TY - JOUR
T1 - Identifying differentially expressed genes in meta-analysis via Bayesian model-based clustering
AU - Jung, Yoon Young
AU - Oh, Man Suk
AU - Shin, Dong Wan
AU - Kang, Seung Ho
AU - Oh, Hyun Sook
PY - 2006/6
Y1 - 2006/6
N2 - A Bayesian model-based clustering approach is proposed for identifying differentially expressed genes in meta-analysis. A Bayesian hierarchical model is used as a scientific tool for combining information from different studies, and a mixture prior is used to separate differentially expressed genes from non-differentially expressed genes. Posterior estimation of the parameters and missing observations are done by using a simple Markov chain Monte Carlo method. From the estimated mixture model, useful measure of significance of a test such as the Bayesian false discovery rate (FDR), the local FDR (Efron et al., 2001), and the integration-driven discovery rate (IDR; Choi et al., 2003) can be easily computed. The model-based approach is also compared with commonly used permutation methods, and it is shown that the model-based approach is superior to the permutation methods when there are excessive under-expressed genes compared to over-expressed genes or vice versa. The proposed method is applied to four publicly available prostate cancer gene expression data sets and simulated data sets.
AB - A Bayesian model-based clustering approach is proposed for identifying differentially expressed genes in meta-analysis. A Bayesian hierarchical model is used as a scientific tool for combining information from different studies, and a mixture prior is used to separate differentially expressed genes from non-differentially expressed genes. Posterior estimation of the parameters and missing observations are done by using a simple Markov chain Monte Carlo method. From the estimated mixture model, useful measure of significance of a test such as the Bayesian false discovery rate (FDR), the local FDR (Efron et al., 2001), and the integration-driven discovery rate (IDR; Choi et al., 2003) can be easily computed. The model-based approach is also compared with commonly used permutation methods, and it is shown that the model-based approach is superior to the permutation methods when there are excessive under-expressed genes compared to over-expressed genes or vice versa. The proposed method is applied to four publicly available prostate cancer gene expression data sets and simulated data sets.
UR - http://www.scopus.com/inward/record.url?scp=33745654577&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=33745654577&partnerID=8YFLogxK
U2 - 10.1002/bimj.200410230
DO - 10.1002/bimj.200410230
M3 - Article
C2 - 16845907
AN - SCOPUS:33745654577
SN - 0323-3847
VL - 48
SP - 435
EP - 450
JO - Biometrische Zeitschrift
JF - Biometrische Zeitschrift
IS - 3
ER -