Microarrays Commons^™

Assessment Of A Cgh-Based Genetic Instability, David A. Engler, Yiping Shen, J F. Gusella, Rebecca A. Betensky

Harvard University Biostatistics Working Paper Series

No abstract provided.

Survival Analysis With Large Dimensional Covariates: An Application In Microarray Studies, David A. Engler, Yi Li

Harvard University Biostatistics Working Paper Series

Use of microarray technology often leads to high-dimensional and low- sample size data settings. Over the past several years, a variety of novel approaches have been proposed for variable selection in this context. However, only a small number of these have been adapted for time-to-event data where censoring is present. Among standard variable selection methods shown both to have good predictive accuracy and to be computationally efficient is the elastic net penalization approach. In this paper, adaptation of the elastic net approach is presented for variable selection both under the Cox proportional hazards model and under an accelerated failure time …

What Is The Best Reference Rna? And Other Questions Regarding The Design And Analysis Of Two-Color Microarray Experiments, Kathleen F. Kerr, Kyle A. Serikawa, Caimiao Wei, Mette A. Peters, Roger E. Bumgarner

UW Biostatistics Working Paper Series

The reference design is a practical and popular choice for microarray studies using two-color platforms. In the reference design, the reference RNA uses half of all array resources, leading investigators to ask: What is the best reference RNA? We propose a novel method for evaluating reference RNAs and present the results of an experiment that was specially designed to evaluate three common choices of reference RNA. We found no compelling evidence in favor of any particular reference. In particular, a commercial reference showed no advantage in our data. Our experimental design also enabled a new way to test the effectiveness …

A Bayesian Hierarchical Model For Spot Fluorescence In Microarrays, Federico Mattia Stefanini

COBRA Preprint Series

Microarray experiments are characterized by the presence of many sources of experimental bias and a remarkably large technical variability. The assessment of differential expression for genes transcribed into a small number of mRNA copies heavily depends on the proper quantification of background fluorescence within spot. The rough model `observed = hybridization plus background' fluorescence is at first reformulated at spot level, then it is embedded into a Bayesian hierarchical model suited for fitting control spots. The novelties of the approach include the background correction performed on the latent mean of replicated spots, and an explicit model for outlying observations at …

On Comparing The Clustering Of Regression Models Method With K-Means Clustering, Li-Xuan Qin, Steven G. Self

Memorial Sloan-Kettering Cancer Center, Dept. of Epidemiology & Biostatistics Working Paper Series

Gene clustering is a common question addressed with microarray data. Previous methods, such as K-means clustering and hierarchical clustering, base gene clustering directly on the observed measurements. A new model-based clustering method, the clustering of regression models (CORM) method, bases the clustering of genes on their relationship to covariates. It explicitly models different sources of variations and bases gene clustering solely on the systematic variation. Both being partitional clustering, CORM is closely related to K-means clustering. In this paper, we discuss the relationship between the two clustering methods in terms of both model formulation and implications on other important aspects …

Conservative Estimation Of Optimal Multiple Testing Procedures, James E. Signorovitch

Harvard University Biostatistics Working Paper Series

No abstract provided.

Statistical Evaluation Of Evidence For Clonal Allelic Alterations In Array-Cgh Experiments, Colin B. Begg, Kevin Eng, Adam Olshen, E S. Venkatraman

Memorial Sloan-Kettering Cancer Center, Dept. of Epidemiology & Biostatistics Working Paper Series

In recent years numerous investigators have conducted genetic studies of pairs of tumor specimens from the same patient to determine whether the tumors share a clonal origin. These studies have the potential to be of considerable clinical significance, especially in clinical settings where the distinction of a new primary cancer and metastatic spread of a previous cancer would lead to radically different indications for treatment. Studies of clonality have typically involved comparison of the patterns of somatic mutations in the tumors at candidate genetic loci to see if the patterns are sufficiently similar to indicate a clonal origin. More recently, …

Power Boosting In Genome-Wide Studies Via Methods For Multivariate Outcomes, Mary J. Emond

UW Biostatistics Working Paper Series

Whole-genome studies are becoming a mainstay of biomedical research. Examples include expression array experiments, comparative genomic hybridization analyses and large case-control studies for detecting polymorphism/disease associations. The tactic of applying a regression model to every locus to obtain test statistics is useful in such studies. However, this approach ignores potential correlation structure in the data that could be used to gain power, particularly when a Bonferroni correction is applied to adjust for multiple testing. In this article, we propose using regression techniques for misspecified multivariate outcomes to increase statistical power over independence-based modeling at each locus. Even when the outcome …

A Robust Measure Of Correlation Between Two Genes On A Microarray, Johanna S. Hardin, Aya Mitani '06, Leanne Hicks, Brian Vankoten

Pomona Faculty Publications and Research

Background

The underlying goal of microarray experiments is to identify gene expression patterns across different experimental conditions. Genes that are contained in a particular pathway or that respond similarly to experimental conditions could be co-expressed and show similar patterns of expression on a microarray. Using any of a variety of clustering methods or gene network analyses we can partition genes of interest into groups, clusters, or modules based on measures of similarity. Typically, Pearson correlation is used to measure distance (or similarity) before implementing a clustering algorithm. Pearson correlation is quite susceptible to outliers, however, an unfortunate characteristic when dealing …