Holt C L, Stauffer C, Wallin J M, Lazaruk K D, Nguyen T, Budowle B, Walsh P S
PE Biosystems, 850 Lincoln Centre Drive, Foster City, CA 94404, USA.
Forensic Sci Int. 2000 Aug 14;112(2-3):91-109. doi: 10.1016/s0379-0738(00)00169-9.
Legitimate genotype frequency estimation for multiallelic loci relies on component allele frequencies, as population surveys represent only a fraction of possible DNA profiles. Multilocus genotypes from two ethnic human populations, African American (n=195) and U.S. Caucasian (n=200), were compiled at 13 STR loci that are used worldwide in forensic investigation (D3S1358, vWA, FGA, D16S539, TH01, TPOX, CSF1PO, D8S1179, D21S11, D18S51, D5S818, D13S317, and D7S820). Sex-specific AmpFlSTR multiplexes provided stringent PCR-based STR typing specifically optimized for multicolor fluorescence detection. Heterozygosity at each STR locus ranged from 0.57 to 0.89 and encompassed from seven (TH01) to twenty-one (D21S11) alleles. Homozygosity tests, tests based on the distinct numbers of observed homozygous and heterozygous classes, log likelihood ratio tests, and exact tests assessed that the degree of divergence from theoretical Hardy-Weinberg proportions for all 13 STRs does not have practical consequence in genotype frequency estimation. Departures from linkage equilibrium, between loci, that imposed significance to forensic calculations were not indicated by observed variance of the number of heterozygous loci or Karlin interclass correlation tests. For forensic casework, reliable multilocus profile estimates may be obtained from the product of component genotype frequencies, each calculated through application of the Hardy-Weinberg equation to population database allele frequency estimates reported here. The average probability that two randomly selected, unrelated individuals possess an identical thirteen-locus DNA profile was one in 1.8x10(15) African Americans and one in 3.8x10(14) U.S. Caucasians.
对于多等位基因座,合法的基因型频率估计依赖于组成等位基因频率,因为群体调查仅代表了可能的DNA图谱的一部分。从两个种族的人群(非裔美国人,n = 195;美国白种人,n = 200)中收集了13个STR基因座的多位点基因型,这些基因座在全球法医调查中广泛使用(D3S1358、vWA、FGA、D16S539、TH01、TPOX、CSF1PO、D8S1179、D21S11、D18S51、D5S818、D13S317和D7S820)。性别特异性的AmpFlSTR多重PCR提供了基于PCR的严格STR分型,专门针对多色荧光检测进行了优化。每个STR基因座的杂合度范围为0.57至0.89,等位基因数量从7个(TH01)到21个(D21S11)不等。纯合性测试、基于观察到的纯合和杂合类别数量差异的测试、对数似然比测试以及精确测试评估得出,所有13个STR与理论哈迪 - 温伯格比例的偏离程度在基因型频率估计中没有实际影响。通过观察杂合基因座数量的方差或卡林类间相关性测试,未发现基因座之间存在对法医计算有显著影响的连锁不平衡。对于法医案件工作,可以从组成基因型频率的乘积中获得可靠的多位点图谱估计值,每个组成基因型频率是通过将哈迪 - 温伯格方程应用于此报告的群体数据库等位基因频率估计值来计算的。两个随机选择的、无亲属关系的个体拥有相同的13个基因座DNA图谱的平均概率在非裔美国人中为1/1.8×10¹⁵,在美国白种人中为1/3.8×10¹⁴。