Experimental factor ontology, also known as EFO, is an open-access ontology of experimental variables particularly those used in molecular biology.[1] The ontology covers variables which include aspects of disease, anatomy, cell type, cell lines, chemical compounds and assay information. EFO is developed and maintained at the EMBL-EBI as a cross-cutting resource for the purposes of curation, querying and data integration[2] in resources such as Ensembl,[3] ChEMBL and Expression Atlas.[4]
 | |
| Content | |
|---|---|
| Description | Biomedical ontology |
| Data types captured | Experimental and sample variables |
| Organisms | Multiple |
| Contact | |
| Research center | European Molecular Biology Laboratory |
| Laboratory | European Bioinformatics Institute |
| Primary citation | [1] |
| Access | |
| Website | EFO |
| Download URL | Download ontology |
| Sparql endpoint | EBI RDF Platform |
| Tools | |
| Web | http://www.ebi.ac.uk/efo |
| Miscellaneous | |
| Data release frequency | monthly |
| Curation policy | Manually curated, text mining |
Scope and access edit
The original aim of EFO was to describe experimental variables in the EBI's Expression Atlas resource.[1][4] This consisted primarily of disease, anatomical regions and cell types. By December 2013 the scope had grown to include several other EMBL-EBI resources and several external projects including CellFinder,[5] cell lines from the ENCODE project and phenotype to SNP information in the NHGRI's Catalog of Published Genome-Wide Association Studies.[6]
EFO makes use of existing biomedical ontologies from the Open Biomedical Ontologies collection in order to improve interoperability with other resources which may also use these same ontologies, such as ChEBI[7] and the Ontology for Biomedical Investigations.
All data in the database is non-proprietary or is derived from a non-proprietary source. It is thus freely accessible and available to anyone. In addition, each data item is fully traceable and explicitly referenced to the original source.
The EFO data is available through a public web interface, BioPortal Web Service hosted at the National Centre for Biomedical Ontology (NCBO)[8] and downloads.
See also edit
References edit
- ^ a b c Malone, J.; Holloway, E.; Adamusiak, T.; Kapushesky, M.; Zheng, J.; Kolesnikov, N.; Zhukova, A.; Brazma, A.; Parkinson, H. (2010). "Modeling sample variables with an Experimental Factor Ontology". Bioinformatics. 26 (8): 1112–8. doi:10.1093/bioinformatics/btq099. PMC 2853691. PMID 20200009.
- ^ Brooksbank, C.; Bergman, M.T.; Apweiler, A.; Birney, E.; Thornton, J. = (2014). "The European Bioinformatics Institute's data resources 2014". Nucleic Acids Research. 42 (Database issue): D18–D25. doi:10.1093/nar/gkt1206. PMC 3964968. PMID 24271396.
- ^ Flicek, P. (2014). "Ensembl 2014". Nucleic Acids Research. 42 (Database issue): D749–D755. doi:10.1093/nar/gkt1196. PMC 3964975. PMID 24316576.
- ^ a b Kapushesky, M.; Emam, I; Holloway, E; Kurnosov, P; Zorin, A; Malone, J; Rustici, G; Williams, E; Parkinson, H; Brazma, A (2010). "Gene Expression Atlas at the European Bioinformatics Institute". Nucleic Acids Research. 38 (Database issue): D690–D698. doi:10.1093/nar/gkp936. PMC 2808905. PMID 19906730.
- ^ Seltmann, S. (2014). "CELDA – an ontology for the comprehensive representation of cells in complex systems". BMC Bioinformatics. 14: 228. doi:10.1186/1471-2105-14-228. PMC 3722091. PMID 23865855.
- ^ Welter, D. (2014). "The NHGRI GWAS Catalog, a curated resource of SNP-trait associations". Nucleic Acids Research. 42 (Database issue): D1001–D1006. doi:10.1093/nar/gkt1229. PMC 3965119. PMID 24316577.
- ^ De Matos, P.; Alcantara, R.; Dekker, A.; Ennis, M.; Hastings, J.; Haug, K.; Spiteri, I.; Turner, S.; Steinbeck, C. (2009). "Chemical Entities of Biological Interest: An update". Nucleic Acids Research. 38 (Database issue): D249–54. doi:10.1093/nar/gkp886. PMC 2808869. PMID 19854951.
- ^ "NCBO BioPortal". Stanford University. Retrieved 4 April 2014.