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Finding disagreement pathway signatures and constructing an ensemble model for cancer classification

机译:查找分歧途径特征并建立癌症分类的整体模型

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摘要

Cancer classification based on molecular level is a relatively routine research procedure with advances in high-throughput molecular profiling techniques. However, the number of genes typically far exceeds the number of the sample size in gene expression studies. The existing gene selection methods are almost based on statistics and machine learning, overlooking relevant biological principles or knowledge while working with biological data. Here, we propose a robust ensemble learning paradigm, which incorporates multiple pathways information, to predict cancer classification. We compare the proposed method with other methods, such as Elastic SCAD and PPDMF, and estimate the classification performance. The results show that the proposed method has the higher performances on most metrics and robust performance. We further investigate the biological mechanism of the ensemble feature genes. The results demonstrate that the ensemble feature genes are associated with drug targets/clinically-relevant cancer. In addition, some core biological pathways and biological process underlying clinically-relevant phenotypes are identified by function annotation. Overall, our research can provide a new perspective for the further study of molecular activities and manifestations of cancer.
机译:基于分子水平的癌症分类是一种相对常规的研究程序,具有高通量分子谱分析技术的进步。然而,在基因表达研究中,基因的数量通常远远超过样本量的数量。现有的基因选择方法几乎基于统计学和机器学习,在处理生物学数据时忽略了相关的生物学原理或知识。在这里,我们提出了一个强大的整体学习范例,该范例结合了多种途径信息,可以预测癌症的分类。我们将提出的方法与其他方法(如Elastic SCAD和PPDMF)进行比较,并估计分类性能。结果表明,该方法在大多数指标上具有较高的性能,并且性能稳定。我们进一步研究集合特征基因的生物学机制。结果表明,集合特征基因与药物靶标/临床相关癌症有关。此外,通过功能注释可以识别一些临床相关表型的核心生物学途径和生物学过程。总的来说,我们的研究可以为进一步研究分子活性和癌症表现提供新的视角。

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