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The eMERGE Network: A consortium of biorepositories linked to electronic medical records data for conducting genomic studies

机译:eMERGE网络:与电子病历数据链接的一组生物储存库,用于进行基因组研究

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Introduction The eMERGE (electronic MEdical Records and GEnomics) Network is an NHGRI-supported consortium of five institutions to explore the utility of DNA repositories coupled to Electronic Medical Record (EMR) systems for advancing discovery in genome science. eMERGE also includes a special emphasis on the ethical, legal and social issues related to these endeavors. Organization The five sites are supported by an Administrative Coordinating Center. Setting of network goals is initiated by working groups: (1) Genomics, (2) Informatics, and (3) Consent & Community Consultation, which also includes active participation by investigators outside the eMERGE funded sites, and (4) Return of Results Oversight Committee. The Steering Committee, comprised of site PIs and representatives and NHGRI staff, meet three times per year, once per year with the External Scientific Panel. Current progress The primary site-specific phenotypes for which samples have undergone genome-wide association study (GWAS) genotyping are cataract and HDL, dementia, electrocardiographic QRS duration, peripheral arterial disease, and type 2 diabetes. A GWAS is also being undertaken for resistant hypertension in ≈2,000 additional samples identified across the network sites, to be added to data available for samples already genotyped. Funded by ARRA supplements, secondary phenotypes have been added at all sites to leverage the genotyping data, and hypothyroidism is being analyzed as a cross-network phenotype. Results are being posted in dbGaP. Other key eMERGE activities include evaluation of the issues associated with cross-site deployment of common algorithms to identify cases and controls in EMRs, data privacy of genomic and clinically-derived data, developing approaches for large-scale meta-analysis of GWAS data across five sites, and a community consultation and consent initiative at each site. Future activities Plans are underway to expand the network in diversity of populations and incorporation of GWAS findings into clinical care. Summary By combining advanced clinical informatics, genome science, and community consultation, eMERGE represents a first step in the development of data-driven approaches to incorporate genomic information into routine healthcare delivery.
机译:引言eMERGE(电子病历和基因组学)网络是由NHGRI支持的五个机构组成的联盟,旨在探索与电子病历(EMR)系统耦合的DNA信息库在基因组科学研究中的应用。 eMERGE还特别强调与这些努力有关的道德,法律和社会问题。组织这五个站点由一个行政协调中心提供支持。网络目标的确定由以下工作组发起:(1)基因组学,(2)信息学和(3)同意与社区咨询,其中还包括eMERGE资助地点以外的调查人员的积极参与,以及(4)结果监督的返回委员会。指导委员会由现场PI和代表以及NHGRI工作人员组成,每年召开三次会议,每年与外部科学小组举行一次会议。当前的进展样本已接受全基因组关联研究(GWAS)基因分型的主要位点特异性表型是白内障和HDL,痴呆,心电图QRS持续时间,外周动脉疾病和2型糖尿病。还在全球各地确定的大约2,000个其他样本中进行了GWAS,用于抗药性高血压,并将其添加到已进行基因分型的样本的可用数据中。在ARRA补充剂的资助下,在所有位点都添加了次级表型以利用基因型数据,甲状腺功能减退症正在作为跨网络表型进行分析。结果正在dbGaP中发布。 eMERGE的其他重要活动包括评估与跨站点部署通用算法相关的问题,以识别EMR中的病例和对照,基因组数据和临床数据的数据保密性,开发对五种GWAS数据进行大规模荟萃分析的方法站点,并在每个站点进行社区咨询和同意。未来的活动计划正在制定中,以扩大不同人群的网络,并将GWAS的发现纳入临床治疗。总结通过整合先进的临床信息学,基因组科学和社区咨询,eMERGE代表了将基因组信息纳入常规医疗保健服务的数据驱动方法开发的第一步。

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