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一种评估 X 染色体标记在亲缘关系测试中效用的通用方法。

A general method to assess the utility of the X-chromosomal markers in kinship testing.

机构信息

Instituto de Patologia e Imunologia Molecular da Universidade do Porto (IPATIMUP), Portugal.

出版信息

Forensic Sci Int Genet. 2012 Mar;6(2):198-207. doi: 10.1016/j.fsigen.2011.04.014. Epub 2011 May 17.

Abstract

In studies involving pedigree reconstruction and kinship estimation, it is acknowledged that some pedigrees have the same algebraic expressions for the joint genotypic probabilities and are, therefore, indistinguishable when considering only genetic information, no matter what the mode of transmission considered. Indeed, although standard forensic practice considers solely unlinked autosomal markers, the existence of pedigrees with the referred theoretical property (that are then said to belong to the same kinship class) is possible when considering any kind of genetic transmission. The research on genetic relatedness has always been linked to the root concept of identity-by-descent (IBD). However, although the basic theoretical core for autosomal transmission has been long formalised, a general method allowing the decision if two pedigrees linking two non-inbred individuals are distinguishable using unlinked autosomal markers along with the respective IBD partitions (and consequently the algebraic expressions for the joint genotypic probabilities) was only recently published. In this work X-chromosomal transmission will be at stake, considering that the analytical framework for X-chromosomal markers has been recently established and the importance of X-chromosome markers for these questions has been steadily growing, particularly in forensics, as a tool both to complement the information given by autosomes in complex kinship testing cases and to differentiate pedigrees belonging to the same autosomal kinship class. Therefore, here it will be presented a formal and mathematically well supported framework where a general counting rule is given, allowing a secure and expeditious decision on the usefulness of typing (unlinked) X-chromosomal markers on pairwise kinship testing involving two non-inbred individuals. Moreover the counting rule now presented allows the derivation of algebraic expressions for the joint genotypic probabilities associated with any pedigree.

摘要

在涉及系谱重建和亲属关系估计的研究中,人们承认,一些系谱具有相同的联合基因型概率的代数表达式,因此,仅考虑遗传信息时,无论考虑哪种遗传模式,它们都是不可区分的。事实上,尽管标准的法医实践仅考虑非连锁的常染色体标记,但当考虑任何类型的遗传传递时,存在具有上述理论特性的系谱(即属于同一亲属关系类别的系谱)是可能的。遗传相关性的研究一直与血缘关系的基本概念(IBD)有关。然而,尽管常染色体传递的基本理论核心已经长期形式化,但直到最近才发表了一种通用方法,可以决定使用非连锁常染色体标记以及各自的 IBD 分区(以及由此产生的联合基因型概率的代数表达式)是否可以区分两个非近亲个体的系谱。在这项工作中,将涉及 X 染色体的传递,因为 X 染色体标记的分析框架最近已经建立,并且 X 染色体标记对于这些问题的重要性一直在稳步增长,特别是在法医领域,作为一种工具,用于补充复杂亲属关系测试案例中常染色体提供的信息,并区分属于同一常染色体亲属关系类别的系谱。因此,这里将介绍一个正式的、数学上有充分支持的框架,其中给出了一个通用的计数规则,允许对涉及两个非近亲个体的成对亲属关系测试中(非连锁)X 染色体标记的有用性进行安全和快速的决策。此外,现在提出的计数规则允许推导出与任何系谱相关联的联合基因型概率的代数表达式。

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