The BioGRID interaction database: 2015 update

Andrew Chatr‐aryamontri(Institute for Research in Immunology and Cancer), Bobby‐Joe Breitkreutz(Mount Sinai Hospital), Rose Oughtred(Princeton University), Lorrie Boucher(Mount Sinai Hospital), Sven Heinicke(Princeton University), Daici Chen(Institute for Research in Immunology and Cancer), Chris Stark(Mount Sinai Hospital), Ashton Breitkreutz(Mount Sinai Hospital), Nadine K. Kolas(Mount Sinai Hospital), Lara O’Donnell(Mount Sinai Hospital), Teresa Reguly(Mount Sinai Hospital), Julie Nixon(University of Edinburgh), Lindsay Ramage(University of Edinburgh), Andrew Winter(University of Edinburgh), Adnane Sellam(Centre hospitalier de l'Université Laval), Christie Chang(Princeton University), Jodi Hirschman(Princeton University), Chandra L. Theesfeld(Princeton University), Jennifer Rust(Princeton University), Michael Livstone(Princeton University), Kara Dolinski(Princeton University), Mike Tyers(Mount Sinai Hospital)
Nucleic Acids Research
November 26, 2014
Cited by 924Open Access
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Abstract

The Biological General Repository for Interaction Datasets (BioGRID: http://thebiogrid.org) is an open access database that houses genetic and protein interactions curated from the primary biomedical literature for all major model organism species and humans. As of September 2014, the BioGRID contains 749,912 interactions as drawn from 43,149 publications that represent 30 model organisms. This interaction count represents a 50% increase compared to our previous 2013 BioGRID update. BioGRID data are freely distributed through partner model organism databases and meta-databases and are directly downloadable in a variety of formats. In addition to general curation of the published literature for the major model species, BioGRID undertakes themed curation projects in areas of particular relevance for biomedical sciences, such as the ubiquitin-proteasome system and various human disease-associated interaction networks. BioGRID curation is coordinated through an Interaction Management System (IMS) that facilitates the compilation interaction records through structured evidence codes, phenotype ontologies, and gene annotation. The BioGRID architecture has been improved in order to support a broader range of interaction and post-translational modification types, to allow the representation of more complex multi-gene/protein interactions, to account for cellular phenotypes through structured ontologies, to expedite curation through semi-automated text-mining approaches, and to enhance curation quality control.


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