Institute of Investigative Genetics, University of North Texas Health Science Center, Fort Worth, TX 76107, USA.
Int J Legal Med. 2010 Sep;124(5):353-61. doi: 10.1007/s00414-009-0400-5. Epub 2009 Dec 22.
Forensic DNA analysis is currently performed using highly discriminating short tandem repeat (STR) markers. SNPs are being investigated as adjunct tools for human identity testing because of their abundance in the human genome, utility for genotyping degraded DNA samples, and amenability to automation. While SNPs can provide an alternative approach, on a per locus basis they have a lower power of discrimination (PD) than STRs. With the discovery of block structures in the human genome, a novel set of SNP markers are available for further exploration of forensic utility. Several neighboring, tightly linked SNPs are inherited together and form a haplotype block, which as a haploblock has a higher discrimination power than the individual SNPs within the block. Candidate haplotype blocks were selected from three major populations (Caucasian, East Asian, and African) using the following parameters: maximum match probability reduction = 0.85, linkage disequilibrium (LD) r(2) ≥ 0.7, maximum F(st) = 0.06, minimum number of SNPs = 3, minimum heterozygosity = 0.2, and minimum number of haplotypes = 3. From the HapMap Phase II data, 253 haploblocks were identified on the 22 autosomal chromosomes. After removing haploblocks deviating from the Hardy-Weinberg equilibrium (HWE) or in LD with other haploblocks, 24 haploblocks remained as candidates for forensic consideration. The cumulative PD of these blocks can reach 10(-12) in the populations studied. The data support within and between haplotype independence even when they are syntenic. We propose guidelines for evidence interpretation that address the application of haplotype blocks for transfer evidence, mixture, and kinship analyses.
法医 DNA 分析目前使用高度区分的短串联重复 (STR) 标记进行。由于 SNP 在人类基因组中的丰富性、对降解 DNA 样本进行基因分型的实用性以及易于自动化,因此它们被作为人类身份测试的辅助工具进行研究。虽然 SNP 可以提供一种替代方法,但就每个基因座而言,它们的鉴别能力 (PD) 低于 STR。随着人类基因组中块结构的发现,一组新的 SNP 标记可用于进一步探索法医用途。几个相邻的紧密连锁的 SNP 一起遗传并形成单倍型块,作为单倍型块,其鉴别能力高于块内的单个 SNP。使用以下参数从三个主要人群(高加索人、东亚人和非洲人)中选择候选单倍型块:最大匹配概率降低 = 0.85、连锁不平衡 (LD) r(2)≥0.7、最大 F(st)=0.06、最小 SNP 数 = 3、最小杂合度 = 0.2 和最小单倍型数 = 3。从 HapMap 第二阶段数据中,在 22 条常染色体上确定了 253 个单倍型块。从 Hardy-Weinberg 平衡 (HWE) 或与其他单倍型块 LD 偏离的单倍型块中去除后,24 个单倍型块仍然是法医考虑的候选者。这些块的累积 PD 在研究人群中可达 10(-12)。即使它们是同线的,数据也支持单倍型内和单倍型间的独立性。我们提出了证据解释的指导方针,以解决单倍型块在转移证据、混合物和亲属关系分析中的应用。