Mattheisen Manuel, Dietter Johannes, Knapp Michael, Baur Max P, Strauch Konstantin
Institute for Medical Biometry, Informatics, and Epidemiology, University of Bonn, Bonn, Germany.
Genet Epidemiol. 2008 Jan;32(1):73-83. doi: 10.1002/gepi.20264.
The asymptotic distribution of [MOD] scores under the null hypothesis of no linkage is only known for affected sib pairs and other types of affected relative pairs. We have extended the GENEHUNTER-MODSCORE program to allow for simulations under the null hypothesis of no linkage to determine the empirical significance of MOD-score results in general situations. We performed simulations with families of different size (one million replicates of 500 families per simulation setting) to thoroughly investigate the impact of the pedigree size on the null distribution of multipoint MOD scores. It is shown that the distribution is dependent on the size and structure of the pedigrees under study. By performing simulations in the context of MOD-score analysis, our new tool efficiently explores the linkage data in a comprehensive way and also provides a valid method to inferentially test for linkage.
在无连锁的零假设下,[MOD] 分数的渐近分布仅在患病同胞对和其他类型的患病亲属对中已知。我们扩展了GENEHUNTER-MODSCORE程序,以允许在无连锁的零假设下进行模拟,从而确定MOD分数结果在一般情况下的经验显著性。我们对不同规模的家系进行了模拟(每个模拟设置对500个家系进行100万次重复),以全面研究家系规模对多点MOD分数零分布的影响。结果表明,该分布取决于所研究家系的规模和结构。通过在MOD分数分析的背景下进行模拟,我们的新工具以全面的方式有效地探索了连锁数据,并且还提供了一种有效的方法来进行连锁的推断性检验。