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PMID: 21269473 Published · epublish English Letter Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

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

BMC medical genomics ·Vol. 4 ·2011-01-26 ·Pages 13

McCarty CA, Chisholm RL, Chute CG, Kullo IJ, Jarvik GP, Larson EB, Li R, Masys DR, Ritchie MD, Roden DM, Struewing JP, Wolf WA, eMERGE Team

Abstract

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. 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. 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. Plans are underway to expand the network in diversity of populations and incorporation of GWAS findings into clinical care. 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.

MeSH Terms
American Recovery and Reinvestment Act Clinical Trials as Topic/methods Diabetes Mellitus, Type 2/genetics Electronic Health Records Genome Genome-Wide Association Study Genotype Humans Hypertension/genetics National Human Genome Research Institute (U.S.) Peripheral Arterial Disease/genetics Population Groups United States
Authors & Affiliations
13 authors, click to expand affiliations / ORCID
McCarty Catherine A
Chisholm Rex L
Chute Christopher G
Kullo Iftikhar J
Jarvik Gail P
Larson Eric B
Li Rongling
Masys Daniel R
Ritchie Marylyn D
Roden Dan M
Struewing Jeffery P
Wolf Wendy A
eMERGE Team
Investigators
70 investigators, click to expand
McCarty Catherine A
Starren Justin
Peissig Peggy
Berg Richard
Rasmussen Luke
Linneman James
Miller Aaron
Choudary Vidhu
Chen Lin
Waudby Carol
Kitchner Terrie
Reeser Jonathan
Fost Norman
Ritchie Marylyn
Wilke Russell A
Chisholm Rex L
Avila Pedro C
Greenland Philip
Hayes M Geoff
Kho Abel
Kibbe Warren A
Lemke Amy A
Lowe William L
Smith Maureen E
Wolf Wendy A
Pacheco Jennifer A
Thompson William K
Humowiecki Joel
Law May
Chute Christopher
Kullo Iftikar
Koenig Barbara
de Andrade Mariza
Bielinski Suzette
Pathak Jyotishman
Savova Guergana
Wu Joel
Henriksen Joan
Ding Keyue
Hart Lacey
Palbicki Jeremy
Larson Eric B
Newton Katherine
Ludman Evette
Spangler Leslie
Hart Gene
Carrell David
Jarvik Gail
Crane Paul
Burke Wylie
Fullerton Stephanie Malia
Trinidad Susan Brown
Carlson Chris
McDavid Andrew
Roden Dan M
Clayton Ellen
Haines Jonathan L
Masys Daniel R
Churchill Larry R
Cornfield Daniel
Crawford Dana
Darbar Dawood
Denny Joshua C
Malin Bradley A
Ritchie Marylyn D
Schildcrout Jonathan S
Xu Hua
Ramirez Andrea Havens
Basford Melissa
Pulley Jill
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Article Info
Journal
BMC medical genomics
Abbr.
BMC Med Genomics
ISSN
1755-8794
Published
2011-01-26
Epub
2011-00-26
Pages
13
Language
English
Region
England
NLM ID
101319628
PMCID
PMC3038887
Subset
IM
Grants
NHGRI NIH HHS · U01-HG-004610 · United States
NHGRI NIH HHS · U01-HG-04603 · United States
NHGRI NIH HHS · U01 HG004603 · United States
NHGRI NIH HHS · U01HG004609 · United States
NHGRI NIH HHS · U01 HG004609 · United States
NHGRI NIH HHS · U01 HG004599 · United States
NHGRI NIH HHS · U01 HG004609-03 · United States
NHGRI NIH HHS · U01 HG004610 · United States
NHGRI NIH HHS · U01-HG-004608 · United States
NHGRI NIH HHS · U01 HG004608 · United States
NHGRI NIH HHS · U01-HG-04599 · United States
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