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韩国人群中基于外显子阵列的全基因组关联研究的实用呼叫方法

Practical Calling Approach for Exome Array-Based Genome-Wide Association Studies in Korean Population.

作者信息

Park Tae-Joon, Heo Lyong, Moon Sanghoon, Kim Young Jin, Oh Ji Hee, Han Sohee, Kim Bong-Jo

机构信息

Division of Structural and Functional Genomics, Center for Genome Science, National Institute of Health, Centers for Disease Control and Prevention, Chungcheongbuk-do 363-700, Republic of Korea.

出版信息

Int J Genomics. 2015;2015:421715. doi: 10.1155/2015/421715. Epub 2015 Dec 27.

DOI:10.1155/2015/421715
PMID:26819946
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4706946/
Abstract

Exome-based genotyping arrays are cost-effective and have recently been used as alternative platforms to whole-exome sequencing. However, the automated clustering algorithm in an exome array has a genotype calling problem in accuracy for identifying rare and low-frequency variants. To address these shortcomings, we present a practical approach for accurate genotype calling using the Illumina Infinium HumanExome BeadChip. We present comparison results and a statistical summary of our genotype data sets. Our data set comprises 14,647 Korean samples. To solve the limitation of automated clustering, we performed manual genotype clustering for the targeted identification of 46,076 variants that were identified using GenomeStudio software. To evaluate the effects of applying custom cluster files, we tested cluster files using 804 independent Korean samples and the same platform. Our study firstly suggests practical guidelines for exome chip quality control in Asian populations and provides valuable insight into an association study using exome chip.

摘要

基于外显子组的基因分型阵列具有成本效益,最近已被用作全外显子组测序的替代平台。然而,外显子组阵列中的自动聚类算法在识别罕见和低频变异的基因型调用准确性方面存在问题。为了解决这些缺点,我们提出了一种使用Illumina Infinium HumanExome BeadChip进行准确基因型调用的实用方法。我们展示了比较结果和基因型数据集的统计摘要。我们的数据集包含14,647个韩国样本。为了解决自动聚类的局限性,我们对使用GenomeStudio软件识别的46,076个变异进行了手动基因型聚类,以进行靶向识别。为了评估应用自定义聚类文件的效果,我们使用804个独立的韩国样本和相同平台测试了聚类文件。我们的研究首先提出了亚洲人群外显子组芯片质量控制的实用指南,并为使用外显子组芯片的关联研究提供了有价值的见解。

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本文引用的文献

1
Illumina human exome genotyping array clustering and quality control.Illumina人类外显子基因分型阵列聚类与质量控制
Nat Protoc. 2014 Nov;9(11):2643-62. doi: 10.1038/nprot.2014.174. Epub 2014 Oct 16.
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The NHGRI GWAS Catalog, a curated resource of SNP-trait associations.NHGRI GWAS Catalog,一个经过精心策划的 SNP 与特征关联资源。
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Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium.人类外显子芯片最佳实践和联合调用:CHARGE 联盟。
韩国男性外显子组稀有变异分析确定了三个导致前列腺癌的新易感基因。
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Population based allele frequencies of disease associated polymorphisms in the Personalized Medicine Research Project.基于人群的个体化医学研究项目中与疾病相关的多态性的等位基因频率。
BMC Genet. 2010 Jun 17;11:51. doi: 10.1186/1471-2156-11-51.
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Next-generation DNA sequencing.下一代DNA测序
Nat Biotechnol. 2008 Oct;26(10):1135-45. doi: 10.1038/nbt1486.
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Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs.单核苷酸多态性(SNPs)、常见拷贝数多态性和罕见拷贝数变异(CNVs)的整合基因型分型与关联分析。
Nat Genet. 2008 Oct;40(10):1253-60. doi: 10.1038/ng.237. Epub 2008 Sep 7.
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PLINK: a tool set for whole-genome association and population-based linkage analyses.PLINK:一个用于全基因组关联分析和基于群体的连锁分析的工具集。
Am J Hum Genet. 2007 Sep;81(3):559-75. doi: 10.1086/519795. Epub 2007 Jul 25.
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topoSNP: a topographic database of non-synonymous single nucleotide polymorphisms with and without known disease association.topoSNP:一个包含有无已知疾病关联的非同义单核苷酸多态性的地形数据库。
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