia data) identified 20 highly significant colon cancer genes and 23 highly significant molecular signatures for refining the acute leukemia phenotype, most of which have been verified either by biological experiments or by alternative analysis approaches. Furthermore, the globally optimal gene subsets identified by the novel approach have so far achieved the highest accuracy for classification of colon cancer tissue types. Establishment of this analysis strategy has offered the promise of advancing microarray technology as a means of deciphering the involved genetic complexities of complex diseases.
机译:微阵列的当前应用集中于生物学类型的精确分类或发现,例如癌症研究中的肿瘤与正常表型。由于缺乏有效的分析方法,在后基因组时代的一些具有挑战性的科学任务,例如从全基因组范围内的基因表达谱中寻找复杂疾病的基因,从而建立相应的基因网络,被广泛忽视了。因此,我们开发了一种创新的整体决策方法,该方法可以有效地执行多个基因挖掘任务。这种方法的应用分析了两个公开可用的数据集(结肠数据和白血病数据),确定了20个高度重要的结肠癌基因和23个非常重要的分子标记,以改善急性白血病的表型,其中大多数已通过生物学实验或通过其他分析方法。此外,迄今为止,通过该新方法鉴定出的全球最佳基因子集已达到结肠癌组织类型分类的最高准确度。这种分析策略的建立提供了发展微阵列技术作为破解复杂疾病遗传复杂性的手段的希望。

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