Dominance on the human genome and non-additive polygenic models for predicting complex traits
人类基因组的优势和用于预测复杂性状的非加性多基因模型
基本信息
- 批准号:10283330
- 负责人:
- 金额:$ 8.28万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2021
- 资助国家:美国
- 起止时间:2021-08-01 至 2023-07-31
- 项目状态:已结题
- 来源:
- 关键词:AccountingAddressAdmixtureAffectBiologicalBiologyCollaborationsCommunitiesComplexComputing MethodologiesData AnalysesDemographyDevelopmentDiseaseEcologyEuropeanEvolutionGeneticGenomeGenomic SegmentGenomicsHumanHuman GenomeIndividualJournalsKnowledgeLightMachine LearningMentorsMethodsMinority GroupsModelingModernizationMutationOutcomePatternPhasePhenotypePlayPopulationPopulation GeneticsPopulation HeterogeneityRecording of previous eventsReportingResearch PersonnelResearch TrainingResolutionRoleSeriesShapesStatistical MethodsStudy SubjectTestingTrainingVariantWorkbasebiobankdisorder riskexperiencefitnessfunctional genomicsgenetic variantgenome wide association studygenome-widegenomic datahuman population geneticsimprovedinsightmachine learning methodnovelpolygenic risk scoreprecision medicinepredictive modelingrisk predictionsimulationtraining opportunitytrait
项目摘要
Project Abstract
Dominance is one of the most fundamental concepts in genetics and has many key implications in population
genetics, as it ultimately determines how selection manifests in a population. However, despite its unarguable
importance, dominance is also one of the least characterized quantities in genetics, especially in humans, with
the major challenge being current methods cannot distinguish dominance from the fitness effect of genomic
variants. This proposed K99/R00 work will systematically address this longstanding problem from a dual-
perspectives, by inferring dominance in humans and quantitatively model its role in shaping the phenotypes of
complex traits and diseases. Specifically, in Aim1, I will develop a powerful machine learning-based method to
infer the realistic distribution of dominance on the human genome in megabase-scale, leveraging archaic
introgressed ancestry in non-African populations that is sensitive to dominance variation in genomic regions. In
Aim 2, I will develop non-additive polygenic models accounting for dominance in full genomic regions to identify
complex traits profiled in UK Biobank that deviate from additive models, improve the accuracy of phenotype and
disease risk predictions, and contribute to an in-depth understanding of complex trait biology. Finally, in Aim 3
(R00 phase), I will extend these approaches to infer dominance variation in worldwide populations and
investigate how dominance, combined with selection and admixture, determines complex trait phenotypes in
diverse human populations. The mentored phase of this work will take place at the Department of Ecology and
Evolutionary Biology at UCLA, where Dr. Zhang will have access to rich training opportunities and be supported
by active scientific communities, including numerous seminar series, journal clubs, and networking activities. Dr.
Kirk Lohmueller (primary mentor) and Dr. Sriram Sankararaman (co-mentor) will train Dr. Zhang in computational
and statistical methods in population genetics, machine learning applications, and large-scale disease
association data analysis. The research trainings, collaborations, and professional development during the K99
phase will assist Dr. Zhang in becoming an independent investigator in human population genetics.
项目摘要
优势是遗传学中最基本的概念之一,对人群具有许多关键意义
遗传学,因为它最终决定了选择如何在人群中表现出来。但是,尽管它毫不掩饰
重要性,优势也是遗传学数量最少的统治之一,尤其是在人类中,
主要的挑战是当前方法无法区分基因组的适应性效应
变体。这项提出的K99/R00工作将系统地解决这一长期存在的问题。
观点,通过推断人类的主导地位,并定量地模拟其在塑造表型中的作用
复杂的特征和疾病。具体来说,在AIM1中,我将开发一种强大的基于机器学习的方法来
推断出巨型巴布斯规模中人类基因组的统治地位的现实分布,利用古老
非非洲种群中的侵入祖先对基因组区域的优势差异敏感。在
AIM 2,我将开发非加性的多基因模型,以确定完整基因组区域的优势
在英国生物库中介绍的复杂性状,偏离添加剂模型,提高表型和
疾病的风险预测,并有助于对复杂性状生物学的深入了解。最后,在目标3中
(r00阶段),我将扩展这些方法以推断全球人口中的优势差异
调查优势如何与选择和混合结合,决定了复杂的性状表型
多样化的人口。这项工作的指导阶段将在生态学系发生,
加州大学洛杉矶分校的进化生物学,张博士将获得丰富的培训机会并得到支持
由活跃的科学社区,包括众多研讨会系列,期刊俱乐部和网络活动。博士
Kirk Lohmueller(主要导师)和Sriram Sankararaman博士(Co-Incermor)将训练Zhang博士的计算
人口遗传学,机器学习应用和大规模疾病的统计方法
协会数据分析。 K99期间的研究培训,合作和专业发展
阶段将帮助张博士成为人口遗传学的独立研究者。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Xinjun Zhang其他文献
Xinjun Zhang的其他文献
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{{ truncateString('Xinjun Zhang', 18)}}的其他基金
Dominance on the human genome and non-additive polygenic models for predicting complex traits
人类基因组的优势和用于预测复杂性状的非加性多基因模型
- 批准号:
10456164 - 财政年份:2021
- 资助金额:
$ 8.28万 - 项目类别:
Dominance on the Human Genome and Non-additive Polygenic Models for Predicting Complex Traits
人类基因组的主导地位和用于预测复杂性状的非加性多基因模型
- 批准号:
10755393 - 财政年份:2021
- 资助金额:
$ 8.28万 - 项目类别:
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