| Literature DB >> 16011696 |
Mahlet G Tadesse1, Joseph G Ibrahim, Robert Gentleman, Sabina Chiaretti, Jerome Ritz, Robin Foa.
Abstract
DNA microarrays in conjunction with statistical models may help gain a deeper understanding of the molecular basis for specific diseases. An intense area of research is concerned with the identification of genes related to particular phenotypes. The technology, however, is subject to various sources of error that may lead to expression readings that are substantially different from the true transcript levels. Few methods for microarray data analysis have accounted for measurement error in a substantial way and that is the purpose of this investigation. We describe a Bayesian error-in-variable model for the analysis of microarray data from a clinical study of patients with acute lymphoblastic leukemia. We focus in particular on the problem of identifying genes whose expression patterns are associated with duration of remission. This is a question of great practical interest since relapse is a major concern in the treatment of this disease. We explore the effects of ignoring the uncertainty in the expression estimates on the selection and ranking of genes.Entities:
Mesh:
Substances:
Year: 2005 PMID: 16011696 DOI: 10.1111/j.1541-0420.2005.00313.x
Source DB: PubMed Journal: Biometrics ISSN: 0006-341X Impact factor: 2.571