Selection of influential genetic markers among a large number of candidates based on effect estimation rather than hypothesis testing -: An approach for genome-wide association studies

被引:10
作者
Stromberg, Ulf [1 ]
Bjork, Jonas [2 ]
Broberg, Karin [1 ]
Mertens, Fredrik [3 ]
Vineis, Paolo [4 ]
机构
[1] Univ Lund Hosp, Dept Occupat & Environm Med, SE-22185 Lund, Sweden
[2] Univ Lund Hosp, Competence Ctr Clin Res, S-22185 Lund, Sweden
[3] Univ Lund Hosp, Dept Clin Genet, Lund, Sweden
[4] Univ London Imperial Coll Sci Technol & Med, Dept Epidemiol & Publ Hlth, London, England
关键词
D O I
10.1097/EDE.0b013e3181632c3d
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
In epidemiologic studies on direct genetic associations, hypothesis testing is primarily considered for evaluating the effects of each candidate genetic marker, eg, single nucleotide polymorphisms. To help investigators protect themselves from over-interpreting statistically significant findings that are not likely to signify a true effect-a problem connected to multiple comparisons - consideration of the false-positive report probability has been proposed. There have also been arguments advocating estimation of effect size rather than hypothesis testing (P value). Here, we propose an estimation-based approach that offers an attractive alternative to the test-based false-positive report probability, when the task is to select promising genetic markers for further analyses. We discuss the potential of this estimation-based approach for genome-wide association studies.
引用
收藏
页码:302 / 308
页数:7
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