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Refining genetic associations in multiple sclerosis

机译:改善多发性硬化症的遗传关联

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Genome-wide association studies involve several hundred thousand markers and, even when quality control is scrupulous, are invariably confounded by residual uncorrected errors that can falsely inflate the apparent difference between cases and controls (so-called genomic inflation).1 As a consequence such studies inevitably generate false positives alongside genuine associations. By use of Bayesian logic and empirical data, the Wellcome Trust Case Control Consortium suggested that association studies in complex disease should involve at least 2000 cases and 2000 controls, at which level they predicted that p values of less than 5xlO~7 would more commonly signify true positives than false positives.
机译:全基因组关联研究涉及数十万个标记,即使严格地进行质量控制,也总是被残留的未校正错误所混淆,这些残留未校正错误会错误地夸大病例与对照之间的表观差异(所谓的基因组膨胀)。1因此,研究不可避免地会产生假阳性以及真正的联想。通过使用贝叶斯逻辑和经验数据,Wellcome Trust病例对照协会建议,复杂疾病的关联研究应至少涉及2000例病例和2000例对照,在该水平上,他们预测p值小于5x10〜7更常见。真假比假阳性。

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