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Arena-Idb: a platform to build human non-coding RNA interaction networks

BACKGROUND: High throughput technologies have provided the scientific community an unprecedented opportunity for large-scale analysis of genomes. Non-coding RNAs (ncRNAs), for a long time believed to be non-functional, are emerging as one of the most important and large family of gene regulators and...

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Autores principales: Bonnici, Vincenzo, Caro, Giorgio De, Constantino, Giorgio, Liuni, Sabino, D’Elia, Domenica, Bombieri, Nicola, Licciulli, Flavio, Giugno, Rosalba
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6191940/
https://www.ncbi.nlm.nih.gov/pubmed/30367585
http://dx.doi.org/10.1186/s12859-018-2298-8
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author Bonnici, Vincenzo
Caro, Giorgio De
Constantino, Giorgio
Liuni, Sabino
D’Elia, Domenica
Bombieri, Nicola
Licciulli, Flavio
Giugno, Rosalba
author_facet Bonnici, Vincenzo
Caro, Giorgio De
Constantino, Giorgio
Liuni, Sabino
D’Elia, Domenica
Bombieri, Nicola
Licciulli, Flavio
Giugno, Rosalba
author_sort Bonnici, Vincenzo
collection PubMed
description BACKGROUND: High throughput technologies have provided the scientific community an unprecedented opportunity for large-scale analysis of genomes. Non-coding RNAs (ncRNAs), for a long time believed to be non-functional, are emerging as one of the most important and large family of gene regulators and key elements for genome maintenance. Functional studies have been able to assign to ncRNAs a wide spectrum of functions in primary biological processes, and for this reason they are assuming a growing importance as a potential new family of cancer therapeutic targets. Nevertheless, the number of functionally characterized ncRNAs is still too poor if compared to the number of new discovered ncRNAs. Thus platforms able to merge information from available resources addressing data integration issues are necessary and still insufficient to elucidate ncRNAs biological roles. RESULTS: In this paper, we describe a platform called Arena-Idb for the retrieval of comprehensive and non-redundant annotated ncRNAs interactions. Arena-Idb provides a framework for network reconstruction of ncRNA heterogeneous interactions (i.e., with other type of molecules) and relationships with human diseases which guide the integration of data, extracted from different sources, via mapping of entities and minimization of ambiguity. CONCLUSIONS: Arena-Idb provides a schema and a visualization system to integrate ncRNA interactions that assists in discovering ncRNA functions through the extraction of heterogeneous interaction networks. The Arena-Idb is available at http://arenaidb.ba.itb.cnr.it
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spelling pubmed-61919402018-10-23 Arena-Idb: a platform to build human non-coding RNA interaction networks Bonnici, Vincenzo Caro, Giorgio De Constantino, Giorgio Liuni, Sabino D’Elia, Domenica Bombieri, Nicola Licciulli, Flavio Giugno, Rosalba BMC Bioinformatics Research BACKGROUND: High throughput technologies have provided the scientific community an unprecedented opportunity for large-scale analysis of genomes. Non-coding RNAs (ncRNAs), for a long time believed to be non-functional, are emerging as one of the most important and large family of gene regulators and key elements for genome maintenance. Functional studies have been able to assign to ncRNAs a wide spectrum of functions in primary biological processes, and for this reason they are assuming a growing importance as a potential new family of cancer therapeutic targets. Nevertheless, the number of functionally characterized ncRNAs is still too poor if compared to the number of new discovered ncRNAs. Thus platforms able to merge information from available resources addressing data integration issues are necessary and still insufficient to elucidate ncRNAs biological roles. RESULTS: In this paper, we describe a platform called Arena-Idb for the retrieval of comprehensive and non-redundant annotated ncRNAs interactions. Arena-Idb provides a framework for network reconstruction of ncRNA heterogeneous interactions (i.e., with other type of molecules) and relationships with human diseases which guide the integration of data, extracted from different sources, via mapping of entities and minimization of ambiguity. CONCLUSIONS: Arena-Idb provides a schema and a visualization system to integrate ncRNA interactions that assists in discovering ncRNA functions through the extraction of heterogeneous interaction networks. The Arena-Idb is available at http://arenaidb.ba.itb.cnr.it BioMed Central 2018-10-15 /pmc/articles/PMC6191940/ /pubmed/30367585 http://dx.doi.org/10.1186/s12859-018-2298-8 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Bonnici, Vincenzo
Caro, Giorgio De
Constantino, Giorgio
Liuni, Sabino
D’Elia, Domenica
Bombieri, Nicola
Licciulli, Flavio
Giugno, Rosalba
Arena-Idb: a platform to build human non-coding RNA interaction networks
title Arena-Idb: a platform to build human non-coding RNA interaction networks
title_full Arena-Idb: a platform to build human non-coding RNA interaction networks
title_fullStr Arena-Idb: a platform to build human non-coding RNA interaction networks
title_full_unstemmed Arena-Idb: a platform to build human non-coding RNA interaction networks
title_short Arena-Idb: a platform to build human non-coding RNA interaction networks
title_sort arena-idb: a platform to build human non-coding rna interaction networks
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6191940/
https://www.ncbi.nlm.nih.gov/pubmed/30367585
http://dx.doi.org/10.1186/s12859-018-2298-8
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