Core C - Genomics, Animal Models and Advanced Phenotyping Core
核心 C - 基因组学、动物模型和高级表型分析核心
基本信息
- 批准号:10403631
- 负责人:
- 金额:$ 38.62万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2013
- 资助国家:美国
- 起止时间:2013-09-05 至 2023-04-30
- 项目状态:已结题
- 来源:
- 关键词:Animal ModelAnimalsBiological AssayBiological ProcessBreedingCardiovascular ModelsCardiovascular systemCellsCenters of Research ExcellenceClinicalCollectionComplementConsultationsCountryCustomData SetDiseaseEnsureEquipmentFacultyFaculty WorkshopFee-for-Service PlansFundingGene ExpressionGenerationsGenesGenetic EngineeringGenomicsGenotypeGoalsGrantHealthHigh PrevalenceHistorically Black Colleges and UniversitiesInbred MouseInbreedingInfrastructureInstitutionInstructionKidneyKidney DiseasesKnockout MiceLettersMaintenanceMeasurementMedical centerMetabolic DiseasesMethodologyMethylationMississippiModelingMolecularMolecular GeneticsMorbidity - disease rateObesityPhasePhenotypePhysiologicalPopulationPreparationProteinsPublicationsRattusResearchResearch PersonnelResearch Project GrantsScientific Advances and AccomplishmentsScientistServicesSmall RNAStudentsSupervisionSystems BiologyTechnical ExpertiseTechniquesTechnologyTrainingTraining and EducationTransgenic MiceTransgenic OrganismsUnited StatesUnited States National Institutes of HealthUniversitiesWorkanimal model developmentbasebioinformatics toolepigenetic regulationepigenomeexome sequencinggenome sequencinggenomic dataimprovedinsightinstrumentationmeetingsmetabolic phenotypemicrobialmortalitymouse modelmultidisciplinarynext generation sequencingnovelservice deliverytraining opportunitytranscriptometranscriptome sequencingundergraduate studentwhole genome
项目摘要
CORE C – GENOMICS, ANIMAL MODELS AND ADVANCED PHENOTYPING
PROJECT SUMMARY/ABSTRACT
The goal of the Cardiorenal and Metabolic Disease Research Center (CMDRC) COBRE is to bring together
a multidisciplinary group of basic, clinical, and population scientists to work synergistically on the theme of
cardiorenal and metabolic diseases. During Phase 1, CMDRC-Core C provided COBRE investigators and
external researchers' access to technical expertise and equipment to perform a wide variety of molecular,
genetic, microarray and gene expression studies that would otherwise not be possible. Core C also provided
investigators at UMMC access to novel transgenic and knockout mouse and rat models of cardiovascular
renal and metabolic disease that are only available at UMMC. In total, CMDRC-Core C completed several
hundred genomic studies as well as generated thousands of animals for detailed phenotyping resulting in
numerous publications and several NIH R01 funded grants. In Phase II, CMDRC-Core C major project, pilot
grants, and external researchers will have access to state-of-the-art genomic technologies through the
Genomics Sub-Core and large collection of animal models (inbred, transgenic, and gene-edited rat and
mouse models) as well as advanced phenotyping methodologies through the Animal Models and Advanced
Phenotyping Sub-Core. Core C has four aims: (1) to provide CMDRC investigators access to technical
expertise and cutting-edge genomic services, including next generation sequencing technologies (RNA
sequencing, 16S microbial sequencing, custom amplicon panels, whole genome sequencing, and exome
sequencing); (2) to provide CMDRC investigators access to large collection of unique animal models of
obesity, cardiorenal and metabolic diseases, along with training in advanced phenotyping techniques; (3) to
provide education and training opportunities for students, trainees, and faculty in genomics technologies and
advanced animal phenotyping; and (4) to provide continuous improvement in existing assays, services, and
enhance technological capabilities through acquisition of new cutting-edge instrumentation that will assist in
sustainability of the Core. Therefore, it is the objective of the CMDRC-Core C to aid investigators in advancing
scientific discovery in obesity, cardiorenal, and metabolic diseases through application of state-of-the-art
genomic technologies, specialized animal models, and advanced physiological measurements to generate
greater insight into these diseases. Aside from CMDRC investigators, continued funding of the COBRE during
Phase II will have a significant impact on providing external researchers (at other Mississippi undergraduate
institutions and Historically Black Colleges and Universities (HBCUs)] access to equipment and expertise that
would otherwise not be available in our region of the country.
