Statistical Methods for Rare Variant Association Studies
Statistical Methods for Rare Variant Association Studies
批准号:
9022785
负责人:
Qiuying Sha
金额:
$43.69万
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-05-17 至 2020-04-30
关键词:
AccountingChargeChromosome MappingCommunitiesComplexComplex Genetic TraitComputer softwareDataData SetDetectionDevelopmentDevelopmental ProcessDiseaseDocumentationEnvironmentEpidemiologistEtiologyFamilyFundingGene FrequencyGenesGeneticGenotypeGrowthGuidelinesIndividualMeasuresMethodologyMethodsMinorPerformancePhenotypePlayPopulationPopulation ControlPositioning AttributeReportingResearchResearch AssistantResearch DesignResearch PersonnelResearch Project GrantsRoleSeriesStatistical MethodsStratificationStudentsTargeted ResearchTechnologyTestingTimeUncertaintyVariantbasecomputerized toolsdesigngenetic pedigreegenetic variantgenome wide association studygraduate studentinterestlecturesnext generation sequencingnovelpopulation basedpublic health relevancerare variantsimulationsimulation softwaresoftware developmentsoundtraitundergraduate studentwhole genome
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): There is increasing interest in detecting associations between rare variants and complex traits, for the following reasons: (1) the common variants identified through genome-wide association studies (GWAS) account for only a small portion of the presumed phenotypic variation and (2) the development of next-generation sequencing technology has made it feasible to directly test all rare variants. Although many statistical methods have been developed for detecting associations between rare variants and complex traits, effectively controlling for population stratification in rare variant association studies i still an open problem. Furthermore, it has been realized that every trait or disease develops over a period of time. If this developmental process is ignored, it reduces the power in rare variant association studies. However, statistical methods for longitudinal phenotypes in rare variant association studies are still underdeveloped. This project explores novel statistical methods to detect rare variants responsible for complex diseases, which include (1) a novel statistical method to control for population stratification in rare variant association studies that is applicale to a wide range of study designs, (2) novel, family-based rare variant association tests that are based on a retrospective view and thus can account for complex and undefined ascertainment of pedigrees, and (3) new rare variant association tests for longitudinal phenotypes that use growth trajectories as a phenotype instead of using phenotype values at one time point. The last specific aim of this project is to use extensive simulation studies to compare the performance of the proposed methods with that of the existing methods, apply the proposed methods to selected real data sets, and develop computer software for the proposed methods and release the software to the scientific community at no charge. If this AREA project can be funded, we will directly support two graduate research assistants majoring in statistical genetics (one full-time support and one
summer support) and two part-time (summer support) senior undergraduate students. The students involved in this project will perform simulation studies and analyze real data sets. Thus,
this project can increase the number of students exposed to meritorious research. The availability of funded research positions provided by this project will enable the investigators to
make significant efforts toward attracting senior undergraduate and graduate students to research. Research results from this project will be also used in reports, presentations and development of short lectures for our statistical genetics seminar series and these research results presented in our seminar can stimulate the research interests of graduate students. Attracting senior undergraduate and graduate students to research and stimulating the research interests of graduate students will greatly enhance the research environment in the department.
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DOI:
10.1038/srep34323
发表时间:
2016-10-03
期刊:
Scientific reports
影响因子:
4.6
作者:
[Liang X, Wang Z, Sha Q, Zhang S]
通讯作者:
Zhang S
A gene based approach to test genetic association based on an optimally weighted combination of multiple traits.
一种基于基因的方法,基于多个性状的最佳加权组合来测试遗传关联。
DOI:
10.1371/journal.pone.0220914
发表时间:
2019
期刊:
PloS one
影响因子:
3.7
作者:
[Zhang,Jianjun, Sha,Qiuying, Liu,Guanfu, Wang,Xuexia]
通讯作者:
Wang,Xuexia
DOI:
10.1371/journal.pone.0190788
发表时间:
2018
期刊:
PloS one
影响因子:
3.7
作者:
[Zhu H, Zhang S, Sha Q]
通讯作者:
Sha Q
DOI:
10.1002/gepi.22124
发表时间:
2018-06
期刊:
Genetic epidemiology
影响因子:
2.1
作者:
[Liang X, Sha Q, Rho Y, Zhang S]
通讯作者:
Zhang S
DOI:
10.1111/ahg.12260
发表时间:
2018-11
期刊:
Annals of human genetics
影响因子:
1.9
作者:
[Liang X, Sha Q, Zhang S]
通讯作者:
Zhang S
Statistical Methods for Family-Based Association Studies
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批准号:8243121
-
项目类别:
-
资助金额:$7.8万
-
财政年份:2012
-
负责人:Qiuying Sha
-
依托单位:
Statistical Methods for Family-Based Association Studies
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批准号:8470203
-
项目类别:
-
资助金额:$7.8万
-
财政年份:2012
-
负责人:Qiuying Sha
-
依托单位:
国内基金
海外基金
CHARGE综合征致病基因CHD7介导的三维转录调控网络研究
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批准号:--
-
项目类别:面上项目
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资助金额:51万元
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批准年份:2022
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负责人:朱艳芬
-
依托单位:
Sema3E在CHARGE综合症中的作用及机制研究
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批准号:81160144
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项目类别:地区科学基金项目
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资助金额:52.0万元
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批准年份:2011
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负责人:徐洪
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依托单位: