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Unlocking the potential of publicly available microarray data using inSilicoDb and inSilicoMerging R/Bioconductor packages

BACKGROUND: With an abundant amount of microarray gene expression data sets available through public repositories, new possibilities lie in combining multiple existing data sets. In this new context, analysis itself is no longer the problem, but retrieving and consistently integrating all this data...

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Autores principales: Taminau, Jonatan, Meganck, Stijn, Lazar, Cosmin, Steenhoff, David, Coletta, Alain, Molter, Colin, Duque, Robin, Schaetzen, Virginie de, Weiss Solís, David Y, Bersini, Hugues, Nowé, Ann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3568420/
https://www.ncbi.nlm.nih.gov/pubmed/23259851
http://dx.doi.org/10.1186/1471-2105-13-335
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author Taminau, Jonatan
Meganck, Stijn
Lazar, Cosmin
Steenhoff, David
Coletta, Alain
Molter, Colin
Duque, Robin
Schaetzen, Virginie de
Weiss Solís, David Y
Bersini, Hugues
Nowé, Ann
author_facet Taminau, Jonatan
Meganck, Stijn
Lazar, Cosmin
Steenhoff, David
Coletta, Alain
Molter, Colin
Duque, Robin
Schaetzen, Virginie de
Weiss Solís, David Y
Bersini, Hugues
Nowé, Ann
author_sort Taminau, Jonatan
collection PubMed
description BACKGROUND: With an abundant amount of microarray gene expression data sets available through public repositories, new possibilities lie in combining multiple existing data sets. In this new context, analysis itself is no longer the problem, but retrieving and consistently integrating all this data before delivering it to the wide variety of existing analysis tools becomes the new bottleneck. RESULTS: We present the newly released inSilicoMerging R/Bioconductor package which, together with the earlier released inSilicoDb R/Bioconductor package, allows consistent retrieval, integration and analysis of publicly available microarray gene expression data sets. Inside the inSilicoMerging package a set of five visual and six quantitative validation measures are available as well. CONCLUSIONS: By providing (i) access to uniformly curated and preprocessed data, (ii) a collection of techniques to remove the batch effects between data sets from different sources, and (iii) several validation tools enabling the inspection of the integration process, these packages enable researchers to fully explore the potential of combining gene expression data for downstream analysis. The power of using both packages is demonstrated by programmatically retrieving and integrating gene expression studies from the InSilico DB repository [https://insilicodb.org/app/].
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spelling pubmed-35684202013-02-11 Unlocking the potential of publicly available microarray data using inSilicoDb and inSilicoMerging R/Bioconductor packages Taminau, Jonatan Meganck, Stijn Lazar, Cosmin Steenhoff, David Coletta, Alain Molter, Colin Duque, Robin Schaetzen, Virginie de Weiss Solís, David Y Bersini, Hugues Nowé, Ann BMC Bioinformatics Software BACKGROUND: With an abundant amount of microarray gene expression data sets available through public repositories, new possibilities lie in combining multiple existing data sets. In this new context, analysis itself is no longer the problem, but retrieving and consistently integrating all this data before delivering it to the wide variety of existing analysis tools becomes the new bottleneck. RESULTS: We present the newly released inSilicoMerging R/Bioconductor package which, together with the earlier released inSilicoDb R/Bioconductor package, allows consistent retrieval, integration and analysis of publicly available microarray gene expression data sets. Inside the inSilicoMerging package a set of five visual and six quantitative validation measures are available as well. CONCLUSIONS: By providing (i) access to uniformly curated and preprocessed data, (ii) a collection of techniques to remove the batch effects between data sets from different sources, and (iii) several validation tools enabling the inspection of the integration process, these packages enable researchers to fully explore the potential of combining gene expression data for downstream analysis. The power of using both packages is demonstrated by programmatically retrieving and integrating gene expression studies from the InSilico DB repository [https://insilicodb.org/app/]. BioMed Central 2012-12-24 /pmc/articles/PMC3568420/ /pubmed/23259851 http://dx.doi.org/10.1186/1471-2105-13-335 Text en Copyright ©2012 Taminau 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
Taminau, Jonatan
Meganck, Stijn
Lazar, Cosmin
Steenhoff, David
Coletta, Alain
Molter, Colin
Duque, Robin
Schaetzen, Virginie de
Weiss Solís, David Y
Bersini, Hugues
Nowé, Ann
Unlocking the potential of publicly available microarray data using inSilicoDb and inSilicoMerging R/Bioconductor packages
title Unlocking the potential of publicly available microarray data using inSilicoDb and inSilicoMerging R/Bioconductor packages
title_full Unlocking the potential of publicly available microarray data using inSilicoDb and inSilicoMerging R/Bioconductor packages
title_fullStr Unlocking the potential of publicly available microarray data using inSilicoDb and inSilicoMerging R/Bioconductor packages
title_full_unstemmed Unlocking the potential of publicly available microarray data using inSilicoDb and inSilicoMerging R/Bioconductor packages
title_short Unlocking the potential of publicly available microarray data using inSilicoDb and inSilicoMerging R/Bioconductor packages
title_sort unlocking the potential of publicly available microarray data using insilicodb and insilicomerging r/bioconductor packages
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3568420/
https://www.ncbi.nlm.nih.gov/pubmed/23259851
http://dx.doi.org/10.1186/1471-2105-13-335
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