Genomics Core
基因组学核心
基本信息
- 批准号:10685624
- 负责人:
- 金额:$ 37.73万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2014
- 资助国家:美国
- 起止时间:2014-05-15 至 2024-07-31
- 项目状态:已结题
- 来源:
- 关键词:ATAC-seqAntibodiesArchitectureBindingBinding SitesBioinformaticsCell LineageCellsChIP-seqChromatinCommon CoreConceptionsCore FacilityDNA sequencingDNA-Binding ProteinsDataData AnalysesData SetData Storage and RetrievalDevelopmentE proteinEnhancersEpigenetic ProcessExperimental DesignsGenomic approachGenomicsGrantHost DefenseHumanIndividualInterventionLaboratoriesMapsMethodsMolecularMusNuclearPatternPopulationPostdoctoral FellowPreparationProceduresProcessPromoter RegionsQuality ControlReagentReproducibilityResearch PersonnelSamplingServicesSignal TransductionSiteSpecific qualifier valueStandardizationSystemT-LymphocyteTechniquesTechnologyTrainingWorkbioinformatics pipelinebioinformatics tooldata acquisitiondata sharingeffector T cellexperimental studygenome-widegenome-wide analysisgenomic locusgraduate studentinnovationinsightinstrumentationlaboratory experimentmembermultidimensional datanovelprogenitorprogramsresponsesample fixationsequencing platformsingle cell analysissingle-cell RNA sequencingskillsstem cellssynergismtechnology platformtranscription factortranscriptome sequencingtranscriptomicsγδ T cells
项目摘要
PROJECT SUMMARY/ABSTRACT
The objective of this program project application is to gain insight into the molecular basis by which genome-
wide remodeling of E box DNA binding protein activity, in response to TCR signals, controls the development
and functional specialization of γδ T cells, which are critically important to host defense. In supporting this effort,
the Genomics Core would provide centralized access to scRNA-Seq, ChIP-Seq, ATAC-Seq and HiC
sequencing platforms to allow large-scale genomic location analysis of transcription factors as well as epigenetic
marks to reveal and describe the chromatin landscapes of αβ and γδ T-lineage cells. The Genomics Core would
generate robust single-cell transcriptomic and small-cell-number epigenetic datasets, epigenetic landscapes as
well as methods to describe the folding patterns of human and murine αβ and γδ T-lineage cells in global terms.
The Genomics Core would assist the participating laboratories for experimental design and work closely with
the participating members of the program to analyze individual, as well as, combined data sets. The Genomics
Core will also continue to generate new bioinformatics pipelines to process genome-wide data sets obtained
from bulk populations as well as data obtained from single cells. Finally, in addition to the provision of core
services, the Genomics Core would be a hub for the training of graduate students and postdoctoral fellows in
the utilization of deep DNA sequencing and associated bioinformatics techniques for the participating
laboratories.
项目摘要/摘要
该计划项目应用的目的是洞悉基因组的分子基础
响应TCR信号的E Box DNA结合蛋白活性的广泛重塑,控制了发展
和γδT细胞的功能专业化,这对于宿主防御至关重要。在支持这项工作时,
基因组学核心将提供对SCRNA-SEQ,CHIP-SEQ,ATAC-SEQ和HIC的集中式访问
测序平台允许转录因子和表观遗传的大规模基因组位置分析
标记揭示和描述αβ和γδT-Linege细胞的染色质景观。基因组核心将
生成健壮的单细胞转录组和小细胞表观遗传数据集,表观遗传景观作为
以及描述人类和鼠αβ和γδT-linege细胞的折叠模式的方法。
基因组学核心将帮助参与的实验室进行实验设计,并紧密合作
该计划的参与成员分析个人以及组合数据集。基因组学
核心还将继续生成新的生物信息学管道,以处理获得的全基因组数据集
从批量种群以及从单个细胞获得的数据。最后,除了提供核心
服务,基因组核心将是培训研究生和博士后研究员的枢纽
参与的深度DNA测序和相关的生物信息学技术的利用
实验室。
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)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
CORNELIS MURRE其他文献
CORNELIS MURRE的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('CORNELIS MURRE', 18)}}的其他基金
Genome-wide networks that modulate the T-lineage cell fate
调节 T 谱系细胞命运的全基因组网络
- 批准号:
8608279 - 财政年份:2014
- 资助金额:
$ 37.73万 - 项目类别:
Molecular and physical mechanisms that underpin the αβ versus γδ T cell fate decision
支持 αβ 与 γδ T 细胞命运决定的分子和物理机制
- 批准号:
10462551 - 财政年份:2014
- 资助金额:
$ 37.73万 - 项目类别:
Molecular and physical mechanisms that underpin the αβ versus γδ T cell fate decision
支持 αβ 与 γδ T 细胞命运决定的分子和物理机制
- 批准号:
10226999 - 财政年份:2014
- 资助金额:
$ 37.73万 - 项目类别:
Molecular and physical mechanisms that underpin the αβ versus γδ T cell fate decision
支持 αβ 与 γδ T 细胞命运决定的分子和物理机制
- 批准号:
10685633 - 财政年份:2014
- 资助金额:
$ 37.73万 - 项目类别:
相似国自然基金
人源化小鼠筛选猴痘抗体及机制研究
- 批准号:82373778
- 批准年份:2023
- 资助金额:48 万元
- 项目类别:面上项目
抗HTNV抗体mRNA修饰MSC在肾综合征出血热治疗中的作用研究
- 批准号:82302487
- 批准年份:2023
- 资助金额:30 万元
- 项目类别:青年科学基金项目
人和小鼠中新冠病毒RBD的免疫原性表位及其互作抗体的表征和结构组学规律的比较研究
- 批准号:32371262
- 批准年份:2023
- 资助金额:50 万元
- 项目类别:面上项目
靶向肿瘤内T细胞的双特异性抗体治疗策略研究
- 批准号:82371845
- 批准年份:2023
- 资助金额:49 万元
- 项目类别:面上项目
靶向DLL3和γδ T细胞的双特异抗体对小细胞肺癌的免疫治疗活性研究
- 批准号:32300783
- 批准年份:2023
- 资助金额:30 万元
- 项目类别:青年科学基金项目
相似海外基金
Role of neonatal lung macrophages in mediating resilience to hyperoxia induced lung injury via TREM2 signaling
新生儿肺巨噬细胞通过 TREM2 信号传导介导高氧诱导肺损伤的恢复能力
- 批准号:
10720557 - 财政年份:2023
- 资助金额:
$ 37.73万 - 项目类别:
Assessing Sox 10's effect on chromatin accessibility in enteric neuron lineage diversification
评估 Sox 10 对肠神经元谱系多样化中染色质可及性的影响
- 批准号:
10749740 - 财政年份:2023
- 资助金额:
$ 37.73万 - 项目类别:
Mapping heritable chromatin loop variants with allele-specific Hi-C analysis
通过等位基因特异性 Hi-C 分析绘制可遗传的染色质环变体图谱
- 批准号:
10583721 - 财政年份:2023
- 资助金额:
$ 37.73万 - 项目类别:
Regulation of the lens transcriptome and chromatin architecture by FOXE3
FOXE3 对晶状体转录组和染色质结构的调节
- 批准号:
10546497 - 财政年份:2022
- 资助金额:
$ 37.73万 - 项目类别:
Project II: Immune regulatory circuits in primary colon cancer and lymph node and liver metastases
项目二:原发性结肠癌及淋巴结和肝转移的免疫调节回路
- 批准号:
10525193 - 财政年份:2022
- 资助金额:
$ 37.73万 - 项目类别: