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arrayMap 2014: an updated cancer genome resource

Somatic copy number aberrations (CNA) represent a mutation type encountered in the majority of cancer genomes. Here, we present the 2014 edition of arrayMap (http://www.arraymap.org), a publicly accessible collection of pre-processed oncogenomic array data sets and CNA profiles, representing a vast...

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Autores principales: Cai, Haoyang, Gupta, Saumya, Rath, Prisni, Ai, Ni, Baudis, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4383937/
https://www.ncbi.nlm.nih.gov/pubmed/25428357
http://dx.doi.org/10.1093/nar/gku1123
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author Cai, Haoyang
Gupta, Saumya
Rath, Prisni
Ai, Ni
Baudis, Michael
author_facet Cai, Haoyang
Gupta, Saumya
Rath, Prisni
Ai, Ni
Baudis, Michael
author_sort Cai, Haoyang
collection PubMed
description Somatic copy number aberrations (CNA) represent a mutation type encountered in the majority of cancer genomes. Here, we present the 2014 edition of arrayMap (http://www.arraymap.org), a publicly accessible collection of pre-processed oncogenomic array data sets and CNA profiles, representing a vast range of human malignancies. Since the initial release, we have enhanced this resource both in content and especially with regard to data mining support. The 2014 release of arrayMap contains more than 64 000 genomic array data sets, representing about 250 tumor diagnoses. Data sets included in arrayMap have been assembled from public repositories as well as additional resources, and integrated by applying custom processing pipelines. Online tools have been upgraded for a more flexible array data visualization, including options for processing user provided, non-public data sets. Data integration has been improved by mapping to multiple editions of the human reference genome, with the majority of the data now being available for the UCSC hg18 as well as GRCh37 versions. The large amount of tumor CNA data in arrayMap can be freely downloaded by users to promote data mining projects, and to explore special events such as chromothripsis-like genome patterns.
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spelling pubmed-43839372015-04-08 arrayMap 2014: an updated cancer genome resource Cai, Haoyang Gupta, Saumya Rath, Prisni Ai, Ni Baudis, Michael Nucleic Acids Res Database Issue Somatic copy number aberrations (CNA) represent a mutation type encountered in the majority of cancer genomes. Here, we present the 2014 edition of arrayMap (http://www.arraymap.org), a publicly accessible collection of pre-processed oncogenomic array data sets and CNA profiles, representing a vast range of human malignancies. Since the initial release, we have enhanced this resource both in content and especially with regard to data mining support. The 2014 release of arrayMap contains more than 64 000 genomic array data sets, representing about 250 tumor diagnoses. Data sets included in arrayMap have been assembled from public repositories as well as additional resources, and integrated by applying custom processing pipelines. Online tools have been upgraded for a more flexible array data visualization, including options for processing user provided, non-public data sets. Data integration has been improved by mapping to multiple editions of the human reference genome, with the majority of the data now being available for the UCSC hg18 as well as GRCh37 versions. The large amount of tumor CNA data in arrayMap can be freely downloaded by users to promote data mining projects, and to explore special events such as chromothripsis-like genome patterns. Oxford University Press 2014-11-26 2015-01-28 /pmc/articles/PMC4383937/ /pubmed/25428357 http://dx.doi.org/10.1093/nar/gku1123 Text en © The Author(s) 2014. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Database Issue
Cai, Haoyang
Gupta, Saumya
Rath, Prisni
Ai, Ni
Baudis, Michael
arrayMap 2014: an updated cancer genome resource
title arrayMap 2014: an updated cancer genome resource
title_full arrayMap 2014: an updated cancer genome resource
title_fullStr arrayMap 2014: an updated cancer genome resource
title_full_unstemmed arrayMap 2014: an updated cancer genome resource
title_short arrayMap 2014: an updated cancer genome resource
title_sort arraymap 2014: an updated cancer genome resource
topic Database Issue
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4383937/
https://www.ncbi.nlm.nih.gov/pubmed/25428357
http://dx.doi.org/10.1093/nar/gku1123
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