Advanced Haplotype Analyses in Coronary Artery Disease
Advanced Haplotype Analyses in Coronary Artery Disease
批准号:
7437286
负责人:
ANDREW S ALLEN
金额:
$14.21万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-08-02 至 2010-06-30
关键词:
AddressAffectAreaBiological AssayCandidate Disease GeneCardiologyCardiovascular DiseasesChromosomesCodeCommunitiesComplementComplexComputer softwareCoronary ArteriosclerosisDNA SequenceDataDevelopmentDevelopment PlansDiseaseDocumentationEnvironmentFailureFamilyFosteringFrequenciesGenerationsGeneticGenetic VariationGenotypeHaplotypesHuman GeneticsHuman Genome ProjectIndividualInternetMapsMentorshipMethodologyMethodsModelingNuclear FamilyParentsPerformanceProceduresProteinsRangeResearchResearch DesignResearch PersonnelSamplingScientistSingle Nucleotide PolymorphismStatistical MethodsStressStructureTechniquesTestingTrainingUniversitiesVariantbasecareerdata structuredisorder riskearly onsetfamily structuregenetic epidemiologygenetic pedigreegenetic variantimprovednovelprobandprogramsresearch studysimulationsoftware developmentstatisticstheoriestooluser friendly software
中文摘要
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英文摘要
DESCRIPTION (provided by applicant):
Modeling human genetic variation is critical to understanding the genetic basis of complex disease. The Human Genome Project has discovered millions of DNA sequence variants (single nucleotide polymorphisms or SNPs), and millions more may exist. As the coding for proteins takes place along chromosomes, SNP organization along each chromosome, the haplotype structure, will be most useful for discovering genetic variants associated with disease. Haplotype-based association studies are powerful procedures for detecting genetic influences on complex diseases. However, association tests of haplotype effects with unphased genotype data can be sensitive to estimates of haplotype frequencies even with family-based study designs and complete genotype information.
The broad objectives of this proposal focus on enhancing the arsenal of statistical methods researchers use to dissect genetic factors in complex diseases. Specifically, we propose to apply results from coarsened-data semi-parametric efficient model theory to derive optimal tests and estimates of haplotype and haplotype interaction effects that are robust to haplotype frequencies using unphased, and possibly missing, genotype data. The data structures we will consider are motivated by those found in the Genetics of Early Onset Cardiovascular Disease (GENECARD) study and the GENECARD Offspring Study. In addition, we propose to apply these newly developed techniques to the GENECARD samples in fine mapping and candidate gene studies.
This research will form the core of a 5-year career development plan for Dr. Andrew Allen under the mentorship of three exceptional researchers, each with expertise that complements one another and represent the three areas addressed in this proposal: cardiology, genetics, and statistics. They propose a career development plan that combines didactic and practical training in genetics, cardiology, and genetic epidemiology with an ongoing research program within the unique research environment of Duke University. This career development plan will foster Dr. Allen's development into an established independent quantitative research scientist with expertise in both methodology for dissecting genetic factors in complex disease and cardiovascular genetics.
期刊论文(18)
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Genome-wide association analysis of rheumatoid arthritis data via haplotype sharing.
通过单倍型共享对类风湿性关节炎数据进行全基因组关联分析。
DOI:
10.1186/1753-6561-3-s7-s30
发表时间:
2009
期刊:
BMC proceedings
影响因子:
--
作者:
[Allen,AndrewS, Satten,GlenA]
通讯作者:
Satten,GlenA
Application of a rank-based genetic association test to age-at-onset data from the Collaborative Study on the Genetics of Alcoholism study.
