Epigenomics Core
Epigenomics Core
批准号:
7943657
负责人:
John Greally
金额:
$2.88万
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:
2010-04-01 至 2015-03-31
关键词:
AdipocytesAdministratorAreaBeta CellBioinformaticsBiologicalBiological AssayCellsChromatinCommitComplications of Diabetes MellitusComputational BiologyCore FacilityDNA MethylationData AnalysesData SetData Storage and RetrievalDevelopmentDiabetes MellitusEducational workshopFosteringGene ExpressionGenerationsGeneticGoalsHepatocyteHigh Performance ComputingHumanImmuneInformaticsInstructionInsulinJournalsKidneyLaboratoriesMetabolic DiseasesMetabolismMethodologyMissionModificationMolecularMolecular GeneticsMutationNeuronsObesityPatientsPopulationPostdoctoral FellowProcessProtocols documentationQuality ControlResearchResearch PersonnelResourcesRodent ModelRoleScientistServicesSkeletal MuscleStudentsSystemTissuesTrainingVascular Endothelial CellWorkblood glucose regulationcandidate identificationcohortcomparativecomputing resourcescost effectivediabetes mellitus geneticsepigenomicshigh throughput screeningimprovedinformation assurancemouse modelrelational databasetool
中文摘要
表观基因组学核心的任务是协助研究人员进行专门的表观基因组学分析
并对这些大型数据集进行全面的数据分析。通过与其他核心的协作努力
在DRTC中,明确的药理、饮食、环境和遗传改变的影响是
以其对葡萄糖动态平衡、胰岛素作用和新陈代谢的影响为特征。的作用
相关组织的基因修饰,如神经元、肝细胞、骨骼肌、脂肪细胞、β
而与葡萄糖动态平衡相关的免疫细胞可以通过彻底的和
在啮齿动物模型中进行了明确的实验。可以在功能上确认候选目标的识别
或者通过产生特定的小鼠模型来反驳,并通过比较在人类种群中进行验证
在多个队列/群体中进行分析。虽然这是一个快速发展的领域,但广泛的专业知识
聚集在爱因斯坦表观基因组学中心,包括分子遗传学,生物信息学和
计算生物学专业知识允许表观基因组学核心为DRTC调查人员提供服务
与了解新陈代谢相关的各种专门的、高质量的方法和工具
疾病过程。为了实现这些目标,表观基因组学核心将:1)向研究人员提供
专业的高通量分子技术资源,包括微阵列和大规模并行
研究DNA甲基化和染色质组织的测序平台;2)提供广泛的质量
所有高通量分析的控制和保证信息,作为每次分析的一部分;3)
提供随时可用的专用系统管理员和程序员、关系数据库服务、
通过计算和统计表观基因组学资源和研究信息学提供高性能的计算资源和数据存储/备份系统;4)就用于所提出的特定生物学问题的最佳实验平台和方案向研究人员提供建议;5)通过每周讲习班和期刊俱乐部传播当前和新的技术发展信息,并促进研究人员的互动;6)在实验室对学生、博士后研究员、研究人员和技术人员进行表观基因组学方法和数据分析方面的培训。所有这些服务都提供给糖尿病研究的新手,以及从事糖尿病相关项目的研究人员,这些项目可以通过使用这一核心的专门知识和设施得到丰富和扩展。
英文摘要
The mission of the Epigenomics Core is to assist investigators in performing specialized epigenomics assays
and comprehensive data analyses of these large datasets. Through collaborative efforts with the other Cores
of the DRTC, the effects of defined pharmacological, dietary, environmental and genetic alterations are
thoroughly characterized for their effects on glucose homeostasis, insulin action, and metabolism. The role of
genetic modifications in relevant tissues, such as neurons, hepatocytes, skeletal muscle, adipocytes, beta
and immune cells that are related to glucose homeostasis can be directly compared by thorough and
definitive experimentation in rodent models. Identification of candidate targets can be functionally confirmed
or refuted by the generation of specific mouse models and validated in human populations by comparative
analyses in multiple cohorts/populations. Although this is a rapidly developing field, the broad expertise
assembled at Einstein's Center for Epigenomics including molecular genetics, bioinformatics and
computational biology expertise allows the Epigenomics Core to provide services to DRTC investigators with
a wide range of specialized, high quality methodologies and tools relevant to understanding metabolic
disease processes. To accomplish these goals, the Epigenomics Core will: 1) make available to investigators
specialized high-throughput molecular technological resources including microarray and massively-parallel
sequencing platforms to study DNA methylation and chromatin organization; 2) provide extensive quality
controls and assurance information for all high-throughput assays, generated as part of each analysis; 3)
provide readily available dedicated systems administrators and programmers, relational database services,
high-performance computing resources and data storage/backup systems through the Computational and Statistical Epigenomics Resource and Research Informatics; 4) advise investigators regarding the best experimental platforms and protocols to use for the specific biological question being asked; 5) disseminate current and new technological development information and foster investigator Interactions through weekly workshops and journal clubs; and 6) provide laboratory training of students, postdoctoral fellows, investigators and technical staff in performing epigenomics methodologies and data analyses. All these services are available to investigators new to diabetes research, as well as to investigators working on diabetes-related projects that can be enriched and extended by the use of the expertise and facilities of this core.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
A Clinical Trial of GenomeDiver for Improved Diagnosis of Pediatric Rare Diseases
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批准号:10689316
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资助金额:$22.41万
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财政年份:2022
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依托单位:
A Clinical Trial of GenomeDiver for Improved Diagnosis of Pediatric Rare Diseases
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批准号:10433004
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资助金额:$28.31万
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依托单位:
Understanding cellular and transcriptional regulatory changes in human aging.
