Performance comparison of one-color and two-color platforms within the MicroArray Quality Control (MAQC) project

被引:373
作者
Patterson, Tucker A.
Lobenhofer, Edward K.
Fulmer-Smentek, Stephanie B.
Collins, Patrick J.
Chu, Tzu-Ming
Bao, Wenjun
Fang, Hong
Kawasaki, Ernest S.
Hager, Janet
Tikhonova, Irina R.
Walker, Stephen J.
Zhang, Liang
Hurban, Patrick
de Longueville, Francoise
Fuscoe, James C.
Tong, Weida
Shi, Leming
Wolfinger, Russell D.
机构
[1] US FDA, Natl Ctr Toxicol Res, Jefferson, AR 72079 USA
[2] Cogenics, Morrisville, NC 27560 USA
[3] Agilent Technol, Integrated Biol Solut, Santa Clara, CA 95052 USA
[4] SAS Inst Inc, Cary, NC 27513 USA
[5] US FDA, Natl Ctr Toxicol Res, ZTech Corp, Jefferson, AR 72079 USA
[6] NCI, Adv Technol Ctr, Bethesda, MD 20892 USA
[7] Yale Univ, WM Keck Biotechnol Resource Lab, New Haven, CT 06511 USA
[8] Wake Forest Univ, Sch Med, Dept Physiol & Pharmacol, Winston Salem, NC 27101 USA
[9] CapitalBio Corp, Beijing 102206, Peoples R China
[10] EAT, Gene Express Chips, B-5000 Namur, Belgium
关键词
D O I
10.1038/nbt1242
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Microarray-based expression profiling experiments typically use either a one-color or a two-color design to measure mRNA abundance. The validity of each approach has been amply demonstrated. Here we provide a simultaneous comparison of results from one- and two-color labeling designs, using two independent RNA samples from the MicroArray Quality Control (MAQC) project, tested on each of three different microarray platforms. The data were evaluated in terms of reproducibility, specificity, sensitivity and accuracy to determine if the two approaches provide comparable results. For each of the three microarray platforms tested, the results show good agreement with high correlation coefficients and high concordance of differentially expressed gene lists within each platform. Cumulatively, these comparisons indicate that data quality is essentially equivalent between the one- and two-color approaches and strongly suggest that this variable need not be a primary factor in decisions regarding experimental microarray design.
引用
收藏
页码:1140 / 1150
页数:11
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