Search results for "A* algorithm"

showing 10 items of 2538 documents

Differential detectability of polymorphic warning signals under varying light environments.

2014

The striking colour-pattern variation of some aposematic species is paradoxical because selection by predators is expected to favour signal uniformity. Although the mechanisms allowing for the maintenance of such variation are not well understood, possible explanations include both non-adaptive processes like drift and gene flow; and adaptive processes, such as an interaction between natural and sexual selection, spatial and temporal variation in selection, a link between behaviour or other fitness-related traits and phenotype, and predators' ability to generalise among different signals. Here we test whether warning-signal polymorphisms, such as that of dyeing poison frogs (Dendrobates tin…

MaleDendrobatesPoison controlSkin PigmentationAposematismBiologyPredationBirdsBehavioral NeuroscienceDiscrimination PsychologicalAnimalsHumansPredatorSelection (genetic algorithm)LightingMechanism (biology)EcologyGeneral Medicinebiology.organism_classificationEvolutionary biologySexual selectionPredatory Behaviorta1181Animal Science and ZoologyFemaleAnuraColor PerceptionBehavioural processes
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Epidemiology of multiple congenital anomalies in Europe : A EUROCAT population-based registry study

2014

BACKGROUND: This study describes the prevalence, associated anomalies, and demographic characteristics of cases of multiple congenital anomalies (MCA) in 19 population-based European registries (EUROCAT) covering 959,446 births in 2004 and 2010.METHODS: EUROCAT implemented a computer algorithm for classification of congenital anomaly cases followed by manual review of potential MCA cases by geneticists. MCA cases are defined as cases with two or more major anomalies of different organ systems, excluding sequences, chromosomal and monogenic syndromes.RESULTS: The combination of an epidemiological and clinical approach for classification of cases has improved the quality and accuracy of the M…

MaleEmbryologyPediatricsEpidemiologyPrenatal diagnosisINFANTSPregnancyEpidemiologyPrevalenceMedicineRegistrieseducation.field_of_studyAutomatic Data ProcessingGeneral MedicineClassificationEpidemiology ; Multiple congenital anomalies ; Classification ; Prevalence ; Prenatal diagnosisComputer algorithmEuropeclassificationcardiovascular systemFemaleepidemiologyPopulation-Based RegistryAlgorithmscirculatory and respiratory physiologymedicine.medical_specialtyPopulationprevalencePrenatal diagnosismultiple congenital anomaliesBIRTH-DEFECTSHumansAbnormalities MultipleMALFORMATIONSRATEScardiovascular diseaseseducationRetrospective StudiesElectronic Data ProcessingPregnancyprenatal diagnosisbusiness.industryPublic healthRetrospective cohort studymedicine.diseasenervous system diseasesPediatrics Perinatology and Child HealthMultiple congenital anomaliesPATTERNSbusinessDevelopmental Biology
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Colour polymorphism torn apart by opposing positive frequency-dependent selection, yet maintained in space.

2015

Summary Polymorphic warning signals in aposematic species are enigmatic because predator learning and discrimination should select for the most common coloration, resulting in positive frequency‐dependent survival selection. Here, we investigated whether differential mating success could create sufficiently strong negative frequency‐dependent selection for rare morphs to explain polymorphic (white and yellow) warning coloration in male wood tiger moths (Parasemia plantaginis). We conducted an experiment in semi‐natural conditions where we estimated mating success for both white and yellow male moths under three different morph frequencies. Contrary to expectations, mating success was positi…

MaleFrequency-dependent selectionColorAposematismBiologyMothsSexual Behavior AnimalParasemia plantaginisAnimalsMatingPredatorreproductive and urinary physiologyEcology Evolution Behavior and SystematicsSelection (genetic algorithm)FinlandPolymorphism GeneticEcologyPigmentationfungibiology.organism_classificationFixation (population genetics)Evolutionary biologySexual selectionAnimal Science and ZoologyFemaleGenetic FitnessThe Journal of animal ecology
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Heritability Estimates of Differences in Arbitrary Embryonic Mortality Traits in Turkeys

