Lin S
Department of Statistics, Ohio State University, Columbus, Ohio 43210-1247, USA.
Hum Hered. 2001;52(4):201-9. doi: 10.1159/000053377.
The chi-square model (CHS) of recombination has been studied extensively, in recent years, for its ability of capturing the process and estimating the level of crossover interference. Exploration thus far shows that this model yields much better fits to human genetic data than Haldane's no-interference model, and the explicit level of interference can be easily estimated as well. This paper provides calculations of sample sizes required to detect interference under CHS for a variety of settings. Two data types, fully informative meioses and phase-unknown backcross families, are studied. Under each setting, we calculate the number of meioses/families needed to ensure that the expected log-likelihood difference between the chi(2) interference model and Haldane's no-interference model exceeds a prespecified threshold. It is found that joint consideration of multiple (more than three) markers dramatically reduces the number of meioses/families needed when compared to an analysis based on three-point data, a traditional setting for detecting interference using three-point tests. The results indicate that the numbers of meioses needed to detect interference under CHS are well within the reach of most genetic mapping studies.
近年来,重组的卡方模型(CHS)因其能够捕捉重组过程并估计交叉干扰水平而受到广泛研究。迄今为止的探索表明,该模型对人类遗传数据的拟合效果比霍尔丹无干扰模型好得多,而且干扰的明确水平也很容易估计。本文提供了在各种情况下检测CHS下干扰所需样本量的计算。研究了两种数据类型,即完全信息性减数分裂和相位未知的回交家系。在每种情况下,我们计算所需的减数分裂数/家系数,以确保卡方干扰模型与霍尔丹无干扰模型之间的预期对数似然差超过预先设定的阈值。结果发现,与基于三点数据(使用三点检验检测干扰的传统设置)的分析相比,联合考虑多个(超过三个)标记可显著减少所需的减数分裂数/家系数。结果表明,在CHS下检测干扰所需的减数分裂数在大多数基因定位研究的能力范围内。