IGF::OT::IGF - B599 SPECIAL STUDIES/ANALYSIS- OTHER
IGF::OT::IGF - B599 SPECIAL STUDIES/ANALYSIS- OTHER
批准号:
10000808
负责人:
J. WES TEASDALE
金额:
$8.96万
依托单位国家:
美国
项目类别:
财政年份:
2015
资助国家:
美国
项目状态:
已结题
起止时间:
2015-09-25 至 2017-09-24
关键词:
AfricanArchivesAsthmaAtrial FibrillationBehavioralBioinformaticsBiological ProcessBiotechnologyChronic Obstructive Airway DiseaseClinicalClinical DataCommunitiesComplexDataData Coordinating CenterDiagnosisDiseaseDyslipidemiasEnsureEuropeanFundingGenetic MarkersGenetic TranscriptionGenomicsGoalsHealthHeart DiseasesHematological DiseaseHispanicsImageIndividualInformaticsLung diseasesMedicineMolecularNational Heart, Lung, and Blood InstituteObesityOutcomePacific Island AmericansParticipantPatternPhasePhenotypePopulationPopulation HeterogeneityPrecision Medicine InitiativePreventionProteomicsResearchResourcesSleep Apnea SyndromesSleep DisordersSystemTrans-Omics for Precision Medicinedisorder riskdisorder subtypegenome sequencingimprovedmetabolic profilemetabolomicsnovelpersonalized medicinephenotypic dataprogramsprotein expressionrepositorytraitwhole genome
中文摘要
反式精准医学组学(TOPMed)是nhlbi范围内的一项倡议,旨在通过整合组学(如基因组学、蛋白质组学、代谢组学)和表型数据,提高我们对HLBS疾病基础生物学过程的理解,以改善这些疾病的预测、预防、诊断和治疗。为了支持NHLBI TOPMed项目,全基因组测序(WGS)项目将收集具有良好表型特征的个体的全基因组测序数据和现有的临床结果数据。该项目旨在确定疾病风险增加或减少的遗传标记,以及那些有助于确定疾病亚型的遗传标记。WGS项目的初始阶段已经从以前nhlbi资助的研究中确定了近2万名参与者进行全基因组测序。第一组参与者包括具有复杂特征(例如,血脂异常)和以下心脏,肺,血液和睡眠(HLBS)疾病的个体:心房颤动,哮喘,慢性阻塞性肺疾病(COPD),肥胖和睡眠呼吸暂停。目标是建立一个新的基因组资源,反映美国人口的多样性。目前的研究参与者中几乎有一半是欧洲血统,其余的是非洲人、西班牙人和太平洋岛民血统。目前,WGS项目由9个参与研究中心、4个测序中心、1个信息学研究中心和1个数据协调中心(DCC)开展。随着项目的进展,预计其他中心将加入该财团。国家生物技术中心将提供档案和生物信息学支持。
英文摘要
Trans-Omics for Precision Medicine (TOPMed) is an NHLBI-wide initiative to generate scientific resources to enhance our understanding of fundamental biological processes that underlie HLBS disorders through the integration of –omics (e.g., genomic, proteomic, metabolomic) and phenotypic data in an effort to improve the prediction, prevention, diagnosis, and treatment of these disorders. To support the NHLBI TOPMed program, the Whole-Genome Sequencing (WGS) project will collect whole-genome sequencing data from individuals with well characterized phenotypes and existing clinical outcome data. This project aims to identify genetic markers of increased or decreased risk of disease, as well as those that help define disease subtypes. The initial phase of the WGS project has identified nearly 20,000 participants from previous NHLBI-funded studies to undergo whole-genome sequencing. This first set of participants includes individuals that have complex traits (e.g., dyslipidemia) and the following heart, lung, blood and sleep (HLBS) disorders: Atrial fibrillation, Asthma, Chronic obstructive pulmonary disease (COPD), Obesity,and Sleep apnea. The objective is to establish a novel genomic resource that is reflective of the diversity of the US population. Almost half of current study participants are of European descent, with the remainder being people of African, Hispanic and Pacific Islander ancestry. Currently, the WGS project is being conducted by nine participating research centers, four sequencing centers, an informatics research center, and a Data Coordinating Center (DCC). As the project progresses, it is anticipated that other centers will join the consortium. The National Center for Biotechnology will provide archival and bioinformatics support.
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IGF::OT::IGF - B599 SPECIAL STUDIES/ANALYSIS- OTHER
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批准号:9173476
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项目类别:
-
资助金额:$107.56万
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财政年份:2015
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负责人:J. WES TEASDALE
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依托单位:
海外基金