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Use of a mixed tissue RNA design for performance assessments on multiple microarray formats.

Authors :
Thompson KL
Rosenzweig BA
Pine PS
Retief J
Turpaz Y
Afshari CA
Hamadeh HK
Damore MA
Boedigheimer M
Blomme E
Ciurlionis R
Waring JF
Fuscoe JC
Paules R
Tucker CJ
Fare T
Coffey EM
He Y
Collins PJ
Jarnagin K
Fujimoto S
Ganter B
Kiser G
Kaysser-Kranich T
Sina J
Sistare FD
Source :
Nucleic acids research [Nucleic Acids Res] 2005 Dec 23; Vol. 33 (22), pp. e187. Date of Electronic Publication: 2005 Dec 23.
Publication Year :
2005

Abstract

The comparability and reliability of data generated using microarray technology would be enhanced by use of a common set of standards that allow accuracy, reproducibility and dynamic range assessments on multiple formats. We designed and tested a complex biological reagent for performance measurements on three commercial oligonucleotide array formats that differ in probe design and signal measurement methodology. The reagent is a set of two mixtures with different proportions of RNA for each of four rat tissues (brain, liver, kidney and testes). The design provides four known ratio measurements of >200 reference probes, which were chosen for their tissue-selectivity, dynamic range coverage and alignment to the same exemplar transcript sequence across all three platforms. The data generated from testing three biological replicates of the reagent at eight laboratories on three array formats provides a benchmark set for both laboratory and data processing performance assessments. Close agreement with target ratios adjusted for sample complexity was achieved on all platforms and low variance was observed among platforms, replicates and sites. The mixed tissue design produces a reagent with known gene expression changes within a complex sample and can serve as a paradigm for performance standards for microarrays that target other species.

Details

Language :
English
ISSN :
1362-4962
Volume :
33
Issue :
22
Database :
MEDLINE
Journal :
Nucleic acids research
Publication Type :
Academic Journal
Accession number :
16377776
Full Text :
https://doi.org/10.1093/nar/gni186