Human Phenotyping Core
人类表型核心
基本信息
- 批准号:10478211
- 负责人:
- 金额:$ 36.85万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2018
- 资助国家:美国
- 起止时间:2018-09-07 至 2023-08-31
- 项目状态:已结题
- 来源:
- 关键词:AddressAutoantibodiesAutoimmune DiseasesBiological AssayBiological MarkersBlood CellsCaringCellsCellular Indexing of Transcriptomes and Epitopes by SequencingCharacteristicsClinicalCompetenceComplexConsultationsDataData AnalysesData SetDatabasesDevelopmentDiagnosticDiseaseEffectivenessEnsureEpigenetic ProcessEquipmentExperimental DesignsFlow CytometryFoundationsFreezingFundingFutureGenerationsGeneticGenetic PolymorphismGenomic DNAGenomicsGenotypeHumanHuman Herpesvirus 4Human ResourcesImmuneImmunologicsImmunophenotypingIndividualInflammatoryInvestigationKnowledgeMeasuresMediator of activation proteinMethodologyMethodsMolecularMolecular ProfilingOklahomaPathogenesisPathway interactionsPatientsPhenotypePlasmaPopulationPreparationProcessProteomicsQuality ControlReproducibilityResearchResearch PersonnelResourcesRheumatismSamplingSerumServicesSiteSpecimenStatistical ModelsSystemTechnical ExpertiseTechnologyTherapeuticTimeTransformed Cell LineVariantbasebiobankchemokineclinical centerclinical phenotypeclinically relevantcomputerized data processingcytokinedata qualitydesignexperienceexperimental studyhuman diseaseimmune functionmolecular phenotypenovelnovel strategiesphenotypic dataprecision medicineprognostic toolprogramsresponsesingle-cell RNA sequencingsuccesstranscriptometranscriptomics
项目摘要
Human Phenotyping Core Project Summary
The rapid development of new approaches to interrogate the immune and inflammatory systems comes
with a growing demand for both technical and conceptual expertise in these methodologies. The Human
Phenotyping Core was created to support these activities within the Oklahoma Rheumatic Disease Resources
Cores Center (ORDRCC). To address the most broadly scientifically interesting and clinically important
questions, our ORDRCC Investigators need access to cutting-edge approaches, such as scRNA-Seq/CITE-
Seq, ChipCytometry, and CyTOF to perform incisive experiments and to generate high-quality, reproducible
data. The Human Phenotyping Core will allow our investigators to ask novel questions regarding the molecular
phenotypes of rheumatic diseases. In addition to providing ORDRCC investigators with high-content
biomolecular phenotyping services, the Human Phenotyping Core in conjunction with the Clinical
Characterization and Biorepository Core (CCBC) will provide access to datasets containing previously
collected genetic, proteomic, and biomolecular phenotypes of clinical subjects whose samples are available
from the CCBC. The tight integration of the Human Phenotyping Core, CCBC and our databases will enable
investigators to efficiently phenotype samples and correlate molecular and cellular phenotypes with clinical
characteristics, to select more homogeneous patients for hypothesis-driven investigation and help provide the
foundational knowledge needed for precision medicine in rheumatic disease care.
By consolidating a range of technologies required for the complete characterization of molecular or
cellular phenotypes into a single unit, the Human Phenotyping Core (HPC) will streamline services to help
ORDRCC investigators in the efficient planning, design, execution and data analysis required for their
individual projects. The HPC will provide experience in performing research using clinical specimens,
technical expertise in a wide range of molecular and bioassays, access to equipment and resources thus
enabling cutting-edge approaches to address research questions, quality control assessment of the data
collected and data processing suitable for higher end statistical modeling of phenotype/clinical associations.
SPECIFIC AIM 1: Assist ORDRCC Investigators, JCIs and Scholars to navigate the stages of project
development, experimental design, resource planning and execution of translational and mechanistic studies
through Core Management and individual consultations.
SPECIFIC AIM 2: Provide access to advanced molecular phenotyping technologies and experienced
technical personnel for efficient execution of advanced experimental data plans.
SPECIFIC AIM 3: Establish processes to ensure data quality control, processing of raw data, and preparation
of data sets for more extensive analysis and statistical modeling.
SPECIFIC AIM 4: Evaluate, assess and implement new cutting-edge technologies for molecular phenotyping.
人类表型分析核心项目摘要
快速发展的新方法来审问免疫和炎症系统来
随着对这些方法的技术和概念专门知识的需求不断增长。人类
创建表型核心是为了支持俄克拉荷马州风湿病资源中的这些活动
核心中心(ORTRCC)。为了解决最广泛的科学有趣和临床重要的
问题,我们的ORDRCC研究人员需要获得尖端的方法,如scRNA-Seq/CITE-
Seq、ChipCytography和CyTOF可执行深入的实验并生成高质量、可重现的结果
数据人类表型核心将允许我们的研究人员提出有关分子生物学的新问题。
风湿性疾病的表型除了为ORDRC研究人员提供高内容的
生物分子表型分析服务,人类表型分析核心与临床
表征和生物储存核心(CCBC)将提供对包含先前
收集的样本可用的临床受试者的遗传、蛋白质组和生物分子表型
来自CCBC。人类表型核心,CCBC和我们的数据库的紧密整合将使
研究人员有效地对样本进行表型分析,并将分子和细胞表型与临床
特征,选择更同质的患者进行假设驱动的研究,并帮助提供
风湿病护理中精准医学所需的基础知识。
通过整合一系列完整表征分子或
细胞表型整合到一个单元中,人类表型核心(HPC)将简化服务,
在有效的规划,设计,执行和数据分析所需的ORDRCC调查,
个别项目。HPC将提供使用临床标本进行研究的经验,
在广泛的分子和生物测定技术专长,获得设备和资源,从而
使尖端的方法来解决研究问题,数据的质量控制评估,
收集和数据处理适用于表型/临床关联的高端统计建模。
具体目标1:协助ORDRCC研究者、JCI和学者指导项目的各个阶段
开发、实验设计、资源规划和执行转化和机制研究
通过核心管理和个人咨询。
具体目标2:提供先进的分子表型技术和经验丰富的
技术人员的高效执行先进的实验数据计划。
具体目标3:建立确保数据质量控制、原始数据处理和准备的流程
用于更广泛的分析和统计建模。
具体目标4:评价,评估和实施新的尖端技术的分子表型。
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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Joel Marvin Guthridge其他文献
Joel Marvin Guthridge的其他文献
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{{ truncateString('Joel Marvin Guthridge', 18)}}的其他基金
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10655219 - 财政年份:2023
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Accelerating Medicines Partnership-Autoimmune and Immunologic Disease Tissue Research Core Admin Supplement: Preclinical Studies in Sjogren's
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- 批准号:
10834635 - 财政年份:2022
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$ 36.85万 - 项目类别:
Accelerating Medicines Partnership-Autoimmune and Immunologic Disease Tissue Research Core
加速药物合作——自身免疫和免疫疾病组织研究核心
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10687729 - 财政年份:2022
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$ 36.85万 - 项目类别:
Accelerating Medicines Partnership-Autoimmune and Immunologic Disease Tissue Research Core
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10452026 - 财政年份:2022
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Accelerating Medicines Partnership-Autoimmune and Immunologic Disease Tissue Research Core
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Ikaros family genes and lupus susceptibility across ethnically diverse populations
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9770772 - 财政年份:2018
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Ikaros family genes and lupus susceptibility across ethnically diverse populations
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10238826 - 财政年份:2018
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