Egeland Thore, Sheehan Nuala
Department of Medical Genetics, Ulleval University Hospital, 0407 Oslo, Norway.
Forensic Sci Int Genet. 2008 Jun;2(3):219-25. doi: 10.1016/j.fsigen.2008.02.006. Epub 2008 Apr 18.
This paper considers identification problems based on DNA marker data. The topics we discuss are general, but we will exemplify them in a simple context. There is DNA available from two persons. There is uncertainty about the relationship between the two individuals and a number of hypotheses describing the possible relationship is available. The task is to determine the most likely pedigree. This problem is fairly standard. However, there are some problems that cannot be solved using DNA from independently segregating loci. For example, the likelihoods for (i) grandparent-grandchild, (ii) uncle-niece and (iii) half-sibs coincide for such DNA data and so these relations cannot be distinguished on the basis of markers normally used for forensic identification problems: the likelihood ratio comparing any pair of hypotheses will be unity. Sometimes, but not in the examples we consider, other sources of DNA like mtDNA or sex chromosomes can help to distinguish between such equally likely possibilities. Prior information can likewise be of use. For instance, age information can exclude alternative (i) above and also indicate that alternative (iii) is apriori more likely than alternative (ii). More generally, the above problems can be solved using linked autosomal markers. To study the problem in detail and understand how linkage works in this regard, we derive an explicit formula for a pair of linked markers. The formula extends to independent pairs of linked markers. While this approach adds to the understanding of the problem, more markers are required to obtain satisfactory results and then the Lander-Green algorithm is needed. Simulation experiments are presented based on a range of scenarios and we conclude that useful results can be obtained using available freeware (MERLIN and R). The main message of this paper is that linked autosomal markers deserve greater attention in forensic genetics and that the required laboratory and statistical analyses can be performed based on existing technology and freeware.
本文探讨基于DNA标记数据的识别问题。我们讨论的主题具有普遍性,但将在一个简单的背景下举例说明。现有来自两个人的DNA。这两个人之间的关系存在不确定性,并且有一些描述可能关系的假设。任务是确定最可能的谱系。这个问题相当标准。然而,存在一些使用独立分离基因座的DNA无法解决的问题。例如,对于此类DNA数据,(i)祖父母 - 孙子女、(ii)叔侄和(iii)半同胞的似然性是一致的,因此这些关系无法根据通常用于法医鉴定问题的标记来区分:比较任何一对假设的似然比将为1。有时,但在我们考虑的例子中并非如此,其他DNA来源如线粒体DNA或性染色体可以帮助区分这些同样可能的可能性。先验信息同样可能有用。例如,年龄信息可以排除上述替代方案(i),并且还表明替代方案(iii)在先天条件下比替代方案(ii)更有可能。更一般地,上述问题可以使用连锁常染色体标记来解决。为了详细研究这个问题并理解连锁在这方面的作用,我们推导出一对连锁标记的显式公式。该公式扩展到独立的连锁标记对。虽然这种方法有助于理解问题,但需要更多的标记才能获得满意的结果,然后需要使用兰德 - 格林算法。基于一系列场景进行了模拟实验,我们得出结论,使用现有的免费软件(MERLIN和R)可以获得有用的结果。本文的主要信息是,连锁常染色体标记在法医遗传学中值得更多关注,并且所需的实验室和统计分析可以基于现有技术和免费软件进行。