首页> 外文会议>2010 IEEE International Conference on Bioinformatics and Biomedicine >Concurrent analysis of copy number variation and gene expression: Application in paired non-smoking female lung cancer patients
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Concurrent analysis of copy number variation and gene expression: Application in paired non-smoking female lung cancer patients

机译:拷贝数变异和基因表达的同时分析:在成对非吸烟女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:这项研究开发了一种通过整合拷贝数(CN)和基因表达(GE)来识别疾病相关途径的方法。为了评估CN和GE之间的相关性,通过仿真评估了合适的窗口大小。利用基因集富集分析(GSEA)分别通过CN,GE及其相关性鉴定可能的途径。这些富集的途径中的每一个都进一步分配了一个分数,以纳入来自CN,GE及其相关性的信息。使用数据集的44名女性非吸烟肺癌患者的正常和肿瘤组织来评估此方法的性能。为了进一步评估这些途径的预测能力,使用仅通过拷贝数,仅基因表达并结合了CN,GE及其相关性的途径,通过支持向量机对患者进行了分类。结果表明,与传统方法相比,该方法具有更高的准确性,灵敏性和特异性。

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