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A class of models for analyzing GeneChip(® )gene expression analysis array data
BACKGROUND: Various analytical methods exist that first quantify gene expression and then analyze differentially expressed genes from Affymetrix GeneChip(® )gene expression analysis array data. These methods differ in the choice of probe measure (quantification of probe hybridization), summarizing m...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC553974/ https://www.ncbi.nlm.nih.gov/pubmed/15710039 http://dx.doi.org/10.1186/1471-2164-6-16 |
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author | Fan, Wenhong Pritchard, Joel I Olson, James M Khalid, Najma Zhao, Lue Ping |
author_facet | Fan, Wenhong Pritchard, Joel I Olson, James M Khalid, Najma Zhao, Lue Ping |
author_sort | Fan, Wenhong |
collection | PubMed |
description | BACKGROUND: Various analytical methods exist that first quantify gene expression and then analyze differentially expressed genes from Affymetrix GeneChip(® )gene expression analysis array data. These methods differ in the choice of probe measure (quantification of probe hybridization), summarizing multiple probe intensities into a gene expression value, and analysis of differential gene expression. Research papers that describe these methods focus on performance, and how their approaches differ from others. To better understand the common features and differences between various methods, and to evaluate their impact on the results of gene expression analysis, we describe a class of models, referred to as generalized probe models (GPMs), which encompass various currently available methods. RESULTS: Using an empirical dataset, we compared different formulations of GPMs, and GPMs with three other commonly used methods, i.e. MAS 5.0, dChip, and RMA. The comparison shows that, on a genome-wide scale , different methods yield similar results if the same probe measures are chosen. CONCLUSION: In this paper we present a general framework, i.e. GPMs, which encompasses various methods. GPMs permit the use of a wide range of probe measures and facilitate appropriate comparison between commonly used methods. We demonstrate that the dissimilar results stem primarily from different choice of probe measures, rather than other factors. |
format | Text |
id | pubmed-553974 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-5539742005-03-11 A class of models for analyzing GeneChip(® )gene expression analysis array data Fan, Wenhong Pritchard, Joel I Olson, James M Khalid, Najma Zhao, Lue Ping BMC Genomics Research Article BACKGROUND: Various analytical methods exist that first quantify gene expression and then analyze differentially expressed genes from Affymetrix GeneChip(® )gene expression analysis array data. These methods differ in the choice of probe measure (quantification of probe hybridization), summarizing multiple probe intensities into a gene expression value, and analysis of differential gene expression. Research papers that describe these methods focus on performance, and how their approaches differ from others. To better understand the common features and differences between various methods, and to evaluate their impact on the results of gene expression analysis, we describe a class of models, referred to as generalized probe models (GPMs), which encompass various currently available methods. RESULTS: Using an empirical dataset, we compared different formulations of GPMs, and GPMs with three other commonly used methods, i.e. MAS 5.0, dChip, and RMA. The comparison shows that, on a genome-wide scale , different methods yield similar results if the same probe measures are chosen. CONCLUSION: In this paper we present a general framework, i.e. GPMs, which encompasses various methods. GPMs permit the use of a wide range of probe measures and facilitate appropriate comparison between commonly used methods. We demonstrate that the dissimilar results stem primarily from different choice of probe measures, rather than other factors. BioMed Central 2005-02-14 /pmc/articles/PMC553974/ /pubmed/15710039 http://dx.doi.org/10.1186/1471-2164-6-16 Text en Copyright © 2005 Fan 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 | Research Article Fan, Wenhong Pritchard, Joel I Olson, James M Khalid, Najma Zhao, Lue Ping A class of models for analyzing GeneChip(® )gene expression analysis array data |
title | A class of models for analyzing GeneChip(® )gene expression analysis array data |
title_full | A class of models for analyzing GeneChip(® )gene expression analysis array data |
title_fullStr | A class of models for analyzing GeneChip(® )gene expression analysis array data |
title_full_unstemmed | A class of models for analyzing GeneChip(® )gene expression analysis array data |
title_short | A class of models for analyzing GeneChip(® )gene expression analysis array data |
title_sort | class of models for analyzing genechip(® )gene expression analysis array data |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC553974/ https://www.ncbi.nlm.nih.gov/pubmed/15710039 http://dx.doi.org/10.1186/1471-2164-6-16 |
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