Search results for "Likelihood Function"

showing 10 items of 114 documents

Molecular basis of adaptive convergence in experimental populations of RNA viruses

2002

Abstract Characterizing the molecular basis of adaptation is one of the most important goals in modern evolutionary genetics. Here, we report a full-genome sequence analysis of 21 independent populations of vesicular stomatitis ribovirus evolved on the same cell type but under different demographic regimes. Each demographic regime differed in the effective viral population size. Evolutionary convergences are widespread both at synonymous and nonsynonymous replacements as well as in an intergenic region. We also found evidence for epistasis among sites of the same and different loci. We explain convergences as the consequence of four factors: (1) environmental homogeneity that supposes an id…

GeneticsNonsynonymous substitutionLikelihood Functionseducation.field_of_studyClonal interferenceHuman evolutionary geneticsPopulation sizePoint mutationPopulationEpistasis GeneticBiologyEvolution MolecularPhylogeneticsEvolutionary biologyGeneticsPoint MutationRNA VirusesEpistasiseducationPhylogenyResearch Article
researchProduct

Recombination drives genome evolution in outbreak-related Legionella pneumophila isolates.

2014

Legionella pneumophila is a strictly environmental pathogen and the etiological agent of legionellosis. It is known that non-vertical processes have a major role in the short-term evolution of pathogens, but little is known about the relevance of these and other processes in environmental bacteria. We report the whole-genome sequencing of 69 L. pneumophila strains linked to recurrent outbreaks in a single location (Alcoy, Spain) over 11 years. We found some examples where the genome sequences of isolates of the same sequence type and outbreak did not cluster together and were more closely related to sequences from different outbreaks. Our analyses identify 16 recombination events responsibl…

Genome evolutionMolecular Sequence DataLegionella pneumophilaPolymorphism Single NucleotideMicrobiologyDisease OutbreaksLegionella pneumophilaEvolution MolecularGeneticsHumansPathogenPhylogenyRecombination GeneticLikelihood FunctionsbiologyBase SequenceModels GeneticOutbreakBayes TheoremGenomicsSequence Analysis DNAbacterial infections and mycosesbiology.organism_classificationVirologyrespiratory tract diseasesSpainbacteriaLegionnaires' DiseaseGenome BacterialNature genetics
researchProduct

Deep metazoan phylogeny: When different genes tell different stories

2013

11 páginas, 4 figuras, 1 tabla.

GenomicsBiologyCnidariaPhylogeneticsGeneticsAnimalsSupermatrixPlacozoaMolecular BiologyGeneEcology Evolution Behavior and SystematicsPhylogenyLong branch attractionGeneticsLikelihood FunctionsModels GeneticPhylogenetic treeCtenophoraBayes TheoremGenomicsRibosomal RNAPoriferaTaxonAnimal evolutionEvolutionary biologyRibosomes
researchProduct

Evidence of Recombination in Intrapatient Populations of Hepatitis C Virus.

2008

Hepatitis C virus (HCV) is a major cause of liver disease worldwide and a potential cause of substantial morbidity and mortality in the future. HCV is characterized by a high level of genetic heterogeneity. Although homologous recombination has been demonstrated in many members of the family Flaviviridae, to which HCV belongs, there are only a few studies reporting recombination on natural populations of HCV, suggesting that these events are rare in vivo. Furthermore, these few studies have focused on recombination between different HCV genotypes/subtypes but there are no reports on the extent of intra-genotype or intra-subtype recombination between viral strains infecting the same patient.…

