Evidence map›Paper›PMID 18803882›Full record

ArticleBMC genomics2008

Evaluating the performance of Affymetrix SNP Array 6.0 platform with 400 Japanese individuals.

Nao Nishida, Asako Koike, Atsushi Tajima, Yuko Ogasawara, Yoshimi Ishibashi, Yasuka Uehara, Ituro Inoue, Katsushi Tokunaga

Abstract readEvaluation Study
In one paragraph

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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0cells of the map it votes in
31citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

31 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Nao NishidaDepartment of Human Genetics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan. nishida-75@umin.ac.jp
Asako Koike
Atsushi Tajima
Yuko Ogasawara
Yoshimi Ishibashi
Yasuka Uehara
Ituro Inoue
Katsushi Tokunaga

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Polymorphism, Single NucleotideAlgorithmsAsian PeopleComputational BiologyGene FrequencyHumansOligonucleotide Array Sequence Analysis

Identifiers

PMID18803882
PMCPMC2566316

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.