4.7 Article

Next generation genome-wide association tool: Design and coverage of a high-throughput European-optimized SNP array

Journal

GENOMICS
Volume 98, Issue 2, Pages 79-89

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ygeno.2011.04.005

Keywords

Microarray; Genome-wide association study; Coverage; Throughput; Single nucleotide polymorphism

Funding

  1. National Institutes of Health [RC2 AG036607, R25 CA112355]
  2. Robert Wood Johnson Foundation
  3. Ellison Medical Foundation
  4. Wayne and Gladys Valley Foundation
  5. Kaiser Permanente

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The success of genome-wide association studies has paralleled the development of efficient genotyping technologies. We describe the development of a next-generation microarray based on the new highly-efficient Affymetrix Axiom genotyping technology that we are using to genotype individuals of European ancestry from the Kaiser Permanente Research Program on Genes, Environment and Health (RPGEH). The array contains 674,517 SNPs, and provides excellent genome-wide as well as gene-based and candidate-SNP coverage. Coverage was calculated using an approach based on imputation and cross validation. Preliminary results for the first 80,301 saliva-derived DNA samples from the RPGEH demonstrate very high quality genotypes, with sample success rates above 94% and over 98% of successful samples having SNP call rates exceeding 98%. At steady state, we have produced 462 million genotypes per week for each Axiom system. The new array provides a valuable addition to the repertoire of tools for large scale genome-wide association studies. (C) 2011 Elsevier Inc. All rights reserved.

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