A big data approach to explore epigenetic heterogeneity and interpret noncoding variants for psychiatric disorders

探索表观遗传异质性并解释精神疾病非编码变异的大数据方法

• 批准号: 10431884
• 负责人: JING ZHANG
• 金额: $ 11.22万
• 依托单位: UNIVERSITY OF CALIFORNIA-IRVINE
• 依托单位国家: 美国
• 财政年份: 2020
• 资助国家: 美国
• 起止时间: 2020-07-17 至 2024-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10431884
• 关键词: Affect; Award; Big Data; Binding; Biochemistry; Biological Assay; Biological Process; Biophysics; Brain; ChIP-seq; Chromatin; Communities; Computer software; Computing Methodologies; Data; Data Scientist; Databases; Dependence; Development; Dimensions; Disease; Distal; Elements; Enhancers; Entropy; Epigenetic Process; Event; Gaussian model; Gene Expression Regulation; Genes; Genetic; Genetic Risk; Genetic Transcription; Genetic Variation; Genome; Genomics; Heritability; Heterogeneity; Human; Incidence; Individual; Knowledge; Learning; Link; Machine Learning; Maps; Mental disorders; Mentorship; Methods; Modeling; Molecular; Nucleic Acid Regulatory Sequences; Patients; Pattern; Phenotype; Population; Prefrontal Cortex; Proteins; Psychiatric Diagnosis; Regulatory Element; Reporter; Reporting; Research; Research Personnel; Resolution; Resources; Risk Factors; Sampling; Scanning; Scoring Method; Shapes; Signal Transduction; Technology; Training; Training Programs; Transcriptional Regulation; Universities; Untranslated RNA; Variant; Work; base; career development; cell type; deep learning; disorder risk; epigenome; experience; experimental study; functional genomics; gene regulatory network; genetic variant; genome-wide; genomic data; genomic locus; genomic profiles; insight; machine learning method; multimodality; multiple omics; neurogenetics; neuropsychiatric disorder; new therapeutic target; novel; novel sequencing technology; open source; programs; promoter; recruit; research and development; risk variant; therapeutic target; transcription factor; transcriptomics; web services

PROJECT ABSTRACT The incidence of diagnosed psychiatric disorders has been increasing for decades, leaving millions of afflicted individuals. Despite the high heritability, their underlying molecular mechanisms remain elusive. Most risk loci are located in noncoding genomic elements without direct effects on protein products. Comprehensive functional annotation and variant impact quantification are essential to provide new molecular insights and discover therapeutic targets. Recent advances in novel sequencing technologies and community efforts to share genomic data provide unprecedented opportunities to understand how genetic variants contribute to psychiatric diseases. This application describes the development of integrative strategies and machine learning methods to combine novel assays (such as STARR-seq) with population-scale genomic profiles to elucidate the genetic regulatory grammar in the human prefrontal cortex (PFC) and to prioritize genetic variants in psychiatric disorders. Specifically, we will (1) dissect the cis- regulatory landscape of the PFC using population-scale epigenetics data, (2) construct multi- model gene regulatory networks by linking distal cis-regulatory elements to genes using chromatin co-variability analyses, (3) integrate genetic, epigenetic, and transcriptional data to identify key transcription factors and variants that contribute to psychiatric disorders. Distinct from existing efforts focusing on one genome, this proposed work presents a truly novel big-data approach for both modeling gene regulation and investigating disease-risk factors by incorporating heterogeneous multi-omics profiles from hundreds of individuals. The resultant comprehensive list of cis-regulatory elements will expand the number of known functional regions in the human brain by at least an order. We will release our methods and resources in the form of web services, distributed open-source software, and annotation databases, which will also benefit other investigators exploring the genetic underpinnings of neuropsychiatric disorders. In addition to its scientific content, this application proposes a comprehensive training program for preparing an independent investigator in computational genomics and neurogenetics. This training will take place at Yale University (in the Dept. of Molecular Biophysics and Biochemistry) under the mentorship of Prof. Mark Gerstein (functional genomics), Prof. Nenad Sestan (neurogenetics), and Prof. Hongyu Zhao (statistical genetics and machine learning). A committee of experienced psychiatric disease experts and data scientists will also provide advice on both scientific research and career development.

项目摘要 几十年来，诊断出的精神疾病的发病率一直在增加， 留下了数百万受折磨的人尽管遗传率很高，但其潜在的分子 机制仍然难以捉摸。大多数风险基因座位于非编码基因组元件中， 直接影响蛋白质产品。全面的功能注释和变体影响 定量分析对于提供新的分子见解和发现治疗靶点至关重要。 新测序技术的最新进展和社区努力分享 基因组数据提供了前所未有的机会，以了解遗传变异如何贡献 精神疾病。本申请描述了综合战略的发展， 机器学习方法将新的测定（如STARR-seq）与群体规模结合起来，联合收割机 基因组图谱，以阐明人类前额叶皮层（PFC）的遗传调控语法 并优先考虑精神疾病的遗传变异。具体来说，我们将（1）解剖顺- 使用群体规模表观遗传学数据的PFC的监管景观，（2）构建多个 通过使用染色质将远端顺式调控元件连接到基因来模拟基因调控网络 协变分析，（3）整合遗传、表观遗传和转录数据，以确定关键的 转录因子和变异导致精神疾病。区别于现有的 专注于一个基因组的努力，这项拟议的工作提出了一个真正新颖的大数据方法， 通过整合基因调控模型和研究疾病风险因素， 来自数百个个体的异质多组学图谱。由此产生的全面 顺式调节元件的列表将扩大人类中已知功能区域的数量。 大脑至少有一个命令。我们将以Web服务的形式发布我们的方法和资源， 分布式开源软件和注释数据库，这也将有利于其他 研究人员正在探索神经精神疾病的遗传基础。 除了其科学的内容，这一申请提出了一个全面的培训， 程序准备在计算基因组学和神经遗传学的独立调查员。 该培训将在耶鲁大学（系内）进行。分子生物物理学和 Mark Gerstein教授（功能基因组学）、Nenad教授 Sestan（神经遗传学）和Hongyu Zhao教授（统计遗传学和机器学习）。一 经验丰富的精神疾病专家和数据科学家委员会也将提供建议 科学研究和职业发展。