TY - JOUR
T1 - A PCR primer bank for quantitative gene expression analysis
AU - Wang, Xiaowei
AU - Seed, Brian
N1 - Funding Information:
We thank our colleagues Yi Yang, Amy Stirman, Shukui Guan, Glenn Short and Najib El Messadi for their contributions. We also thank Mason Freeman and Harry Bjorkbacka for useful discussions and primer testing. This research was supported by PGA grant U01 HL66678 from the National Heart, Lung and Blood Institute.
Publisher Copyright:
© Oxford University Press 2003; all rights reserved.
PY - 2003/12/15
Y1 - 2003/12/15
N2 - Although gene expression profiling by microarray analysis is a useful tool for assessing global levels of transcriptional activity, variability associated with the data sets usually requires that observed differences be validated by some other method, such as real-time quantitative polymerase chain reaction (real-time PCR). However, non-specific amplification of non-target genes is frequently observed in the latter, confounding the analysis in ~40% of real-time PCR attempts when primer-specific labels are not used. Here we present an experimentally validated algorithm for the identification of transcript-specific PCR primers on a genomic scale that can be applied to real-time PCR with sequence-independent detection methods. An online database, PrimerBank, has been created for researchers to retrieve primer information for their genes of interest. PrimerBank currently contains 147 404 primers encompassing most known human and mouse genes. The primer design algorithm has been tested by conventional and real-time PCR for a subset of 112 primer pairs with a success rate of 98.2%.
AB - Although gene expression profiling by microarray analysis is a useful tool for assessing global levels of transcriptional activity, variability associated with the data sets usually requires that observed differences be validated by some other method, such as real-time quantitative polymerase chain reaction (real-time PCR). However, non-specific amplification of non-target genes is frequently observed in the latter, confounding the analysis in ~40% of real-time PCR attempts when primer-specific labels are not used. Here we present an experimentally validated algorithm for the identification of transcript-specific PCR primers on a genomic scale that can be applied to real-time PCR with sequence-independent detection methods. An online database, PrimerBank, has been created for researchers to retrieve primer information for their genes of interest. PrimerBank currently contains 147 404 primers encompassing most known human and mouse genes. The primer design algorithm has been tested by conventional and real-time PCR for a subset of 112 primer pairs with a success rate of 98.2%.
UR - http://www.scopus.com/inward/record.url?scp=85074914953&partnerID=8YFLogxK
U2 - 10.1093/nar/gng154
DO - 10.1093/nar/gng154
M3 - Article
C2 - 14654707
AN - SCOPUS:85074914953
SN - 0305-1048
VL - 31
JO - Nucleic acids research
JF - Nucleic acids research
IS - 24
M1 - e154
ER -