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Cross-platform comparison of SYBR(® )Green real-time PCR with TaqMan PCR, microarrays and other gene expression measurement technologies evaluated in the MicroArray Quality Control (MAQC) study

BACKGROUND: The MicroArray Quality Control (MAQC) project evaluated the inter- and intra-platform reproducibility of seven microarray platforms and three quantitative gene expression assays in profiling the expression of two commercially available Reference RNA samples (Nat Biotechnol 24:1115-22, 20...

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Autores principales: Arikawa, Emi, Sun, Yanyang, Wang, Jie, Zhou, Qiong, Ning, Baitang, Dial, Stacey L, Guo, Lei, Yang, Jingping
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2491643/
https://www.ncbi.nlm.nih.gov/pubmed/18620571
http://dx.doi.org/10.1186/1471-2164-9-328
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author Arikawa, Emi
Sun, Yanyang
Wang, Jie
Zhou, Qiong
Ning, Baitang
Dial, Stacey L
Guo, Lei
Yang, Jingping
author_facet Arikawa, Emi
Sun, Yanyang
Wang, Jie
Zhou, Qiong
Ning, Baitang
Dial, Stacey L
Guo, Lei
Yang, Jingping
author_sort Arikawa, Emi
collection PubMed
description BACKGROUND: The MicroArray Quality Control (MAQC) project evaluated the inter- and intra-platform reproducibility of seven microarray platforms and three quantitative gene expression assays in profiling the expression of two commercially available Reference RNA samples (Nat Biotechnol 24:1115-22, 2006). The tested microarrays were the platforms from Affymetrix, Agilent Technologies, Applied Biosystems, GE Healthcare, Illumina, Eppendorf and the National Cancer Institute, and quantitative gene expression assays included TaqMan(® )Gene Expression PCR Assay, Standardized (Sta) RT-PCR™ and QuantiGene(®). The data showed great consistency in gene expression measurements across different microarray platforms, different technologies and test sites. However, SYBR(® )Green real-time PCR, another common technique utilized by half of all real-time PCR users for gene expression measurement, was not addressed in the MAQC study. In the present study, we compared the performance of SYBR Green PCR with TaqMan PCR, microarrays and other quantitative technologies using the same two Reference RNA samples as the MAQC project. We assessed SYBR Green real-time PCR using commercially available RT(2 )Profiler™ PCR Arrays from SuperArray, containing primer pairs that have been experimentally validated to ensure gene-specificity and high amplification efficiency. RESULTS: The SYBR Green PCR Arrays exhibit good reproducibility among different users, PCR instruments and test sites. In addition, the SYBR Green PCR Arrays have the highest concordance with TaqMan PCR, and a high level of concordance with other quantitative methods and microarrays that were evaluated in this study in terms of fold-change correlation and overlap of lists of differentially expressed genes. CONCLUSION: These data demonstrate that SYBR Green real-time PCR delivers highly comparable results in gene expression measurement with TaqMan PCR and other high-density microarrays.
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spelling pubmed-24916432008-07-31 Cross-platform comparison of SYBR(® )Green real-time PCR with TaqMan PCR, microarrays and other gene expression measurement technologies evaluated in the MicroArray Quality Control (MAQC) study Arikawa, Emi Sun, Yanyang Wang, Jie Zhou, Qiong Ning, Baitang Dial, Stacey L Guo, Lei Yang, Jingping BMC Genomics Research Article BACKGROUND: The MicroArray Quality Control (MAQC) project evaluated the inter- and intra-platform reproducibility of seven microarray platforms and three quantitative gene expression assays in profiling the expression of two commercially available Reference RNA samples (Nat Biotechnol 24:1115-22, 2006). The tested microarrays were the platforms from Affymetrix, Agilent Technologies, Applied Biosystems, GE Healthcare, Illumina, Eppendorf and the National Cancer Institute, and quantitative gene expression assays included TaqMan(® )Gene Expression PCR Assay, Standardized (Sta) RT-PCR™ and QuantiGene(®). The data showed great consistency in gene expression measurements across different microarray platforms, different technologies and test sites. However, SYBR(® )Green real-time PCR, another common technique utilized by half of all real-time PCR users for gene expression measurement, was not addressed in the MAQC study. In the present study, we compared the performance of SYBR Green PCR with TaqMan PCR, microarrays and other quantitative technologies using the same two Reference RNA samples as the MAQC project. We assessed SYBR Green real-time PCR using commercially available RT(2 )Profiler™ PCR Arrays from SuperArray, containing primer pairs that have been experimentally validated to ensure gene-specificity and high amplification efficiency. RESULTS: The SYBR Green PCR Arrays exhibit good reproducibility among different users, PCR instruments and test sites. In addition, the SYBR Green PCR Arrays have the highest concordance with TaqMan PCR, and a high level of concordance with other quantitative methods and microarrays that were evaluated in this study in terms of fold-change correlation and overlap of lists of differentially expressed genes. CONCLUSION: These data demonstrate that SYBR Green real-time PCR delivers highly comparable results in gene expression measurement with TaqMan PCR and other high-density microarrays. BioMed Central 2008-07-11 /pmc/articles/PMC2491643/ /pubmed/18620571 http://dx.doi.org/10.1186/1471-2164-9-328 Text en Copyright © 2008 Arikawa et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Arikawa, Emi
Sun, Yanyang
Wang, Jie
Zhou, Qiong
Ning, Baitang
Dial, Stacey L
Guo, Lei
Yang, Jingping
Cross-platform comparison of SYBR(® )Green real-time PCR with TaqMan PCR, microarrays and other gene expression measurement technologies evaluated in the MicroArray Quality Control (MAQC) study
title Cross-platform comparison of SYBR(® )Green real-time PCR with TaqMan PCR, microarrays and other gene expression measurement technologies evaluated in the MicroArray Quality Control (MAQC) study
title_full Cross-platform comparison of SYBR(® )Green real-time PCR with TaqMan PCR, microarrays and other gene expression measurement technologies evaluated in the MicroArray Quality Control (MAQC) study
title_fullStr Cross-platform comparison of SYBR(® )Green real-time PCR with TaqMan PCR, microarrays and other gene expression measurement technologies evaluated in the MicroArray Quality Control (MAQC) study
title_full_unstemmed Cross-platform comparison of SYBR(® )Green real-time PCR with TaqMan PCR, microarrays and other gene expression measurement technologies evaluated in the MicroArray Quality Control (MAQC) study
title_short Cross-platform comparison of SYBR(® )Green real-time PCR with TaqMan PCR, microarrays and other gene expression measurement technologies evaluated in the MicroArray Quality Control (MAQC) study
title_sort cross-platform comparison of sybr(® )green real-time pcr with taqman pcr, microarrays and other gene expression measurement technologies evaluated in the microarray quality control (maqc) study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2491643/
https://www.ncbi.nlm.nih.gov/pubmed/18620571
http://dx.doi.org/10.1186/1471-2164-9-328
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