Search results for "Conti"

showing 10 items of 3486 documents

Improving the Representativeness of a Simple Random Sample: An Optimization Model and Its Application to the Continuous Sample of Working Lives

2020

This paper proposes an optimization model for selecting a larger subsample that improves the representativeness of a simple random sample previously obtained from a population larger than the population of interest. The problem formulation involves convex mixed-integer nonlinear programming (convex MINLP) and is, therefore, NP-hard. However, the solution is found by maximizing the size of the subsample taken from a stratified random sample with proportional allocation and restricting it to a p-value large enough to achieve a good fit to the population of interest using Pearson&rsquo

General MathematicsPopulation0211 other engineering and technologiessubsamplingSample (statistics)02 engineering and technologyRepresentativeness heuristic:CIENCIAS ECONÓMICAS [UNESCO]Nonlinear programming0502 economics and businessStatisticsComputer Science (miscellaneous)Chi-square testchi-square testp-value050207 economicseducationEngineering (miscellaneous)Mathematicseducation.field_of_study021103 operations researchlcsh:Mathematics05 social sciencesUNESCO::CIENCIAS ECONÓMICASp-valueSimple random samplelcsh:QA1-939Stratified samplingOptimización matemáticacontinuous sample of working livesEconomía públicaoptimizationMathematics
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New insights on partial trisomy 3q syndrome: de novo 3q27.1-q29 duplication in a newborn with pre and postnatal overgrowth and assisted reproductive …

2023

Abstract Background Duplications of the long arm of chromosome 3 are rare, and associated to a well-defined contiguous gene syndrome known as partial trisomy 3q syndrome. It has been first described in 1966 by Falek et al., and since then around 100 patients have been reported. Clinical manifestations include characteristic facial dysmorphic features, microcephaly, hirsutism, congenital heart disease, genitourinary anomalies, hand and feet abnormalities, growth disturbances and intellectual disability. Most of cases are due to unbalanced translocations, inherited from a parent carrying a balanced aberration (reciprocal translocation or inversion), and rarely the genomic anomaly arises de no…

General MedicineChromosome 3 Contiguous gene syndrome Prenatal diagnosis ART a-CGH Case reportItalian Journal of Pediatrics
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Count data in psychological applied research.

2006

As some authors have noticed in fields other than psychology, level of measurement and distributional characteristics of count data are commonly not taken into account, so that they are analysed as normally distributed continuous variables, and therefore some general linear model is applied. In this work, we review a random sample of 457 articles published in the last four years in journals with the highest impact factor in the Journal Citation Reports (JCR Social Sciences Edition) of the Institute for Scientific Information. The goals are to know how often count variables appear in psychological applied research and which data analyses are used when dealing with count response variables. …

General linear modelImpact factor05 social sciences050401 social sciences methodsContinuous variableLevel of measurement0504 sociology0502 economics and businessStatisticsHumansApplied researchCitationPsychology050203 business & managementGeneral PsychologyCount dataPsychology AppliedPsychological reports
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Adaptive interpolation with maximum order close to discontinuities

2022

Abstract Adaptive rational interpolation has been designed in the context of image processing as a new nonlinear technique that avoids the Gibbs phenomenon when we approximate a discontinuous function. In this work, we present a generalization to this method giving explicit expressions for all the weights for any order of the algorithm. It has a similar behavior to weighted essentially non oscillatory (WENO) technique but the design of the weights in this case is more simple. Also, we propose a new way to construct them obtaining the maximum order near the discontinuities. Some experiments are performed to demonstrate our results and to compare them with standard methods.

GeneralizationApplied MathematicsImage processingContext (language use)Classification of discontinuitiesGibbs phenomenonComputational MathematicsNonlinear systemsymbols.namesakeSimple (abstract algebra)symbolsApplied mathematicsInterpolationMathematicsApplied Mathematics and Computation
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Comparative architectural aspects of regions of conserved synteny on human chromosome 11p15.3 and mouse chromosome 7 (including genes WEE1 and LMO1)

2001

Human chromosome 11p15.3 is associated with chromosome aberrations in the Beckwith Wiedemann Syndrome and implicated in the pathogenesis of different tumor types including lung cancer and leukemias. To date, only single tumor-relevant genes with linkage to this region (e.g. LMO1) have been found suggesting that this region may harbor additional potential disease associated genes. Although this genomic area has been studied for years, the exact order of genes/chromosome markers between D11S572 and the WEE1 gene locus remained unclear. Using the FISH technique and PAC clones of the flanking markers we determined the order of the genomic markers. Based on these clones we established a PAC cont…

Genetic Markerscongenital hereditary and neonatal diseases and abnormalitiesBeckwith–Wiedemann syndromeCell Cycle ProteinsBiologyChromosomesEvolution MolecularContig MappingMiceChromosome regionsGene OrderMetalloproteinsGeneticsmedicineAnimalsHumansCloning MolecularMolecular BiologyGeneConserved SequenceIn Situ Hybridization FluorescenceGenetics (clinical)Repetitive Sequences Nucleic AcidSyntenyOncogene ProteinsGeneticsChromosome 7 (human)Base CompositionChromosomes Human Pair 11Nuclear ProteinsChromosomeSequence Analysis DNALIM Domain ProteinsProtein-Tyrosine Kinasesmedicine.diseaseAT Rich SequenceGC Rich SequenceDNA-Binding ProteinsChromosome 3CpG IslandsChromosome 21Transcription FactorsCytogenetic and Genome Research
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Plant speciation in continental island floras as exemplified byNigellain the Aegean Archipelago

2008

Continental shelf island systems, created by rising sea levels, provide a premier setting for studying the effects of geographical isolation on non-adaptive radiation and allopatric speciation brought about by genetic drift. The Aegean Archipelago forms a highly fragmented complex of mostly continental shelf islands that have become disconnected from each other and the mainland in relatively recent geological times (ca<5.2 Ma). These ecologically fairly homogenous islands thus provide a suitable biogeographic context for assessing the relative influences of past range fragmentation, colonization, gene flow and drift on taxon diversification. Indeed, recent molecular biogeographic studies…

Genetic SpeciationPopulationAllopatric speciationBiologyGeneral Biochemistry Genetics and Molecular BiologyGenetic driftCluster AnalysisAmplified Fragment Length Polymorphism AnalysiseducationPhylogenyDemographyNigellageographyeducation.field_of_studygeography.geographical_feature_categoryGeographyGreeceModels GeneticContinental shelfEcologyGenetic DriftIncipient speciationPhylogeographyGenetics PopulationGenetic SpeciationArchipelagoGeneral Agricultural and Biological SciencesResearch ArticlePhilosophical Transactions of the Royal Society B: Biological Sciences
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Distributed and Lumped Parameter Models for the Characterization of High Throughput Bioreactors

2016

Next generation bioreactors are being developed to generate multiple human cell-based tissue analogs within the same fluidic system, to better recapitulate the complexity and interconnection of human physiology. The effective development of these devices requires a solid understanding of their interconnected fluidics, to predict the transport of nutrients and waste through the constructs and improve the design accordingly. In this work, we focus on a specific model of bioreactor, with multiple input/outputs, aimed at gen- erating osteochondral constructs, i.e., a biphasic construct in which one side is cartilagi- nous in nature, while the other is osseous. We next develop a general computat…

Genetics and Molecular Biology (all)0301 basic medicineComputer scienceDistributed computinglcsh:Medicine02 engineering and technologyMedicine (all); Biochemistry Genetics and Molecular Biology (all); Agricultural and Biological Sciences (all)BiochemistryOxygenPLLA bioreactor computational modelMedicine and Health SciencesFluid dynamicslcsh:ScienceThroughput (business)Flow RateMultidisciplinaryPhysicsSimulation and ModelingMedicine (all)Classical MechanicsVolumetric flow rateChemistryConnective TissuePhysical SciencesAnatomyResearch ArticleChemical ElementsCell Physiology0206 medical engineeringMicrofluidicschemistry.chemical_elementFluid MechanicsResearch and Analysis MethodsContinuum Mechanics03 medical and health sciencesBioreactorFluidicsFluid Flowlcsh:RBiology and Life SciencesBiological TransportFluid DynamicsCell BiologyConstruct (python library)020601 biomedical engineeringCell MetabolismOxygenMetabolismBiological TissueCartilage030104 developmental biologyAgricultural and Biological Sciences (all)chemistryFlow (mathematics)lcsh:QPorous mediumPLOS ONE
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Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder

