Biological assessment of robust noise models in microarray data analysis

被引:24
作者
Posekany, A. [1 ]
Felsenstein, K. [2 ]
Sykacek, P. [1 ]
机构
[1] Univ Nat Resources & Life Sci, Dept Biotechnol, Chair Bioinformat, A-1180 Vienna, Austria
[2] Vienna Univ Technol, Dept Stat, A-1040 Vienna, Austria
关键词
DIFFERENTIALLY EXPRESSED GENES; NONPARAMETRIC METHODS; NORMALIZATION; TRANSCRIPTOME; MECHANISMS; ONTOLOGY; OBESITY; MICE; TOOL;
D O I
10.1093/bioinformatics/btr018
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Although several recently proposed analysis packages for microarray data can cope with heavy-tailed noise, many applications rely on Gaussian assumptions. Gaussian noise models foster computational efficiency. This comes, however, at the expense of increased sensitivity to outlying observations. Assessing potential insufficiencies of Gaussian noise in microarray data analysis is thus important and of general interest. Results: We propose to this end assessing different noise models on a large number of microarray experiments. The goodness of fit of noise models is quantified by a hierarchical Bayesian analysis of variance model, which predicts normalized expression values as a mixture of a Gaussian density and t-distributions with adjustable degrees of freedom. Inference of differentially expressed genes is taken into consideration at a second mixing level. For attaining far reaching validity, our investigations cover a wide range of analysis platforms and experimental settings. As the most striking result, we find irrespective of the chosen preprocessing and normalization method in all experiments that a heavy-tailed noise model is a better fit than a simple Gaussian. Further investigations revealed that an appropriate choice of noise model has a considerable influence on biological interpretations drawn at the level of inferred genes and gene ontology terms. We conclude from our investigation that neglecting the over dispersed noise in microarray data can mislead scientific discovery and suggest that the convenience of Gaussian-based modelling should be replaced by non-parametric approaches or other methods that account for heavy-tailed noise.
引用
收藏
页码:807 / 814
页数:8
相关论文
共 58 条
  • [1] Understanding endothelial cell apoptosis: what can the transcriptome, glycome and proteome reveal?
    Affara, Muna
    Dunmore, Benjamin
    Savoie, Christopher
    Imoto, Seiya
    Tamada, Yoshinori
    Araki, Hiromitsu
    Charnock-Jones, D. Stephen
    Miyano, Satoru
    Print, Cristin
    [J]. PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2007, 362 (1484) : 1469 - 1487
  • [2] FatiGO:: a web tool for finding significant associations of Gene Ontology terms with groups of genes
    Al-Shahrour, F
    Díaz-Uriarte, R
    Dopazo, J
    [J]. BIOINFORMATICS, 2004, 20 (04) : 578 - 580
  • [3] Gene Ontology: tool for the unification of biology
    Ashburner, M
    Ball, CA
    Blake, JA
    Botstein, D
    Butler, H
    Cherry, JM
    Davis, AP
    Dolinski, K
    Dwight, SS
    Eppig, JT
    Harris, MA
    Hill, DP
    Issel-Tarver, L
    Kasarskis, A
    Lewis, S
    Matese, JC
    Richardson, JE
    Ringwald, M
    Rubin, GM
    Sherlock, G
    [J]. NATURE GENETICS, 2000, 25 (01) : 25 - 29
  • [4] Gene selection using a two-level hierarchical Bayesian model
    Bae, K
    Mallick, BK
    [J]. BIOINFORMATICS, 2004, 20 (18) : 3423 - 3430
  • [5] A Bayesian framework for the analysis of microarray expression data: regularized t-test and statistical inferences of gene changes
    Baldi, P
    Long, AD
    [J]. BIOINFORMATICS, 2001, 17 (06) : 509 - 519
  • [6] Berger J. O., 1994, Test, V3, P5, DOI 10.1007/BF02562676
  • [7] Bernardo J. M., 1994, Bayesian theory, DOI 10.1002/9780470316870
  • [8] Incipient Alzheimer's disease: Microarray correlation analyses reveal major transcriptional and tumor suppressor responses
    Blalock, EM
    Geddes, JW
    Chen, KC
    Porter, NM
    Markesbery, WR
    Landfield, PW
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (07) : 2173 - 2178
  • [9] A comparison of normalization methods for high density oligonucleotide array data based on variance and bias
    Bolstad, BM
    Irizarry, RA
    Åstrand, M
    Speed, TP
    [J]. BIOINFORMATICS, 2003, 19 (02) : 185 - 193
  • [10] Cameron DA, 2005, MOL VIS, V11, P775