Nascimento Fabrícia F, Mehta Sanjay R, Little Susan J, Volz Erik M
MRC Centre for Global Infectious Disease Analysis and the Department of Infectious Disease Epidemiology, Imperial College London, London, UK.
Division of Infectious Diseases, University of California San Diego, San Diego, CA, USA.
Epidemics. 2025 Jul 16;52:100846. doi: 10.1016/j.epidem.2025.100846.
The robustness and statistical efficiency of phylodynamic models have been tested by many investigators. However, little attention has been given to model specification and inductive bias that can occur if the model is misspecified or provides an overly simplistic representation of the evolutionary process. Here, we carried out a study involving the simulation of HIV epidemics using a complex model and calibrated to men who have sex with men from San Diego, USA. We then used this epidemic trajectory to simulate genealogies, sequence alignments equivalent to HIV partial pol gene and the complete genome. We proceeded to estimate migration rates using a simplistic representation of the epidemiological model by testing model-based phylodynamics and phylogeographic methods. We observed that even though there were some biases on the estimates using a simplistic representation of the epidemiological model, we were still able to estimate the migration rates depending on the method and sample size used in the analyses.
许多研究人员已经测试了系统动力学模型的稳健性和统计效率。然而,如果模型设定错误或对进化过程提供过于简单的表示,那么很少有人关注模型设定和归纳偏差可能会出现的情况。在这里,我们进行了一项研究,使用一个复杂模型模拟艾滋病毒流行情况,并根据美国圣地亚哥男男性行为者的数据进行校准。然后,我们利用这个流行轨迹来模拟谱系、等同于艾滋病毒部分pol基因和完整基因组的序列比对。我们通过测试基于模型的系统动力学和系统地理学方法,使用流行病学模型的简单表示来估计迁移率。我们观察到,尽管使用流行病学模型的简单表示进行估计存在一些偏差,但根据分析中使用的方法和样本量,我们仍然能够估计迁移率。