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dc.contributor.authorAmes, RM
dc.contributor.authorMoney, D
dc.contributor.authorGhatge, VP
dc.contributor.authorWhelan, S
dc.contributor.authorLovell, SC
dc.date.accessioned2016-07-07T11:23:00Z
dc.date.issued2011-10-28
dc.description.abstractMotivation: Recent large-scale studies of individuals within a population have demonstrated that there is widespread variation in copy number in many gene families. In addition, there is increasing evidence that the variation in gene copy number can give rise to substantial phenotypic effects. In some cases, these variations have been shown to be adaptive. These observations show that a full understanding of the evolution of biological function requires an understanding of gene gain and gene loss. Accurate, robust evolutionary models of gain and loss events are, therefore, required. Results: We have developed weighted parsimony and maximum likelihood methods for inferring gain and loss events. To test these methods, we have used Markov models of gain and loss to simulate data with known properties. We examine three models: a simple birth–death model, a single rate model and a birth–death innovation model with parameters estimated from Drosophila genome data. We find that for all simulations maximum likelihood-based methods are very accurate for reconstructing the number of duplication events on the phylogenetic tree, and that maximum likelihood and weighted parsimony have similar accuracy for reconstructing the ancestral state. Our implementations are robust to different model parameters and provide accurate inferences of ancestral states and the number of gain and loss events. For ancestral reconstruction, we recommend weighted parsimony because it has similar accuracy to maximum likelihood, but is much faster. For inferring the number of individual gene loss or gain events, maximum likelihood is noticeably more accurate, albeit at greater computational cost.en_GB
dc.description.sponsorshipBiotechnology and Biological Sciences Research Council, UK.en_GB
dc.identifier.citationVol. 28, No. 1, pp. 48 - 55en_GB
dc.identifier.doi10.1093/bioinformatics/btr592
dc.identifier.urihttp://hdl.handle.net/10871/22438
dc.language.isoenen_GB
dc.publisherOxford University Pressen_GB
dc.relation.urlhttp://bioinformatics.oxfordjournals.org/content/28/1/48.fullen_GB
dc.rightsThis is the author accepted manuscript. The final version is available from Oxford University Press via the DOI in this record.en_GB
dc.titleDetermining the evolutionary history of gene familiesen_GB
dc.typeArticleen_GB
dc.date.available2016-07-07T11:23:00Z
dc.identifier.issn1367-4803
dc.descriptionPublisheden_GB
dc.identifier.eissn1460-2059
dc.identifier.journalBioinformaticsen_GB


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