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Statistical monitoring of weak spots for improvement of normalization and ratio estimates in microarrays
BACKGROUND: Several aspects of microarray data analysis are dependent on identification of genes expressed at or near the limits of detection. For example, regression-based normalization methods rely on the premise that most genes in compared samples are expressed at similar levels and therefore req...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2004
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC415561/ https://www.ncbi.nlm.nih.gov/pubmed/15128432 http://dx.doi.org/10.1186/1471-2105-5-53 |
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author | Dozmorov, Igor Knowlton, Nicholas Tang, Yuhong Centola, Michael |
author_facet | Dozmorov, Igor Knowlton, Nicholas Tang, Yuhong Centola, Michael |
author_sort | Dozmorov, Igor |
collection | PubMed |
description | BACKGROUND: Several aspects of microarray data analysis are dependent on identification of genes expressed at or near the limits of detection. For example, regression-based normalization methods rely on the premise that most genes in compared samples are expressed at similar levels and therefore require accurate identification of nonexpressed genes (additive noise) so that they can be excluded from the normalization procedure. Moreover, key regulatory genes can maintain stringent control of a given response at low expression levels. If arbitrary cutoffs are used for distinguishing expressed from nonexpressed genes, some of these key regulatory genes may be unnecessarily excluded from the analysis. Unfortunately, no accurate method for differentiating additive noise from genes expressed at low levels is currently available. RESULTS: We developed a multistep procedure for analysis of mRNA expression data that robustly identifies the additive noise in a microarray experiment. This analysis is predicated on the fact that additive noise signals can be accurately identified by both distribution and statistical analysis. CONCLUSIONS: Identification of additive noise in this manner allows exclusion of noncorrelated weak signals from regression-based normalization of compared profiles thus maximizing the accuracy of these methods. Moreover, genes expressed at very low levels can be clearly identified due to the fact that their expression distribution is stable and distinguishable from the random pattern of additive noise. |
format | Text |
id | pubmed-415561 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-4155612004-05-21 Statistical monitoring of weak spots for improvement of normalization and ratio estimates in microarrays Dozmorov, Igor Knowlton, Nicholas Tang, Yuhong Centola, Michael BMC Bioinformatics Methodology Article BACKGROUND: Several aspects of microarray data analysis are dependent on identification of genes expressed at or near the limits of detection. For example, regression-based normalization methods rely on the premise that most genes in compared samples are expressed at similar levels and therefore require accurate identification of nonexpressed genes (additive noise) so that they can be excluded from the normalization procedure. Moreover, key regulatory genes can maintain stringent control of a given response at low expression levels. If arbitrary cutoffs are used for distinguishing expressed from nonexpressed genes, some of these key regulatory genes may be unnecessarily excluded from the analysis. Unfortunately, no accurate method for differentiating additive noise from genes expressed at low levels is currently available. RESULTS: We developed a multistep procedure for analysis of mRNA expression data that robustly identifies the additive noise in a microarray experiment. This analysis is predicated on the fact that additive noise signals can be accurately identified by both distribution and statistical analysis. CONCLUSIONS: Identification of additive noise in this manner allows exclusion of noncorrelated weak signals from regression-based normalization of compared profiles thus maximizing the accuracy of these methods. Moreover, genes expressed at very low levels can be clearly identified due to the fact that their expression distribution is stable and distinguishable from the random pattern of additive noise. BioMed Central 2004-05-05 /pmc/articles/PMC415561/ /pubmed/15128432 http://dx.doi.org/10.1186/1471-2105-5-53 Text en Copyright © 2004 Dozmorov et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL. |
spellingShingle | Methodology Article Dozmorov, Igor Knowlton, Nicholas Tang, Yuhong Centola, Michael Statistical monitoring of weak spots for improvement of normalization and ratio estimates in microarrays |
title | Statistical monitoring of weak spots for improvement of normalization and ratio estimates in microarrays |
title_full | Statistical monitoring of weak spots for improvement of normalization and ratio estimates in microarrays |
title_fullStr | Statistical monitoring of weak spots for improvement of normalization and ratio estimates in microarrays |
title_full_unstemmed | Statistical monitoring of weak spots for improvement of normalization and ratio estimates in microarrays |
title_short | Statistical monitoring of weak spots for improvement of normalization and ratio estimates in microarrays |
title_sort | statistical monitoring of weak spots for improvement of normalization and ratio estimates in microarrays |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC415561/ https://www.ncbi.nlm.nih.gov/pubmed/15128432 http://dx.doi.org/10.1186/1471-2105-5-53 |
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