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使用内部大规模平行测序平台对韩国人群23个常染色体STR基因座基于序列的多样性进行研究。

Sequence-based diversity of 23 autosomal STR loci in Koreans investigated using an in-house massively parallel sequencing panel.

作者信息

Kim Eun Hye, Lee Hwan Young, Kwon So Yeun, Lee Eun Young, Yang Woo Ick, Shin Kyoung-Jin

机构信息

Department of Forensic Medicine, Yonsei University College of Medicine, 50-1 Yonsei-ro, Seodaemun-gu, Seoul 03722, Republic of Korea.

Department of Forensic Medicine, Yonsei University College of Medicine, 50-1 Yonsei-ro, Seodaemun-gu, Seoul 03722, Republic of Korea; Brain Korea 21 PLUS Project for Medical Science, Yonsei University, 50-1 Yonsei-ro, Seodaemun-gu, Seoul 03722, Republic of Korea.

出版信息

Forensic Sci Int Genet. 2017 Sep;30:134-140. doi: 10.1016/j.fsigen.2017.07.001. Epub 2017 Jul 9.

Abstract

As DNA databases continue to grow and international cooperation increases, forensic STR loci have expanded to increase the discriminatory power and inter-database compatibility. Current capillary electrophoresis (CE) and/or massively parallel sequencing (MPS)-based commercial STR analysis systems reflect such changing trends of expanding STR loci. Due to the general gains of larger multiplexing and the detection of sequence variation, the application of MPS technology to STR analysis has further improved discrimination and is expected to aid in mixture interpretation by increasing the effective number of alleles. However, high-throughput analysis has rarely been reported for forensic DNA databasing. In this study, we present the sequencing results from 250 Korean samples at 23 commonly used STR loci (D1S1656, TPOX, D2S441, D2S1338, D3S1358, FGA, CSF1PO, D5S818, D6S1043, D7S820, D8S1179, D10S1248, TH01, vWA, D12S391, D13S317, Penta E, D16S539, D18S51, D19S433, D21S11, Penta D, and D22S1045) using an in-house assay designed for MPS. All amplicons in the multiplex exhibited a size range of 77 to 217 base pairs, and the barcoded library for the MPS run was easily prepared using a PCR-based library preparation method followed by sequencing on a MiSeq System (Illumina). We compared the STR genotyping results with those obtained using CE and scrutinized the sequence variations in both the targeted STR and flanking regions. MPS results of 23 autosomal STRs were 99.97% concordant with those of CE results. D12S391 and D21S11 exhibited, respectively, the highest number of alleles and genotypes by the MPS analysis. Single nucleotide polymorphisms and insertion and deletions (Indels) were observed in the flanking regions of D1S1656, D2S441, D5S818, D7S820, D13S317, D16S539, D21S11, and Penta D. Consequently, an MPS analysis of an expanded set of STRs, as demonstrated in the population statistics of a Korean population, will be of great practical use in forensic genetics.

摘要

随着DNA数据库持续增长以及国际合作不断增加,法医STR基因座已得到扩展,以增强鉴别能力和数据库间的兼容性。当前基于毛细管电泳(CE)和/或大规模平行测序(MPS)的商业STR分析系统反映了STR基因座这种不断变化的扩展趋势。由于普遍实现了更大的复合扩增以及对序列变异的检测,MPS技术在STR分析中的应用进一步提高了鉴别能力,并有望通过增加有效等位基因数量来辅助混合样本解读。然而,针对法医DNA数据库的高通量分析鲜有报道。在本研究中,我们展示了使用为MPS设计的内部检测方法对250份韩国样本在23个常用STR基因座(D1S1656、TPOX、D2S441、D2S1338、D3S1358、FGA、CSF1PO、D5S818、D6S1043、D7S820、D8S1179、D10S1248、TH01、vWA D12S391、D13S317、Penta E、D16S539、D18S51、D19S433、D21S11、Penta D和D22S1045)上的测序结果。复合扩增中的所有扩增子大小范围为77至217个碱基对,并且使用基于PCR的文库制备方法很容易制备用于MPS运行的带条形码文库,随后在MiSeq系统(Illumina)上进行测序。我们将STR基因分型结果与使用CE获得的结果进行了比较,并仔细检查了目标STR及其侧翼区域的序列变异。23个常染色体STR的MPS结果与CE结果的一致性为99.97%。通过MPS分析,D12S391和D21S11分别表现出最高的等位基因数和基因型数。在D1S1656、D2S441、D5S818、D7S820、D13S317、D16S539、D21S11和Penta D的侧翼区域观察到单核苷酸多态性以及插入和缺失(Indels)。因此,如在韩国人群的群体统计中所展示的,对一组扩展的STR进行MPS分析在法医遗传学中将具有很大的实际用途。

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