The X-chromosome is often excluded from genome-wide association studies because of analytical challenges. Some of the problems, such as the random, skewed or no X-inactivation model uncertainty, have been investigated. Other considerations have received little to no attention, such as the value in considering non-additive and gene-sex interaction effects, and the inferential consequence of choosing different baseline alleles (i.e.\ the reference vs.\ the alternative allele). Here we propose a unified and flexible regression-based association test for X-chromosomal variants. We provide theoretical justifications for its robustness in the presence of various model uncertainties, as well as for its improved power when compared with the existing approaches under certain scenarios. For completeness, we also revisit the autosomes and show that the proposed framework leads to a more robust approach than the standard method. Finally, we provide supporting evidence by revisiting several published association studies. Supplementary materials for this article are available online.
翻译:由于分析方面的挑战,X-染色体往往被排除在全基因组协会研究之外,有些问题,如随机、偏斜或无X-不活动模型的不确定性,已经调查过;其他考虑因素很少得到重视,甚至没有引起注意,例如考虑非增加和基因-性别相互作用效应的价值,以及选择不同基线所有物的推论后果(即参考与替代所有物的推论)。我们在这里提议对X-染色体变异物进行统一和灵活的回归式联合测试。我们提供了理论理由,说明在存在各种模型不确定性的情况下,这种变异物具有稳健性,而且与某些情况下的现有方法相比,其功率有所提高。关于完整性,我们还重新审视了拟议框架,并表明采用比标准方法更稳健的方法。最后,我们通过重新研究若干已公布的协会研究来提供证据支持。这一文章的补充材料可在网上查阅。