Design and coverage of high throughput genotyping arrays optimized for individuals of East Asian, African American, and Latino race/ethnicity using imputation and a novel hybrid SNP selection algorithm
- 31 December 2011
- journal article
- Published by Elsevier BV in Genomics
- Vol. 98 (6), 422-430
- https://doi.org/10.1016/j.ygeno.2011.08.007
Abstract
No abstract availableKeywords
Funding Information
- National Institutes of Health (RC2 AG036607)
- Robert Wood Johnson Foundation
- Ellison Medical Foundation
- Wayne and Gladys Valley Foundation
- Kaiser Permanente
- NIH (R25 CA112355)
This publication has 29 references indexed in Scilit:
- Next generation genome-wide association tool: Design and coverage of a high-throughput European-optimized SNP arrayGenomics, 2011
- MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypesGenetic Epidemiology, 2010
- Integrating common and rare genetic variation in diverse human populationsNature, 2010
- Biological, clinical and population relevance of 95 loci for blood lipidsNature, 2010
- The Pharmacogenomics of Membrane Transporters Project: Research at the Interface of Genomics and Transporter PharmacologyClinical Pharmacology & Therapeutics, 2009
- Genotype-Imputation Accuracy across Worldwide Human PopulationsAmerican Journal of Human Genetics, 2009
- A second generation human haplotype map of over 3.1 million SNPsNature, 2007
- A new multipoint method for genome-wide association studies by imputation of genotypesNature Genetics, 2007
- Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controlsNature, 2007
- Efficiency and power in genetic association studiesNature Genetics, 2005