GenotypeHepatitis C virusHepacivirusPublic Health and Epidemiology/Infectious Diseaseslcsh:MedicineHepacivirusVirology/Immune Evasionmedicine.disease_causeAntiviral AgentsGenetics and Genomics/Population GeneticsGenotypemedicineNS5Alcsh:SciencePhylogenyRecombination GeneticGeneticsLikelihood FunctionsGenomeMultidisciplinaryModels GeneticbiologyGenetic heterogeneitylcsh:RGenetic Variationvirus diseasesRNA virusbiology.organism_classificationGenetics and Genomics/Microbial Evolution and GenomicsVirologyVirology/Virus Evolution and Symbiosislcsh:QComputational Biology/Population GeneticsHomologous recombinationAlgorithmsSoftwareRecombinationResearch Article
researchProduct

Population genetic analysis of bi-allelic structural variants from low-coverage sequence data with an expectation-maximization algorithm

2014

Background Population genetics and association studies usually rely on a set of known variable sites that are then genotyped in subsequent samples, because it is easier to genotype than to discover the variation. This is also true for structural variation detected from sequence data. However, the genotypes at known variable sites can only be inferred with uncertainty from low coverage data. Thus, statistical approaches that infer genotype likelihoods, test hypotheses, and estimate population parameters without requiring accurate genotypes are becoming popular. Unfortunately, the current implementations of these methods are intended to analyse only single nucleotide and short indel variation…

GenotypingGenotypePopulation geneticsPopulationPopulation geneticsBiologyBiochemistryReference biasStructural variation03 medical and health sciences0302 clinical medicineStructural BiologyGenotypeStatisticsHumans1000 Genomes ProjecteducationMolecular BiologyAlleles030304 developmental biologySampling biasGenetic associationGeneticsLikelihood Functions0303 health scienceseducation.field_of_studyGenomePolymorphism GeneticGenètica de poblacionsApplied MathematicsHigh-Throughput Nucleotide SequencingGenomicsComputer Science ApplicationsGenotype frequencyGenetics PopulationStructural variationSoftwareAlgorithms030217 neurology & neurosurgeryMaximum likelihood
researchProduct

Dental services utilization between 1977 and 1995 by Finnish adolescents of different socioeconomic levels.

1998

Equal distribution of health care services has long been a major goal of health policy in the Nordic countries. According to these guidelines, every child is expected to have an examination and treatment at least every second year. The aim of this study was to analyze the trends and, in particular, the socioeconomic differences in dental visits between 1977 and 1995. The data were collected as part of a nationwide research program, the Adolescent Health and Lifestyle Survey, which began in 1977. Every second year a self-administered questionnaire was mailed to a representative sample of 14-, 16- and 18-year-old Finns. The sample sizes in the surveys varied from 2422 to 9556, making a total …

GerontologyMaleParentsToothbrushingAdolescentHealth BehaviorOral HealthRural HealthSocial classCohort Studies03 medical and health sciences0302 clinical medicineSex FactorsSurveys and QuestionnairesHealth careMedicineHumansSocial inequality030212 general & internal medicineOccupationsDental CareGeneral DentistrySocioeconomic statusLife StyleHealth policyFinlandLikelihood Functionsbusiness.industry4. EducationRural healthHealth PolicyPublic Health Environmental and Occupational HealthUrban Health030206 dentistry3. Good healthSocial ClassAdolescent BehaviorEducational StatusFemalebusinessCohort studyDemographyAdolescent healthCommunity dentistry and oral epidemiology
researchProduct

Influence of immigration and other factors on caries in 12- and 15-yr-old children.

2007

In recent years the Valencia region has undergone mass immigration, mainly of people from eastern Europe, North Africa, and Latin America. The objective of this study was to assess the effect of immigration on caries prevalence and experience in 12- and 15-yr-old children in the Valencia region, and to relate this to other socio-economic and oral hygiene-related variables. The data were obtained from the epidemiological study of oral health carried out in the Valencia Region in 2004. The study group comprised 478, 12-yr-old children and 401, 15-yr-old children. Immigration status, age, toothbrushing frequency, and intake of cariogenic foods between meals showed significant association in a …