1971

Abstract INTRODUCTION SPECIFIC embryonic abnormalities in Broad Breasted Bronze turkeys which contributed to low hatchability were classified into eight groups which are referred to as traits in this paper. References to these traits or similar abnormalities in chickens and turkeys are shown in Table 1. The objective of this study was to determine the differences in the rates, relative to unhatched fertile eggs, at which these specific traits could be changed by artificial selection which was accompanied by inbreeding. Rapid changes would indicate the traits more responsive to selection. MATERIALS AND METHODS Four different strains of Broad Breasted Bronze turkeys were introduced as eggs to…

MaleGeneticsTurkeysmedia_common.quotation_subjectZoologyFertilityChick EmbryoGeneral MedicineHeritabilityBiologyBody weightCongenital AbnormalitiesFertilityAnimalsFemaleInbreedingAnimal Science and ZoologySelection GeneticInbreedingPoultry DiseasesSelection (genetic algorithm)media_commonPoultry Science
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Reproductive isolation among allopatric Drosophila montana populations

2014

An outstanding goal in speciation research is to trace the mode and tempo of the evolution of barriers to gene flow. Such research benefits from studying incipient speciation, in which speciation between populations has not yet occurred, but where multiple potential mechanisms of reproductive isolation (RI: i.e., premating, postmating-prezygotic (PMPZ), and postzygotic barriers) may act. We used such a system to investigate these barriers among allopatric populations of Drosophila montana. In all heteropopulation crosses we found premating (sexual) isolation, which was either symmetric or asymmetric depending on the population pair compared. Postmating isolation was particularly strong in c…

MaleGeneticseducation.field_of_studyDrosophila montanaReproductive IsolationGenetic SpeciationPopulationAllopatric speciationReproductive isolationIncipient speciationBiologyEcological speciationGene flowEvolutionary biologyGenetic algorithmGeneticsAnimalsta1181DrosophilaFemaleGeneral Agricultural and Biological ScienceseducationEcology Evolution Behavior and SystematicsEvolution
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Quantitative measure of sexual selection with respect to the operational sex ratio: a comparison of selection indices

2006

Despite numerous indices proposed to predict the evolution of mating systems, a unified measure of sexual selection has remained elusive. Three previous studies have compared indices of sexual selection under laboratory conditions. Here, we use a genetic study to compare the most widely used measures of sexual selection in natural populations. We explored the mating and reproductive successes of male and female bank voles,Clethrionomys glareolus, across manipulated operational sex ratios (OSRs) by genotyping all adult and pup bank voles on 13 islands using six microsatellite loci. We used Bateman's principles (IsandIand Bateman gradients) and selection coefficients (s′ andβ′) to evaluate, f…

MaleGenotypeBiologyGeneral Biochemistry Genetics and Molecular BiologyAnimalsBody SizeBateman's principleTestosteroneSex RatioOperational sex ratioMatingSelection (genetic algorithm)General Environmental ScienceGeneral Immunology and MicrobiologyEcologyArvicolinaeReproductionGeneral MedicineMating Preference AnimalMating systembiology.organism_classificationBank voleSexual selectionFemaleGeneral Agricultural and Biological SciencesSex ratioDemographyResearch Article
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Attenuation of disease phenotype through alternative translation initiation in low-penetrance retinoblastoma

2006

Hereditary predisposition to retinoblastoma (RB) is caused by germline mutations in the retinoblastoma 1 (RB1) gene and transmits as an autosomal dominant trait. In the majority of cases disease develops in greater than 90% of carriers. However, reduced penetrance with a large portion of disease-free carrier is seen in some families. Unambiguous identification of the predisposing mutation in these families is important for accurate risk prediction in relatives and their genetic counseling but also provides conceptual information regarding the relationship between the RB1 genotype and the disease phenotype. In this study we report a novel mutation detected in 10 individuals of an extended fa…

MaleGenotypeDNA Mutational AnalysisGreen Fluorescent ProteinsMolecular Sequence DataPenetranceBiologyRetinoblastoma ProteinFrameshift mutationExonGermline mutationGeneticsmedicineHumansGenetic Predisposition to DiseaseAmino Acid SequenceRNA MessengerChildFrameshift MutationPeptide Chain Initiation TranslationalGenetics (clinical)GeneticsRetinoblastomaRetinoblastomaInfantAutosomal dominant traitExonsmedicine.diseasePenetranceAlternative SplicingPhenotypeCodon NonsenseHereditary RetinoblastomaMutation (genetic algorithm)FemaleHuman Mutation
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Signatures of selection in the genome of Swedish warmblood horses selected for sport performance

