ArticleBMC bioinformatics2008
Assessment of protein set coherence using functional annotations.
Article in BMC bioinformatics, 2008. 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.
- Functional annotation of hierarchical modularity.PloS one · 2012Article
- AIGO: towards a unified framework for the analysis and the inter-comparison of GO functional annotations.BMC bioinformatics · 2011Article
- Quantification of protein group coherence and pathway assignment using functional association.BMC bioinformatics · 2011Article
- GO-based functional dissimilarity of gene sets.BMC bioinformatics · 2011Article
- Assessing the functional coherence of modules found in multiple-evidence networks from Arabidopsis.BMC bioinformatics · 2011Article
- Functional cohesion of gene sets determined by latent semantic indexing of PubMed abstracts.PloS one · 2011Article
- Functional characterization and topological modularity of molecular interaction networks.BMC bioinformatics · 2010Article
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3 authors.
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Abstract
backgroundAnalysis of large-scale experimental datasets frequently produces one or more sets of proteins that are subsequently mined for functional interpretation and validation. To this end, a number of computational methods have been devised that rely on the analysis of functional annotations. Although current methods provide valuable information (e.g. significantly enriched annotations, pairwise functional similarities), they do not specifically measure the degree of homogeneity of a protein set.
resultsIn this work we present a method that scores the degree of functional homogeneity, or coherence, of a set of proteins on the basis of the global similarity of their functional annotations. The method uses statistical hypothesis testing to assess the significance of the set in the context of the functional space of a reference set. As such, it can be used as a first step in the validation of sets expected to be homogeneous prior to further functional interpretation.
conclusionWe evaluate our method by analysing known biologically relevant sets as well as random ones. The known relevant sets comprise macromolecular complexes, cellular components and pathways described for Saccharomyces cerevisiae, which are mostly significantly coherent. Finally, we illustrate the usefulness of our approach for validating 'functional modules' obtained from computational analysis of protein-protein interaction networks. Matlab code and supplementary data are available at http://www.cnb.csic.es/~monica/coherence/
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