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On incomplete sampling under birth-death models and connections to the sampling-based coalescent.

机译:关于出生死亡模型下的不完全抽样以及与基于抽样的合并的联系。

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The constant rate birth-death process is used as a stochastic model for many biological systems, for example phylogenies or disease transmission. As the biological data are usually not fully available, it is crucial to understand the effect of incomplete sampling. In this paper, we analyze the constant rate birth-death process with incomplete sampling. We derive the density of the bifurcation events for trees on n leaves which evolved under this birth-death-sampling process. This density is used for calculating prior distributions in Bayesian inference programs and for efficiently simulating trees. We show that the birth-death-sampling process can be interpreted as a birth-death process with reduced rates and complete sampling. This shows that joint inference of birth rate, death rate and sampling probability is not possible. The birth-death-sampling process is compared to the sampling-based population genetics model, the coalescent. It is shown that despite many similarities between these two models, the distribution of bifurcation times remains different even in the case of very large population sizes. We illustrate these findings on an Hepatitis C virus dataset from Egypt. We show that the transmission times estimates are significantly different-the widely used Gamma statistic even changes its sign from negative to positive when switching from the coalescent to the birth-death process.
机译:恒定速率的生死过程被用作许多生物系统(例如系统发育或疾病传播)的随机模型。由于通常无法完全获得生物学数据,因此了解不完整采样的影响至关重要。在本文中,我们分析了不完全抽样的恒定比率出生-死亡过程。我们推导了在这种出生-死亡采样过程中进化的n个叶子上树木的分叉事件的密度。此密度用于计算贝叶斯推理程序中的先验分布,并有效地模拟树木。我们表明,出生死亡采样过程可以解释为出生率降低且采样完整的死亡过程。这表明不可能共同推断出生率,死亡率和抽样概率。将出生-死亡采样过程与基于采样的种群遗传模型(聚结)进行了比较。结果表明,尽管这两个模型之间有许多相似之处,但即使在人口规模非常大的情况下,分叉时间的分布仍然不同。我们在来自埃及的丙型肝炎病毒数据集上说明了这些发现。我们表明,传输时间的估计值存在显着差异-广泛使用的Gamma统计量甚至在从合并过程转换为出生死亡过程时,其符号也从负变为正。

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