ArticleBMC bioinformatics2005
AVID: an integrative framework for discovering functional relationships among proteins.
Article in BMC bioinformatics, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed.
- SamPler - a novel method for selecting parameters for gene functional annotation routines.BMC bioinformatics · 2019Article
- Walking the interactome to identify human miRNA-disease associations through the functional link between miRNA targets and disease genes.BMC systems biology · 2013Article
- Genes2FANs: connecting genes through functional association networks.BMC bioinformatics · 2012Article
- Recent advances in clustering methods for protein interaction networks.BMC genomics · 2010Article
- A genomewide functional network for the laboratory mouse.PLoS computational biology · 2008Article
- High-precision high-coverage functional inference from integrated data sources.BMC bioinformatics · 2008Article
- Accessing and integrating data and knowledge for biomedical research.Yearbook of medical informatics · 2008Review
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2 authors.
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Abstract
backgroundDetermining the functions of uncharacterized proteins is one of the most pressing problems in the post-genomic era. Large scale protein-protein interaction assays, global mRNA expression analyses and systematic protein localization studies provide experimental information that can be used for this purpose. The data from such experiments contain many false positives and false negatives, but can be processed using computational methods to provide reliable information about protein-protein relationships and protein function. An outstanding and important goal is to predict detailed functional annotation for all uncharacterized proteins that is reliable enough to effectively guide experiments.
resultsWe present AVID, a computational method that uses a multi-stage learning framework to integrate experimental results with sequence information, generating networks reflecting functional similarities among proteins. We illustrate use of the networks by making predictions of detailed Gene Ontology (GO) annotations in three categories: molecular function, biological process, and cellular component. Applied to the yeast Saccharomyces cerevisiae, AVID provides 37,451 pair-wise functional linkages between 4,191 proteins. These relationships are approximately 65-78% accurate, as assessed by cross-validation testing. Assignments of highly detailed functional descriptors to proteins, based on the networks, are estimated to be approximately 67% accurate for GO categories describing molecular function and cellular component and approximately 52% accurate for terms describing biological process. The predictions cover 1,490 proteins with no previous annotation in GO and also assign more detailed functions to many proteins annotated only with less descriptive terms. Predictions made by AVID are largely distinct from those made by other methods. Out of 37,451 predicted pair-wise relationships, the greatest number shared in common with another method is 3,413.
conclusionAVID provides three networks reflecting functional associations among proteins. We use these networks to generate new, highly detailed functional predictions for roughly half of the yeast proteome that are reliable enough to drive targeted experimental investigations. The predictions suggest many specific, testable hypotheses. All of the data are available as downloadable files as well as through an interactive website at http://web.mit.edu/biology/keating/AVID. Thus, AVID will be a valuable resource for experimental biologists.
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