基于等级的遗传关联检验的应用到酒精中毒遗传学协作研究中的年龄大量数据。
DOI:
10.1186/1471-2156-6-s1-s53
发表时间:
2005-12-30
期刊:
BMC GENETICS
影响因子:
2.9
作者:
[Li, YJ, Martin, ER, Zhang, L, Allen, AS]
通讯作者:
Allen, AS
DOI:
10.1186/1471-2156-6-s1-s69
发表时间:
2005-12-30
期刊:
BMC GENETICS
影响因子:
2.9
作者:
[Allen, AS, Satten, GA]
通讯作者:
Satten, GA
Stratification-score matching improves correction for confounding by population stratification in case-control association studies.
分层得分匹配改善了病例对照关联研究中人口分层混淆的校正。
DOI:
10.1002/gepi.21611
发表时间:
2012-04
期刊:
GENETIC EPIDEMIOLOGY
影响因子:
2.1
作者:
[Epstein, Michael P., Duncan, Richard, Broadaway, K. Alaine, He, Min, Allen, Andrew S., Satten, Glen A.]
通讯作者:
Satten, Glen A.
DOI:
10.1186/1753-6561-1-s1-s123
发表时间:
2007
期刊:
BMC proceedings
影响因子:
--
作者:
[Allen AS, Satten GA]
通讯作者:
Satten GA
共 8 条
Design, prediction, and prioritization of systematic perturbations of the human genome
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批准号:10665666
-
项目类别:
-
资助金额:$72.98万
-
财政年份:2021
-
负责人:ANDREW S ALLEN
-
依托单位:
Design, prediction, and prioritization of systematic perturbations of the human genome
-
批准号:10473740
-
项目类别:
-
资助金额:$72.98万
-
财政年份:2021
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负责人:ANDREW S ALLEN
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依托单位:
Design, prediction, and prioritization of systematic perturbations of the human genome
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批准号:10295506
-
项目类别:
-
资助金额:$35.37万
-
财政年份:2021
-
负责人:ANDREW S ALLEN
-
依托单位:
The Duke FUNCTION Center: Pioneering the comprehensive identification of combinatorial noncoding causes of disease
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批准号:10271500
-
项目类别:
-
资助金额:$248.99万
-
财政年份:2020
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负责人:ANDREW S ALLEN
-
依托单位:
Quantifying the genetic diversity of human regulatory element activity
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批准号:10404498
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项目类别:
-
资助金额:$76.48万
-
财政年份:2019
-
负责人:ANDREW S ALLEN
-
依托单位:
Robust Methods for the Efficient Analysis and Integration of DNA Sequence Data
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批准号:7692191
-
项目类别:
-
资助金额:$23.4万
-
财政年份:2008
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负责人:ANDREW S ALLEN
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依托单位:
Robust Methods for the Efficient Analysis and Integration of DNA Sequence Data
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批准号:8064557
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项目类别:
-
资助金额:$20.99万
-
财政年份:2008
-
负责人:ANDREW S ALLEN
-
依托单位:
Robust Methods for the Efficient Analysis and Integration of DNA Sequence Data
-
批准号:7892941
-
项目类别:
-
资助金额:$23.4万
-
财政年份:2008
-
负责人:ANDREW S ALLEN
-
依托单位:
Advanced Haplotype Analyses in Coronary Artery Disease
-
批准号:6934516
-
项目类别:
-
资助金额:$14.21万
-
财政年份:2004
-
负责人:ANDREW S ALLEN
-
依托单位:
Advanced Haplotype Analyses in Coronary Artery Disease
-
批准号:7279291
-
项目类别:
-
资助金额:$14.21万
-
财政年份:2004
-
负责人:ANDREW S ALLEN
-
依托单位:
Advanced Haplotype Analyses in Coronary Artery Disease
-
批准号:6815671
-
项目类别:
-
资助金额:$14.21万
-
财政年份:2004
-
负责人:ANDREW S ALLEN
-
依托单位:
Advanced Haplotype Analyses in Coronary Artery Disease
-
批准号:7094069
-
项目类别:
-
资助金额:$14.21万
-
财政年份:2004
-
负责人:ANDREW S ALLEN
-
依托单位:
海外基金