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不完全连锁不平衡下全基因组扫描中的稳健检验

Robust Tests in Genome-Wide Scans under Incomplete Linkage Disequilibrium.

作者信息

Zheng Gang, Joo Jungnam, Zaykin Dmitri, Wu Colin, Geller Nancy

机构信息

Office of Biostatistics Research, Division of Population and Prevention Sciences, National Heart, Lung and Blood Institute, 6701 Rockledge Drive, MSC 7913, Bethesda, MD 20892, U.S.A.

Biostatistics Branch, National Institute of Environmental Health Sciences, Mail Drop A3-03, Research Triangle Park, NC 27709, U.S.A.

出版信息

Stat Sci. 2009 Nov;24(4):503-516. doi: 10.1214/09-sts314. Epub 2010 Apr 20.

Abstract

When genetic markers are in complete linkage disequilibrium with disease loci, it has been shown that the efficiency robust tests, including maximum (minimum) type statistics and the procedure with genetic model selection, are often preferred to either a single trend test or Pearson's chi-squared test in candidate-gene studies and genome-wide scans. We consider a more general two-locus model where linkage disequilibrium is allowed to vary, and examine the impact of penetrances at the marker locus when genetic models are defined at the disease locus. Robust statistics are then reviewed and their efficiency and robustness are compared through simulations in genome-wide scans of 300,000 markers under the two-locus model. Applications of the robust tests to Wellcome Trust Case-Control Consortium (2007) are illustrated.

摘要

当遗传标记与疾病位点处于完全连锁不平衡状态时,研究表明,在候选基因研究和全基因组扫描中,包括最大(最小)型统计量以及遗传模型选择程序在内的稳健检验效率,通常优于单趋势检验或Pearson卡方检验。我们考虑一个更一般的双位点模型,其中允许连锁不平衡有所变化,并在疾病位点定义遗传模型时,研究标记位点外显率的影响。然后回顾稳健统计量,并通过在双位点模型下对30万个标记进行全基因组扫描的模拟,比较它们的效率和稳健性。文中还举例说明了稳健检验在威康信托病例对照协会(2007年)中的应用。

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