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批准号:10427922
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项目类别:
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资助金额:$7.2万
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财政年份:2018
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负责人:John Greally
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依托单位:
UNDERSTANDING CELLULAR AND TRANSCRIPTIONAL REGULATORY CHANGES IN HUMAN AGING
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批准号:10667773
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项目类别:
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资助金额:$8.64万
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财政年份:2018
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负责人:John Greally
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依托单位:
The Einstein-Montefiore Diversity, Equity, Inclusion, and Accessibility (DEIA) Mentorship program
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批准号:10605137
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项目类别:
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资助金额:$41.71万
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财政年份:2018
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负责人:John Greally
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依托单位:
UNDERSTANDING CELLULAR AND TRANSCRIPTIONAL REGULATORY CHANGES IN HUMAN AGING
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批准号:10407046
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项目类别:
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资助金额:$71.28万
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财政年份:2018
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负责人:John Greally
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依托单位:
Project 2: Molecular signatures for ME/CFS sub-types
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批准号:10246407
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项目类别:
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资助金额:$26.43万
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财政年份:2017
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负责人:John Greally
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依托单位:
Mapping and Functional Analysis of RNA:DNA Hybrid-Forming Loci
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批准号:8316684
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项目类别:
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资助金额:$25.05万
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财政年份:2012
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负责人:John Greally
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依托单位:
Mapping and Functional Analysis of RNA:DNA Hybrid-Forming Loci
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批准号:8529570
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项目类别:
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资助金额:$20.14万
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财政年份:2012
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负责人:John Greally
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依托单位:
In vivo imaging of X inactivation
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批准号:9185246
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项目类别:
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资助金额:$19.08万
-
财政年份:2010
-
负责人:John Greally
-
依托单位:
In vivo imaging of X inactivation
-
批准号:8267685
-
项目类别:
-
资助金额:$59.63万
-
财政年份:2010
-
负责人:John Greally
-
依托单位:
In vivo imaging of X inactivation
-
批准号:8470606
-
项目类别:
-
资助金额:$56.71万
-
财政年份:2010
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负责人:John Greally
-
依托单位:
In vivo imaging of X inactivation
-
批准号:8662216
-
项目类别:
-
资助金额:$38.23万
-
财政年份:2010
-
负责人:John Greally
-
依托单位:
In vivo imaging of X inactivation
-
批准号:8142157
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项目类别:
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资助金额:$60.82万
-
财政年份:2010
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负责人:John Greally
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依托单位:
Genome-wide DNA Methylation Profiles Associated with Abnormal Intrauterine Growth
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批准号:8488298
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项目类别:
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资助金额:$33.69万
-
财政年份:2009
-
负责人:John Greally
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依托单位:
Genome-wide DNA Methylation Profiles Associated with Abnormal Intrauterine Growth
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批准号:7928865
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项目类别:
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资助金额:$41.09万
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财政年份:2009
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负责人:John Greally
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依托单位:
Epigenetics Landscape of Chronic Kidney Disease
-
批准号:7930689
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项目类别:
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资助金额:$36.98万
-
财政年份:2009
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负责人:John Greally
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依托单位:
Genome-wide DNA Methylation Profiles Associated with Abnormal Intrauterine Growth
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批准号:8301705
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项目类别:
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资助金额:$39.44万
-
财政年份:2009
-
负责人:John Greally
-
依托单位:
Epigenetics Landscape of Chronic Kidney Disease
-
批准号:8524098
-
项目类别:
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资助金额:$30.56万
-
财政年份:2009
-
负责人:John Greally
-
依托单位:
Epigenetics Landscape of Chronic Kidney Disease
-
批准号:7727134
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项目类别:
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资助金额:$37.35万
-
财政年份:2009
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负责人:John Greally
-
依托单位:
海外基金