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Robust identification of transcriptional regulatory networks using a Gibbs sampler on outlier sum statistic.

机译:使用基于异常值和统计量的Gibbs采样器对转录调控网络进行可靠的鉴定。

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MOTIVATION: Identification of transcriptional regulatory networks (TRNs) is of significant importance in computational biology for cancer research, providing a critical building block to unravel disease pathways. However, existing methods for TRN identification suffer from the inclusion of excessive 'noise' in microarray data and false-positives in binding data, especially when applied to human tumor-derived cell line studies. More robust methods that can counteract the imperfection of data sources are therefore needed for reliable identification of TRNs in this context. RESULTS: In this article, we propose to establish a link between the quality of one target gene to represent its regulator and the uncertainty of its expression to represent other target genes. Specifically, an outlier sum statistic was used to measure the aggregated evidence for regulation events between target genes and their corresponding transcription factors. A Gibbs sampling method was then developed to estimate the marginal distribution of the outlier sum statistic, hence, to uncover underlying regulatory relationships. To evaluate the effectiveness of our proposed method, we compared its performance with that of an existing sampling-based method using both simulation data and yeast cell cycle data. The experimental results show that our method consistently outperforms the competing method in different settings of signal-to-noise ratio and network topology, indicating its robustness for biological applications. Finally, we applied our method to breast cancer cell line data and demonstrated its ability to extract biologically meaningful regulatory modules related to estrogen signaling and action in breast cancer. Availability and implementation: The Gibbs sampler MATLAB package is freely available at http://www.cbil.ece.vt.edu/software.htm. CONTACT: xuan@vt.edu SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
机译:动机:转录调控网络(TRNs)的识别在癌症研究的计算生物学中非常重要,为揭示疾病途径提供了重要的基础。但是,现有的TRN鉴定方法在微阵列数据中包含过多的“噪音”,在结合数据中包含假阳性,尤其是在应用于人类肿瘤来源的细胞系研究时。因此,在这种情况下,需要更强大的方法来抵消数据源的缺陷,以便可靠地识别TRN。结果:在本文中,我们建议在代表一个调控基因的一个靶基因的质量与代表其他靶基因的表达的不确定性之间建立联系。具体而言,使用异常值总和统计量度目标基因及其相应转录因子之间调控事件的汇总证据。然后开发了一种吉布斯抽样方法来估计异常值和统计量的边际分布,从而发现潜在的监管关系。为了评估我们提出的方法的有效性,我们使用模拟数据和酵母细胞周期数据将其性能与现有的基于采样的方法进行了比较。实验结果表明,在信噪比和网络拓扑的不同设置下,我们的方法始终优于竞争方法,表明其在生物学应用中的鲁棒性。最后,我们将我们的方法应用于乳腺癌细胞系数据,并证明了其提取与乳腺癌中雌激素信号传导和作用有关的生物学意义上的调控模块的能力。可用性和实现:Gibbs采样器MATLAB软件包可从http://www.cbil.ece.vt.edu/software.htm免费获得。联系人:xuan@vt.edu补充信息:补充数据可从在线生物信息学获得。

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