Genomics and Molecular Resources Core
基因组学和分子资源核心
基本信息
- 批准号:10007633
- 负责人:
- 金额:$ 11.86万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2016
- 资助国家:美国
- 起止时间:2016-09-21 至 2021-08-31
- 项目状态:已结题
- 来源:
- 关键词:AddressAdultAgeAutoantigensAutoimmune ProcessBioinformaticsBiological AssayCRISPR/Cas technologyCaliforniaChildhoodClinicalClinical DataCollaborationsCollectionConsultationsDataData AnalysesDatabase and Analysis PortalDiseaseEnsureEpigenetic ProcessFacultyFlow CytometryFutureGenerationsGenomicsGoalsGrowthImmuneImmunologicsImmunologyImmunophenotypingIndividualInfrastructureInternationalLaboratoriesLaboratory PersonnelLaboratory ResearchLeadershipLymphocyteManagement Information SystemsMass Spectrum AnalysisMedicineMolecularMonitorMutationPatientsPhenotypePlayPluripotent Stem CellsProcessProductionProteomicsQuality ControlResearchResearch InfrastructureResearch PersonnelResourcesRheumatismRheumatologyRoleSamplingSan FranciscoSecureServicesSignal TransductionSoftware ToolsSpecimenStatistical Data InterpretationSystemTechnologyTestingTrainingUniversitiesWorkbasebiobankclinical phenotypecytokineexperiencegenome editinggenomic toolshuman datahuman subjectinnovationinterestmicrobiome analysismolecular phenotypenew technologynoveloutreachphenotypic dataprecision medicineranpirnasesample collectionservice coordinationsuccesstool
项目摘要
PROJECT SUMMARY/ABSTRACT – Genomics and Molecular Resources Core
The overall goal of our Center is to advance precision medicine in the rheumatic diseases. The Genomics and
Molecular Resources (GMR) Core will play a critical role in our Center by facilitating access to biospecimens
from well-characterized rheumatic disease patients, and providing consultative and coordination services to
ensure appropriate use of genomics, proteomics, and other molecular technologies that have the potential to
advance precision medicine in rheumatology. The GMR Core will streamline laboratory research
infrastructure, including acquisition, processing, storage and management of biospecimens by consolidating
existing rheumatology biospecimens at UCSF and establishing a state-of-the-art Laboratory Information
Management System (LIMS) that will enable us to expand sample collection and create an accessible
biorepository. These activities will occur within the laboratory of Dr. Pui-Yan Kwok, Co-Director of the GMR
Core, whose experience as Faculty Director of the UCSF Genomics Core over the past decade makes him
highly qualified to direct these activities. Core leadership will also provide consultation related to the
appropriate application of genomics and molecular assays (including proteomic and immunologic phenotyping)
and will serve as a liaison between investigators and laboratory personnel to ensure that consistently high
quality genomic and molecular phenotyping data are obtained. A panel of genomics and molecular
phenotyping experts will serve as consultants for P30 investigators and projects, covering a wide range of
expertise including genomics, epigenetics, proteomics, immune phenotyping, lymphocyte signaling,
microbiome analysis, and production of pluripotent stem cells. The GMR Core will work closely with the
Human Subjects and Clinical Phenotyping (HSCP) Core to coordinate selection of the appropriate rheumatic
disease patients and clinical data for Center studies, and with the Integrative Bioinformatics (IB) Core to
integrate genomic and molecular data with clinical data for statistical analysis. Key strengths of the GMR Core
include the substantial existing rheumatic disease biospecimens that will be consolidated and centrally
managed using a state-of-the-art LIMS; internationally renowned experts in genomics and molecular
phenotyping for rheumatic, autoimmune and other disorders; facilities for generating state-of-the-art genomics
and other molecular phenotyping data from human biospecimens; and visibility locally, nationally, and
internationally to facilitate outreach activities of the Center to advance precision medicine in rheumatic disease
research.
