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Matching of array CGH and gene expression microarray features for the purpose of integrative genomic analyses
BACKGROUND: An increasing number of genomic studies interrogating more than one molecular level is published. Bioinformatics follows biological practice, and recent years have seen a surge in methodology for the integrative analysis of genomic data. Often such analyses require knowledge of which ele...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3475006/ https://www.ncbi.nlm.nih.gov/pubmed/22559006 http://dx.doi.org/10.1186/1471-2105-13-80 |
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author | van Wieringen, Wessel N Unger, Kristian Leday, Gwenaël GR Krijgsman, Oscar de Menezes, Renée X Ylstra, Bauke van de Wiel, Mark A |
author_facet | van Wieringen, Wessel N Unger, Kristian Leday, Gwenaël GR Krijgsman, Oscar de Menezes, Renée X Ylstra, Bauke van de Wiel, Mark A |
author_sort | van Wieringen, Wessel N |
collection | PubMed |
description | BACKGROUND: An increasing number of genomic studies interrogating more than one molecular level is published. Bioinformatics follows biological practice, and recent years have seen a surge in methodology for the integrative analysis of genomic data. Often such analyses require knowledge of which elements of one platform link to those of another. Although important, many integrative analyses do not or insufficiently detail the matching of the platforms. RESULTS: We describe, illustrate and discuss six matching procedures. They are implemented in the R-package sigaR (available from Bioconductor). The principles underlying the presented matching procedures are generic, and can be combined to form new matching approaches or be applied to the matching of other platforms. Illustration of the matching procedures on a variety of data sets reveals how the procedures differ in the use of the available data, and may even lead to different results for individual genes. CONCLUSIONS: Matching of data from multiple genomics platforms is an important preprocessing step for many integrative bioinformatic analysis, for which we present six generic procedures, both old and new. They have been implemented in the R-package sigaR, available from Bioconductor. |
format | Online Article Text |
id | pubmed-3475006 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34750062012-10-19 Matching of array CGH and gene expression microarray features for the purpose of integrative genomic analyses van Wieringen, Wessel N Unger, Kristian Leday, Gwenaël GR Krijgsman, Oscar de Menezes, Renée X Ylstra, Bauke van de Wiel, Mark A BMC Bioinformatics Software BACKGROUND: An increasing number of genomic studies interrogating more than one molecular level is published. Bioinformatics follows biological practice, and recent years have seen a surge in methodology for the integrative analysis of genomic data. Often such analyses require knowledge of which elements of one platform link to those of another. Although important, many integrative analyses do not or insufficiently detail the matching of the platforms. RESULTS: We describe, illustrate and discuss six matching procedures. They are implemented in the R-package sigaR (available from Bioconductor). The principles underlying the presented matching procedures are generic, and can be combined to form new matching approaches or be applied to the matching of other platforms. Illustration of the matching procedures on a variety of data sets reveals how the procedures differ in the use of the available data, and may even lead to different results for individual genes. CONCLUSIONS: Matching of data from multiple genomics platforms is an important preprocessing step for many integrative bioinformatic analysis, for which we present six generic procedures, both old and new. They have been implemented in the R-package sigaR, available from Bioconductor. BioMed Central 2012-05-04 /pmc/articles/PMC3475006/ /pubmed/22559006 http://dx.doi.org/10.1186/1471-2105-13-80 Text en Copyright ©2012 van Wieringen 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 | Software van Wieringen, Wessel N Unger, Kristian Leday, Gwenaël GR Krijgsman, Oscar de Menezes, Renée X Ylstra, Bauke van de Wiel, Mark A Matching of array CGH and gene expression microarray features for the purpose of integrative genomic analyses |
title | Matching of array CGH and gene expression microarray features for the purpose of integrative genomic analyses |
title_full | Matching of array CGH and gene expression microarray features for the purpose of integrative genomic analyses |
title_fullStr | Matching of array CGH and gene expression microarray features for the purpose of integrative genomic analyses |
title_full_unstemmed | Matching of array CGH and gene expression microarray features for the purpose of integrative genomic analyses |
title_short | Matching of array CGH and gene expression microarray features for the purpose of integrative genomic analyses |
title_sort | matching of array cgh and gene expression microarray features for the purpose of integrative genomic analyses |
topic | Software |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3475006/ https://www.ncbi.nlm.nih.gov/pubmed/22559006 http://dx.doi.org/10.1186/1471-2105-13-80 |
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