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CTen: a web-based platform for identifying enriched cell types from heterogeneous microarray data
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 i...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3473317/ https://www.ncbi.nlm.nih.gov/pubmed/22953731 http://dx.doi.org/10.1186/1471-2164-13-460 |
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author | Shoemaker, Jason E Lopes, Tiago JS Ghosh, Samik Matsuoka, Yukiko Kawaoka, Yoshihiro Kitano, Hiroaki |
author_facet | Shoemaker, Jason E Lopes, Tiago JS Ghosh, Samik Matsuoka, Yukiko Kawaoka, Yoshihiro Kitano, Hiroaki |
author_sort | Shoemaker, Jason E |
collection | PubMed |
description | 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/~jshoemaker/cten/ |
format | Online Article Text |
id | pubmed-3473317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34733172012-10-18 CTen: a web-based platform for identifying enriched cell types from heterogeneous microarray data Shoemaker, Jason E Lopes, Tiago JS Ghosh, Samik Matsuoka, Yukiko Kawaoka, Yoshihiro Kitano, Hiroaki BMC Genomics Software 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/~jshoemaker/cten/ BioMed Central 2012-09-06 /pmc/articles/PMC3473317/ /pubmed/22953731 http://dx.doi.org/10.1186/1471-2164-13-460 Text en Copyright ©2012 Shoemaker et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Software Shoemaker, Jason E Lopes, Tiago JS Ghosh, Samik Matsuoka, Yukiko Kawaoka, Yoshihiro Kitano, Hiroaki CTen: a web-based platform for identifying enriched cell types from heterogeneous microarray data |
title | CTen: a web-based platform for identifying enriched cell types from heterogeneous microarray data |
title_full | CTen: a web-based platform for identifying enriched cell types from heterogeneous microarray data |
title_fullStr | CTen: a web-based platform for identifying enriched cell types from heterogeneous microarray data |
title_full_unstemmed | CTen: a web-based platform for identifying enriched cell types from heterogeneous microarray data |
title_short | CTen: a web-based platform for identifying enriched cell types from heterogeneous microarray data |
title_sort | cten: a web-based platform for identifying enriched cell types from heterogeneous microarray data |
topic | Software |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3473317/ https://www.ncbi.nlm.nih.gov/pubmed/22953731 http://dx.doi.org/10.1186/1471-2164-13-460 |
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