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INTERFEROME v2.0: an updated database of annotated interferon-regulated genes
Interferome v2.0 (http://interferome.its.monash.edu.au/interferome/) is an update of an earlier version of the Interferome DB published in the 2009 NAR database edition. Vastly improved computational infrastructure now enables more complex and faster queries, and supports more data sets from types I...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3531205/ https://www.ncbi.nlm.nih.gov/pubmed/23203888 http://dx.doi.org/10.1093/nar/gks1215 |
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author | Rusinova, Irina Forster, Sam Yu, Simon Kannan, Anitha Masse, Marion Cumming, Helen Chapman, Ross Hertzog, Paul J. |
author_facet | Rusinova, Irina Forster, Sam Yu, Simon Kannan, Anitha Masse, Marion Cumming, Helen Chapman, Ross Hertzog, Paul J. |
author_sort | Rusinova, Irina |
collection | PubMed |
description | Interferome v2.0 (http://interferome.its.monash.edu.au/interferome/) is an update of an earlier version of the Interferome DB published in the 2009 NAR database edition. Vastly improved computational infrastructure now enables more complex and faster queries, and supports more data sets from types I, II and III interferon (IFN)-treated cells, mice or humans. Quantitative, MIAME compliant data are collected, subjected to thorough, standardized, quantitative and statistical analyses and then significant changes in gene expression are uploaded. Comprehensive manual collection of metadata in v2.0 allows flexible, detailed search capacity including the parameters: range of -fold change, IFN type, concentration and time, and cell/tissue type. There is no limit to the number of genes that can be used to search the database in a single query. Secondary analysis such as gene ontology, regulatory factors, chromosomal location or tissue expression plots of IFN-regulated genes (IRGs) can be performed in Interferome v2.0, or data can be downloaded in convenient text formats compatible with common secondary analysis programs. Given the importance of IFN to innate immune responses in infectious, inflammatory diseases and cancer, this upgrade of the Interferome to version 2.0 will facilitate the identification of gene signatures of importance in the pathogenesis of these diseases. |
format | Online Article Text |
id | pubmed-3531205 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-35312052013-01-03 INTERFEROME v2.0: an updated database of annotated interferon-regulated genes Rusinova, Irina Forster, Sam Yu, Simon Kannan, Anitha Masse, Marion Cumming, Helen Chapman, Ross Hertzog, Paul J. Nucleic Acids Res Articles Interferome v2.0 (http://interferome.its.monash.edu.au/interferome/) is an update of an earlier version of the Interferome DB published in the 2009 NAR database edition. Vastly improved computational infrastructure now enables more complex and faster queries, and supports more data sets from types I, II and III interferon (IFN)-treated cells, mice or humans. Quantitative, MIAME compliant data are collected, subjected to thorough, standardized, quantitative and statistical analyses and then significant changes in gene expression are uploaded. Comprehensive manual collection of metadata in v2.0 allows flexible, detailed search capacity including the parameters: range of -fold change, IFN type, concentration and time, and cell/tissue type. There is no limit to the number of genes that can be used to search the database in a single query. Secondary analysis such as gene ontology, regulatory factors, chromosomal location or tissue expression plots of IFN-regulated genes (IRGs) can be performed in Interferome v2.0, or data can be downloaded in convenient text formats compatible with common secondary analysis programs. Given the importance of IFN to innate immune responses in infectious, inflammatory diseases and cancer, this upgrade of the Interferome to version 2.0 will facilitate the identification of gene signatures of importance in the pathogenesis of these diseases. Oxford University Press 2013-01 2012-11-29 /pmc/articles/PMC3531205/ /pubmed/23203888 http://dx.doi.org/10.1093/nar/gks1215 Text en © The Author(s) 2012. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/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 | Articles Rusinova, Irina Forster, Sam Yu, Simon Kannan, Anitha Masse, Marion Cumming, Helen Chapman, Ross Hertzog, Paul J. INTERFEROME v2.0: an updated database of annotated interferon-regulated genes |
title | INTERFEROME v2.0: an updated database of annotated interferon-regulated genes |
title_full | INTERFEROME v2.0: an updated database of annotated interferon-regulated genes |
title_fullStr | INTERFEROME v2.0: an updated database of annotated interferon-regulated genes |
title_full_unstemmed | INTERFEROME v2.0: an updated database of annotated interferon-regulated genes |
title_short | INTERFEROME v2.0: an updated database of annotated interferon-regulated genes |
title_sort | interferome v2.0: an updated database of annotated interferon-regulated genes |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3531205/ https://www.ncbi.nlm.nih.gov/pubmed/23203888 http://dx.doi.org/10.1093/nar/gks1215 |
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