The effect of oligonucleotide microarray data pre-processing on the analysis of patient-cohort studies

<p>Abstract</p> <p>Background</p> <p>Intensity values measured by Affymetrix microarrays have to be both normalized, to be able to compare different microarrays by removing non-biological variation, and summarized, generating the final probe set expression values. Vario...

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Main Authors: Reinders Marcel JT, Valk Peter JM, Lowenberg Bob, Staal Frank JT, Verhaak Roel GW, de Ridder Dick
Format: Article
Language:English
Published: BMC 2006-03-01
Series:BMC Bioinformatics
Online Access:http://www.biomedcentral.com/1471-2105/7/105
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author Reinders Marcel JT
Valk Peter JM
Lowenberg Bob
Staal Frank JT
Verhaak Roel GW
de Ridder Dick
author_facet Reinders Marcel JT
Valk Peter JM
Lowenberg Bob
Staal Frank JT
Verhaak Roel GW
de Ridder Dick
author_sort Reinders Marcel JT
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Intensity values measured by Affymetrix microarrays have to be both normalized, to be able to compare different microarrays by removing non-biological variation, and summarized, generating the final probe set expression values. Various pre-processing techniques, such as dChip, GCRMA, RMA and MAS have been developed for this purpose. This study assesses the effect of applying different pre-processing methods on the results of analyses of large Affymetrix datasets. By focusing on practical applications of microarray-based research, this study provides insight into the relevance of pre-processing procedures to biology-oriented researchers.</p> <p>Results</p> <p>Using two publicly available datasets, i.e., gene-expression data of 285 patients with Acute Myeloid Leukemia (AML, Affymetrix HG-U133A GeneChip) and 42 samples of tumor tissue of the embryonal central nervous system (CNS, Affymetrix HuGeneFL GeneChip), we tested the effect of the four pre-processing strategies mentioned above, on (1) expression level measurements, (2) detection of differential expression, (3) cluster analysis and (4) classification of samples. In most cases, the effect of pre-processing is relatively small compared to other choices made in an analysis for the AML dataset, but has a more profound effect on the outcome of the CNS dataset. Analyses on individual probe sets, such as testing for differential expression, are affected most; supervised, multivariate analyses such as classification are far less sensitive to pre-processing.</p> <p>Conclusion</p> <p>Using two experimental datasets, we show that the choice of pre-processing method is of relatively minor influence on the final analysis outcome of large microarray studies whereas it can have important effects on the results of a smaller study. The data source (platform, tissue homogeneity, RNA quality) is potentially of bigger importance than the choice of pre-processing method.</p>
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spelling doaj.art-a60f012bb41c45b7b2d82f847008ff6b2022-12-21T19:14:05ZengBMCBMC Bioinformatics1471-21052006-03-017110510.1186/1471-2105-7-105The effect of oligonucleotide microarray data pre-processing on the analysis of patient-cohort studiesReinders Marcel JTValk Peter JMLowenberg BobStaal Frank JTVerhaak Roel GWde Ridder Dick<p>Abstract</p> <p>Background</p> <p>Intensity values measured by Affymetrix microarrays have to be both normalized, to be able to compare different microarrays by removing non-biological variation, and summarized, generating the final probe set expression values. Various pre-processing techniques, such as dChip, GCRMA, RMA and MAS have been developed for this purpose. This study assesses the effect of applying different pre-processing methods on the results of analyses of large Affymetrix datasets. By focusing on practical applications of microarray-based research, this study provides insight into the relevance of pre-processing procedures to biology-oriented researchers.</p> <p>Results</p> <p>Using two publicly available datasets, i.e., gene-expression data of 285 patients with Acute Myeloid Leukemia (AML, Affymetrix HG-U133A GeneChip) and 42 samples of tumor tissue of the embryonal central nervous system (CNS, Affymetrix HuGeneFL GeneChip), we tested the effect of the four pre-processing strategies mentioned above, on (1) expression level measurements, (2) detection of differential expression, (3) cluster analysis and (4) classification of samples. In most cases, the effect of pre-processing is relatively small compared to other choices made in an analysis for the AML dataset, but has a more profound effect on the outcome of the CNS dataset. Analyses on individual probe sets, such as testing for differential expression, are affected most; supervised, multivariate analyses such as classification are far less sensitive to pre-processing.</p> <p>Conclusion</p> <p>Using two experimental datasets, we show that the choice of pre-processing method is of relatively minor influence on the final analysis outcome of large microarray studies whereas it can have important effects on the results of a smaller study. The data source (platform, tissue homogeneity, RNA quality) is potentially of bigger importance than the choice of pre-processing method.</p>http://www.biomedcentral.com/1471-2105/7/105
spellingShingle Reinders Marcel JT
Valk Peter JM
Lowenberg Bob
Staal Frank JT
Verhaak Roel GW
de Ridder Dick
The effect of oligonucleotide microarray data pre-processing on the analysis of patient-cohort studies
BMC Bioinformatics
title The effect of oligonucleotide microarray data pre-processing on the analysis of patient-cohort studies
title_full The effect of oligonucleotide microarray data pre-processing on the analysis of patient-cohort studies
title_fullStr The effect of oligonucleotide microarray data pre-processing on the analysis of patient-cohort studies
title_full_unstemmed The effect of oligonucleotide microarray data pre-processing on the analysis of patient-cohort studies
title_short The effect of oligonucleotide microarray data pre-processing on the analysis of patient-cohort studies
title_sort effect of oligonucleotide microarray data pre processing on the analysis of patient cohort studies
url http://www.biomedcentral.com/1471-2105/7/105
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