首页> 外文会议>International Conference on Advanced Data Mining and Applications(ADMA 2006); 20060814-16; Xi'an(CN) >Application of Factor Analysis on Mycobacterium Tuberculosis Transcriptional Responses for Drug Clustering, Drug Target, and Pathway Detections
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Application of Factor Analysis on Mycobacterium Tuberculosis Transcriptional Responses for Drug Clustering, Drug Target, and Pathway Detections

机译:因子分析在结核分枝杆菌转录反应中用于药物聚类,药物靶标和途径检测的应用

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Recently, the differential transcriptional responses of Mycobacterium tuberculosis to drug and growth-inhibitory conditions were monitored to generate a data set of 436 microarray profiles. These profiles were valuably used for grouping drugs, identifying drug targets and detecting related pathways, based on various conventional methods; such as Pearson correlation, hierarchical clustering, and statistical tests. These conventional clustering methods used the high dimensionality of gene space to reveal drug groups basing on the similarity of expression levels of all genes. In this study, we applied the factor analysis with these conventional methods for drug clustering, drug target detection and pathway detection. The latent variables or factors of gene expression levels in loading space from factor analysis allowed the hierarchical clustering to discover true drug groups. The t-test method was applied to identify drug targets which most significantly associated with each drug cluster. Then, gene ontology was used to detect pathway associations for each group of drug targets.
机译:最近,监测了结核分枝杆菌对药物和生长抑制条件的差异转录反应,以产生436个微阵列图谱的数据集。这些配置文件可根据各种常规方法宝贵地用于对药物进行分组,确定药物靶标和检测相关途径。例如Pearson相关性,层次聚类和统计测试。这些常规的聚类方法利用基因空间的高维性,基于所有基因表达水平的相似性揭示药物组。在这项研究中,我们将因子分析与这些常规方法一起用于药物聚类,药物靶标检测和途径检测。来自因子分析的负载空间中基因表达水平的潜在变量或因子允许层次聚类发现真正的药物组。应用t检验方法确定与每种药物簇最相关的药物靶标。然后,使用基因本体论来检测每组药物靶标的通路关联。

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