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首页> 外文期刊>Journal of Integrative Bioinformatics >Transcription Network Analysis by A Sparse Binary Factor Analysis Algorithm
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Transcription Network Analysis by A Sparse Binary Factor Analysis Algorithm

机译:稀疏二元因子分析算法转录网络分析

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Summary Transcription factor activities (TFAs), rather than expression levels, control gene expres- sion and provide valuable information for investigating TF-gene regulations. The underly- ing bimodal or switch-like patterns of TFAs may play important roles in gene regulation. Network Component Analysis (NCA) is a popular method to deduce TFAs and TF-gene control strengths from microarray data. However, it does not directly examine the bimodal- ity of TFAs and it needs the TF-gene connection topology to be a priori known. In this paper, we modify NCA to model gene expression regulation by Binary Factor Analysis (BFA), which directly captures switch-like patterns of TFAs. Moreover, sparse technique is employed on the mixing matrix of BFA, and thus the proposed sparse BYY-BFA al- gorithm, developed under Bayesian Ying-Yang (BYY) learning framework, can not only uncover the latent TFA profile’s switch-like patterns, but also be capable of automatically shutting off the unnecessary connections. Simulation study demonstrates the effectiveness of BYY-BFA, and a preliminary application to Saccharomyces cerevisiae cell cycle data and Escherichia coli carbon source transition data shows that the reconstructed binary pat- terns of TFAs by BYY-BFA are consistent with the ups and downs of TFAs by NCA, and that BYY-BFA also works well when the network topology is unknown.
机译:发明内容转录因子活性(TFA),而不是表达水平,对照基因表达,并提供了研究TF-基因规定的有价值的信息。 TFA的下面的双峰或交换样图案可能在基因调节中起重要作用。网络分量分析(NCA)是一种普遍的方法,用于推导TFAS和TF-基因控制强度的微阵列数据。但是,它没有直接检查TFAS的双峰,它需要TF-Gene连接拓扑,以证实优先考虑。在本文中,我们通过二元因子分析(BFA)来修饰NCA以模拟基因表达调节,直接捕获TFA的开关样模式。此外,在BFA的混合基质上采用稀疏技术,因此提出的稀疏Byy-BFA Al-Gorithm,在贝叶斯ying-yang(Byy)学习框架下,不仅可以揭示潜伏的TFA型材的交换式图案,但也能够自动关闭不必要的连接。仿真研究证明了BY-BFA的有效性,以及对酿酒酵母细胞周期数据和大肠杆菌碳源转换数据的初步应用表明,Byy-BFA的TFA的重建二进制图案与TFA的UPS和下降一致通过NCA,当网络拓扑未知时,Byy-BFA也很好地运行。

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