Data quality control in genetic case-control association studies

被引:860
|
作者
Anderson, Carl A. [1 ,2 ]
Pettersson, Fredrik H. [1 ]
Clarke, Geraldine M. [1 ]
Cardon, Lon R. [3 ]
Morris, Andrew P. [1 ]
Zondervan, Krina T. [1 ]
机构
[1] Univ Oxford, Wellcome Trust Ctr Human Genet, Genet & Genom Epidemiol Unit, Oxford, England
[2] Wellcome Trust Sanger Inst, Cambridge, England
[3] GlaxoSmithKline, King Of Prussia, PA USA
基金
英国惠康基金;
关键词
GENOME-WIDE ASSOCIATION; RISK LOCI; STRATIFICATION; TOOL;
D O I
10.1038/nprot.2010.116
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This protocol details the steps for data quality assessment and control that are typically carried out during case-control association studies. The steps described involve the identification and removal of DNA samples and markers that introduce bias. These critical steps are paramount to the success of a case-control study and are necessary before statistically testing for association. We describe how to use PLINK, a tool for handling SNP data, to perform assessments of failure rate per individual and per SNP and to assess the degree of relatedness between individuals. We also detail other quality-control procedures, including the use of SMARTPCA software for the identification of ancestral outliers. These platforms were selected because they are user-friendly, widely used and computationally efficient. Steps needed to detect and establish a disease association using case-control data are not discussed here. Issues concerning study design and marker selection in case-control studies have been discussed in our earlier protocols. This protocol, which is routinely used in our labs, should take approximately 8 h to complete.
引用
收藏
页码:1564 / 1573
页数:10
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