DNA mixture interpretation based on the continuous model

Sho Manabe, Keiji Tamaki
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引用次数: 1

Abstract

In forensic science, the interpretation of DNA mixture proˆles and small amounts or degraded DNA proˆles is challenging due to di‹culties in evaluating the contribution of the person of interest ( e.g., victim and suspect ) . In recent years, some probabilistic genotyping software programs based on a continuous model were developed to promote the interpretation of complex DNA proˆles. The model uses quantitative information of peak heights in the DNA proˆle and considers the eŠect of stutters and allelic drop-out. Therefore, the model is eŠective for interpreting complex DNA proˆles, and some software based on the model that has been applied to actual caseworks. This review provides the concept of probabilistic genotyping based on a continuous model. We explain calculation principles of likelihood ratios, weight values, and expected peak heights in the continuous model. We also discuss the current issues of software validation, management of artifact peaks, and the estimation of the number of contributors.
基于连续模型的DNA混合解释
在法医科学中,由于在评估相关人员(例如受害者和嫌疑人)的贡献方面存在困难,因此对混合DNA样本和少量或降解DNA样本的解释具有挑战性。近年来,开发了一些基于连续模型的概率基因分型软件程序,以促进复杂DNA序列的解释。该模型使用DNA序列中峰高的定量信息,并考虑口吃和等位基因脱落的eŠect。因此,该模型是解释复杂DNA序列的eŠective,一些基于该模型的软件已经应用到实际案例中。本文综述了基于连续模型的概率基因分型的概念。我们解释了连续模型中似然比、权重值和预期峰值高度的计算原理。我们还讨论了软件验证、工件峰值的管理以及贡献者数量的估计等当前问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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