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人群遗传分析 NGM STR 基因座。

Population genetic analyses of the NGM STR loci.

机构信息

Institute of Investigative Genetics, University of North Texas Health Science Center, Fort Worth, TX 76107, USA.

出版信息

Int J Legal Med. 2011 Jan;125(1):101-9. doi: 10.1007/s00414-010-0516-7. Epub 2010 Sep 29.

Abstract

The AmpFlSTR® NGM™ PCR Amplification Kit enables amplification of 15 autosomal short tandem repeat (STR) loci. The loci are the ten STRs in the SGM Plus® Kit plus the EDNAP and ENSFI recommended STRs D10S1248, D22S1045, D2S441, D1S1656, and D12S391. Allele frequency and other forensically relevant statistics data were generated for the NGM loci in three US population groups (African Americans, Caucasians, and Hispanics). The analyses support that the NGM multiplex is one of the most informative STR multiplex kits available to the forensic science community. At the population level, there are no more detectable departures from expectations of the independence of alleles within as well as between loci than would be expected due to chance, even for the two syntenic loci vWA and D12S391; however, linkage analysis in three large pedigree families shows close linkage between these two loci with a recombination fraction of 0.108. Therefore, in contrast to the practices in calculating the rarity of a DNA profile, for kinship analyses independence between the loci, vWA and D12S391 cannot be assumed.

摘要

AmpFlSTR® NGM™ PCR 扩增试剂盒可扩增 15 个常染色体短串联重复(STR)基因座。这些基因座是 SGM Plus®试剂盒中的 10 个 STR 基因座加上 EDNAP 和 ENSFI 推荐的 STR 基因座 D10S1248、D22S1045、D2S441、D1S1656 和 D12S391。在三个美国人群体(非裔美国人、白人和西班牙裔)中,对 NGM 基因座的等位基因频率和其他法医学相关统计数据进行了生成。分析结果表明,NGM 多重扩增试剂盒是法医学领域最具信息量的 STR 多重扩增试剂盒之一。在群体水平上,即使对于两个连锁基因座 vWA 和 D12S391,也没有比由于偶然因素而预期的更多可检测到的等位基因之间以及基因座之间的独立性偏差;然而,对三个大型家系的连锁分析表明,这两个基因座之间存在紧密连锁,重组分数为 0.108。因此,与计算 DNA 图谱稀有性的做法相反,对于亲缘关系分析,不能假设基因座 vWA 和 D12S391 之间是独立的。

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