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Human microRNA target analysis and gene ontology clustering by GOmir, a novel stand-alone application
BACKGROUND: microRNAs (miRNAs) are single-stranded RNA molecules of about 20–23 nucleotides length found in a wide variety of organisms. miRNAs regulate gene expression, by interacting with target mRNAs at specific sites in order to induce cleavage of the message or inhibit translation. Predicting o...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2697644/ https://www.ncbi.nlm.nih.gov/pubmed/19534746 http://dx.doi.org/10.1186/1471-2105-10-S6-S20 |
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author | Roubelakis, Maria G Zotos, Pantelis Papachristoudis, Georgios Michalopoulos, Ioannis Pappa, Kalliopi I Anagnou, Nicholas P Kossida, Sophia |
author_facet | Roubelakis, Maria G Zotos, Pantelis Papachristoudis, Georgios Michalopoulos, Ioannis Pappa, Kalliopi I Anagnou, Nicholas P Kossida, Sophia |
author_sort | Roubelakis, Maria G |
collection | PubMed |
description | BACKGROUND: microRNAs (miRNAs) are single-stranded RNA molecules of about 20–23 nucleotides length found in a wide variety of organisms. miRNAs regulate gene expression, by interacting with target mRNAs at specific sites in order to induce cleavage of the message or inhibit translation. Predicting or verifying mRNA targets of specific miRNAs is a difficult process of great importance. RESULTS: GOmir is a novel stand-alone application consisting of two separate tools: JTarget and TAGGO. JTarget integrates miRNA target prediction and functional analysis by combining the predicted target genes from TargetScan, miRanda, RNAhybrid and PicTar computational tools as well as the experimentally supported targets from TarBase and also providing a full gene description and functional analysis for each target gene. On the other hand, TAGGO application is designed to automatically group gene ontology annotations, taking advantage of the Gene Ontology (GO), in order to extract the main attributes of sets of proteins. GOmir represents a new tool incorporating two separate Java applications integrated into one stand-alone Java application. CONCLUSION: GOmir (by using up to five different databases) introduces miRNA predicted targets accompanied by (a) full gene description, (b) functional analysis and (c) detailed gene ontology clustering. Additionally, a reverse search initiated by a potential target can also be conducted. GOmir can freely be downloaded BRFAA. |
format | Text |
id | pubmed-2697644 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26976442009-06-16 Human microRNA target analysis and gene ontology clustering by GOmir, a novel stand-alone application Roubelakis, Maria G Zotos, Pantelis Papachristoudis, Georgios Michalopoulos, Ioannis Pappa, Kalliopi I Anagnou, Nicholas P Kossida, Sophia BMC Bioinformatics Proceedings BACKGROUND: microRNAs (miRNAs) are single-stranded RNA molecules of about 20–23 nucleotides length found in a wide variety of organisms. miRNAs regulate gene expression, by interacting with target mRNAs at specific sites in order to induce cleavage of the message or inhibit translation. Predicting or verifying mRNA targets of specific miRNAs is a difficult process of great importance. RESULTS: GOmir is a novel stand-alone application consisting of two separate tools: JTarget and TAGGO. JTarget integrates miRNA target prediction and functional analysis by combining the predicted target genes from TargetScan, miRanda, RNAhybrid and PicTar computational tools as well as the experimentally supported targets from TarBase and also providing a full gene description and functional analysis for each target gene. On the other hand, TAGGO application is designed to automatically group gene ontology annotations, taking advantage of the Gene Ontology (GO), in order to extract the main attributes of sets of proteins. GOmir represents a new tool incorporating two separate Java applications integrated into one stand-alone Java application. CONCLUSION: GOmir (by using up to five different databases) introduces miRNA predicted targets accompanied by (a) full gene description, (b) functional analysis and (c) detailed gene ontology clustering. Additionally, a reverse search initiated by a potential target can also be conducted. GOmir can freely be downloaded BRFAA. BioMed Central 2009-06-16 /pmc/articles/PMC2697644/ /pubmed/19534746 http://dx.doi.org/10.1186/1471-2105-10-S6-S20 Text en Copyright © 2009 Roubelakis et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Proceedings Roubelakis, Maria G Zotos, Pantelis Papachristoudis, Georgios Michalopoulos, Ioannis Pappa, Kalliopi I Anagnou, Nicholas P Kossida, Sophia Human microRNA target analysis and gene ontology clustering by GOmir, a novel stand-alone application |
title | Human microRNA target analysis and gene ontology clustering by GOmir, a novel stand-alone application |
title_full | Human microRNA target analysis and gene ontology clustering by GOmir, a novel stand-alone application |
title_fullStr | Human microRNA target analysis and gene ontology clustering by GOmir, a novel stand-alone application |
title_full_unstemmed | Human microRNA target analysis and gene ontology clustering by GOmir, a novel stand-alone application |
title_short | Human microRNA target analysis and gene ontology clustering by GOmir, a novel stand-alone application |
title_sort | human microrna target analysis and gene ontology clustering by gomir, a novel stand-alone application |
topic | Proceedings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2697644/ https://www.ncbi.nlm.nih.gov/pubmed/19534746 http://dx.doi.org/10.1186/1471-2105-10-S6-S20 |
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