项目摘要/摘要 - 基因组学和分子资源核心
我们中心的总体目标是进步风湿性疾病中的精确药物。基因组学和
分子资源(GMR)核心将通过支持获得生物测量来在我们的中心发挥关键作用
来自特征良好的风湿病患者,并提供协商和协调服务
确保适当使用具有潜力的基因组学,蛋白质组学和其他分子技术
风湿病学的预先精确医学。 GMR核心将简化实验室研究
基础架构,包括通过合并对生物测量的收购,处理,存储和管理
在UCSF的现有风湿病生物测量并建立最先进的实验室信息
管理系统(LIMS)将使我们能够扩展样本收集并创建一个可访问的
生物座席。这些活动将发生在GMR联合主任Pui-Yan Kwok博士的实验室内。
核心,他在过去十年中担任UCSF基因组学核心核心核心的经验使他
高度有资格指导这些活动。核心领导还将提供与
适当应用基因组学和分子测定(包括蛋白质组学和免疫表型)
并将作为调查人员和实验室人员之间的联络
获得质量基因组和分子表型数据。基因组学和分子面板
表型专家将担任P30调查人员和项目的顾问,涵盖广泛的
专业知识包括基因组学,表观遗传学,蛋白质组学,免疫表型,淋巴细胞信号传导,
微生物组分析和多能干细胞的产生。 GMR核心将与
人类受试者和临床表型(HSCP)核心,以协调适当的风湿性选择
疾病患者和中心研究的临床数据,以及综合生物信息学(IB)核心
综合基因组和分子数据与临床数据进行统计分析。 GMR核心的关键优势
包括将巩固并集中的现有风湿性疾病生物测量
使用最先进的LIM进行了管理;国际知名的基因组学专家和分子专家
风湿性,自身免疫性和其他疾病的表型;生成最先进基因组学的设施
以及来自人类生物测量的其他分子表型数据;在本地,全国和
在国际上促进中心的外展活动,以促进风湿病的精确医学
研究。
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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Pui-Yan KWOK其他文献
Pui-Yan KWOK的其他文献
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{{ truncateString('Pui-Yan KWOK', 18)}}的其他基金
Genomic sequencing to aid diagnosis in pediatric and prenatal practice: Examining clinical utility, ethical implications, payer coverage, and data integration in a diverse population.
基因组测序有助于儿科和产前实践中的诊断:检查不同人群的临床效用、伦理影响、付款人覆盖范围和数据整合。
- 批准号:
10359980 - 财政年份:2017
- 资助金额:
$ 11.86万 - 项目类别:
Genomic sequencing to aid diagnosis in pediatric and prenatal practice: Examining clinical utility, ethical implications, payer coverage, and data integration in a diverse population.
基因组测序有助于儿科和产前实践中的诊断:检查不同人群的临床效用、伦理影响、付款人覆盖范围和数据整合。
- 批准号:
9538816 - 财政年份:2017
- 资助金额:
$ 11.86万 - 项目类别:
Genomic sequencing to aid diagnosis in pediatric and prenatal practice: Examining clinical utility, ethical implications, payer coverage, and data integration in a diverse population.
基因组测序有助于儿科和产前实践中的诊断:检查不同人群的临床效用、伦理影响、付款人覆盖范围和数据整合。
- 批准号:
9327452 - 财政年份:2017
- 资助金额:
$ 11.86万 - 项目类别:
Genomic sequencing to aid diagnosis in pediatric and prenatal practice: Examining clinical utility, ethical implications, payer coverage, and data integration in a diverse population.
基因组测序有助于儿科和产前实践中的诊断:检查不同人群的临床效用、伦理影响、付款人覆盖范围和数据整合。
- 批准号:
9929780 - 财政年份:2017
- 资助金额:
$ 11.86万 - 项目类别:
Genomic sequencing to aid diagnosis in pediatric and prenatal practice: Examining clinical utility, ethical implications, payer coverage, and data integration in a diverse population.
基因组测序有助于儿科和产前实践中的诊断:检查不同人群的临床效用、伦理影响、付款人覆盖范围和数据整合。
- 批准号:
9926108 - 财政年份:2017
- 资助金额:
$ 11.86万 - 项目类别:
Sequencing of Newborn Blood Spot DNA to Improve and Expand Newborn Screening
新生儿血斑 DNA 测序可改善和扩大新生儿筛查
- 批准号:
9562276 - 财政年份:2013
- 资助金额:
$ 11.86万 - 项目类别:
Sequencing of Newborn Blood Spot DNA to Improve and Expand Newborn Screening
新生儿血斑 DNA 测序可改善和扩大新生儿筛查
- 批准号:
8915730 - 财政年份:2013
- 资助金额:
$ 11.86万 - 项目类别:
Sequencing of Newborn Blood Spot DNA to Improve and Expand Newborn Screening
新生儿血斑 DNA 测序可改善和扩大新生儿筛查
- 批准号:
9105532 - 财政年份:2013
- 资助金额:
$ 11.86万 - 项目类别:
Sequencing of Newborn Blood Spot DNA to Improve and Expand Newborn Screening
新生儿血斑 DNA 测序可改善和扩大新生儿筛查
- 批准号:
9351187 - 财政年份:2013
- 资助金额:
$ 11.86万 - 项目类别:
Sequencing of Newborn Blood Spot DNA to Improve and Expand Newborn Screening
新生儿血斑 DNA 测序可改善和扩大新生儿筛查
- 批准号:
9485694 - 财政年份:2013
- 资助金额:
$ 11.86万 - 项目类别:
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