Sparse graphical models for exploring gene expression data

被引:276
作者
Dobra, A
Hans, C
Jones, B
Nevins, JR
Yao, GA
West, M
机构
[1] Duke Univ, ISDS, Durham, NC 27708 USA
[2] Duke Univ, Dept Mol Genet & Microbiol, Durham, NC 27708 USA
[3] Stat & Appl Math Sci Inst, Res Triangle Pk, NC 27709 USA
基金
美国国家卫生研究院;
关键词
Bayesian regression analysis; compositional networks; estrogen receptor gene and pathway; ER pathway; gene expression; graphical models; model selection; Rb-E2F genes and pathway; transitive gene expression pathways;
D O I
10.1016/j.jmva.2004.02.009
中图分类号
O21 [概率论与数理统计]; C8 [统计学];
学科分类号
020208 ; 070103 ; 0714 ;
摘要
We discuss the theoretical structure and constructive methodology for large-scale graphical models, motivated by their potential in evaluating and aiding the exploration of patterns of association in gene expression data. The theoretical discussion covers basic ideas and connections between Gaussian graphical models, dependency networks and specific classes of directed acyclic graphs we refer to as compositional networks. We describe a constructive approach to generating interesting graphical models for very high-dimensional distributions that builds on the relationships between these various stylized graphical representations. Issues of consistency of models and priors across dimension are key. The resulting methods are of value in evaluating patterns of association in large-scale gene expression data with a view to generating biological insights about genes related to a known molecular pathway or set of specified genes. Some initial examples relate to the estrogen receptor pathway in breast cancer, and the Rb-E2F cell proliferation control pathway. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:196 / 212
页数:17
相关论文
共 30 条
  • [1] Transcription factor GATA-6 activates expression of gastroprotective trefoil genes TFF1 and TFF2
    Al-azzeh, ED
    Fegert, P
    Blin, N
    Gött, P
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 2000, 1490 (03): : 324 - 332
  • [2] Andersson SA, 1997, ANN STAT, V25, P505
  • [3] *AT T RES LABS, GRAPH OP SOURC GRAPH
  • [4] pS2 gene expression in HepG2 cells:: Complex regulation through crosstalk between the estrogen receptor α, an estrogen-responsive element, and the activator protein 1 response element
    Barkhem, T
    Haldosén, LA
    Gustafsson, JÅ
    Nilsson, S
    [J]. MOLECULAR PHARMACOLOGY, 2002, 61 (06) : 1273 - 1283
  • [5] Hepatocyte nuclear factor 3 (winged helix domain) activates trefoil factor gene TFF1 through a binding motif adjacent to the TATAA box
    Beck, S
    Sommer, P
    Silva, ED
    Blin, N
    Gött, P
    [J]. DNA AND CELL BIOLOGY, 1999, 18 (02) : 157 - 164
  • [6] HYPER MARKOV LAWS IN THE STATISTICAL-ANALYSIS OF DECOMPOSABLE GRAPHICAL MODELS
    DAWID, AP
    LAURITZEN, SL
    [J]. ANNALS OF STATISTICS, 1993, 21 (03) : 1272 - 1317
  • [7] DAWID AP, 1981, BIOMETRIKA, V68, P265, DOI 10.1093/biomet/68.1.265
  • [8] The regulation of E2F by pRB-family proteins
    Dyson, N
    [J]. GENES & DEVELOPMENT, 1998, 12 (15) : 2245 - 2262
  • [9] Geiger D, 2002, ANN STAT, V30, P1412
  • [10] Giudici P., 1996, Statistics, P621