Frontiers in Genetics (Dec 2014)

Imputation and quality control steps for combining multiple genome-wide datasets

  • Shefali S Verma,
  • Mariza ede Andrade,
  • Gerard eTromp,
  • Helena eKuivaniemi,
  • Elizabeth ePugh,
  • Bahram eNamjou,
  • Shubhabrata eMukherjee,
  • Gail P Jarvik,
  • Leah Claire Kottyan,
  • Amber eBurt,
  • Yuki eBradford,
  • Gretta D Armstrong,
  • Kimberly eDerr,
  • Dana eCrawford,
  • Jonathan L Haines,
  • Rongling eLi,
  • David eCrosslin,
  • Marylyn D Ritchie

DOI
https://doi.org/10.3389/fgene.2014.00370
Journal volume & issue
Vol. 5

Abstract

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The electronic MEdical Records and GEnomics (eMERGE) network brings together DNA biobanks linked to electronic health records (EHRs) from multiple institutions. Approximately 52,000 DNA samples from distinct individuals have been genotyped using genome-wide SNP arrays across the nine sites of the network. The eMERGE Coordinating Center and the Genomics Workgroup developed a pipeline to impute and merge genomic data across the different SNP arrays to maximize sample size and power to detect associations with a variety of clinical endpoints. The 1000 Genomes cosmopolitan reference panel was used for imputation. Imputation results were evaluated using the following metrics: accuracy of imputation, allelic R2 (estimated correlation between the imputed and true genotypes), and the relationship between allelic R2 and minor allele frequency. Computation time and memory resources required by two different software packages (BEAGLE and IMPUTE2) were also evaluated. A number of challenges were encountered due to the complexity of using two different imputation software packages, multiple ancestral populations, and many different genotyping platforms. We present lessons learned and describe the pipeline implemented here to impute and merge genomic data sets. The eMERGE imputed dataset will serve as a valuable resource for discovery, leveraging the clinical data that can be mined from the EHR.

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