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在某些缺失情况下,根据DNA多位点指纹计算父权概率。

Calculating paternity probabilities from DNA multilocus fingerprints in some cases of deficiency.

作者信息

Yassouridis A, Epplen J T

机构信息

Max-Planck-Institut für Psychiatrie, München, Germany.

出版信息

Electrophoresis. 1993 Oct;14(10):978-85. doi: 10.1002/elps.11501401156.

Abstract

Paternity determination via DNA multilocus fingerprints in normal trio cases, namely when the fingerprints of the trio mother, child and putative father are available, is performed on a routine basis. But in cases of deficiency, where the DNA fingerprint of mother or putative father is missing, there exists no systematic, analytical way for paternity calculations, even in cases where DNA fingerprints of other persons related to the missing individual are available. The aim of this paper is to establish a mathematical, analytical background, that enables paternity calculations in cases of deficiency if complementary information can be obtained from the DNA fingerprints of at least one of the parents of the missing individual. Using the basic outline of our previously described procedure, the formulas for paternity calculations also allow mutations.

摘要

在常规的三联体案例中,即当三联体母亲、孩子和推定父亲的指纹均可用时,通过DNA多位点指纹进行亲子鉴定是常规操作。但在存在缺失情况时,即母亲或推定父亲的DNA指纹缺失,即使有与缺失个体相关的其他人的DNA指纹,也不存在用于亲子鉴定计算的系统分析方法。本文的目的是建立一个数学分析背景,以便在可以从缺失个体的至少一位父母的DNA指纹中获得补充信息的缺失情况下进行亲子鉴定计算。使用我们之前描述的程序的基本框架,亲子鉴定计算的公式也允许突变。

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