Archive
Local FDR estimation for low-dimensional data
M. Padilla and D. R. Bickel, “Estimators of the local false discovery rate designed for small numbers of tests,” Statistical Applications in Genetics and Molecular Biology 11 (5), art. 4 (2012). Full article | 2010 & 2012 preprints
How to combine statistical methods
D. R. Bickel, “Game-theoretic probability combination with applications to resolving conflicts between statistical methods,” International Journal of Approximate Reasoning 53, 880-891 (2012). Full article | 2011 preprint | Slides | Simple explanation
This paper proposes both a novel solution to the problem of combining probability distributions and a framework for using the new method to combine the results of differing statistical methods that may legitimately be used to analyze the same data set. While the paper emphasizes theoretical development, it is motivated by the need to combine two conflicting estimators of the probability of differential gene expression.
Estimating probabilities of enrichment
Z. Yang, Z. Li, and D. R. Bickel, “Empirical Bayes estimation of posterior probabilities of enrichment,” Technical Report, Ottawa Institute of Systems Biology, Technical Report, Ottawa Institute of Systems Biology, arXiv:1201.0153 (2011). Full preprint | 2010 seed
This paper adapts novel empirical Bayes methods for the problem of detecting enrichment in the form of differential representation of genes associated with a biological category with respect to a list of genes identified as differentially expressed. A microarray case study illustrates the methods using Gene Ontology (GO) terms, and a simulation study compares their performance. We report that which enrichment methods work best depends strongly on how many GO terms or other biological categories are of interest.
Combining inferences from different methods
D. R. Bickel, “Resolving conflicts between statistical methods by probability combination: Application to empirical Bayes analyses of genomic data,” Technical Report, Ottawa Institute of Systems Biology, arXiv:1111.6174 (2011). Full preprint
This paper proposes a solution to the problem of combining the results of differing statistical methods that may legitimately be used to analyze the same data set. The motivating application is the combination of two estimators of the probability of differential gene expression: one uses an empirical null distribution, and the other uses the theoretical null distribution. Since there is usually not any reliable way to predict which null distribution will perform better for a given data set and since the choice between them often has a large impact on the conclusions, the proposed hedging strategy addresses a pressing need in statistical genomics. Many other applications are also mentioned in the abstract and described in the introduction.
Minimax strength of statistical evidence
D. R. Bickel, “A predictive approach to measuring the strength of statistical evidence for single and multiple comparisons,” Canadian Journal of Statistics 39, 610–631 (2011). Full text | Revised preprint | 2010 draft
This paper introduces a novel approach to the multiple comparisons problem by generalizing a promising method of model selection developed by information theorists. The first two sections present that method and its main advantages over conventional approaches without burdening statisticians with unfamiliar terms from coding theory. A quantitative proteomics case study facilitates application of the new method to the analysis of data sets involving multiple biological features. The theorems describe its operating characteristics.
The cited medium-scale paper presented previous minimum description length (MDL) methods. Unlike those methods, the new MDL methods of the current paper are based on a conflation of the normalized maximum likelihood (NML) with the weighted likelihood (WL). The previous MDL methods are used in the CJS article for comparison with its NML/WL methods.
Software for local false discovery rate estimation
LFDR-MLE is a suite of R functions for the estimation of local false discovery rates by maximum likelihood under a two-group parametric mixture model of test statistics.
Unknown Bayes factor approximation
D. R. Bickel, “Measuring support for a hypothesis about a random parameter without estimating its unknown prior,” Technical Report, Ottawa Institute of Systems Biology, arXiv:1101.0305 (2011). Full preprint
Quantifying evidence for enrichment
Z. Yang and D. R. Bickel, “Minimum description length measures of evidence for enrichment,” Technical Report, Ottawa Institute of Systems Biology, COBRA Preprint Series, Article 76, available at biostats.bepress.com/cobra/ps/art76 (2010). Full preprint
Quantifying evidence for genetic association
Y. Yang and D. R. Bickel, “Minimum description length and empirical Bayes methods of identifying SNPs associated with disease,” Technical Report, Ottawa Institute of Systems Biology, COBRA Preprint Series, Article 74, available at biostats.bepress.com/cobra/ps/art74 (2010).
This manuscript adapts two new evidential, information-theoretic methods to the problem of detecting SNPs associated with disease on the basis of genome-wide association data. Both an application to coronary artery disease and an extensive set of simulation studies indicate that these parametric methods tend to be more reliable than a popular semi-parametric approach to estimating local false discovery rates. In addition, the paper reports that one of the two novel methods performs better than the other.
The abstract and the discussion section of the preprint provide more detailed summaries.
Normalized maximum weighted likelihood
D. R. Bickel, “Statistical inference optimized with respect to the observed sample for single or multiple comparisons,” Technical Report, Ottawa Institute of Systems Biology, arXiv:1010.0694 (2010). Full preprint
David Bickel, statistician 
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