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Full-Text Articles in Computational Biology
Penalized Likelihood And Bayesian Methods For Sparse Contingency Tables: An Analysis Of Alternative Splicing In Full-Length Cdna Libraries, Corinne Dahinden, Giovanni Parmigiani, Mark C. Emerick, Peter Buhlmann
Penalized Likelihood And Bayesian Methods For Sparse Contingency Tables: An Analysis Of Alternative Splicing In Full-Length Cdna Libraries, Corinne Dahinden, Giovanni Parmigiani, Mark C. Emerick, Peter Buhlmann
Johns Hopkins University, Dept. of Biostatistics Working Papers
We develop methods to perform model selection and parameter estimation in loglinear models for the analysis of sparse contingency tables to study the interaction of two or more factors. Typically, datasets arising from so-called full-length cDNA libraries, in the context of alternatively spliced genes, lead to such sparse contingency tables. Maximum Likelihood estimation of log-linear model coefficients fails to work because of zero cell entries. Therefore new methods are required to estimate the coefficients and to perform model selection. Our suggestions include computationally efficient penalization (Lasso-type) approaches as well as Bayesian methods using MCMC. We compare these procedures in a …
Estimating Genome-Wide Copy Number Using Allele Specific Mixture Models, Wenyi Wang , Benilton Caravalho, Nate Miller, Jonathan Pevsner, Aravinda Chakravarti, Rafael A. Irizarry
Estimating Genome-Wide Copy Number Using Allele Specific Mixture Models, Wenyi Wang , Benilton Caravalho, Nate Miller, Jonathan Pevsner, Aravinda Chakravarti, Rafael A. Irizarry
Johns Hopkins University, Dept. of Biostatistics Working Papers
Genomic changes such as copy number alterations are thought to be one of the major underlying causes of human phenotypic variation among normal and disease subjects [23,11,25,26,5,4,7,18]. These include chromosomal regions with so-called copy number alterations: instead of the expected two copies, a section of the chromosome for a particular individual may have zero copies (homozygous deletion), one copy (hemizygous deletions), or more than two copies (amplifications). The canonical example is Down syndrome which is caused by an extra copy of chromosome 21. Identification of such abnormalities in smaller regions has been of great interest, because it is believed to …
Fdr And Bayesian Multiple Comparisons Rules, Peter Muller, Giovanni Parmigiani, Kenneth Rice
Fdr And Bayesian Multiple Comparisons Rules, Peter Muller, Giovanni Parmigiani, Kenneth Rice
Johns Hopkins University, Dept. of Biostatistics Working Papers
We discuss Bayesian approaches to multiple comparison problems, using a decision theoretic perspective to critically compare competing approaches. We set up decision problems that lead to the use of FDR-based rules and generalizations. Alternative definitions of the probability model and the utility function lead to different rules and problem-specific adjustments. Using a loss function that controls realized FDR we derive an optimal Bayes rule that is a variation of the Benjamini and Hochberg (1995) procedure. The cutoff is based on increments in ordered posterior probabilities instead of ordered p- values. Throughout the discussion we take a Bayesian perspective. In particular, …
Exploration, Normalization, And Genotype Calls Of High Density Oligonucleotide Snp Array Data, Benilton Carvalho, Terence P. Speed, Rafael A. Irizarry
Exploration, Normalization, And Genotype Calls Of High Density Oligonucleotide Snp Array Data, Benilton Carvalho, Terence P. Speed, Rafael A. Irizarry
Johns Hopkins University, Dept. of Biostatistics Working Papers
In most microarray technologies, a number of critical steps are required to convert raw intensity measurements into the data relied upon by data analysts, biologists and clinicians. These data manipulations, referred to as preprocessing, can influence the quality of the ultimate measurements. In the last few years, the high-throughput measurement of gene expression is the most popular application of microarray technology. For this application, various groups have demonstrated that the use of modern statistical methodology can substantially improve accuracy and precision of gene expression measurements, relative to ad-hoc procedures introduced by designers and manufacturers of the technology. Currently, other applications …
Multivariate Analysis And Visualization Of Splicing Correlations In Single-Gene Transcriptomes, Mark C. Emerick, Giovanni Parmigiani, William S. Agnew
Multivariate Analysis And Visualization Of Splicing Correlations In Single-Gene Transcriptomes, Mark C. Emerick, Giovanni Parmigiani, William S. Agnew
Johns Hopkins University, Dept. of Biostatistics Working Papers
Through ‘combinatorial splicing’, RNA metabolism may create enormous structural diversity in the proteome. Functional interactions among multiple alternative domains can have a disproportionate impact on the phenotype, requiring integrated RNA-level regulation of molecular composition. Splicing correlations within molecules expressed from a single gene, where these effects would be greatest, provide valuable clues to functional relationships and targets for splicing regulation. We present tools to visualize complex splicing patterns in full-length cDNA libraries. Developmental changes in pair-wise correlations are presented vectorially in ‘clock plots’ and linkage grids. Higher-order correlations are assessed via a loglinear model and Monte Carlo analysis with an …
Feature-Level Exploration Of The Choe Et Al. Affymetrix Genechip Control Dataset, Rafael A. Irizarry, Leslie Cope, Zhijin Wu
Feature-Level Exploration Of The Choe Et Al. Affymetrix Genechip Control Dataset, Rafael A. Irizarry, Leslie Cope, Zhijin Wu
Johns Hopkins University, Dept. of Biostatistics Working Papers
We describe why the Choe et al. control dataset should not be used to assess GeneChip expression measures.