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

摘要

BackgroundThe 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 RT² Profiler™ PCR Arrays from SuperArray, containing primer pairs that have been experimentally validated to ensure gene-specificity and high amplification efficiency.