Bayesian hierarchical model for identifying changes in gene expression from microarray experiments

被引:62
作者
Broët, P
Richardson, S
Radvanyi, F
机构
[1] Hop Paul Brousse, INSERM, U472, F-94807 Villejuif, France
[2] Univ Paris 11, Fac Med, Orsay, France
[3] Univ London Imperial Coll Sci Technol & Med, Dept Epidemiol & Publ Hlth, London W2 1PG, England
[4] Inst Curie, Sect Rech, CNRS, UMR 144, F-75248 Paris, France
关键词
Bayesian hierarchical model; gene expression analysis; DNA microarrays; Markov chain Monte Carlo methods; normal mixtures;
D O I
10.1089/106652702760277381
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Recent developments in microarrays technology enable researchers to study simultaneously the expression of thousands of genes from one cell line or tissue sample. This new technology is often used to assess changes in mRNA expression upon a specified transfection for a cell line in order to identify target genes. For such experiments, the range of differential expression is moderate, and teasing out the modified genes is challenging and calls for detailed modeling. The aim of this paper is to propose a methodological framework for studies that investigate differential gene expression through microarrays technology that is based on a fully Bayesian mixture approach (Richardson and Green, 1997). A case study that investigated those genes that were differentially expressed in two cell lines (normal and modified by a gene transfection) is provided to illustrate the performance and usefulness of this approach.
引用
收藏
页码:671 / 683
页数:13
相关论文
共 17 条
[1]  
[Anonymous], 2000, WILEY SERIES PROBABI
[2]  
[Anonymous], 1993, Resampling-based multiple testing: Examples and methods for P-value adjustment
[3]   Exploring the new world of the genome with DNA microarrays [J].
Brown, PO ;
Botstein, D .
NATURE GENETICS, 1999, 21 (Suppl 1) :33-37
[4]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[5]   Computational methods for the identification of differential and coordinated gene expression [J].
Claverie, JM .
HUMAN MOLECULAR GENETICS, 1999, 8 (10) :1821-1832
[6]  
DUDOIT S, 2000, 578 U CAL BERK DEP S
[7]  
Efron B., 2000, MICROARRAYS THEIR US
[8]  
Green PJ, 1995, BIOMETRIKA, V82, P711, DOI 10.2307/2337340
[9]   Functional discovery via a compendium of expression profiles [J].
Hughes, TR ;
Marton, MJ ;
Jones, AR ;
Roberts, CJ ;
Stoughton, R ;
Armour, CD ;
Bennett, HA ;
Coffey, E ;
Dai, HY ;
He, YDD ;
Kidd, MJ ;
King, AM ;
Meyer, MR ;
Slade, D ;
Lum, PY ;
Stepaniants, SB ;
Shoemaker, DD ;
Gachotte, D ;
Chakraburtty, K ;
Simon, J ;
Bard, M ;
Friend, SH .
CELL, 2000, 102 (01) :109-126
[10]   Analysis of variance for gene expression microarray data [J].
Kerr, MK ;
Martin, M ;
Churchill, GA .
JOURNAL OF COMPUTATIONAL BIOLOGY, 2000, 7 (06) :819-837