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Pattern recognition in gene expression profiling using DNA array: a comparative study of different statistical methods applied to cancer classification.

机译:使用DNA阵列进行基因表达谱分析中的模式识别:对不同统计方法应用于癌症分类的比较研究。

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Large-scale parallel measurements of the expression of many thousands genes are now available with high-density array made with collections of cDNA fragments, or oligonucleotide corresponding to different transcripts. These technologies have been applied to cancer investigations since the availability of such a large number of markers makes DNA array a powerful diagnostic tool for tumour and patient classification. Over the last two years, a series of computational tools have been developed for the analysis of different aspects of gene profiling. Our work tries to compare a series of supervised statistical techniques on the basis of their ability to correctly classify different types of tumours. A simulation approach was initially used to control the huge source of variation among and between patients, and to evaluate the ability of algorithms to classify tumours in relation to different types of experimental variables. Different techniques for reduction of data dimension were then added to the discriminant analysis and compared according to their ability to capture the main genetic information. The simulation results have been tested by applying the selected classification algorithms to two experimental microarray datasets of human cancers, and by measuring the correspondent rates of misclassification. Our analyses identify in these datasets a series of genes principally involved in tumour characterization. The functional role of these discriminant transcripts is discussed.
机译:现在可以使用高密度阵列对数千种基因的表达进行大规模并行测量,该阵列由cDNA片段或对应于不同转录本的寡核苷酸组成。这些技术已被用于癌症研究,因为如此大量的标记使DNA阵列成为用于肿瘤和患者分类的强大诊断工具。在过去的两年中,已经开发出了一系列用于分析基因谱分析各个方面的计算工具。我们的工作试图根据其对不同类型的肿瘤正确分类的能力来比较一系列监督统计技术。最初使用一种模拟方法来控制患者之间以及患者之间的巨大变异源,并评估算法根据不同类型的实验变量对肿瘤进行分类的能力。然后将不同的减少数据维度的技术添加到判别分析中,并根据它们捕获主要遗传信息的能力进行比较。通过将选定的分类算法应用于人类癌症的两个实验性微阵列数据集,并通过测量相应的错误分类率,对模拟结果进行了测试。我们的分析在这些数据集中确定了一系列主要涉及肿瘤表征的基因。这些判别笔录的功能作用进行了讨论。

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