Epistatic and Cross Tissue Analysis for Human Gene Expression Traits
Epistatic and Cross Tissue Analysis for Human Gene Expression Traits
批准号:
8144822
负责人:
JUN S LIU
金额:
$28.4万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-09-17 至 2013-07-31
关键词:
AddressAffectArchitectureBayesian MethodBinding SitesBiological ProcessChromosome MappingCodeCommunitiesComplexDNADataDiseaseGene ExpressionGenesGeneticGenetic EpistasisGenetic VariationGenomicsGenotypeGoalsHumanIndividualIntercistronic RegionIntronsLightLinear RegressionsLinkMapsMethodsModelingMolecularMotivationMusOrganismPhenotypePredispositionRegulator GenesScienceSourceStatistical MethodsStructureSystemTissuesVariantVitelliform macular dystrophybasecohortdisease phenotypedisorder riskfallsgenome wide association studyhuman diseaseinfancymodel developmentnovelpublic health relevanceresearch studysimulationsuccesstraittranscription factoruser friendly software
中文摘要
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英文摘要
DESCRIPTION (provided by applicant):
Epistatic and cross-tissue analysis for human gene expression traits Genome wide association studies (GWAS) have delivered unprecedented rates of discovery associating variations in DNA with common human diseases. However, how these SNPs affect human diseases are not clear in most cases. Gene expression is the intermediate between SNPs and disease phenotypes. Methods to maximally leverage gene expression and genetic variation information collected in human cohorts over multiple tissues show great promise for characterizing not only the genetic architecture of disease but the molecule networks that define disease. The long-term goal of this application is to develop and implement novel statistical methods to identify networks of genes affecting an individual's susceptibility to complex phenotypes like disease. Here, we propose several model developments that not only enhance our power to detect eQTL in single or multiple tissues, but that identify eQTL and interactions among eQTL in the molecular network contexts that define biological processes associated with disease: (1) A Bayesian modeling approach that simultaneously models the total distribution of all genes and all markers will be developed. The strength of our approach will be its ability to detect epistasis with high power when the marginal effects are weak, addressing a key weakness of all other eQTL mapping methods. (2) A likelihood based approach for inferring causal relationships that also incorporates transcription factor binding site information will be developed. (3) An approach for linking subnetworks in different tissues to diseases will be developed. Also a method to dissect causal/ reactive relationships between tissues will be developed. (4) The proposed methods will be extensively validated via simulations and, more importantly, on multi-tissue mouse and human cohort data we have generated. All methods will be implemented in user-friendly software and made available to the scientific community.
PUBLIC HEALTH RELEVANCE:
Epistatic and cross-tissue analysis for human gene expression traits Gene expression is the intermediate between SNPs and disease phenotypes. Methods to maximimally leverage gene expression and genetic variation information collected in human cohorts over multiple tissues show great promise for characterizing not only the genetic architecture of disease but the molecule networks that define disease. We propose several model developments that not only enhance our power to detect eQTL in single or multiple tissues, but that identify eQTL and interactions among eQTL in the molecular network contexts that define biological processes associated with disease.
期刊论文(2)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1080/01621459.2015.1049746
发表时间:
2015
期刊:
Journal of the American Statistical Association
影响因子:
3.7
作者:
[Jiang B, Liu JS]
通讯作者:
Liu JS
Epistatic and Cross Tissue Analysis for Human Gene Expression Traits
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批准号:7935037
-
项目类别:
-
资助金额:$30.38万
-
财政年份:2010
-
负责人:JUN S LIU
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依托单位:
B BURGDORFERI FLAGELLA
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批准号:8168602
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项目类别:
-
资助金额:$1.08万
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财政年份:2010
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负责人:JUN S LIU
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依托单位:
THE INHIBITORY ROLE OF INTEGRIN ?5 IN ADIPOCYTE DIFFERENTIATION
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批准号:7960498
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项目类别:
-
资助金额:$6.47万
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财政年份:2009
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负责人:JUN S LIU
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依托单位:
THE INHIBITORY ROLE OF INTEGRIN ?5 IN ADIPOCYTE DIFFERENTIATION
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批准号:7720905
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项目类别:
-
资助金额:$7.37万
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财政年份:2008
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负责人:JUN S LIU
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依托单位:
Systems Biology of Sporulation in Bacillus Subtilis
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批准号:7161841
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项目类别:
-
资助金额:$32.29万
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财政年份:2006
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负责人:JUN S LIU
-
依托单位:
Systems Biology of Sporulation in Bacillus Subtilis
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批准号:7650273
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项目类别:
-
资助金额:$31.85万
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财政年份:2006
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负责人:JUN S LIU
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依托单位:
Systems Biology of Sporulation in Bacillus Subtilis
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批准号:7253393
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项目类别:
-
资助金额:$31.85万
-
财政年份:2006
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负责人:JUN S LIU
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依托单位:
Systems Biology of Sporulation in Bacillus Subtilis
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批准号:7460720
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项目类别:
-
资助金额:$31.85万
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财政年份:2006
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负责人:JUN S LIU
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依托单位:
Computational Haplotype Analysis for SNPs
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批准号:6463868
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项目类别:
-
资助金额:$35.1万
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财政年份:2002
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负责人:JUN S LIU
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依托单位:
Center for Computational Study of Biological Systems
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批准号:6792647
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项目类别:
-
资助金额:$62.32万
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财政年份:2002
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负责人:JUN S LIU
-
依托单位:
Computational Haplotype Analysis for SNPs
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批准号:6896558
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项目类别:
-
资助金额:$32.6万
-
财政年份:2002
-
负责人:JUN S LIU
-
依托单位:
Computational Haplotype Analysis for SNPs
-
批准号:6765828
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项目类别:
-
资助金额:$32.6万
-
财政年份:2002
-
负责人:JUN S LIU
-
依托单位:
Bayesian Inference of Haplotypes and Genetic Interactions
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批准号:7919529
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项目类别:
-
资助金额:$23.76万
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财政年份:2002
-
负责人:JUN S LIU
-
依托单位:
Bayesian Inference of Haplotypes and Genetic Interactions
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批准号:7485155
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项目类别:
-
资助金额:$23.86万
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财政年份:2002
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负责人:JUN S LIU
-
依托单位:
Computational Haplotype Analysis for SNPs
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批准号:6603789
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项目类别:
-
资助金额:$32.6万
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财政年份:2002
-
负责人:JUN S LIU
-
依托单位:
Bayesian Inference of Haplotypes and Genetic Interactions
-
批准号:7143839
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项目类别:
-
资助金额:$24.24万
-
财政年份:2002
-
负责人:JUN S LIU
-
依托单位:
Bayesian Inference of Haplotypes and Genetic Interactions
-
批准号:7648162
-
项目类别:
-
资助金额:$24.0万
-
财政年份:2002
-
负责人:JUN S LIU
-
依托单位:
Bayesian Inference of Haplotypes and Genetic Interactions
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批准号:7292735
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项目类别:
-
资助金额:$23.67万
-
财政年份:2002
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负责人:JUN S LIU
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依托单位:
海外基金