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

被引:464
作者
McCarty, Catherine A. [1 ]
Chisholm, Rex L. [2 ]
Chute, Christopher G. [3 ]
Kullo, Iftikhar J. [4 ]
Jarvik, Gail P. [5 ]
Larson, Eric B. [6 ]
Li, Rongling [7 ]
Masys, Daniel R. [8 ]
Ritchie, Marylyn D. [9 ]
Roden, Dan M. [10 ]
Struewing, Jeffery P. [7 ]
Wolf, Wendy A. [2 ]
机构
[1] Marshfield Clin Res Fdn, Ctr Human Genet, Marshfield, WI 54449 USA
[2] Northwestern Univ, Ctr Genet Med, Chicago, IL 60611 USA
[3] Mayo Clin, Div Biomed Stat & Informat, Rochester, MN 55905 USA
[4] Mayo Clin, Div Cardiovasc Dis, Rochester, MN 55905 USA
[5] Univ Washington, Dept Genome Sci, Seattle, WA 98195 USA
[6] Grp Hlth Res Inst, Seattle, WA 98101 USA
[7] NHGRI, Off Populat Genom, Bethesda, MD 20892 USA
[8] Vanderbilt Univ, Sch Med, Dept Biomed Informat, Nashville, TN 37232 USA
[9] Vanderbilt Univ, Sch Med, Ctr Human Genet Res, Nashville, TN 37231 USA
[10] Vanderbilt Univ, Sch Med, Dept Pharmacol, Nashville, TN 37232 USA
关键词
ALZHEIMER-DISEASE; RISK; DEMENTIA; BIOBANK; UPDATE; OLDER;
D O I
10.1186/1755-8794-4-13
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
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 approximate to 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.
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页数:11
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