Cargando…

eDGAR: a database of Disease-Gene Associations with annotated Relationships among genes

BACKGROUND: Genetic investigations, boosted by modern sequencing techniques, allow dissecting the genetic component of different phenotypic traits. These efforts result in the compilation of lists of genes related to diseases and show that an increasing number of diseases is associated with multiple...

Descripción completa

Detalles Bibliográficos
Autores principales: Babbi, Giulia, Martelli, Pier Luigi, Profiti, Giuseppe, Bovo, Samuele, Savojardo, Castrense, Casadio, Rita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5558190/
https://www.ncbi.nlm.nih.gov/pubmed/28812536
http://dx.doi.org/10.1186/s12864-017-3911-3
_version_ 1783257352649048064
author Babbi, Giulia
Martelli, Pier Luigi
Profiti, Giuseppe
Bovo, Samuele
Savojardo, Castrense
Casadio, Rita
author_facet Babbi, Giulia
Martelli, Pier Luigi
Profiti, Giuseppe
Bovo, Samuele
Savojardo, Castrense
Casadio, Rita
author_sort Babbi, Giulia
collection PubMed
description BACKGROUND: Genetic investigations, boosted by modern sequencing techniques, allow dissecting the genetic component of different phenotypic traits. These efforts result in the compilation of lists of genes related to diseases and show that an increasing number of diseases is associated with multiple genes. Investigating functional relations among genes associated with the same disease contributes to highlighting molecular mechanisms of the pathogenesis. RESULTS: We present eDGAR, a database collecting and organizing the data on gene/disease associations as derived from OMIM, Humsavar and ClinVar. For each disease-associated gene, eDGAR collects information on its annotation. Specifically, for lists of genes, eDGAR provides information on: i) interactions retrieved from PDB, BIOGRID and STRING; ii) co-occurrence in stable and functional structural complexes; iii) shared Gene Ontology annotations; iv) shared KEGG and REACTOME pathways; v) enriched functional annotations computed with NET-GE; vi) regulatory interactions derived from TRRUST; vii) localization on chromosomes and/or co-localisation in neighboring loci. The present release of eDGAR includes 2672 diseases, related to 3658 different genes, for a total number of 5729 gene-disease associations. 71% of the genes are linked to 621 multigenic diseases and eDGAR highlights their common GO terms, KEGG/REACTOME pathways, physical and regulatory interactions. eDGAR includes a network based enrichment method for detecting statistically significant functional terms associated to groups of genes. CONCLUSIONS: eDGAR offers a resource to analyze disease-gene associations. In multigenic diseases genes can share physical interactions and/or co-occurrence in the same functional processes. eDGAR is freely available at: edgar.biocomp.unibo.it ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-3911-3) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5558190
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-55581902017-08-16 eDGAR: a database of Disease-Gene Associations with annotated Relationships among genes Babbi, Giulia Martelli, Pier Luigi Profiti, Giuseppe Bovo, Samuele Savojardo, Castrense Casadio, Rita BMC Genomics Research BACKGROUND: Genetic investigations, boosted by modern sequencing techniques, allow dissecting the genetic component of different phenotypic traits. These efforts result in the compilation of lists of genes related to diseases and show that an increasing number of diseases is associated with multiple genes. Investigating functional relations among genes associated with the same disease contributes to highlighting molecular mechanisms of the pathogenesis. RESULTS: We present eDGAR, a database collecting and organizing the data on gene/disease associations as derived from OMIM, Humsavar and ClinVar. For each disease-associated gene, eDGAR collects information on its annotation. Specifically, for lists of genes, eDGAR provides information on: i) interactions retrieved from PDB, BIOGRID and STRING; ii) co-occurrence in stable and functional structural complexes; iii) shared Gene Ontology annotations; iv) shared KEGG and REACTOME pathways; v) enriched functional annotations computed with NET-GE; vi) regulatory interactions derived from TRRUST; vii) localization on chromosomes and/or co-localisation in neighboring loci. The present release of eDGAR includes 2672 diseases, related to 3658 different genes, for a total number of 5729 gene-disease associations. 71% of the genes are linked to 621 multigenic diseases and eDGAR highlights their common GO terms, KEGG/REACTOME pathways, physical and regulatory interactions. eDGAR includes a network based enrichment method for detecting statistically significant functional terms associated to groups of genes. CONCLUSIONS: eDGAR offers a resource to analyze disease-gene associations. In multigenic diseases genes can share physical interactions and/or co-occurrence in the same functional processes. eDGAR is freely available at: edgar.biocomp.unibo.it ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-3911-3) contains supplementary material, which is available to authorized users. BioMed Central 2017-08-11 /pmc/articles/PMC5558190/ /pubmed/28812536 http://dx.doi.org/10.1186/s12864-017-3911-3 Text en © The Author(s). 2017 Open AccessThis 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
Babbi, Giulia
Martelli, Pier Luigi
Profiti, Giuseppe
Bovo, Samuele
Savojardo, Castrense
Casadio, Rita
eDGAR: a database of Disease-Gene Associations with annotated Relationships among genes
title eDGAR: a database of Disease-Gene Associations with annotated Relationships among genes
title_full eDGAR: a database of Disease-Gene Associations with annotated Relationships among genes
title_fullStr eDGAR: a database of Disease-Gene Associations with annotated Relationships among genes
title_full_unstemmed eDGAR: a database of Disease-Gene Associations with annotated Relationships among genes
title_short eDGAR: a database of Disease-Gene Associations with annotated Relationships among genes
title_sort edgar: a database of disease-gene associations with annotated relationships among genes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5558190/
https://www.ncbi.nlm.nih.gov/pubmed/28812536
http://dx.doi.org/10.1186/s12864-017-3911-3
work_keys_str_mv AT babbigiulia edgaradatabaseofdiseasegeneassociationswithannotatedrelationshipsamonggenes
AT martellipierluigi edgaradatabaseofdiseasegeneassociationswithannotatedrelationshipsamonggenes
AT profitigiuseppe edgaradatabaseofdiseasegeneassociationswithannotatedrelationshipsamonggenes
AT bovosamuele edgaradatabaseofdiseasegeneassociationswithannotatedrelationshipsamonggenes
AT savojardocastrense edgaradatabaseofdiseasegeneassociationswithannotatedrelationshipsamonggenes
AT casadiorita edgaradatabaseofdiseasegeneassociationswithannotatedrelationshipsamonggenes