Kling Daniel
Department of Forensic Services, Oslo University Hospital, P.O. Box 4950, Nydalen, 0424, Oslo, Norway.
Int J Legal Med. 2018 Mar;132(2):361-371. doi: 10.1007/s00414-017-1612-8. Epub 2017 May 26.
Recent progress in forensic genetics has introduced a number of closely located short tandem repeat (STR) markers on the X chromosome. Inevitably, dependencies arise that have to be accounted for. This paper will in detail explore the complex statistical interpretation of X-chromosomal STR markers, focusing on likelihood calculations. Specifically, we will investigate how the phase uncertainty of haplotypes comes into play in the statistical evaluations and what curious effects this phenomenon can have. The starting point is the different real cases where the weight of evidence has provided unexpected results that require further investigation in order to be fully understood. We will touch upon subjects such as association between alleles, recombinations, and mutations. The aim of this study is to facilitate a better understanding of the interaction between the concepts in addition to provide an understanding why good estimates of haplotype frequencies are crucial. The individual subjects have been discussed in other fields, whereas this study will focus on forensic applications where few studies have been conducted relating to the understanding of how these concepts interact.
法医遗传学的最新进展引入了许多位于X染色体上紧密相邻的短串联重复序列(STR)标记。不可避免地,会出现一些必须加以考虑的依赖性。本文将详细探讨X染色体STR标记的复杂统计解释,重点是似然计算。具体而言,我们将研究单倍型的相位不确定性在统计评估中如何发挥作用,以及这种现象可能产生哪些奇特的影响。起点是不同的实际案例,在这些案例中,证据权重产生了意想不到的结果,需要进一步调查才能完全理解。我们将涉及等位基因之间的关联、重组和突变等主题。本研究的目的是促进对这些概念之间相互作用的更好理解,此外还要理解为什么单倍型频率的良好估计至关重要。其他领域已经讨论过各个主题,而本研究将专注于法医应用,在该领域,关于理解这些概念如何相互作用的研究很少。