CTen: a web-based platform for identifying enriched cell types from heterogeneous microarray data

被引:78
|
作者
Shoemaker, Jason E. [1 ]
Lopes, Tiago J. S. [1 ]
Ghosh, Samik [2 ]
Matsuoka, Yukiko [1 ,2 ]
Kawaoka, Yoshihiro [1 ,3 ,4 ]
Kitano, Hiroaki [1 ,2 ,5 ,6 ]
机构
[1] JST ERATO KAWAOKA Infect Induced Host Responses P, Tokyo, Japan
[2] Syst Biol Inst, Tokyo, Japan
[3] Univ Wisconsin, Sch Vet Med, Dept Pathobiol Sci, Influenza Res Inst, Madison, WI 53706 USA
[4] Univ Tokyo, Inst Med Sci, Dept Microbiol & Immunol, Div Virol, Tokyo, Japan
[5] Sony Comp Sci Labs Inc, Tokyo, Japan
[6] Okinawa Inst Sci & Technol, Open Biol Unit, Okinawa, Japan
来源
BMC GENOMICS | 2012年 / 13卷
关键词
Cell type enrichment; Microarray data; Deconvolution; Influenza; Systems immunology; IMMUNE-RESPONSE; GENE; TRANSCRIPTOMES; BIOLOGY; SYSTEMS; VIRUS;
D O I
10.1186/1471-2164-13-460
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
Background: Interpreting in vivo sampled microarray data is often complicated by changes in the cell population demographics. To put gene expression into its proper biological context, it is necessary to distinguish differential gene transcription from artificial gene expression induced by changes in the cellular demographics. Results: CTen (cell type enrichment) is a web-based analytical tool which uses our highly expressed, cell specific (HECS) gene database to identify enriched cell types in heterogeneous microarray data. The web interface is designed for differential expression and gene clustering studies, and the enrichment results are presented as heatmaps or downloadable text files. Conclusions: In this work, we use an independent, cell-specific gene expression data set to assess CTen's performance in accurately identifying the appropriate cell type and provide insight into the suggested level of enrichment to optimally minimize the number of false discoveries. We show that CTen, when applied to microarray data developed from infected lung tissue, can correctly identify the cell signatures of key lymphocytes in a highly heterogeneous environment and compare its performance to another popular bioinformatics tool. Furthermore, we discuss the strong implications cell type enrichment has in the design of effective microarray workflow strategies and show that, by combining CTen with gene expression clustering, we may be able to determine the relative changes in the number of key cell types. CTen is available at http://www.influenza-x.org/similar to jshoemaker/cten/
引用
收藏
页数:11
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