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PMID: 11747616 Published · ppublish English Journal Article

Assessing gene significance from cDNA microarray expression data via mixed models.

Wolfinger RD, Gibson G, Wolfinger ED, Bennett L, Hamadeh H, Bushel P, Afshari C, Paules RS

Abstract

The determination of a list of differentially expressed genes is a basic objective in many cDNA microarray experiments. We present a statistical approach that allows direct control over the percentage of false positives in such a list and, under certain reasonable assumptions, improves on existing methods with respect to the percentage of false negatives. The method accommodates a wide variety of experimental designs and can simultaneously assess significant differences between multiple types of biological samples. Two interconnected mixed linear models are central to the method and provide a flexible means to properly account for variability both across and within genes. The mixed model also provides a convenient framework for evaluating the statistical power of any particular experimental design and thus enables a researcher to a priori select an appropriate number of replicates. We also suggest some basic graphics for visualizing lists of significant genes. Analyses of published experiments studying human cancer and yeast cells illustrate the results.

MeSH Terms
Computational Biology Gene Expression Profiling/statistics & numerical data Genes, Fungal Humans Lymphoma, B-Cell/genetics Models, Genetic Models, Statistical Oligonucleotide Array Sequence Analysis/statistics & numerical data Saccharomyces cerevisiae/genetics
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Wolfinger R D
SAS Institute Inc., Cary, NC 27513, USA. russ.wolfinger@sas.com
Gibson G
Wolfinger E D
Bennett L
Hamadeh H
Bushel P
Afshari C
Paules R S
Article Info
Journal
Journal of computational biology : a journal of computational molecular cell biology
Abbr.
J Comput Biol
ISSN
1066-5277
Published
2001-00-00
Pages
625-37
Language
English
Region
United States
NLM ID
9433358
Subset
IM
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