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An algorithm for automatic evaluation of the spot quality in two-color DNA microarray experiments
BACKGROUND: Although DNA microarray technologies are very powerful for the simultaneous quantitative characterization of thousands of genes, the quality of the obtained experimental data is often far from ideal. The measured microarrays images represent a regular collection of spots, and the intensi...
Autores principales: | , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2005
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1369007/ https://www.ncbi.nlm.nih.gov/pubmed/16336688 http://dx.doi.org/10.1186/1471-2105-6-293 |
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author | Novikov, Eugene Barillot, Emmanuel |
author_facet | Novikov, Eugene Barillot, Emmanuel |
author_sort | Novikov, Eugene |
collection | PubMed |
description | BACKGROUND: Although DNA microarray technologies are very powerful for the simultaneous quantitative characterization of thousands of genes, the quality of the obtained experimental data is often far from ideal. The measured microarrays images represent a regular collection of spots, and the intensity of light at each spot is proportional to the DNA copy number or to the expression level of the gene whose DNA clone is spotted. Spot quality control is an essential part of microarray image analysis, which must be carried out at the level of individual spot identification. The problem is difficult to formalize due to the diversity of instrumental and biological factors that can influence the result. RESULTS: For each spot we estimate the ratio of measured fluorescence intensities revealing differential gene expression or change in DNA copy numbers between the test and control samples. We also define a set of quality characteristics and a model for combining these characteristics into an overall spot quality value. We have developed a training procedure to evaluate the contribution of each individual characteristic in the overall quality. This procedure uses information available from replicated spots, located in the same array or over a set of replicated arrays. It is assumed that unspoiled replicated spots must have very close ratios, whereas poor spots yield greater diversity in the obtained ratio estimates. CONCLUSION: The developed procedure provides an automatic tool to quantify spot quality and to identify different types of spot deficiency occurring in DNA microarray technology. Quality values assigned to each spot can be used either to eliminate spots or to weight contribution of each ratio estimate in follow-up analysis procedures. |
format | Text |
id | pubmed-1369007 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-13690072006-02-28 An algorithm for automatic evaluation of the spot quality in two-color DNA microarray experiments Novikov, Eugene Barillot, Emmanuel BMC Bioinformatics Methodology Article BACKGROUND: Although DNA microarray technologies are very powerful for the simultaneous quantitative characterization of thousands of genes, the quality of the obtained experimental data is often far from ideal. The measured microarrays images represent a regular collection of spots, and the intensity of light at each spot is proportional to the DNA copy number or to the expression level of the gene whose DNA clone is spotted. Spot quality control is an essential part of microarray image analysis, which must be carried out at the level of individual spot identification. The problem is difficult to formalize due to the diversity of instrumental and biological factors that can influence the result. RESULTS: For each spot we estimate the ratio of measured fluorescence intensities revealing differential gene expression or change in DNA copy numbers between the test and control samples. We also define a set of quality characteristics and a model for combining these characteristics into an overall spot quality value. We have developed a training procedure to evaluate the contribution of each individual characteristic in the overall quality. This procedure uses information available from replicated spots, located in the same array or over a set of replicated arrays. It is assumed that unspoiled replicated spots must have very close ratios, whereas poor spots yield greater diversity in the obtained ratio estimates. CONCLUSION: The developed procedure provides an automatic tool to quantify spot quality and to identify different types of spot deficiency occurring in DNA microarray technology. Quality values assigned to each spot can be used either to eliminate spots or to weight contribution of each ratio estimate in follow-up analysis procedures. BioMed Central 2005-12-09 /pmc/articles/PMC1369007/ /pubmed/16336688 http://dx.doi.org/10.1186/1471-2105-6-293 Text en Copyright © 2005 Novikov and Barillot; 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 Novikov, Eugene Barillot, Emmanuel An algorithm for automatic evaluation of the spot quality in two-color DNA microarray experiments |
title | An algorithm for automatic evaluation of the spot quality in two-color DNA microarray experiments |
title_full | An algorithm for automatic evaluation of the spot quality in two-color DNA microarray experiments |
title_fullStr | An algorithm for automatic evaluation of the spot quality in two-color DNA microarray experiments |
title_full_unstemmed | An algorithm for automatic evaluation of the spot quality in two-color DNA microarray experiments |
title_short | An algorithm for automatic evaluation of the spot quality in two-color DNA microarray experiments |
title_sort | algorithm for automatic evaluation of the spot quality in two-color dna microarray experiments |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1369007/ https://www.ncbi.nlm.nih.gov/pubmed/16336688 http://dx.doi.org/10.1186/1471-2105-6-293 |
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