PedigreeBreedingModels, GeneticGenetic MarkersGenetic LinkageLod ScoreChromosome MappingGenotypeGenes, DominantHaplotypesPhenotypeMicrosatellite RepeatsUtahInbreedingAllelesQuantitative Trait LociConsanguinityMutationInheritance PatternsQuantitative Trait, HeritableGenetic Predisposition to DiseaseComputer SimulationFamily HealthPolymorphism, Single NucleotideLikelihood FunctionsDNA Mutational AnalysisPenetranceHeterozygoteLinkage DisequilibriumAlgorithmsGenes, RecessiveMolecular Sequence DataGenetic VariationGenome, HumanSoftwareChromosomes, Human, Pair 1Founder EffectGenealogy and HeraldryNuclear FamilyGenetic TestingGenetic HeterogeneityBase SequenceHip Dysplasia, CanineSequence Analysis, DNAFamilyGenetics, PopulationGene FrequencyAge of OnsetChromosomes, Human, Pair 2Models, StatisticalHeterozygote DetectionMultifactorial InheritancePaternityPolymerase Chain ReactionOptic Atrophy, Hereditary, LeberGenome-Wide Association StudyMarkov ChainsHomozygoteChromosomes, Human, Pair 3Monte Carlo MethodProbabilityChromosomes, Human, Pair 6Oligonucleotide Array Sequence AnalysisExonsReproducibility of ResultsChromosomes, Human, Pair 7Genetic Diseases, InbornPolymorphism, GeneticChromosomes, Human, Pair 10Chromosomes, Human, Pair 5Gene Expression ProfilingSyndromeDNA, MitochondrialAmishAdult ChildrenPolymorphism, Restriction Fragment LengthPalauX ChromosomeChromosomes, Human, Pair 12PhylogenyAsian Continental Ancestry GroupGenetics, MedicalMutation, MissenseHeredityChromosomes, Human, Pair 4Point MutationComputational BiologyChromosomes, Human, Pair 19Genetic LociCluster Analysis