McQueen Matthew B, Blacker Deborah, Laird Nan M
Department of Epidemiology, Harvard School of Public Health, Boston, MA 02115, USA.
Am J Hum Genet. 2006 Jun;78(6):914-21. doi: 10.1086/503920. Epub 2006 Mar 29.
Nonparametric linkage strategies often involve estimation of identity by descent (IBD) with the use of affected sibling pairs. Methods for IBD estimation are well established and have been successful for mapping complex traits. However, the majority of linkage approaches involving IBD have focused on statistical testing, rather than on the effect estimates themselves. Through a bootstrap procedure developed for linkage-scan data sets, we provide standard errors for the estimated mean IBD that are broadly applicable. Applications that benefit from the availability of standard errors include effect-size estimates and confidence intervals; meta-analyses, including tests for heterogeneity; and discordant-sibling-pair evaluation. We demonstrate the use of estimated mean IBD and its standard errors in the National Institute of Mental Health Human Genetics Initiative linkage samples for bipolar disorder and Alzheimer disease. Mean IBD and its standard errors are valuable tools for the further assessment and evaluation of linkage-scan samples involving complex disease.
非参数连锁策略通常涉及利用患病同胞对来估计同源染色体同一性(IBD)。IBD估计方法已经成熟,并且在复杂性状定位方面取得了成功。然而,大多数涉及IBD的连锁分析方法都集中在统计检验上,而不是效应估计本身。通过为连锁扫描数据集开发的自助程序,我们提供了广泛适用的估计平均IBD的标准误差。受益于标准误差可用性的应用包括效应大小估计和置信区间;荟萃分析,包括异质性检验;以及不一致同胞对评估。我们展示了估计平均IBD及其标准误差在国立精神卫生研究所双相情感障碍和阿尔茨海默病人类遗传学倡议连锁样本中的应用。平均IBD及其标准误差是进一步评估和评价涉及复杂疾病的连锁扫描样本的有价值工具。