Rowold Diane J, Herrera Rene J
Department of Biological Sciences, Florida International University, University Park Campus, Miami, FL 33199, USA.
Forensic Sci Int. 2005 Jun 30;151(1):59-69. doi: 10.1016/j.forsciint.2004.07.007.
This study is an investigation of genetic variation among the CODIS (combined DNA index system) STR (short tandem repeat) reference collections. The analysis was conducted in two parts. The first is an overall comparison (G-test) of allelic frequency distributions for 12 STR loci among 19 forensic databases representing various major groups and ethnic populations. In the second phase of the study, the impact of database replacement on DNA profile frequencies and inclusion probabilities is examined. The G-test results reveal clear allelic frequency differences among the major divisions, and, in some cases, among ethnically distinct subdivisions of the same major group affiliation. Other results indicate that database substitution may sometimes lead to substantial alterations in individual inclusion probabilities. Furthermore, there are numerous instances in which an allele present in some databases is missing in others. Fortunately, in most cases, these effects may not be forensically significant due to the increased discriminatory power of the STR markers employed in the CODIS system. However, differences in inclusion probabilities may become critical in situations in which DNA quantity is severely limited and/or compromised by degradation since, in these cases, the power of forensic STR analysis may be mitigated by reducing the number of informative loci.
本研究是对联合DNA索引系统(CODIS)短串联重复序列(STR)参考样本库之间的基因变异进行的一项调查。分析分两部分进行。第一部分是对代表不同主要群体和种族人群的19个法医数据库中12个STR基因座的等位基因频率分布进行全面比较(G检验)。在研究的第二阶段,考察了数据库替换对DNA图谱频率和个体识别概率的影响。G检验结果显示,在主要群体之间,以及在某些情况下,在同一主要群体归属的不同种族细分群体之间,等位基因频率存在明显差异。其他结果表明,数据库替换有时可能导致个体识别概率发生重大变化。此外,在许多情况下,某些数据库中存在的等位基因在其他数据库中缺失。幸运的是,在大多数情况下,由于CODIS系统中使用的STR标记的鉴别能力增强,这些影响在法医上可能并不显著。然而,在DNA数量严重受限和/或因降解而受损的情况下,个体识别概率的差异可能变得至关重要,因为在这些情况下,法医STR分析的能力可能会因信息性基因座数量的减少而降低。