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A novel parametric approach to mine gene regulatory relationship from microarray datasets

机译:从微阵列数据集挖掘基因调控关系的新型参数方法

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摘要

Background: Microarray has been widely used to measure the gene expression level on the genome scale in the current decade. Many algorithms have been developed to reconstruct gene regulatory networks based on microarray data. Unfortunately, most of these models and algorithms focus on global properties of the expression of genes in regulatory networks. And few of them are able to offer intuitive parameters. We wonder whether some simple but basic characteristics of microarray datasets can be found to identify the potential gene regulatory relationship. Results: Based on expression correlation, expression level variation and vectors derived from microarray expression levels, we first introduced several novel parameters to measure the characters of regulating gene pairs. Subsequently, we used the na飗e Bayesian network to integrate these features as well as the functional coannotation between transcription factors and their target genes. Then, based on the character of time-delay from the expression profile, we were able to predict the existence and direction of the regulatory relationship respectively. Conclusions: Several novel parameters have been proposed and integrated to identify the regulatory relationship. This new model is proved to be of higher efficacy than that of individual features. It is believed that our parametric approach can serve as a fast approach for regulatory relationship mining.
机译:背景:在最近十年中,微阵列已被广泛用于在基因组规模上测量基因表达水平。已经开发了许多算法来基于微阵列数据重建基因调控网络。不幸的是,这些模型和算法大多数都集中在调节网络中基因表达的全局特性上。他们中很少有人能够提供直观的参数。我们想知道是否可以找到微阵列数据集的一些简单但基本的特征来识别潜在的基因调控关系。结果:基于表达相关性,表达水平变异和从微阵列表达水平衍生的载体,我们首先引入了几个新颖的参数来测量调节基因对的特征。随后,我们使用na飗e贝叶斯网络来整合这些特征以及转录因子与其靶基因之间的功能共注释。然后,基于来自表达谱的时间延迟的特征,我们能够分别预测调节关系的存在和方向。结论:已经提出并整合了几个新颖的参数来识别调节关系。事实证明,该新模型比单个特征具有更高的功效。可以相信,我们的参数方法可以用作监管关系挖掘的快速方法。

著录项

  • 来源
  • 会议地点 Hangzhou(CN);Hangzhou(CN)
  • 作者单位

    State Key Laboratory of Proteomics, Beijing Proteome Research Center,Beijing Institute of Radiation Medicine, Beijing 102206, China;

    State Key Laboratory of Proteomics, Beijing Proteome Research Center,Beijing Institute of Radiation Medicine, Beijing 102206, China;

    State Key Laboratory of Proteomics, Beijing Proteome Research Center,Beijing Institute of Radiation Medicine, Beijing 102206, China Department of Chemistry and Biology, College of Science, National University of Defense Technology, Changsha 410073, China;

    State Key Laboratory of Proteomics, Beijing Proteome Research Center,Beijing Institute of Radiation Medicine, Beijing 102206, China;

    State Key Laboratory of Proteomics, Beijing Proteome Research Center, Beijing Institute of Radiation Medicine, Beijing 102206, China;

  • 会议组织
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 基因理论;基因理论;
  • 关键词

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