Patient-based cross-platform comparison of oligonucleotide microarray expression profiles.

Standard

Patient-based cross-platform comparison of oligonucleotide microarray expression profiles. / Schlingemann, Joerg; Habtemichael, Negusse; Ittrich, Carina; Toedt, Grischa; Kramer, Heidi; Hambek, Markus; Knecht, Rainald; Lichter, Peter; Stauber, Roland; Hahn, Meinhard.

in: LAB INVEST, Jahrgang 85, Nr. 8, 8, 2005, S. 1024-1039.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Schlingemann, J, Habtemichael, N, Ittrich, C, Toedt, G, Kramer, H, Hambek, M, Knecht, R, Lichter, P, Stauber, R & Hahn, M 2005, 'Patient-based cross-platform comparison of oligonucleotide microarray expression profiles.', LAB INVEST, Jg. 85, Nr. 8, 8, S. 1024-1039. <http://www.ncbi.nlm.nih.gov/pubmed/16205657?dopt=Citation>

APA

Schlingemann, J., Habtemichael, N., Ittrich, C., Toedt, G., Kramer, H., Hambek, M., Knecht, R., Lichter, P., Stauber, R., & Hahn, M. (2005). Patient-based cross-platform comparison of oligonucleotide microarray expression profiles. LAB INVEST, 85(8), 1024-1039. [8]. http://www.ncbi.nlm.nih.gov/pubmed/16205657?dopt=Citation

Vancouver

Schlingemann J, Habtemichael N, Ittrich C, Toedt G, Kramer H, Hambek M et al. Patient-based cross-platform comparison of oligonucleotide microarray expression profiles. LAB INVEST. 2005;85(8):1024-1039. 8.

Bibtex

@article{a2f09d9228e645c6bab4896fa602ea4b,
title = "Patient-based cross-platform comparison of oligonucleotide microarray expression profiles.",
abstract = "The comparison of gene expression measurements obtained with different technical approaches is of substantial interest in order to clarify whether inter-platform differences may conceal biologically significant information. To address this concern, we analyzed gene expression in a set of head and neck squamous cell carcinoma patients, using both spotted oligonucleotide microarrays made from a large collection of 70-mer probes and commercial arrays produced by in situ synthesis of sets of multiple 25-mer oligonucleotides per gene. Expression measurements were compared for 4425 genes represented on both platforms, which revealed strong correlations between the corresponding data sets. Of note, a global tendency towards smaller absolute ratios was observed when using the 70-mer probes. Real-time quantitative reverse transcription PCR measurements were conducted to verify expression ratios for a subset of genes and achieved good agreement regarding both array platforms. In conclusion, similar profiles of relative gene expression were obtained using arrays of either single 70-mer or multiple short 25-mer oligonucleotide probes per gene. Although qualitative assessments of the expression of individual genes have to be made with caution, our results indicate that the comparison of gene expression profiles generated on these platforms will help to discover disease-related gene signatures in general.",
author = "Joerg Schlingemann and Negusse Habtemichael and Carina Ittrich and Grischa Toedt and Heidi Kramer and Markus Hambek and Rainald Knecht and Peter Lichter and Roland Stauber and Meinhard Hahn",
year = "2005",
language = "Deutsch",
volume = "85",
pages = "1024--1039",
journal = "LAB INVEST",
issn = "0023-6837",
publisher = "NATURE PUBLISHING GROUP",
number = "8",

}

RIS

TY - JOUR

T1 - Patient-based cross-platform comparison of oligonucleotide microarray expression profiles.

AU - Schlingemann, Joerg

AU - Habtemichael, Negusse

AU - Ittrich, Carina

AU - Toedt, Grischa

AU - Kramer, Heidi

AU - Hambek, Markus

AU - Knecht, Rainald

AU - Lichter, Peter

AU - Stauber, Roland

AU - Hahn, Meinhard

PY - 2005

Y1 - 2005

N2 - The comparison of gene expression measurements obtained with different technical approaches is of substantial interest in order to clarify whether inter-platform differences may conceal biologically significant information. To address this concern, we analyzed gene expression in a set of head and neck squamous cell carcinoma patients, using both spotted oligonucleotide microarrays made from a large collection of 70-mer probes and commercial arrays produced by in situ synthesis of sets of multiple 25-mer oligonucleotides per gene. Expression measurements were compared for 4425 genes represented on both platforms, which revealed strong correlations between the corresponding data sets. Of note, a global tendency towards smaller absolute ratios was observed when using the 70-mer probes. Real-time quantitative reverse transcription PCR measurements were conducted to verify expression ratios for a subset of genes and achieved good agreement regarding both array platforms. In conclusion, similar profiles of relative gene expression were obtained using arrays of either single 70-mer or multiple short 25-mer oligonucleotide probes per gene. Although qualitative assessments of the expression of individual genes have to be made with caution, our results indicate that the comparison of gene expression profiles generated on these platforms will help to discover disease-related gene signatures in general.

AB - The comparison of gene expression measurements obtained with different technical approaches is of substantial interest in order to clarify whether inter-platform differences may conceal biologically significant information. To address this concern, we analyzed gene expression in a set of head and neck squamous cell carcinoma patients, using both spotted oligonucleotide microarrays made from a large collection of 70-mer probes and commercial arrays produced by in situ synthesis of sets of multiple 25-mer oligonucleotides per gene. Expression measurements were compared for 4425 genes represented on both platforms, which revealed strong correlations between the corresponding data sets. Of note, a global tendency towards smaller absolute ratios was observed when using the 70-mer probes. Real-time quantitative reverse transcription PCR measurements were conducted to verify expression ratios for a subset of genes and achieved good agreement regarding both array platforms. In conclusion, similar profiles of relative gene expression were obtained using arrays of either single 70-mer or multiple short 25-mer oligonucleotide probes per gene. Although qualitative assessments of the expression of individual genes have to be made with caution, our results indicate that the comparison of gene expression profiles generated on these platforms will help to discover disease-related gene signatures in general.

M3 - SCORING: Zeitschriftenaufsatz

VL - 85

SP - 1024

EP - 1039

JO - LAB INVEST

JF - LAB INVEST

SN - 0023-6837

IS - 8

M1 - 8

ER -