Zeng Xiangpei, Warshauer David H, King Jonathan L, Churchill Jennifer D, Chakraborty Ranajit, Budowle Bruce
Institute of Applied Genetics, Department of Molecular and Medical Genetics, University of North Texas Health Science Center, 3500 Camp Bowie Blvd., Fort Worth, Texas, 76107, USA.
Center of Excellence in Genomic Medicine Research (CEGMR), King Abdulaziz University, Jeddah, Saudi Arabia.
Int J Legal Med. 2016 Jul;130(4):891-896. doi: 10.1007/s00414-016-1333-4. Epub 2016 Feb 25.
Ancestry informative markers (AIMs) can be used to determine population affiliation of the donors of forensic samples. In order to examine ancestry evaluations of the four major populations in the USA, 23 highly informative AIMs were identified from the International HapMap project. However, the efficacy of these 23 AIMs could not be fully evaluated in silico. In this study, these 23 SNPs were multiplexed to test their actual performance in ancestry evaluations. Genotype data were obtained from 189 individuals collected from four American populations. One SNP (rs12149261) on chromosome 16 was removed from this panel because it was duplicated on chromosome 1. The resultant 22-AIMs panel was able to empirically resolve the four major populations as in the in silico study. Eight individuals were assigned to a different group than indicated on their samples. The assignments of the 22 AIMs for these samples were consistent with AIMs results from the ForenSeq(TM) panel. No departures from Hardy-Weinberg equilibrium (HWE) and linkage disequilibrium (LD) were detected for all 22 SNPs in four US populations (after removing the eight problematic samples). The principal component analysis (PCA) results indicated that 181 individuals from these populations were assigned to the expected groups. These 22 SNPs can contribute to the candidate AIMs pool for potential forensic identification purposes in major US populations.
祖先信息标记(AIMs)可用于确定法医样本捐赠者的群体归属。为了研究美国四大群体的祖先评估情况,从国际人类基因组单体型图计划中鉴定出23个高度信息丰富的AIMs。然而,这23个AIMs的效能无法在计算机模拟中得到充分评估。在本研究中,将这23个单核苷酸多态性(SNPs)进行多重检测,以测试它们在祖先评估中的实际性能。基因型数据来自从四个美国群体收集的189个人。由于1号染色体上存在重复,位于16号染色体上的一个SNP(rs12149261)被从该面板中移除。最终得到的22个AIMs面板能够像在计算机模拟研究中那样,从经验上区分这四大群体。有8个人被分配到与其样本所显示的不同群体。这些样本的22个AIMs的分配结果与ForenSeq™面板的AIMs结果一致。在四个美国群体中(去除8个有问题的样本后),对所有22个SNP均未检测到偏离哈迪-温伯格平衡(HWE)和连锁不平衡(LD)的情况。主成分分析(PCA)结果表明,这些群体中的181个人被分配到预期的群体中。这22个SNP可有助于为美国主要群体潜在的法医鉴定目的构建候选AIMs库。