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DBNorm: normalizing high-density oligonucleotide microarray data based on distributions
BACKGROUND: Data from patients with rare diseases is often produced using different platforms and probe sets because patients are widely distributed in space and time. Aggregating such data requires a method of normalization that makes patient records comparable. RESULTS: This paper proposed DBNorm,...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5706403/ https://www.ncbi.nlm.nih.gov/pubmed/29187149 http://dx.doi.org/10.1186/s12859-017-1912-5 |
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author | Meng, Qinxue Catchpoole, Daniel Skillicorn, David Kennedy, Paul J. |
author_facet | Meng, Qinxue Catchpoole, Daniel Skillicorn, David Kennedy, Paul J. |
author_sort | Meng, Qinxue |
collection | PubMed |
description | BACKGROUND: Data from patients with rare diseases is often produced using different platforms and probe sets because patients are widely distributed in space and time. Aggregating such data requires a method of normalization that makes patient records comparable. RESULTS: This paper proposed DBNorm, implemented as an R package, is an algorithm that normalizes arbitrarily distributed data to a common, comparable form. Specifically, DBNorm merges data distributions by fitting functions to each of them, and using the probability of each element drawn from the fitted distribution to merge it into a global distribution. DBNorm contains state-of-the-art fitting functions including Polynomial, Fourier and Gaussian distributions, and also allows users to define their own fitting functions if required. CONCLUSIONS: The performance of DBNorm is compared with z-score, average difference, quantile normalization and ComBat on a set of datasets, including several that are publically available. The performance of these normalization methods are compared using statistics, visualization, and classification when class labels are known based on a number of self-generated and public microarray datasets. The experimental results show that DBNorm achieves better normalization results than conventional methods. Finally, the approach has the potential to be applicable outside bioinformatics analysis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-017-1912-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5706403 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57064032017-12-06 DBNorm: normalizing high-density oligonucleotide microarray data based on distributions Meng, Qinxue Catchpoole, Daniel Skillicorn, David Kennedy, Paul J. BMC Bioinformatics Software BACKGROUND: Data from patients with rare diseases is often produced using different platforms and probe sets because patients are widely distributed in space and time. Aggregating such data requires a method of normalization that makes patient records comparable. RESULTS: This paper proposed DBNorm, implemented as an R package, is an algorithm that normalizes arbitrarily distributed data to a common, comparable form. Specifically, DBNorm merges data distributions by fitting functions to each of them, and using the probability of each element drawn from the fitted distribution to merge it into a global distribution. DBNorm contains state-of-the-art fitting functions including Polynomial, Fourier and Gaussian distributions, and also allows users to define their own fitting functions if required. CONCLUSIONS: The performance of DBNorm is compared with z-score, average difference, quantile normalization and ComBat on a set of datasets, including several that are publically available. The performance of these normalization methods are compared using statistics, visualization, and classification when class labels are known based on a number of self-generated and public microarray datasets. The experimental results show that DBNorm achieves better normalization results than conventional methods. Finally, the approach has the potential to be applicable outside bioinformatics analysis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-017-1912-5) contains supplementary material, which is available to authorized users. BioMed Central 2017-11-29 /pmc/articles/PMC5706403/ /pubmed/29187149 http://dx.doi.org/10.1186/s12859-017-1912-5 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Software Meng, Qinxue Catchpoole, Daniel Skillicorn, David Kennedy, Paul J. DBNorm: normalizing high-density oligonucleotide microarray data based on distributions |
title | DBNorm: normalizing high-density oligonucleotide microarray data based on distributions |
title_full | DBNorm: normalizing high-density oligonucleotide microarray data based on distributions |
title_fullStr | DBNorm: normalizing high-density oligonucleotide microarray data based on distributions |
title_full_unstemmed | DBNorm: normalizing high-density oligonucleotide microarray data based on distributions |
title_short | DBNorm: normalizing high-density oligonucleotide microarray data based on distributions |
title_sort | dbnorm: normalizing high-density oligonucleotide microarray data based on distributions |
topic | Software |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5706403/ https://www.ncbi.nlm.nih.gov/pubmed/29187149 http://dx.doi.org/10.1186/s12859-017-1912-5 |
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