Skip Navigation

This Article
Right arrow FREE Full Text (Print PDF) Freely available
Right arrow FREE Full Text (Screen PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (40)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by He, Y. D.
Right arrow Articles by Stoughton, R. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by He, Y. D.
Right arrow Articles by Stoughton, R. B.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Bioinformatics Vol. 19 no. 8 2003
Pages 956-965
© 2003 Oxford University Press

Microarray standard data set and figures of merit for comparing data processing methods and experiment designs

Yudong D. He , Hongyue Dai , Eric E. Schadt , Guy Cavet , Stephen W. Edwards , Sergey B. Stepaniants , Sven Duenwald , Robert Kleinhanz , Allan R. Jones , Daniel D. Shoemaker and Roland B. Stoughton *

Rosetta Inpharmatics Inc.,{dagger},12 040 115th Avenue Northeast, Kirkland, WA 98034, USA

Received on July 24, 2002 ; revised on October 16, 2002 and December 17, 2002 ; accepted on December 22, 2002

Motivation: There is a very large and growing level of effort toward improving the platforms, experiment designs, and data analysis methods for microarray expression profiling. Along with a growing richness in the approaches there is a growing confusion among most scientists as to how to make objective comparisons and choices between them for different applications. There is a need for a standard framework for the microarray community to compare and improve analytical and statistical methods.

Results: We report on a microarray data set comprising 204 in-situ synthesized oligonucleotide arrays, each hybridized with two-color cDNA samples derived from 20 different human tissues and cell lines. Design of the ~ 24 000 60mer oligonucleotides that report ~2500 known genes on the arrays, and design of the hybridization experiments, were carried out in a way that supports the performance assessment of alternative data processing approaches and of alternative experiment and array designs. We also propose standard figures of merit for success in detecting individual differential expression changes or expression levels, and for detecting similarities and differences in expression patterns across genes and experiments. We expect this data set and the proposed figures of merit will provide a standard framework for much of the microarray community to compare and improve many analytical and statistical methods relevant to microarray data analysis, including image processing, normalization, error modeling, combining of multiple reporters per gene, use of replicate experiments, and sample referencing schemes in measurements based on expression change.

Availability/Supplementary information: Expression data and supplementary information are available at http://www.rii.com/publications/2003/HE_SDS.htm

Contact: yudong_he{at}merck.com

* To whom correspondence should be addressed.

{dagger} A wholly owned subsidiary of Merck & Co., Inc.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Genome ResHome page
M. P. Keller, Y. Choi, P. Wang, D. Belt Davis, M. E. Rabaglia, A. T. Oler, D. S. Stapleton, C. Argmann, K. L. Schueler, S. Edwards, et al.
A gene expression network model of type 2 diabetes links cell cycle regulation in islets with diabetes susceptibility
Genome Res., May 1, 2008; 18(5): 706 - 716.
[Abstract] [Full Text] [PDF]


Home page
Physiol. GenomicsHome page
K. H. Clodfelter, G. D. Miles, V. Wauthier, M. G. Holloway, X. Zhang, P. Hodor, W. J. Ray, and D. J. Waxman
Role of STAT5a in regulation of sex-specific gene expression in female but not male mouse liver revealed by microarray analysis
Physiol Genomics, September 11, 2007; 31(1): 63 - 74.
[Abstract] [Full Text] [PDF]


Home page
Circ. Res.Home page
S. S. Wang, E. E. Schadt, H. Wang, X. Wang, L. Ingram-Drake, W. Shi, T. A. Drake, and A. J. Lusis
Identification of Pathways for Atherosclerosis in Mice: Integration of Quantitative Trait Locus Analysis and Global Gene Expression Data
Circ. Res., August 3, 2007; 101(3): e11 - e30.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
P. Stafford and M. Brun
Three methods for optimization of cross-laboratory and cross-platform microarray expression data
Nucleic Acids Res., May 11, 2007; 35(10): e72 - e72.
[Abstract] [Full Text] [PDF]


Home page
Genome ResHome page
X. Yang, E. E. Schadt, S. Wang, H. Wang, A. P. Arnold, L. Ingram-Drake, T. A. Drake, and A. J. Lusis
Tissue-specific expression and regulation of sexually dimorphic genes in mice
Genome Res., August 1, 2006; 16(8): 995 - 1004.
[Abstract] [Full Text] [PDF]


Home page
BioinformaticsHome page
L. Weng, H. Dai, Y. Zhan, Y. He, S. B. Stepaniants, and D. E. Bassett
Rosetta error model for gene expression analysis
Bioinformatics, May 1, 2006; 22(9): 1111 - 1121.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
K. L. Thompson, B. A. Rosenzweig, P. S. Pine, J. Retief, Y. Turpaz, C. A. Afshari, H. K. Hamadeh, M. A. Damore, M. Boedigheimer, E. Blomme, et al.
Use of a mixed tissue RNA design for performance assessments on multiple microarray formats
Nucleic Acids Res., December 23, 2005; 33(22): e187 - e187.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
J. I. Young, E. P. Hong, J. C. Castle, J. Crespo-Barreto, A. B. Bowman, M. F. Rose, D. Kang, R. Richman, J. M. Johnson, S. Berget, et al.
Inaugural Article: Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2
PNAS, December 6, 2005; 102(49): 17551 - 17558.
[Abstract] [Full Text] [PDF]


Home page
Genome ResHome page
S. Doss, E. E. Schadt, T. A. Drake, and A. J. Lusis
Cis-acting expression quantitative trait loci in mice
Genome Res., May 1, 2005; 15(5): 681 - 691.
[Abstract] [Full Text] [PDF]


Home page
DiabetesHome page
R. C. Davis, E. E. Schadt, A. C.L. Cervino, M. Peterfy, and A. J. Lusis
Ultrafine Mapping of SNPs From Mouse Strains C57BL/6J, DBA/2J, and C57BLKS/J for Loci Contributing to Diabetes and Atherosclerosis Susceptibility
Diabetes, April 1, 2005; 54(4): 1191 - 1199.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
C. K. Raymond, J. Castle, P. Garrett-Engele, C. D. Armour, Z. Kan, N. Tsinoremas, and J. M. Johnson
Expression of Alternatively Spliced Sodium Channel {alpha}-Subunit Genes: UNIQUE SPLICING PATTERNS ARE OBSERVED IN DORSAL ROOT GANGLIA
J. Biol. Chem., October 29, 2004; 279(44): 46234 - 46241.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. ProteomicsHome page
Q. Tian, S. B. Stepaniants, M. Mao, L. Weng, M. C. Feetham, M. J. Doyle, E. C. Yi, H. Dai, V. Thorsson, J. Eng, et al.
Integrated Genomic and Proteomic Analyses of Gene Expression in Mammalian Cells
Mol. Cell. Proteomics, October 1, 2004; 3(10): 960 - 969.
[Abstract] [Full Text] [PDF]


Home page
Mol. Pharmacol.Home page
D. P. Hartley, X. Dai, Y. D. He, E. J. Carlini, B. Wang, S.-e. W. Huskey, R. G. Ulrich, T. H. Rushmore, R. Evers, and D. C. Evans
Activators of the Rat Pregnane X Receptor Differentially Modulate Hepatic and Intestinal Gene Expression
Mol. Pharmacol., May 1, 2004; 65(5): 1159 - 1171.
[Abstract] [Full Text]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.