ArticleBMC genomics2008
Evaluating the performance of Affymetrix SNP Array 6.0 platform with 400 Japanese individuals.
Article in BMC genomics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.
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Who cites it
31 citing papers in PubMed.
- Genome-wide linkage and regional association study of blood pressure response to the cold pressor test in Han Chinese: the genetic epidemiology network of salt sensitivity study.Circulation. Cardiovascular genetics · 2014Trial
- Genome-wide linkage and positional candidate gene study of blood pressure response to dietary potassium intervention: the genetic epidemiology network of salt sensitivity study.Circulation. Cardiovascular genetics · 2010Trial
- Homologous recombination deficiency (HRD) testing landscape: clinical applications and technical validation for routine diagnostics.Biomarker research · 2025Review
- Demographic history of Ryukyu islanders at the southern part of the Japanese Archipelago inferred from whole-genome resequencing data.Journal of human genetics · 2023Article
- A pipeline for sample tagging of whole genome bisulfite sequencing data using genotypes of whole genome sequencing.BMC genomics · 2023Article
- Morphobiometrical characteristics of indigenous chicken ecotype populations in Rwanda.Tropical animal health and production · 2020Article
- SNP genotype calling and quality control for multi-batch-based studies.Genes & genomics · 2019Article
- Genetic and genomic stability across lymphoblastoid cell line expansions.BMC research notes · 2018Article
- Re-evaluating data quality of dog mitochondrial, Y chromosomal, and autosomal SNPs genotyped by SNP array.Zoological research · 2016Article
- Associations of Variants in the CACNA1A and CACNA1C Genes With Longitudinal Blood Pressure Changes and Hypertension Incidence: The GenSalt Study.American journal of hypertension · 2016Article
- Understanding of HLA-conferred susceptibility to chronic hepatitis B infection requires HLA genotyping-based association analysis.Scientific reports · 2016Article
- Associations of Renin-Angiotensin-Aldosterone System Genes With Blood Pressure Changes and Hypertension Incidence.American journal of hypertension · 2015Article
- Unique characteristics of the Ainu population in Northern Japan.Journal of human genetics · 2015Article
- Associations of Endothelial System Genes With Blood Pressure Changes and Hypertension Incidence: The GenSalt Study.American journal of hypertension · 2015Article
- Associations of epithelial sodium channel genes with blood pressure: the GenSalt study.Journal of human hypertension · 2015Article
- Genome-wide linkage and positional association analyses identify associations of novel AFF3 and NTM genes with triglycerides: the GenSalt study.Journal of genetics and genomics = Yi chuan xue bao · 2015Article
- Associations of epithelial sodium channel genes with blood pressure changes and hypertension incidence: the GenSalt study.American journal of hypertension · 2014Article
- Validation and assessment of variant calling pipelines for next-generation sequencing.Human genomics · 2014Article
- Article
- RNA-Seq optimization with eQTL gold standards.BMC genomics · 2013Article
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Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundWith improvements in genotyping technologies, genome-wide association studies with hundreds of thousands of SNPs allow the identification of candidate genetic loci for multifactorial diseases in different populations. However, genotyping errors caused by genotyping platforms or genotype calling algorithms may lead to inflation of false associations between markers and phenotypes. In addition, the number of SNPs available for genome-wide association studies in the Japanese population has been investigated using only 45 samples in the HapMap project, which could lead to an inaccurate estimation of the number of SNPs with low minor allele frequencies. We genotyped 400 Japanese samples in order to estimate the number of SNPs available for genome-wide association studies in the Japanese population and to examine the performance of the current SNP Array 6.0 platform and the genotype calling algorithm "Birdseed".
resultsAbout 20% of the 909,622 SNP markers on the array were revealed to be monomorphic in the Japanese population. Consequently, 661,599 SNPs were available for genome-wide association studies in the Japanese population, after excluding the poorly behaving SNPs. The Birdseed algorithm accurately determined the genotype calls of each sample with a high overall call rate of over 99.5% and a high concordance rate of over 99.8% using more than 48 samples after removing low-quality samples by adjusting QC criteria.
conclusionOur results confirmed that the SNP Array 6.0 platform reached the level reported by the manufacturer, and thus genome-wide association studies using the SNP Array 6.0 platform have considerable potential to identify candidate susceptibility or resistance genetic factors for multifactorial diseases in the Japanese population, as well as in other populations.
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