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首页> 外文期刊>ScientificWorldJournal >Biomarker Identification for Prostate Cancer and Lymph NodeMetastasis from Microarray Data and Protein Interaction NetworkUsing Gene Prioritization Method
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Biomarker Identification for Prostate Cancer and Lymph NodeMetastasis from Microarray Data and Protein Interaction NetworkUsing Gene Prioritization Method

机译:来自微阵列数据和蛋白质相互作用网络基因优先化方法的前列腺癌和淋巴结术的生物标志物鉴定

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Finding a genetic disease-related gene is not a trivial task. Therefore, computational methods are needed to present clues to the biomedical community to explore genes that are more likely to be related to a specific disease as biomarker. We present biomarker identification problem using gene prioritization method called gene prioritization from microarray data based on shortest paths, extended with structural and biological properties and edge flux using voting scheme (GP-MIDAS-VXEF). The method is based on finding relevant interactions on protein interaction networks, then scoring the genes using shortest paths and topological analysis, integrating the results using a voting scheme and a biological boosting. We applied two experiments, one is prostate primary and normal samples and the other is prostate primary tumor with and without lymph nodes metastasis. We used 137 truly prostate cancer genes as benchmark. In the first experiment, GP-MIDAS-VXEF outperforms all the other state-of-the-art methods in the benchmark by retrieving the truest related genes from the candidate set in the top 50 scores found. We applied the same technique to infer the significant biomarkers in prostate cancer with lymph nodes metastasis which is not established well.
机译:寻找相关的遗传疾病相关基因不是琐碎的任务。因此,需要计算方法来向生物医学群落呈现线索以探索更可能与特定疾病与生物标志物相关的基因。我们使用基于最短路径的基因优先级化方法呈现了基因优先化方法的生物标志物鉴定问题,使用投票方案(GP-MIDAS-VXEF)延伸了结构和生物学性质和边缘通量。该方法是基于蛋白质相互作用网络的相关相互作用,然后使用最短路径和拓扑分析进行评分基因,使用投票方案和生物升压整合结果。我们应用了两个实验,一种是前列腺初级和正常样本,另一个是前列腺原发性肿瘤,没有淋巴结转移。我们使用了137个真正前列腺癌基因作为基准。在第一个实验中,GP-MIDAS-VXEF通过从发现的前50个分数中的候选集中检索了基准测试中的所有其他最先进的方法。我们施加了相同的技术来推断出前列腺癌中的重要生物标志物与淋巴结转移,这是不确定的。

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