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TarBase 6.0: capturing the exponential growth of miRNA targets with experimental support
As the relevant literature and the number of experiments increase at a super linear rate, databases that curate and collect experimentally verified microRNA (miRNA) targets have gradually emerged. These databases attempt to provide efficient access to this wealth of experimental data, which is scatt...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3245116/ https://www.ncbi.nlm.nih.gov/pubmed/22135297 http://dx.doi.org/10.1093/nar/gkr1161 |
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author | Vergoulis, Thanasis Vlachos, Ioannis S. Alexiou, Panagiotis Georgakilas, George Maragkakis, Manolis Reczko, Martin Gerangelos, Stefanos Koziris, Nectarios Dalamagas, Theodore Hatzigeorgiou, Artemis G. |
author_facet | Vergoulis, Thanasis Vlachos, Ioannis S. Alexiou, Panagiotis Georgakilas, George Maragkakis, Manolis Reczko, Martin Gerangelos, Stefanos Koziris, Nectarios Dalamagas, Theodore Hatzigeorgiou, Artemis G. |
author_sort | Vergoulis, Thanasis |
collection | PubMed |
description | As the relevant literature and the number of experiments increase at a super linear rate, databases that curate and collect experimentally verified microRNA (miRNA) targets have gradually emerged. These databases attempt to provide efficient access to this wealth of experimental data, which is scattered in thousands of manuscripts. Aim of TarBase 6.0 (http://www.microrna.gr/tarbase) is to face this challenge by providing a significant increase of available miRNA targets derived from all contemporary experimental techniques (gene specific and high-throughput), while incorporating a powerful set of tools in a user-friendly interface. TarBase 6.0 hosts detailed information for each miRNA–gene interaction, ranging from miRNA- and gene-related facts to information specific to their interaction, the experimental validation methodologies and their outcomes. All database entries are enriched with function-related data, as well as general information derived from external databases such as UniProt, Ensembl and RefSeq. DIANA microT miRNA target prediction scores and the relevant prediction details are available for each interaction. TarBase 6.0 hosts the largest collection of manually curated experimentally validated miRNA–gene interactions (more than 65 000 targets), presenting a 16.5–175-fold increase over other available manually curated databases. |
format | Online Article Text |
id | pubmed-3245116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-32451162012-01-10 TarBase 6.0: capturing the exponential growth of miRNA targets with experimental support Vergoulis, Thanasis Vlachos, Ioannis S. Alexiou, Panagiotis Georgakilas, George Maragkakis, Manolis Reczko, Martin Gerangelos, Stefanos Koziris, Nectarios Dalamagas, Theodore Hatzigeorgiou, Artemis G. Nucleic Acids Res Articles As the relevant literature and the number of experiments increase at a super linear rate, databases that curate and collect experimentally verified microRNA (miRNA) targets have gradually emerged. These databases attempt to provide efficient access to this wealth of experimental data, which is scattered in thousands of manuscripts. Aim of TarBase 6.0 (http://www.microrna.gr/tarbase) is to face this challenge by providing a significant increase of available miRNA targets derived from all contemporary experimental techniques (gene specific and high-throughput), while incorporating a powerful set of tools in a user-friendly interface. TarBase 6.0 hosts detailed information for each miRNA–gene interaction, ranging from miRNA- and gene-related facts to information specific to their interaction, the experimental validation methodologies and their outcomes. All database entries are enriched with function-related data, as well as general information derived from external databases such as UniProt, Ensembl and RefSeq. DIANA microT miRNA target prediction scores and the relevant prediction details are available for each interaction. TarBase 6.0 hosts the largest collection of manually curated experimentally validated miRNA–gene interactions (more than 65 000 targets), presenting a 16.5–175-fold increase over other available manually curated databases. Oxford University Press 2012-01 2011-11-30 /pmc/articles/PMC3245116/ /pubmed/22135297 http://dx.doi.org/10.1093/nar/gkr1161 Text en © The Author(s) 2011. 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 Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Vergoulis, Thanasis Vlachos, Ioannis S. Alexiou, Panagiotis Georgakilas, George Maragkakis, Manolis Reczko, Martin Gerangelos, Stefanos Koziris, Nectarios Dalamagas, Theodore Hatzigeorgiou, Artemis G. TarBase 6.0: capturing the exponential growth of miRNA targets with experimental support |
title | TarBase 6.0: capturing the exponential growth of miRNA targets with experimental support |
title_full | TarBase 6.0: capturing the exponential growth of miRNA targets with experimental support |
title_fullStr | TarBase 6.0: capturing the exponential growth of miRNA targets with experimental support |
title_full_unstemmed | TarBase 6.0: capturing the exponential growth of miRNA targets with experimental support |
title_short | TarBase 6.0: capturing the exponential growth of miRNA targets with experimental support |
title_sort | tarbase 6.0: capturing the exponential growth of mirna targets with experimental support |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3245116/ https://www.ncbi.nlm.nih.gov/pubmed/22135297 http://dx.doi.org/10.1093/nar/gkr1161 |
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