Yanxun Xu, Jie Zhang, Yuan Yuan, Riten Mitra, Peter Müller, Yuan Ji
{"title":"A Bayesian Graphical Model for Integrative Analysis of TCGA Data.","authors":"Yanxun Xu, Jie Zhang, Yuan Yuan, Riten Mitra, Peter Müller, Yuan Ji","doi":"10.1109/GENSIPS.2012.6507747","DOIUrl":null,"url":null,"abstract":"<p><p>We integrate three TCGA data sets including measurements on matched DNA copy numbers (C), DNA methylation (M), and mRNA expression (E) over 500+ ovarian cancer samples. The integrative analysis is based on a Bayesian graphical model treating the three types of measurements as three vertices in a network. The graph is used as a convenient way to parameterize and display the dependence structure. Edges connecting vertices infer specific types of regulatory relationships. For example, an edge between M and E and a lack of edge between C and E implies methylation-controlled transcription, which is robust to copy number changes. In other words, the mRNA expression is sensitive to methylational variation but not copy number variation. We apply the graphical model to each of the genes in the TCGA data independently and provide a comprehensive list of inferred profiles. Examples are provided based on simulated data as well.</p>","PeriodicalId":73289,"journal":{"name":"IEEE International Workshop on Genomic Signal Processing and Statistics : [proceedings]. IEEE International Workshop on Genomic Signal Processing and Statistics","volume":"2012 ","pages":"135-138"},"PeriodicalIF":0.0000,"publicationDate":"2012-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4387199/pdf/nihms673684.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"IEEE International Workshop on Genomic Signal Processing and Statistics : [proceedings]. IEEE International Workshop on Genomic Signal Processing and Statistics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/GENSIPS.2012.6507747","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
We integrate three TCGA data sets including measurements on matched DNA copy numbers (C), DNA methylation (M), and mRNA expression (E) over 500+ ovarian cancer samples. The integrative analysis is based on a Bayesian graphical model treating the three types of measurements as three vertices in a network. The graph is used as a convenient way to parameterize and display the dependence structure. Edges connecting vertices infer specific types of regulatory relationships. For example, an edge between M and E and a lack of edge between C and E implies methylation-controlled transcription, which is robust to copy number changes. In other words, the mRNA expression is sensitive to methylational variation but not copy number variation. We apply the graphical model to each of the genes in the TCGA data independently and provide a comprehensive list of inferred profiles. Examples are provided based on simulated data as well.
我们整合了三个 TCGA 数据集,包括 500 多个卵巢癌样本中匹配的 DNA 拷贝数(C)、DNA 甲基化(M)和 mRNA 表达(E)的测量数据。整合分析基于贝叶斯图模型,将三种测量结果视为网络中的三个顶点。图形是参数化和显示依赖结构的便捷方法。连接顶点的边推断出特定类型的调控关系。例如,M 和 E 之间有边,而 C 和 E 之间没有边,这意味着甲基化控制的转录对拷贝数变化具有稳健性。换句话说,mRNA 表达对甲基化变化敏感,而对拷贝数变化不敏感。我们将图形模型独立应用于 TCGA 数据中的每一个基因,并提供了一份推断出的概况综合列表。我们还提供了基于模拟数据的示例。