核心 C – 基因组学、动物模型和高级表型分析
项目概要/摘要
心肾和代谢疾病研究中心 (CMDRC) COBRE 的目标是将
由基础、临床和人口科学家组成的多学科小组,就以下主题协同工作
心肾和代谢疾病。在第一阶段,CMDRC-Core C 提供了 COBRE 研究人员和
外部研究人员获得技术专业知识和设备来执行各种分子、
原本不可能进行的遗传、微阵列和基因表达研究。还提供了核心C
UMMC 的研究人员获得新型转基因和基因敲除小鼠和大鼠心血管模型
肾脏和代谢疾病仅在 UMMC 提供。总共,CMDRC-Core C 完成了多项
数百个基因组研究以及数千只动物进行详细的表型分析,从而产生
许多出版物和多项 NIH R01 资助的赠款。第二阶段,CMDRC-Core C重大项目,试点
赠款,外部研究人员将可以通过以下方式获得最先进的基因组技术
基因组学子核心和大量动物模型(近交系、转基因和基因编辑的大鼠和
小鼠模型)以及通过动物模型和高级表型分析方法
表型子核心。核心 C 有四个目标:(1) 为 CMDRC 调查人员提供技术支持
专业知识和尖端基因组服务,包括下一代测序技术(RNA
测序、16S 微生物测序、定制扩增子组合、全基因组测序和外显子组
测序); (2) 为 CMDRC 研究人员提供大量独特的动物模型
肥胖、心肾和代谢疾病,以及先进表型分析技术的培训; (3) 至
为学生、实习生和教师提供基因组学技术方面的教育和培训机会
先进的动物表型分析; (4) 不断改进现有的检测、服务和
通过购买新的尖端仪器来增强技术能力,这将有助于
核心的可持续性。因此,CMDRC-Core C 的目标是帮助调查人员推进
通过应用最先进的技术对肥胖、心肾和代谢疾病进行科学发现
基因组技术、专门的动物模型和先进的生理测量来产生
对这些疾病有更深入的了解。除了 CMDRC 调查员之外,COBRE 在
第二阶段将对提供外部研究人员(密西西比州其他本科生)产生重大影响。
机构和传统黑人学院和大学 (HBCU)] 获得设备和专业知识
否则将无法在我们国家的地区使用。
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 }}
MICHAEL R GARRETT其他文献
MICHAEL R GARRETT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('MICHAEL R GARRETT', 18)}}的其他基金
Omics, Bioinformatics and Flow Cytometry Core
组学、生物信息学和流式细胞术核心
- 批准号:
10630580 - 财政年份:2023
- 资助金额:
$ 38.62万 - 项目类别:
Core A- Administration, Education, and Mentoring
核心 A- 管理、教育和指导
- 批准号:
10553865 - 财政年份:2023
- 资助金额:
$ 38.62万 - 项目类别:
Genetic Targets of Hypertension End Organ Damage
高血压终末器官损伤的遗传靶标
- 批准号:
10198017 - 财政年份:2018
- 资助金额:
$ 38.62万 - 项目类别:
Genetic Targets of Hypertension End Organ Damage
高血压终末器官损伤的遗传靶标
- 批准号:
9920359 - 财政年份:2018
- 资助金额:
$ 38.62万 - 项目类别:
Core C - Genomics, Animal Models and Advanced Phenotyping Core
核心 C - 基因组学、动物模型和高级表型分析核心
- 批准号:
10159921 - 财政年份:2013
- 资助金额:
$ 38.62万 - 项目类别:
Genetics of Renal End Organ Damage in Hypertension
高血压肾终末器官损伤的遗传学
- 批准号:
8477235 - 财政年份:2009
- 资助金额:
$ 38.62万 - 项目类别:
Genetics of Renal End Organ Damage in Hypertension
高血压肾终末器官损伤的遗传学
- 批准号:
8289584 - 财政年份:2009
- 资助金额:
$ 38.62万 - 项目类别:
相似海外基金
The earliest exploration of land by animals: from trace fossils to numerical analyses
动物对陆地的最早探索:从痕迹化石到数值分析
- 批准号:
EP/Z000920/1 - 财政年份:2025
- 资助金额:
$ 38.62万 - 项目类别:
Fellowship
Animals and geopolitics in South Asian borderlands
南亚边境地区的动物和地缘政治
- 批准号:
FT230100276 - 财政年份:2024
- 资助金额:
$ 38.62万 - 项目类别:
ARC Future Fellowships
The function of the RNA methylome in animals
RNA甲基化组在动物中的功能
- 批准号:
MR/X024261/1 - 财政年份:2024
- 资助金额:
$ 38.62万 - 项目类别:
Fellowship
Ecological and phylogenomic insights into infectious diseases in animals
对动物传染病的生态学和系统发育学见解
- 批准号:
DE240100388 - 财政年份:2024
- 资助金额:
$ 38.62万 - 项目类别:
Discovery Early Career Researcher Award
Zootropolis: Multi-species archaeological, ecological and historical approaches to animals in Medieval urban Scotland
Zootropolis:苏格兰中世纪城市动物的多物种考古、生态和历史方法
- 批准号:
2889694 - 财政年份:2023
- 资助金额:
$ 38.62万 - 项目类别:
Studentship
Using novel modelling approaches to investigate the evolution of symmetry in early animals.
使用新颖的建模方法来研究早期动物的对称性进化。
- 批准号:
2842926 - 财政年份:2023
- 资助金额:
$ 38.62万 - 项目类别:
Studentship
Study of human late fetal lung tissue and 3D in vitro organoids to replace and reduce animals in lung developmental research
研究人类晚期胎儿肺组织和 3D 体外类器官在肺发育研究中替代和减少动物
- 批准号:
NC/X001644/1 - 财政年份:2023
- 资助金额:
$ 38.62万 - 项目类别:
Training Grant
RUI: Unilateral Lasing in Underwater Animals
RUI:水下动物的单侧激光攻击
- 批准号:
2337595 - 财政年份:2023
- 资助金额:
$ 38.62万 - 项目类别:
Continuing Grant
RUI:OSIB:The effects of high disease risk on uninfected animals
RUI:OSIB:高疾病风险对未感染动物的影响
- 批准号:
2232190 - 财政年份:2023
- 资助金额:
$ 38.62万 - 项目类别:
Continuing Grant
A method for identifying taxonomy of plants and animals in metagenomic samples
一种识别宏基因组样本中植物和动物分类的方法
- 批准号:
23K17514 - 财政年份:2023
- 资助金额:
$ 38.62万 - 项目类别:
Grant-in-Aid for Challenging Research (Exploratory)














{{item.name}}会员




