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Identifying the Gene Signatures from Gene-Pathway Bipartite Network Guarantees the Robust Model Performance on Predicting the Cancer Prognosis

机译:从基因途径双向网络中识别基因签名可确保预测癌症预后的稳健模型性能

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摘要

For the purpose of improving the prediction of cancer prognosis in the clinical researches, various algorithms have been developed to construct the predictive models with the gene signatures detected by DNA microarrays. Due to the heterogeneity of the clinical samples, the list of differentially expressed genes (DEGs) generated by the statistical methods or the machine learning algorithms often involves a number of false positive genes, which are not associated with the phenotypic differences between the compared clinical conditions, and subsequently impacts the reliability of the predictive models. In this study, we proposed a strategy, which combined the statistical algorithm with the gene-pathway bipartite networks, to generate the reliable lists of cancer-related DEGs and constructed the models by using support vector machine for predicting the prognosis of three types of cancers, namely, breast cancer, acute myeloma leukemia, and glioblastoma. Our results demonstrated that, combined with the gene-pathway bipartite networks, our proposed strategy can efficiently generate the reliable cancer-related DEG lists for constructing the predictive models. In addition, the model performance in the swap analysis was similar to that in the original analysis, indicating the robustness of the models in predicting the cancer outcomes.
机译:为了改善临床研究中对癌症预后的预测,已开发出各种算法来构建具有DNA微阵列检测到的基因特征的预测模型。由于临床样品的异质性,通过统计方法或机器学习算法生成的差异表达基因(DEG)列表通常涉及许多假阳性基因,这些假阳性基因与所比较的临床情况之间的表型差异无关,进而影响预测模型的可靠性。在这项研究中,我们提出了一种将统计算法与基因途径双向网络相结合的策略,以生成与癌症相关的DEG的可靠列表,并使用支持向量机构建模型来预测三种类型的癌症的预后即乳腺癌,急性骨髓瘤白血病和胶质母细胞瘤。我们的结果表明,结合基因途径双向网络,我们提出的策略可以有效地生成可靠的癌症相关DEG列表,以构建预测模型。此外,交换分析中的模型性能与原始分析中的模型性能相似,表明模型在预测癌症结局方面的鲁棒性。

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