HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype.

Abstract
The Electronic Medical Records and Genomics (eMERGE) network is a network of medical centers with electronic medical records linked to existing biorepository samples for genomic discovery and genomic medicine research. The network sought to unify the genetic results from 78 Illumina and Affymetrix genotype array batches from 12 contributing medical centers for joint association analysis of 83,717 human participants. In this report, we describe the imputation of eMERGE results and methods to create the unified imputed merged set of genome-wide variant genotype data. We imputed the data using the Michigan Imputation Server, which provides a missing single-nucleotide variant genotype imputation service using the minimac3 imputation algorithm with the Haplotype Reference Consortium genotype reference set. We describe the quality control and filtering steps used in the generation of this data set and suggest generalizable quality thresholds for imputation and phenotype association studies. To test the merged imputed genotype set, we replicated a previously reported chromosome 6 HLA-B herpes zoster (shingles) association and discovered a novel zoster-associated loci in an epigenetic binding site near the terminus of chromosome 3 (3p29).
AuthorsIan B Stanaway, Taryn O Hall, Elisabeth A Rosenthal, Melody Palmer, Vivek Naranbhai, Rachel Knevel, Bahram Namjou-Khales, Robert J Carroll, Krzysztof Kiryluk, Adam S Gordon, Jodell Linder, Kayla Marie Howell, Brandy M Mapes, Frederick T J Lin, Yoonjung Yoonie Joo, M Geoffrey Hayes, Ali G Gharavi, Sarah A Pendergrass, Marylyn D Ritchie, Mariza de Andrade, Damien C Croteau-Chonka, Soumya Raychaudhuri, Scott T Weiss, Matt Lebo, Sami S Amr, David Carrell, Eric B Larson, Christopher G Chute, Laura Jarmila Rasmussen-Torvik, Megan J Roy-Puckelwartz, Patrick Sleiman, Hakon Hakonarson, Rongling Li, Elizabeth W Karlson, Josh F Peterson, Iftikhar J Kullo, Rex Chisholm, Joshua Charles Denny, Gail P Jarvik, eMERGE Network, David R Crosslin
JournalGenetic epidemiology (Genet Epidemiol) Vol. 43 Issue 1 Pg. 63-81 (02 2019) ISSN: 1098-2272 [Electronic] United States
PMID30298529 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)
Copyright© 2018 The Authors. Genetic Epidemiology Published by Wiley Periodicals, Inc.
Topics
  • Algorithms
  • Black People (genetics)
  • Chromosomes, Human (genetics)
  • Electronic Health Records
  • Female
  • Genetic Predisposition to Disease
  • Genome-Wide Association Study
  • Haplotypes (genetics)
  • Herpes Zoster (genetics)
  • Homozygote
  • Humans
  • Male
  • Phenotype
  • Polymorphism, Single Nucleotide (genetics)
  • Principal Component Analysis
  • White People (genetics)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: