Search results for "IMPUTATION"

showing 7 items of 57 documents

Examining facial emotion recognition as an intermediate phenotype for psychosis: Findings from the EUGEI study

2022

The EUGEI project was supported by the European Community’s Seventh Framework Program under grant agreement No. HEALTH-F2- 2009-241909 (Project EU-GEI). Dr. Arango was supported by the Spanish Ministry of Science and Innovation; Instituto de Salud Carlos III (SAM16-PE07CP1, PI16/02012, PI19/024); CIBERSAM (...)

AdultMalePsychosisGENETIC RISKInterviews as Topic03 medical and health sciencesSTRUCTURED INTERVIEW0302 clinical medicinePolygenic risk scoreRisk FactorsSocial cognitionIMPUTATIONmedicineHumansPOLYGENIC RISKEmotion recognitionAssociation (psychology)Biological PsychiatryEmotionPharmacologyIntermediate phenotypebusiness.industrySiblingsUNAFFECTED SIBLINGSRegression analysisASSOCIATIONGenomicsmedicine.diseaseSocial cognition030227 psychiatrySchizotypal traitsINDIVIDUALSPolygenic risk scoresPhenotypePsychotic DisordersSchizophreniaRELIABILITYStructured interviewSchizophreniaFemalebusinessFacial Recognition030217 neurology & neurosurgeryClinical psychologyProgress in Neuro-Psychopharmacology and Biological Psychiatry
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Imputation Procedures in Surveys Using Nonparametric and Machine Learning Methods: An Empirical Comparison

2020

Abstract Nonparametric and machine learning methods are flexible methods for obtaining accurate predictions. Nowadays, data sets with a large number of predictors and complex structures are fairly common. In the presence of item nonresponse, nonparametric and machine learning procedures may thus provide a useful alternative to traditional imputation procedures for deriving a set of imputed values used next for the estimation of study parameters defined as solution of population estimating equation. In this paper, we conduct an extensive empirical investigation that compares a number of imputation procedures in terms of bias and efficiency in a wide variety of settings, including high-dimens…

FOS: Computer and information sciencesStatistics and ProbabilityStatistics::ApplicationsEmpirical comparisonbusiness.industryComputer scienceApplied MathematicsNonparametric statisticsMachine learningcomputer.software_genreStatistics - ComputationVariety (cybernetics)Methodology (stat.ME)Set (abstract data type)Statistics::MethodologyImputation (statistics)Artificial intelligenceStatistics Probability and UncertaintybusinesscomputerStatistics - MethodologyComputation (stat.CO)Social Sciences (miscellaneous)Journal of Survey Statistics and Methodology
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Polygenic Risk Scores and Physical Activity

2020

Supplemental digital content is available in the text.

MaleMultifactorial InheritanceEpidemiologyheritabilityNorthern finlandDISEASEhidden heritability0302 clinical medicineRisk FactorsMISSING HERITABILITYAccelerometryMedicineOrthopedics and Sports Medicine315 Sport and fitness sciencesgeneskrooniset tauditFinlandAged 80 and overeducation.field_of_studyFramingham Risk ScoreBIRTH COHORTexerciseHERITABILITYObjective measurementriskitekijätMiddle Aged3. Good healthComputingMethodologies_DOCUMENTANDTEXTPROCESSINGFemaleHEALTHgeenitutkimusBirth cohortfyysinen aktiivisuusAdultSingle variableAdolescentGenotypePopulationPhysical activityEXERCISEPhysical Therapy Sports Therapy and RehabilitationFitness TrackersGENOTYPE IMPUTATIONPolymorphism Single Nucleotideperinnöllinen alttiusYoung Adult03 medical and health sciencesHumansGENOME-WIDE ASSOCIATIONgeneeducationperinnöllisyysAgedgeenitbusiness.industryHIDDEN HERITABILITY030229 sport sciencesGENEperimäPolygenic risk scoreSelf ReportbusinessGenome-Wide Association StudyDemographyMedicine & Science in Sports & Exercise
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CLUSTERING INCOMPLETE SPECTRAL DATA WITH ROBUST METHODS

2018

Abstract. Missing value imputation is a common approach for preprocessing incomplete data sets. In case of data clustering, imputation methods may cause unexpected bias because they may change the underlying structure of the data. In order to avoid prior imputation of missing values the computational operations must be projected on the available data values. In this paper, we apply a robust nan-K-spatmed algorithm to the clustering problem on hyperspectral image data. Robust statistics, such as multivariate medians, are more insensitive to outliers than classical statistics relying on the Gaussian assumptions. They are, however, computationally more intractable due to the lack of closed-for…

lcsh:Applied optics. PhotonicsMultivariate statisticsComputer scienceGaussianCorrelation clusteringRobust statisticsspectral datacomputer.software_genrelcsh:Technologysymbols.namesakeCURE data clustering algorithmImputation (statistics)interpolointiCluster analysisK-meansnan-K-spatmedlcsh:Tk-means clusteringlcsh:TA1501-1820robust statistical methodsMissing dataData setlcsh:TA1-2040OutliersymbolsData mininglcsh:Engineering (General). Civil engineering (General)computerclustering
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A low-frequency haplotype spanning SLX4/FANCP constitutes a new risk locus for early-onset breast cancer (<60 years) and is associated with reduce…

