Evidence map›Paper›PMID 26230274›Full record

ArticlePloS one2015

Optimal Threshold Determination for Interpreting Semantic Similarity and Particularity: Application to the Comparison of Gene Sets and Metabolic Pathways Using GO and ChEBI.

Charles Bettembourg, Christian Diot, Olivier Dameron

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Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

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6citing papers in PubMed
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6 citing papers in PubMed.

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5 · Who and what money

Authors and funding

3 authors.

Charles BettembourgUniversité de Rennes 1, Rennes, France; INRA, UMR1348 PEGASE, Saint-Gilles, France; Agrocampus OUEST, UMR1348 PEGASE, Rennes, France; IRISA, Campus de Beaulieu, Rennes, France; INRIA, Rennes, France.
Christian DiotINRA, UMR1348 PEGASE, Saint-Gilles, France; Agrocampus OUEST, UMR1348 PEGASE, Rennes, France.
Olivier DameronUniversité de Rennes 1, Rennes, France; IRISA, Campus de Beaulieu, Rennes, France; INRIA, Rennes, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe analysis of gene annotations referencing back to Gene Ontology plays an important role in the interpretation of high-throughput experiments results. This analysis typically involves semantic similarity and particularity measures that quantify the importance of the Gene Ontology annotations. However, there is currently no sound method supporting the interpretation of the similarity and particularity values in order to determine whether two genes are similar or whether one gene has some significant particular function. Interpretation is frequently based either on an implicit threshold, or an arbitrary one (typically 0.5). Here we investigate a method for determining thresholds supporting the interpretation of the results of a semantic comparison.

resultsWe propose a method for determining the optimal similarity threshold by minimizing the proportions of false-positive and false-negative similarity matches. We compared the distributions of the similarity values of pairs of similar genes and pairs of non-similar genes. These comparisons were performed separately for all three branches of the Gene Ontology. In all situations, we found overlap between the similar and the non-similar distributions, indicating that some similar genes had a similarity value lower than the similarity value of some non-similar genes. We then extend this method to the semantic particularity measure and to a similarity measure applied to the ChEBI ontology. Thresholds were evaluated over the whole HomoloGene database. For each group of homologous genes, we computed all the similarity and particularity values between pairs of genes. Finally, we focused on the PPAR multigene family to show that the similarity and particularity patterns obtained with our thresholds were better at discriminating orthologs and paralogs than those obtained using default thresholds.

conclusionWe developed a method for determining optimal semantic similarity and particularity thresholds. We applied this method on the GO and ChEBI ontologies. Qualitative analysis using the thresholds on the PPAR multigene family yielded biologically-relevant patterns.

Indexed as

AlgorithmsComputational BiologyGene OntologyHumansMetabolic Networks and PathwaysMolecular Sequence AnnotationMultigene FamilyPeroxisome Proliferator-Activated ReceptorsSemanticsPeroxisome Proliferator-Activated Receptors

Identifiers

PMID26230274
PMCPMC4521860

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.