Biospecimen & Biomarker Development Core
生物样本
基本信息
- 批准号:10657446
- 负责人:
- 金额:$ 7.07万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2022
- 资助国家:美国
- 起止时间:2022-07-01 至 2027-06-30
- 项目状态:未结题
- 来源:
- 关键词:AdultAliquotBar CodesBiochemical MarkersBiologicalBiological AssayBiological MarkersBlood specimenCatalogsCharacteristicsChemopreventionCirrhosisClinicalClinical DataCollectionComprehensive Cancer CenterDNADataDatabasesDetectionDevelopmentDiabetes MellitusEnsureEquipment and supply inventoriesFunctional disorderFutureGenetic MarkersGoalsHealth protectionIndividualInstitutionInvestigationKnowledgeLabelLinkLocationMalignant neoplasm of liverMedicineMetabolicMetabolic dysfunctionMetabolic syndromeModelingObesityParticipantPatient ParticipationPatientsPlasmaPopulationPopulation SciencesPopulations at RiskPreparationPreventionPrevention strategyPrimary carcinoma of the liver cellsProceduresProcessProspective cohortProtocols documentationResearchResearch PersonnelResearch Project GrantsResource SharingResourcesRisk FactorsRisk ReductionSamplingSerumServicesShippingSpecimen HandlingStandardizationTestingTexasTimeTranslational ResearchValidationWorkassay developmentbiobankbiomarker developmentbiomarker discoverybiomarker validationclinical research sitecohortcollegecostcost effectivenesscost estimateearly detection biomarkersethnic disparityethnic diversityfatty liver diseasefollow-upmortalitynovel markerphenotypic biomarkerprofessorprogramsprotective factorsracial disparityracial diversityresearch studysuccesssynergism
项目摘要
ABSTRACT—Biospecimen and Biomarker Development Core
The goal of the Program Project (PP) is to reduce the burden of hepatocellular carcinoma (HCC)-related mortality
through better understanding of contemporary risk factors (e.g., phenotypic, biochemical and genetic markers of
metabolic dysfunction) and preventive strategies (e.g., chemoprevention) of HCC related to metabolic
(dysfunction) associated fatty liver disease (MAFLD). To accomplish our goal, will need repeated collection,
shipping, processing and storage of thousands of blood samples that can be linked to demographic and clinical
data. These samples come from participants at one of eight clinical sites of the Texas HCC Consortium (THCCC)
prospective cohort. We propose 3 Projects, 2 shared resource Cores: Biospecimen and Biomarker
Development Core (BBDC) and Data and Analysis Core, and the Administrative Core.
The primary objectives of the BBDC are 1) to produce high-quality DNA, plasma, and serum for research
projects using standardized collection and processing procedures and 2) to spearhead biomarker assay
development and validation that supports the projects in the PP. The aims of the BBDC are to (1) receive,
process, and catalog all blood samples from patients participating in the THCCC; (2) Allocate and distribute
appropriate research samples to investigators and projects, and work with the biospecimen prioritization group
to prioritize samples; (3) Develop and conduct HCC biomarker assays and analyses as needed for Projects; and
(4) Maintain a biobank of well-annotated samples for future research.
The BBDC will serve as the central location to fully support these functions using previously developed standard
operating procedures. The BBDC will work closely with the Data and Analysis Core to maintain the sample
inventory database, produce labels with unique sample barcodes, and produce lists of patients with specific
characteristics, so the samples needed can be pulled for analysis. The BBDC will also provide up-to-date and
accurate data on sample availability and ensure that the Projects receive optimal samples for the proposed
analyses. Centralizing specimen processing and storage ensures consistent, high-quality sample preparation
that will help achieve the goals of the Projects and minimize costs. The BBDC will also ensure accurate
recordkeeping and guard patient protected health information. Importantly, the Core will provide expertise in
biomarker assay development and application, oversee sample preparation, profile additional targets and liaise
with institutional cores. Thus, the BBDC will provide indispensable services critical for the scientific and
operational success of the PP.
生物标本和生物标志物开发核心
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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Michael E Scheurer其他文献
Germline Genetic Testing and Survival Outcomes Among Children With Rhabdomyosarcoma
横纹肌肉瘤儿童的种系基因检测和生存结果
- DOI:
- 发表时间:
2024 - 期刊:
- 影响因子:13.8
- 作者:
Bailey A Martin;He Li;Michael E Scheurer;Dana L Casey;Shannon Dugan;Deborah A Marquez;D. Muzny;Richard A. Gibbs;D. Barkauskas;David Hall;Douglas R Stewart;J. Schiffman;Matthew T McEvoy;Javed Khan;D. Malkin;C. Linardic;B. Crompton;J. Shern;S. Skapek;R. Venkatramani;Douglas S. Hawkins;A. Sabo;Sharon E. Plon;Philip J. Lupo - 通讯作者:
Philip J. Lupo
Michael E Scheurer的其他文献
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{{ truncateString('Michael E Scheurer', 18)}}的其他基金
Sex and racial/ethnic differences in B-ALL genomics
B-ALL 基因组学中的性别和种族/民族差异
- 批准号:
10555358 - 财政年份:2022
- 资助金额:
$ 7.07万 - 项目类别:
Ethnic disparities in methotrexate neurotoxicity among children and adolescents with ALL
患有 ALL 的儿童和青少年中甲氨蝶呤神经毒性的种族差异
- 批准号:
10289496 - 财政年份:2021
- 资助金额:
$ 7.07万 - 项目类别:
Admixture analysis of acute lymphoblastic leukemia in African American children: the ADMIRAL Study
非裔美国儿童急性淋巴细胞白血病的混合分析:ADMIRAL 研究
- 批准号:
10307680 - 财政年份:2021
- 资助金额:
$ 7.07万 - 项目类别:
Ethnic disparities in methotrexate neurotoxicity among children and adolescents with ALL
患有 ALL 的儿童和青少年中甲氨蝶呤神经毒性的种族差异
- 批准号:
10683990 - 财政年份:2021
- 资助金额:
$ 7.07万 - 项目类别:
Ethnic disparities in methotrexate neurotoxicity among children and adolescents with ALL
患有 ALL 的儿童和青少年中甲氨蝶呤神经毒性的种族差异
- 批准号:
10472703 - 财政年份:2021
- 资助金额:
$ 7.07万 - 项目类别:
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