ArticleBMC biotechnology2001
A simple method for statistical analysis of intensity differences in microarray-derived gene expression data.
Article in BMC biotechnology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
6 citing papers in PubMed.
- NONPARAMETRIC ESTIMATION OF GENEWISE VARIANCE FOR MICROARRAY DATA.Annals of statistics · 2010Article
- Variance estimation in the analysis of microarray data.Journal of the Royal Statistical Society. Series B, Statistical methodology · 2009Article
- Nonparametric variance estimation in the analysis of microarray data: a measurement error approach.Biometrika · 2008Article
- Variation in fiberoptic bead-based oligonucleotide microarrays: dispersion characteristics among hybridization and biological replicate samples.Biology direct · 2006Article
- Ranked prediction of p53 targets using hidden variable dynamic modeling.Genome biology · 2006Article
- Sources of variability and effect of experimental approach on expression profiling data interpretation.BMC bioinformatics · 2002Article
Corrections and comments
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Authors and funding
2 authors.
Funding
Abstract
backgroundMicroarray experiments offer a potent solution to the problem of making and comparing large numbers of gene expression measurements either in different cell types or in the same cell type under different conditions. Inferences about the biological relevance of observed changes in expression depend on the statistical significance of the changes. In lieu of many replicates with which to determine accurate intensity means and variances, reliable estimates of statistical significance remain problematic. Without such estimates, overly conservative choices for significance must be enforced.
resultsA simple statistical method for estimating variances from microarray control data which does not require multiple replicates is presented. Comparison of datasets from two commercial entities using this difference-averaging method demonstrates that the standard deviation of the signal scales at a level intermediate between the signal intensity and its square root. Application of the method to a dataset related to the beta-catenin pathway yields a larger number of biologically reasonable genes whose expression is altered than the ratio method.
conclusionsThe difference-averaging method enables determination of variances as a function of signal intensities by averaging over the entire dataset. The method also provides a platform-independent view of important statistical properties of microarray data.
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