2019

Abstract Background A growing demand for improved physical skills and mental attitude in modern sport horses has led to strong selection for performance in many warmblood studbooks. The aim of this study was to detect genomic regions with low diversity, and therefore potentially under selection, in Swedish Warmblood horses (SWB) by analysing high-density SNP data. To investigate if such signatures could be the result of selection for equestrian sport performance, we compared our SWB SNP data with those from Exmoor ponies, a horse breed not selected for sport performance traits. Results The genomic scan for homozygous regions identified long runs of homozygosity (ROH) shared by more than 85%…

MaleGenotyping TechniquesPerformanceDIVERSITYBreedingRuns of HomozygosityHorseGenomeHISTORYInbreedingHOMOZYGOSITYGenetics & Heredity0303 health sciencesSnp dataeducation.field_of_studyHomozygoteRUNSASSOCIATIONGenomics04 agricultural and veterinary sciencesBreedDIFFERENTIATIONWarmbloodFemaleLife Sciences & BiomedicineTRAITSResearch ArticleSportsBiotechnologyGENESlcsh:QH426-470lcsh:BiotechnologyPopulationBiologyRuns of homozygosityPolymorphism Single Nucleotide03 medical and health scienceslcsh:TP248.13-248.65GeneticsAnimalsHorsesFunctional studieseducationSelection (genetic algorithm)030304 developmental biologyScience & Technology0402 animal and dairy scienceSelection signature040201 dairy & animal sciencelcsh:GeneticsBiotechnology & Applied MicrobiologyEvolutionary biologyWIDE SCANHaplotype homozygosityBMC Genomics
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Relative Age Effect in the Sport Environment. Role of Physical Fitness and Cognitive Function in Youth Soccer Players

2019

The need to achieve short-term competitive outcomes in sports may influence the emergence of talent selection strategies, which could bias individuals&rsquo

MaleHealth Toxicology and MutagenesisPhysical fitnesslcsh:MedicineAthletic PerformanceArticle050105 experimental psychologyDevelopmental psychology03 medical and health sciencesCognition0302 clinical medicineGames RecreationalSoccerHumansAttention0501 psychology and cognitive sciencesCognitive skillChildYouth sport talent selectionyouth sport talent selectionSelection (genetic algorithm)biologymaturationAthletesbusiness.industrylcsh:R05 social sciencesAge FactorsPublic Health Environmental and Occupational HealthRAECognition030229 sport sciencesAnthropometryRelative age effectbiology.organism_classificationattentionCross-Sectional StudiesAthletesPhysical FitnessSpainMaturation (Psychology)FemaleNull hypothesisbusinessPsychologyInternational Journal of Environmental Research and Public Health
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Multiple identification of a particular type of hereditary C1q deficiency in the Turkish population: review of the cases and additional genetic and f…

1997

Complete selective deficiencies of the complement component C1q are rare genetic disorders that are associated with recurrent infections and a high prevalence of lupus erythematosus-like symptoms. All C1q deficiencies studied at the genetic level revealed single-base mutations leading to termination codons, frameshifts or amino acid exchanges and these were thought to be responsible for the defects as no other aberrations were found. One particular mutation, leading to a stop codon in the C1qA gene, was first identified in members of a Gypsy family from the Slovak Republic. The same mutation has been found in all cases of C1q deficiency from Turkey that have been investigated. Here we prese…

MaleHeterozygoteSlovakiaTurkish populationRomaTurkeyGenetic counselingMolecular Sequence DataPopulationBiologyPolymerase Chain ReactionGenetic analysisGeneticsHumansPoint MutationAmino Acid SequenceeducationGeneGenetics (clinical)Geneticseducation.field_of_studyBase SequenceComplement C1qImmunologic Deficiency SyndromesHuman geneticsStop codonPedigreeChild PreschoolMutation (genetic algorithm)Codon TerminatorFemalePolymorphism Restriction Fragment LengthHuman Genetics
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