...
首页> 外文期刊>BMC Bioinformatics >Bayesian hierarchical model for transcriptional module discovery by jointly modeling gene expression and ChIP-chip data
【24h】

Bayesian hierarchical model for transcriptional module discovery by jointly modeling gene expression and ChIP-chip data

机译:通过联合建模基因表达和ChIP芯片数据的转录模块发现的贝叶斯层次模型

获取原文
           

摘要

Background Transcriptional modules (TM) consist of groups of co-regulated genes and transcription factors (TF) regulating their expression. Two high-throughput (HT) experimental technologies, gene expression microarrays and Chromatin Immuno-Precipitation on Chip (ChIP-chip), are capable of producing data informative about expression regulatory mechanism on a genome scale. The optimal approach to joint modeling of data generated by these two complementary biological assays, with the goal of identifying and characterizing TMs, is an important open problem in computational biomedicine. Results We developed and validated a novel probabilistic model and related computational procedure for identifying TMs by jointly modeling gene expression and ChIP-chip binding data. We demonstrate an improved functional coherence of the TMs produced by the new method when compared to either analyzing expression or ChIP-chip data separately or to alternative approaches for joint analysis. We also demonstrate the ability of the new algorithm to identify novel regulatory relationships not revealed by ChIP-chip data alone. The new computational procedure can be used in more or less the same way as one would use simple hierarchical clustering without performing any special transformation of data prior to the analysis. The R and C-source code for implementing our algorithm is incorporated within the R package gimmR which is freely available at http://eh3.uc.edu/gimm. Conclusion Our results indicate that, whenever available, ChIP-chip and expression data should be analyzed within the unified probabilistic modeling framework, which will likely result in improved clusters of co-regulated genes and improved ability to detect meaningful regulatory relationships. Given the good statistical properties and the ease of use, the new computational procedure offers a worthy new tool for reconstructing transcriptional regulatory networks.
机译:背景转录模块(TM)由共同调节的基因和调节其表达的转录因子(TF)组成。两种高通量(HT)实验技术,即基因表达微阵列和染色质免疫沉淀芯片(ChIP-chip),能够产生有关基因组规模表达调控机制的信息。由这两个互补的生物学分析生成的数据的联合建模的最佳方法,以识别和表征TM为目标,是计算生物医学中一个重要的开放性问题。结果我们通过联合建模基因表达和ChIP芯片结合数据,开发并验证了一种用于识别TM的新型概率模型和相关计算程序。与单独分析表达或ChIP芯片数据或与联合分析的替代方法相比,我们证明了通过新方法产生的TM的功能一致性得到了改善。我们还证明了该新算法能够识别仅通过ChIP芯片数据无法揭示的新颖监管关系的能力。可以以与使用简单的层次聚类大致相同的方式使用新的计算过程,而无需在分析之前对数据进行任何特殊的转换。用于实现我们算法的R和C源代码包含在R包gimmR中,该包可从http://eh3.uc.edu/gimm免费获得。结论我们的结果表明,只要有可能,均应在统一的概率建模框架内分析ChIP芯片和表达数据,这可能会改善共同调控基因的簇,并提高检测有意义的调控关系的能力。鉴于良好的统计特性和易用性,新的计算程序为重构转录调控网络提供了有价值的新工具。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号