Powerful Inference and Prediction for Genetic Association
Powerful Inference and Prediction for Genetic Association
批准号:
8238373
负责人:
Wei Pan
金额:
$35.86万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-03-10 至 2014-12-31
关键词:
AccountingAffectArrhythmiaAtrial FibrillationBiologicalCandidate Disease GeneCardiacCommunitiesComplexComputer softwareDataData AnalysesDevelopmentDiagnosticDimensionsDiseaseDisease OutcomeDocumentationEquationFamilyFrequenciesGenesGeneticGenetic HeterogeneityGenotypeGoalsGroup StructureGroupingHereditary DiseaseHospitalizationIndividualKnowledgeLeadLinear ModelsMapsMedicineMethodologyMethodsModelingNetwork-basedOther GeneticsPathway interactionsPhasePopulationPredispositionPreventivePublic DomainsPublishingResearchResearch DesignResourcesRisk FactorsStatistical MethodsStructureTechniquesTestingVariantWritingbasecohortgene environment interactiongenetic associationgenetic variantgenome wide association studyhuman diseaseinnovationinstrumentnovelpublic health relevancesoftware developmenttheoriestooltrait
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Genetic association studies aim to map disease genes through comparisons of frequencies of genetic variants among affected and unaffected individuals. Due to usually weak associations between genetic variants and disease, it is critical to apply powerful statistical tests to maximize the chance to locate disease loci. We propose developing novel and powerful multi-locus methods based on penalized regression to detect genetic association for population- or family-based studies with un- phased genotype data. Specifically, statistical methods and theory will be developed and evaluated for statistical inference and prediction based on penalized regression with novel nonconvex penalties for linear models, generalized linear models and generalized estimating equations. We will apply the developed methods to large cohorts in the Candidate gene Association Resource (CARe) for multi- locus analysis to discover atrial fibrillation (AF)-associated variants, possibly by considering gene by gene and gene by environment interactions. Known and newly discovered genetic and other risk factors will be used to predict AF.
PUBLIC HEALTH RELEVANCE: This proposed research is expected not only to contribute valuable analysis tools to the elucidation of genetic components of complex human diseases and traits, but also to advance statistical methodology and theory for high-dimensional data,
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