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Kernel-based method for feature selection and disease diagnosis using transcriptomics data

机译:基于核的转录组学特征选择和疾病诊断方法

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Global transcriptome profiling is the foundation of systems biology and has been extensively used in biomarker discovery. Tools have been developed to extract meaningful biological information and useful gene features from transcriptomics data. However, there is no commonly accepted method for such purposes. The first IMPROVER (industrial methodology for process verification of research) challenge was launched to assess and verify classification methods using transcriptomics data from clinical samples. We established a computational approach that combined a kernel Fisher discriminant classifier and a feature selection scheme, which used scaled alignment selection and recursive feature elimination methods. A simple and reliable batch effect correction approach was also used. With this approach, a set of informative genes, i.e., biomarker candidates, could be identified for disease diagnosis and classification. We applied this approach to the sbv IMPROVER Challenge and achieved the highest rank in the psoriasis sub-challenge. Here, we describe our methodology and results for the sub-challenge.
机译:全局转录组图谱分析是系统生物学的基础,已被广泛用于生物标志物的发现。已经开发了从转录组学数据中提取有意义的生物学信息和有用的基因特征的工具。但是,没有用于这种目的的普遍接受的方法。发起了第一个IMPROVER(研究过程验证的工业方法)挑战,以使用临床样本的转录组学数据评估和验证分类方法。我们建立了一种将核Fisher判别式分类器和特征选择方案相结合的计算方法,该方法使用了比例尺对齐选择和递归特征消除方法。还使用了一种简单可靠的批量效果校正方法。通过这种方法,可以鉴定一组信息基因,即生物标志物候选物,用于疾病诊断和分类。我们将此方法应用于sbv IMPROVER挑战赛,并在银屑病亚挑战赛中获得最高排名。在这里,我们描述了子挑战的方法论和结果。

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