GerontologyMaleToothbrushingmedicine.medical_specialtyLatin AmericansAdolescentmedia_common.quotation_subjectImmigrationDental CariesSocial classStatistics NonparametricPublic health serviceDiet CariogenicRisk groupsAfrica NorthernSurveys and QuestionnairesEpidemiologyPrevalenceMedicineHumansEurope EasternChildGeneral Dentistrymedia_commonLikelihood Functionsbusiness.industryDMF IndexAge FactorsRegression analysisEmigration and ImmigrationLatin AmericaSpainRegression AnalysisFemalePredictive variablesbusinessDemographyEuropean journal of oral sciences
researchProduct

Nonparametric clustering of seismic events

2006

In this paper we propose a clustering technique, based on the maximization of the likelihood function defined from the generalization of a model for seismic activity (ETAS model, (Ogata (1988))), iteratively changing the partitioning of the events. In this context it is useful to apply models requiring the distinction between independent events (i.e. the background seismicity) and strongly correlated ones. This technique develops nonparametric estimation methods of the point process intensity function. To evaluate the goodness of fit of the model, from which the clustering method is implemented, residuals process analysis is used.

Goodness of fitGeneralizationComputer scienceNonparametric statisticsContext (language use)Maximization.Cluster analysisLikelihood functionAlgorithmPoint process
researchProduct

Mutations in KIAA0586 Cause Lethal Ciliopathies Ranging from a Hydrolethalus Phenotype to Short-Rib Polydactyly Syndrome

2015

KIAA0586, the human ortholog of chicken TALPID3, is a centrosomal protein that is essential for primary ciliogenesis. Its disruption in animal models causes defects attributed to abnormal hedgehog signaling; these defects include polydactyly and abnormal dorsoventral patterning of the neural tube. Here, we report homozygous mutations of KIAA0586 in four families affected by lethal ciliopathies ranging from a hydrolethalus phenotype to short-rib polydactyly. We show defective ciliogenesis, as well as abnormal response to SHH-signaling activation in cells derived from affected individuals, consistent with a role of KIAA0586 in primary cilia biogenesis. Whereas centriolar maturation seemed una…

Heart Defects CongenitalMolecular Sequence DataCell Cycle ProteinsBiologyShort Rib-Polydactyly SyndromeCiliopathies03 medical and health sciencesFatal OutcomeCiliogenesisReportGLI3GeneticsmedicineHumansGenetics(clinical)Europe EasternGenetics (clinical)030304 developmental biologyGenetics0303 health sciencesLikelihood FunctionsShort rib – polydactyly syndromePolydactylyBase SequenceCilium030305 genetics & hereditySequence Analysis DNAmedicine.diseasePhenotypeHuman geneticsHedgehog signaling pathwayFounder EffectPedigreePhenotypeCodon NonsenseCentriolar satelliteErratumHand Deformities CongenitalCiliary Motility DisordersHydrocephalus
researchProduct

Hessian PDF reweighting meets the Bayesian methods

2014

We discuss the Hessian PDF reweighting - a technique intended to estimate the effects that new measurements have on a set of PDFs. The method stems straightforwardly from considering new data in a usual $\chi^2$-fit and it naturally incorporates also non-zero values for the tolerance, $\Delta\chi^2>1$. In comparison to the contemporary Bayesian reweighting techniques, there is no need to generate large ensembles of PDF Monte-Carlo replicas, and the observables need to be evaluated only with the central and the error sets of the original PDFs. In spite of the apparently rather different methodologies, we find that the Hessian and the Bayesian techniques are actually equivalent if the $\Delta…

Hessian matrixNuclear TheoryComputer scienceBayesian probabilityFOS: Physical sciencesObservableExponential functionStatistics::ComputationSet (abstract data type)Nuclear Theory (nucl-th)High Energy Physics - Phenomenologysymbols.namesakeHigh Energy Physics - Phenomenology (hep-ph)Simple (abstract algebra)symbolsApplied mathematicsLikelihood functionNuclear theory
researchProduct