2017

Only a fraction of breast cancer (BC) cases can be yet explained by mutations in genes or genomic variants discovered in linkage, genome-wide association and sequencing studies. The known genes entailing medium or high risk for BC are strongly enriched for a function in DNA double strand repair. Thus, aiming at identifying low frequency variants conferring an intermediate risk, we here investigated 17 variants (MAF: 0.01-0.1) in 10 candidate genes involved in DNA repair or cell cycle control. In an exploration cohort of 437 cases and 1189 controls, we show the variant rs3810813 in the SLX4/FANCP gene to be significantly associated with both BC (≤60 years; OR = 2.6(1.6-3.9), p = 1.6E-05) and…

0301 basic medicineGeneticsCancer ResearchCandidate geneHaplotypeLocus (genetics)Single-nucleotide polymorphismBiologyPenetrance03 medical and health sciences030104 developmental biologyOncologyAlleleAllele frequencyImputation (genetics)International Journal of Cancer
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The population genomics of archaeological transition in west Iberia: Investigation of ancient substructure using imputation and haplotype-based metho…

2017

We analyse new genomic data (0.05–2.95x) from 14 ancient individuals from Portugal distributed from the Middle Neolithic (4200–3500 BC) to the Middle Bronze Age (1740–1430 BC) and impute genomewide diploid genotypes in these together with published ancient Eurasians. While discontinuity is evident in the transition to agriculture across the region, sensitive haplotype-based analyses suggest a significant degree of local hunter-gatherer contribution to later Iberian Neolithic populations. A more subtle genetic influx is also apparent in the Bronze Age, detectable from analyses including haplotype sharing with both ancient and modern genomes, D-statistics and Y-chromosome lineages. However, t…

0301 basic medicineMaleCancer ResearchHistoryHereditySteppePopulation geneticsGenetic LinkagePopulation geneticsStone AgeSocial SciencesQH426-470Population genomics0302 clinical medicineddc:590Databases GeneticGenetics(clinical)Sequencing dataGenetics (clinical)MigrationGenetics0303 health sciencesgeography.geographical_feature_categoryGenomeAncient DNAGeographyPaleogeneticsGeologyGenomicsCChumanitiesPositive selectionEuropeGenetic MappingPhylogeographyGeographyBiogeographyArchaeologyNeolithic PeriodlanguageFemaleResearch Articlelcsh:QH426-470GenotypeIntrogressionVariant GenotypesAdmixtureBiologyInsightsAssociation03 medical and health sciencesAgeBronze AgeGeneticsHumansGenetic variationQH426Molecular BiologyEcology Evolution Behavior and Systematics030304 developmental biologyEvolutionary BiologyChromosomes Human YHuman genomePopulation BiologyPortugalGenome HumanHaplotypeEcology and Environmental SciencesBiology and Life SciencesPaleontologyGenetic VariationGeologic TimeDnaSequence Analysis DNAArchaeologylanguage.human_languagePhylogeographylcsh:Genetics030104 developmental biologyAncient DNAGenetics PopulationHaplotypesEvolutionary biologyEarth SciencesIberiaPortuguesePaleogenetics030217 neurology & neurosurgeryImputation (genetics)Population GeneticsPLoS Genetics
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L'imputazione dei dati mancanti: l'effetto sui parametri di un Extended Logistic Rasch Model

2008

Il problema dei dati mancanti è abbastanza comune nella ricerca empirica, specialmente nelle scienze sociali in cui il tentativo di misurazione di quantità non direttamente osservabili (variabili latenti)avviene attraverso la somministrazione di test o questionari costituiti da più item. I modelli statistici finalizzati alla soluzione di tale problema richiedono, in genere, un elevato numero di osservazioni per ogni unità coinvolta nell’analisi. In un contesto multivariato il problema si amplifica, poiché nel modello sono considerati più item per ciascuna osservazione: la probabilità, quindi, di avere almeno un dato mancante non è irrilevante ed è, inoltre, crescente al crescere del numero …

Multiple Imputation Rasch Model Valutazione Qualità della Didattica ‘Taratura’ del questionarioSettore SECS-S/05 - Statistica Sociale
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