2008

Contains fulltext : 69243.pdf (Publisher’s version ) (Closed access) Genetic contribution to the development of attention deficit hyperactivity disorder (ADHD) is well established. Seven independent genome-wide linkage scans have been performed to map loci that increase the risk for ADHD. Although significant linkage signals were identified in some of the studies, there has been limited replications between the various independent datasets. The current study gathered the results from all seven of the ADHD linkage scans and performed a Genome Scan Meta Analysis (GSMA) to identify the genomic region with most consistent linkage evidence across the studies. Genome-wide significant linkage (P(S…

Genetics and epigenetic pathways of disease [NCMLS 6]Genetic LinkageEuropean Continental Ancestry GroupMedizinGenome ScanBiologyNeuroinformatics [DCN 3]Mental health [NCEBP 9]Genetic determinismWhite PeopleArticleChromosomesGenomic disorders and inherited multi-system disorders [IGMD 3]03 medical and health sciencesCellular and Molecular Neuroscience0302 clinical medicineGene mappingCognitive neurosciences [UMCN 3.2]Genetic linkageGenetic predispositionmedicinePerception and Action [DCN 1]Attention deficit hyperactivity disorderHumansddc:610Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie Psychosomatik und Psychotherapie des Kindes- und JugendaltersGenetics (clinical)030304 developmental biologyProbabilityLinkage (software)Genetics0303 health sciencesGenomeGenome HumanPair 16Chromosome Mappingmedicine.diseasePsychiatry and Mental healthGenetic defects of metabolism [UMCN 5.1]Attention Deficit Disorder with HyperactivityMeta-analysisLod ScoreFunctional Neurogenomics [DCN 2]030217 neurology & neurosurgeryChromosomes Human Pair 16HumanAmerican Journal of Medical Genetics. Part B: Neuropsychiatric Genetics
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A genome-wide association study identifies Arabidopsis thaliana genes that contribute to differences in the outcome of infection with two Turnip mosa…

2021

Viruses lie in a continuum between generalism and specialism depending on their ability to infect more or less hosts. While generalists are able to successfully infect a wide variety of hosts, specialists are limited to one or a few. Even though generalists seem to gain an advantage due to their wide host range, they usually pay a pleiotropic fitness cost within each host. On the contrary, a specialist has maximal fitness within its own host. A relevant yet poorly explored question is whether viruses differ in the way they interact with their hosts’ gene expression depending on their degree of specialization. Using a genome-wide association study approach, we have identified host genes whos…

GeneticsSpecialism-generalism continuumbiologyHost (biology)Strain (biology)Host-rangePotyvirusPotyvirusLocus (genetics)Genome-wide association studybiology.organism_classificationVirus evolutionMicrobiologyPhenotypeVirologyViral evolutionGWASEmerging virusesGeneVirus Evolution
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Genomic structure and paralogous regions of the inversion breakpoint occurring between human chromosome 3p12.3 and orangutan chromosome 2.

2003

Intrachromosomal duplications play a significant role in human genome pathology and evolution. To better understand the molecular basis of evolutionary chromosome rearrangements, we performed molecular cytogenetic and sequence analyses of the breakpoint region that distinguishes human chromosome 3p12.3 and orangutan chromosome 2. FISH with region-specific BAC clones demonstrated that the breakpoint-flanking sequences are duplicated intrachromosomally on orangutan 2 and human 3q21 as well as at many pericentromeric and subtelomeric sites throughout the genomes. Breakage and rearrangement of the human 3p12.3-homologous region in the orangutan lineage were associated with a partial loss of dup…

Genome evolutionHerpesvirus 4 HumanPan troglodytesBiologyHybrid CellsChimpanzee genome projectEvolution MolecularContig MappingChromosome 19Pongo pygmaeusGeneticsAnimalsHumansLymphocytesMolecular BiologyGenetics (clinical)In Situ Hybridization FluorescenceChromosomal inversionCell Line TransformedSequence DeletionGeneticsHuman evolutionary geneticsCercopithecidaeChromosome BreakageGenome projectChromosomes MammalianChromosome InversionChromosomes Human Pair 3Chromosome breakageChromosome 21Cytogenetic and genome research
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