Department of Epidemiology and Biostatistics, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Genes (Basel). 2022 May 9;13(5):847. doi: 10.3390/genes13050847.
Although the X chromosome accounts for about 5% of the human genes, it is routinely excluded from genome-wide association studies probably due to its unique structure and complex biological patterns. While some statistical methods have been proposed for testing the association between X chromosomal markers and diseases, very a few of them can adjust for covariates. Unfortunately, those methods that can incorporate covariates either need to specify an X chromosome inactivation model or require the permutation procedure to compute the value. In this article, we proposed a novel analytic approach based on logistic regression that allows for covariates and does not need to specify the underlying X chromosome inactivation pattern. Simulation studies showed that our proposed method controls the size well and has robust performance in power across various practical scenarios. We applied the proposed method to analyze Graves' disease data to show its usefulness in practice.
虽然 X 染色体约占人类基因的 5%,但由于其独特的结构和复杂的生物学模式,它通常被排除在全基因组关联研究之外。虽然已经提出了一些用于检测 X 染色体标记物与疾病之间关联的统计方法,但很少有方法可以调整协变量。不幸的是,那些可以包含协变量的方法要么需要指定 X 染色体失活模型,要么需要进行置换过程来计算 值。在本文中,我们提出了一种基于逻辑回归的新分析方法,该方法允许包含协变量,并且不需要指定潜在的 X 染色体失活模式。模拟研究表明,我们提出的方法很好地控制了大小,并且在各种实际情况下具有稳健的功效。我们应用所提出的方法来分析格雷夫斯病数据,以显示其在实践中的有用性。