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A probe-treatment-reference (PTR) model for the analysis of oligonucleotide expression microarrays
BACKGROUND: Microarray pre-processing usually consists of normalization and summarization. Normalization aims to remove non-biological variations across different arrays. The normalization algorithms generally require the specification of reference and target arrays. The issue of reference selection...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2375129/ https://www.ncbi.nlm.nih.gov/pubmed/18410691 http://dx.doi.org/10.1186/1471-2105-9-194 |
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author | Ge, Huanying Cheng, Chao Li, Lei M |
author_facet | Ge, Huanying Cheng, Chao Li, Lei M |
author_sort | Ge, Huanying |
collection | PubMed |
description | BACKGROUND: Microarray pre-processing usually consists of normalization and summarization. Normalization aims to remove non-biological variations across different arrays. The normalization algorithms generally require the specification of reference and target arrays. The issue of reference selection has not been fully addressed. Summarization aims to estimate the transcript abundance from normalized intensities. In this paper, we consider normalization and summarization jointly by a new strategy of reference selection. RESULTS: We propose a Probe-Treatment-Reference (PTR) model to streamline normalization and summarization by allowing multiple references. We estimate parameters in the model by the Least Absolute Deviations (LAD) approach and implement the computation by median polishing. We show that the LAD estimator is robust in the sense that it has bounded influence in the three-factor PTR model. This model fitting, implicitly, defines an "optimal reference" for each probe-set. We evaluate the effectiveness of the PTR method by two Affymetrix spike-in data sets. Our method reduces the variations of non-differentially expressed genes and thereby increases the detection power of differentially expressed genes. CONCLUSION: Our results indicate that the reference effect is important and should be considered in microarray pre-processing. The proposed PTR method is a general framework to deal with the issue of reference selection and can readily be applied to existing normalization algorithms such as the invariant-set, sub-array and quantile method. |
format | Text |
id | pubmed-2375129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-23751292008-05-12 A probe-treatment-reference (PTR) model for the analysis of oligonucleotide expression microarrays Ge, Huanying Cheng, Chao Li, Lei M BMC Bioinformatics Methodology Article BACKGROUND: Microarray pre-processing usually consists of normalization and summarization. Normalization aims to remove non-biological variations across different arrays. The normalization algorithms generally require the specification of reference and target arrays. The issue of reference selection has not been fully addressed. Summarization aims to estimate the transcript abundance from normalized intensities. In this paper, we consider normalization and summarization jointly by a new strategy of reference selection. RESULTS: We propose a Probe-Treatment-Reference (PTR) model to streamline normalization and summarization by allowing multiple references. We estimate parameters in the model by the Least Absolute Deviations (LAD) approach and implement the computation by median polishing. We show that the LAD estimator is robust in the sense that it has bounded influence in the three-factor PTR model. This model fitting, implicitly, defines an "optimal reference" for each probe-set. We evaluate the effectiveness of the PTR method by two Affymetrix spike-in data sets. Our method reduces the variations of non-differentially expressed genes and thereby increases the detection power of differentially expressed genes. CONCLUSION: Our results indicate that the reference effect is important and should be considered in microarray pre-processing. The proposed PTR method is a general framework to deal with the issue of reference selection and can readily be applied to existing normalization algorithms such as the invariant-set, sub-array and quantile method. BioMed Central 2008-04-14 /pmc/articles/PMC2375129/ /pubmed/18410691 http://dx.doi.org/10.1186/1471-2105-9-194 Text en Copyright © 2008 Ge 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 | Methodology Article Ge, Huanying Cheng, Chao Li, Lei M A probe-treatment-reference (PTR) model for the analysis of oligonucleotide expression microarrays |
title | A probe-treatment-reference (PTR) model for the analysis of oligonucleotide expression microarrays |
title_full | A probe-treatment-reference (PTR) model for the analysis of oligonucleotide expression microarrays |
title_fullStr | A probe-treatment-reference (PTR) model for the analysis of oligonucleotide expression microarrays |
title_full_unstemmed | A probe-treatment-reference (PTR) model for the analysis of oligonucleotide expression microarrays |
title_short | A probe-treatment-reference (PTR) model for the analysis of oligonucleotide expression microarrays |
title_sort | probe-treatment-reference (ptr) model for the analysis of oligonucleotide expression microarrays |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2375129/ https://www.ncbi.nlm.nih.gov/pubmed/18410691 http://dx.doi.org/10.1186/1471-2105-9-194 |
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