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Progenetix: 12 years of oncogenomic data curation
DNA copy number aberrations (CNAs) can be found in the majority of cancer genomes and are crucial for understanding the potential mechanisms underlying tumor initiation and progression. Since the first release in 2001, the Progenetix project (http://www.progenetix.org) has provided a reference resou...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3965091/ https://www.ncbi.nlm.nih.gov/pubmed/24225322 http://dx.doi.org/10.1093/nar/gkt1108 |
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author | Cai, Haoyang Kumar, Nitin Ai, Ni Gupta, Saumya Rath, Prisni Baudis, Michael |
author_facet | Cai, Haoyang Kumar, Nitin Ai, Ni Gupta, Saumya Rath, Prisni Baudis, Michael |
author_sort | Cai, Haoyang |
collection | PubMed |
description | DNA copy number aberrations (CNAs) can be found in the majority of cancer genomes and are crucial for understanding the potential mechanisms underlying tumor initiation and progression. Since the first release in 2001, the Progenetix project (http://www.progenetix.org) has provided a reference resource dedicated to provide the most comprehensive collection of genome-wide CNA profiles. Reflecting the application of comparative genomic hybridization techniques to tens of thousands of cancer genomes, over the past 12 years our data curation efforts have resulted in a more than 60-fold increase in the number of cancer samples presented through Progenetix. In addition, new data exploration tools and visualization options have been added. In particular, the gene-specific CNA frequency analysis should facilitate the assignment of cancer genes to related cancer types. In addition, the new user file processing interface allows users to take advantage of the online tools, including various data representation options for proprietary data pre-publication. In this update article, we report recent improvements of the database in terms of content, user interface and online tools. |
format | Online Article Text |
id | pubmed-3965091 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-39650912014-03-25 Progenetix: 12 years of oncogenomic data curation Cai, Haoyang Kumar, Nitin Ai, Ni Gupta, Saumya Rath, Prisni Baudis, Michael Nucleic Acids Res VI. Genomic variation, diseases and drugs DNA copy number aberrations (CNAs) can be found in the majority of cancer genomes and are crucial for understanding the potential mechanisms underlying tumor initiation and progression. Since the first release in 2001, the Progenetix project (http://www.progenetix.org) has provided a reference resource dedicated to provide the most comprehensive collection of genome-wide CNA profiles. Reflecting the application of comparative genomic hybridization techniques to tens of thousands of cancer genomes, over the past 12 years our data curation efforts have resulted in a more than 60-fold increase in the number of cancer samples presented through Progenetix. In addition, new data exploration tools and visualization options have been added. In particular, the gene-specific CNA frequency analysis should facilitate the assignment of cancer genes to related cancer types. In addition, the new user file processing interface allows users to take advantage of the online tools, including various data representation options for proprietary data pre-publication. In this update article, we report recent improvements of the database in terms of content, user interface and online tools. Oxford University Press 2014-01-01 2013-11-12 /pmc/articles/PMC3965091/ /pubmed/24225322 http://dx.doi.org/10.1093/nar/gkt1108 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by/3.0/), which permits non-commercial reuse, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | VI. Genomic variation, diseases and drugs Cai, Haoyang Kumar, Nitin Ai, Ni Gupta, Saumya Rath, Prisni Baudis, Michael Progenetix: 12 years of oncogenomic data curation |
title | Progenetix: 12 years of oncogenomic data curation |
title_full | Progenetix: 12 years of oncogenomic data curation |
title_fullStr | Progenetix: 12 years of oncogenomic data curation |
title_full_unstemmed | Progenetix: 12 years of oncogenomic data curation |
title_short | Progenetix: 12 years of oncogenomic data curation |
title_sort | progenetix: 12 years of oncogenomic data curation |
topic | VI. Genomic variation, diseases and drugs |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3965091/ https://www.ncbi.nlm.nih.gov/pubmed/24225322 http://dx.doi.org/10.1093/nar/gkt1108 |
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