4/5/2016
A new version of DisGeNET has been released!!!!
DisGeNET version 4.0 has been released! DisGeNET is a discovery platform integrating information on gene-disease associations from several public data sources and the literature. Developed by the Integrative Biomedical Informatics group of GRIB, DisGeNET integrates expert-curated databases with text-mined data, and it is one of the largest available repositories of its kind. The new release of DisGeNET contains more than 400,000 gene-disease associations, comprising around 17,000 genes, and more than 15,000 diseases and phenotypes. Some of the new features of the current release include:
- New expert-curated databases
- Information on more than 45,000 SNPs associated to diseases
- New annotations of genes to phenotypes
- The DisGeNET Gene-Disease association type ontology updated with new association types
- New features to prioritize genes: the Disease Specificity Index and Disease Pleiotropy Index
- Integration of the Disease Ontology and the Human Phenotype Ontology
and more...
For further details, visit the DisGeNET website and follow us at twitter @DisGeNET
Article references:
- Piñero J, Queralt-Rosinach N, Bravo À, Deu-Pons J, Bauer-Mehren A, Baron M, Sanz F, Furlong LI. DisGeNET: a discovery platform for the dynamical exploration of human diseases and their genes. Database (Oxford), 2015. PMID: 25877637 . DOI: 10.1093/database/bav028.
- Queralt-Rosinach N, Piñero J, Bravo A, Sanz F, Furlong LI. DisGeNET-RDF: Harnessing the Innovative Power of the Semantic Web to Explore the Genetic Basis of Diseases. Bioinformatics, 2016. DOI: 10.1093/ bioinformatics/ btw214.