State Key Laboratory of Proteomics, Beijing Proteome Research Center, Beijing Institute of Radiation Medicine, Beijing 102206, China.
BMC Bioinformatics. 2010 Dec 14;11 Suppl 11(Suppl 11):S15. doi: 10.1186/1471-2105-11-S11-S15.
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.
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 naïve Bayesian network to integrate these features as well as the functional co-annotation 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.
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.
在过去十年中,微阵列已被广泛用于测量基因组规模上的基因表达水平。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侧重于调控网络中基因表达的全局特性。而且很少有模型能够提供直观的参数。我们想知道是否可以找到一些简单但基本的微阵列数据集特征来识别潜在的基因调控关系。
基于表达相关性、表达水平变化以及微阵列表达水平衍生的向量,我们首先引入了几个新的参数来衡量调控基因对的特征。随后,我们使用朴素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,基于表达谱的时滞特征,我们能够分别预测调控关系的存在和方向。
已经提出并整合了几个新的参数来识别调控关系。该新模型被证明比单独使用特征的模型具有更高的功效。我们相信,我们的参数方法可以作为一种快速的调控关系挖掘方法。