STRmix™报告中的结果和诊断指南

IF 2.1 Q1 CRIMINOLOGY & PENOLOGY
Laura Russell, Stuart Cooper, R. Wivell, Zane Kerr, Duncan A. Taylor, J. Buckleton, J. Bright
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引用次数: 20

摘要

直到最近,法医DNA图谱解释主要是一个人工的、耗时的过程,由分析人员使用启发式方法来确定那些可以合理解释恢复的图谱的基因型组合。概率基因分型(PG)现在已经成为解释DNA分析证据的普遍方法。由于PG的复杂性需要使用算法和现代计算能力,一些评论家将其称为“黑箱”方法。在这里,我们讨论STRmix™输出中提供的丰富信息,STRmix™是连续PG系统的一个例子。我们将讨论分析人员如何对这些信息进行评估,以给予结果的信心,或表明进一步的解释可能是有必要的。具体来说,我们讨论了STRmix™输出的“主要”和“次要”诊断,并给出了可能观察到的值的一些背景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A guide to results and diagnostics within a STRmix™ report
Until recently, forensic DNA profile interpretation was predominantly a manual, time consuming process undertaken by analysts using heuristics to determine those genotype combinations that could reasonably explain a recovered profile. Probabilistic genotyping (PG) has now become commonplace in the interpretation of DNA profiling evidence. As the complexity of PG necessitates the use of algorithms and modern computing power it has been dubbed by some critics as a ‘black box’ approach. Here we discuss the wealth of information that is provided within the output of STRmix™, one example of a continuous PG system. We discuss how this information can be evaluated by analysts either to give confidence in the results or to indicate that further interpretation may be warranted. Specifically, we discuss the ‘primary’ and ‘secondary’ diagnostics output by STRmix™ and give some context to the values that may be observed.
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