A cross-platform analysis of 14,177 expression quantitative trait loci derived from lymphoblastoid cell lines

  1. William OC Cookson2,5
  1. 1 Harvard School of Public Health;
  2. 2 National Heart and Lung Institute, Imperial College London, London SW3 6LY, UK;
  3. 3 Centre National de Genotypage, 91057 Evry Cedex, France;
  4. 4 Center for Statistical Genetics, School of Public Health, University of Michigan, Ann Arbor, MI 4810
  1. * Corresponding author; email: w.cookson{at}imperial.ac.uk

Abstract

Gene expression levels can be an important link DNA between variation and phenotypic manifestations. Our previous map of global gene expression based on approximately 400K SNPs and 50K transcripts in 400 sib pairs from the MRCA family panel has been widely used to interpret the results of GWAS. Here, we more than double the size of our initial dataset with expression data on 550 additional individuals from the MRCE family panel using the Illumina whole genome expression array. We have used new statistical methods for dimension reduction to account for non-genetic effects in estimates of expression levels and we have also included SNPs imputed from the 1000 Genomes Project. Our methods reduced false discovery rates and increased the number of eQTLs mapped either locally or at a distance (i.e. in cis or trans) from 1,534 in the MRCA dataset to 4,452 (with <5% FDR). Imputation of 1000 Genomes SNPs further increased the number of eQTLs to 7,302. Using the same methods and imputed SNPs in the newly acquired MRCE dataset we identified eQTLs for 9000 genes. The combined results identify strong local and distant effects for transcripts from 14,177 genes.

  • Received May 1, 2012.
  • Accepted December 27, 2012.

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