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Evaluation of DNA microarray results with quantitative gene expression platforms.
Nat Biotechnol ; 24(9): 1115-22, 2006 Sep.
Article em En | MEDLINE | ID: mdl-16964225
ABSTRACT
We have evaluated the performance characteristics of three quantitative gene expression technologies and correlated their expression measurements to those of five commercial microarray platforms, based on the MicroArray Quality Control (MAQC) data set. The limit of detection, assay range, precision, accuracy and fold-change correlations were assessed for 997 TaqMan Gene Expression Assays, 205 Standardized RT (Sta)RT-PCR assays and 244 QuantiGene assays. TaqMan is a registered trademark of Roche Molecular Systems, Inc. We observed high correlation between quantitative gene expression values and microarray platform results and found few discordant measurements among all platforms. The main cause of variability was differences in probe sequence and thus target location. A second source of variability was the limited and variable sensitivity of the different microarray platforms for detecting weakly expressed genes, which affected interplatform and intersite reproducibility of differentially expressed genes. From this analysis, we conclude that the MAQC microarray data set has been validated by alternative quantitative gene expression platforms thus supporting the use of microarray platforms for the quantitative characterization of gene expression.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Garantia da Qualidade dos Cuidados de Saúde / Análise de Sequência com Séries de Oligonucleotídeos / Perfilação da Expressão Gênica Tipo de estudo: Diagnostic_studies / Evaluation_studies Idioma: En Revista: Nat Biotechnol Ano de publicação: 2006 Tipo de documento: Article
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Garantia da Qualidade dos Cuidados de Saúde / Análise de Sequência com Séries de Oligonucleotídeos / Perfilação da Expressão Gênica Tipo de estudo: Diagnostic_studies / Evaluation_studies Idioma: En Revista: Nat Biotechnol Ano de publicação: 2006 Tipo de documento: Article