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PMID: 10964511 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Direct comparison of GeneChip and SAGE on the quantitative accuracy in transcript profiling analysis.

Genomics ·Vol. 68 ·No. 2 ·2000-09-01 ·Pages 136-43

Ishii M, Hashimoto S, Tsutsumi S, Wada Y, Matsushima K, Kodama T, Aburatani H

Abstract

Among the high-throughput, comprehensive technological methods used to analyze transcript expression levels, array-based hybridization and serial analysis of gene expression (SAGE) are currently the most common approaches. To compare the quantitative accuracy of oligonucleotide array and SAGE, both methods were carried out on identical RNA specimens prepared from human blood monocytes and granulocyte-macrophage colony-stimulating factor (GM-CSF)-induced macrophages. For SAGE analysis, 57,560 and 57,463 tags were obtained from monocytes and macrophages, respectively, resulting in approximately 28,000 different tags, while oligo array hybridization was performed with GeneChip (Affymetrix), which represents approximately 6000 transcripts. These two methods correlated quite well in both absolute expression analyses and comparative analyses during differentiation. The correlation was better for genes with higher expression levels and greater changes in expression. This finding suggests that GeneChip technology is reasonably reliable for quantitative analysis of expression profiling and would be appropriate as a common platform upon which to build a gene expression database.

MeSH Terms
Gene Expression Profiling Granulocyte-Macrophage Colony-Stimulating Factor/pharmacology Humans Macrophages/cytology,drug effects,metabolism Monocytes/cytology,metabolism Oligonucleotide Array Sequence Analysis RNA, Messenger/analysis,genetics Reproducibility of Results
Chemicals
RNA, Messenger Granulocyte-Macrophage Colony-Stimulating Factor
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Ishii M
Genome Science Division, Research Center for Advanced Science and Technology, Tokyo, Japan.
Hashimoto S
Tsutsumi S
Wada Y
Matsushima K
Kodama T
Aburatani H
Article Info
Journal
Genomics
Abbr.
Genomics
ISSN
0888-7543
Published
2000-09-01
Pages
136-43
Language
English
Region
United States
NLM ID
8800135
Subset
IM
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