Flexible empirical Bayes models for differential gene expression.
Details
Serval ID
serval:BIB_C13886118110
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Flexible empirical Bayes models for differential gene expression.
Journal
Bioinformatics
ISSN
1367-4811 (Electronic)
ISSN-L
1367-4803
Publication state
Published
Issued date
01/02/2007
Peer-reviewed
Oui
Volume
23
Number
3
Pages
328-335
Language
english
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Publication Status: ppublish
Abstract
Inference about differential expression is a typical objective when analyzing gene expression data. Recently, Bayesian hierarchical models have become increasingly popular for this type of problem. The two most common hierarchical models are the hierarchical Gamma-Gamma (GG) and Lognormal-Normal (LNN) models. However, to facilitate inference, some unrealistic assumptions have been made. One such assumption is that of a common coefficient of variation across genes, which can adversely affect the resulting inference.
In this paper, we extend both the GG and LNN modeling frameworks to allow for gene-specific variances and propose EM based algorithms for parameter estimation. The proposed methodology is evaluated on three experimental datasets: one cDNA microarray experiment and two Affymetrix spike-in experiments. The two extended models significantly reduce the false positive rate while keeping a high sensitivity when compared to the originals. Finally, using a simulation study we show that the new frameworks are also more robust to model misspecification.
The R code for implementing the proposed methodology can be downloaded at http://www.stat.ubc.ca/~c.lo/FEBarrays.
The supplementary material is available at http://www.stat.ubc.ca/~c.lo/FEBarrays/supp.pdf.
In this paper, we extend both the GG and LNN modeling frameworks to allow for gene-specific variances and propose EM based algorithms for parameter estimation. The proposed methodology is evaluated on three experimental datasets: one cDNA microarray experiment and two Affymetrix spike-in experiments. The two extended models significantly reduce the false positive rate while keeping a high sensitivity when compared to the originals. Finally, using a simulation study we show that the new frameworks are also more robust to model misspecification.
The R code for implementing the proposed methodology can be downloaded at http://www.stat.ubc.ca/~c.lo/FEBarrays.
The supplementary material is available at http://www.stat.ubc.ca/~c.lo/FEBarrays/supp.pdf.
Keywords
Algorithms, Bayes Theorem, Data Interpretation, Statistical, Gene Expression Profiling/methods, Logistic Models, Models, Genetic, Models, Statistical, Oligonucleotide Array Sequence Analysis/methods
Pubmed
Web of science
Create date
28/02/2022 11:45
Last modification date
23/03/2024 7:24