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Concurrent analysis of copy number variation and gene expression: Application in paired non-smoking female lung cancer patients

机译:拷贝数变异与基因表达的并发分析:在成对的非吸烟雌性肺癌患者中的应用

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This study developed a method to identify disease-correlated pathways by integrating copy numbers (CN) and gene expression (GE). To evaluate the correlation between CN and GE, a suitable window size was assessed by simulation. Gene Set Enrichment Analysis (GSEA) was utilized to identify the possible pathways by CN, GE, and their correlations, respectively. Each of those enriched pathways was further assigned a score to incorporate the information from CN, GE, and their correlations. A dataset of 44 female nonsmoking lung cancer patients with both normal and tumor tissues was used to evaluate the performance of this method. To further appraise the predicting abilities of those pathways, patients were classified by support vector machines using the pathways identified by only copy number, only gene expression and incorporating CN, GE, and their correlations. The results showed that the proposed method earned higher accuracy, sensitivity and specificity than traditional methods.
机译:本研究开发了一种通过整合拷贝数(CN)和基因表达(GE)来鉴定疾病相关途径的方法。为了评估CN和GE之间的相关性,通过模拟评估合适的窗口大小。基因设定富集分析(GSEA)分别用于分别鉴定CN,GE及其相关性的可能途径。进一步分配了这些富集的途径中的每一个,以将来自CN,GE及其相关性的信息合并。使用正常和肿瘤组织的44名雌性非莫味肺癌患者的数据集评估该方法的性能。为了进一步评估这些途径的预测能力,通过使用仅由仅拷贝数鉴定的途径,仅掺入CN,GE及其相关性的途径来分类患者的支持载体机。结果表明,该方法赢得了比传统方法更高的准确性,敏感性和特异性。

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