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微单倍型在法医学遗传学中应用的研究进展。

Research progress on application of microhaplotype in forensic genetics.

机构信息

1. Department of Pathology and Pathophysiology, School of Basic Medical Sciences, Zhejiang University, Hangzhou 310058, China.

2. Forensic Science Center, Zhejiang University, Hangzhou 310029, China.

出版信息

Zhejiang Da Xue Xue Bao Yi Xue Ban. 2021 Dec 25;50(6):777-782. doi: 10.3724/zdxbyxb-2021-0180.

Abstract

As a novel genetic marker, microhaplotype can be applied in the field of forensic genetics. Microhaplotype has the advantages of high polymorphism, low mutation rate, no stutter products and short amplification fragments. Microhaplotype can effectively detect mixture, and quantitatively analyze the contributors of mixture. DNA with severe fragmentation can be successfully genotyped by microhaplotype. It can be used as ancestry informative marker to effectively divide the global continental population according to genetic structure. Microhaplotype system can provide more information than traditional short tandem repeat and help to identify complex relationships. It can provide new ideas for tumor source identification, cell line identification and prenatal paternity testing. Here we review the applications of microhaplotype, intending to provide references for forensic practice.

摘要

作为一种新型的遗传标记,微单倍型可应用于法医遗传学领域。微单倍型具有多态性高、突变率低、无 stutter 产物、扩增片段短等优点。微单倍型可有效检测混合样本,并对混合样本的贡献者进行定量分析。严重碎片化的 DNA 可通过微单倍型成功进行基因分型。它可以用作祖先信息标记,根据遗传结构有效地将全球大陆人群进行划分。微单倍型系统比传统的短串联重复序列提供更多的信息,有助于识别复杂的关系。它可为肿瘤来源鉴定、细胞系鉴定和产前亲子鉴定提供新思路。本文综述了微单倍型的应用,旨在为法医实践提供参考。

相似文献

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Research progress on application of microhaplotype in forensic genetics.微单倍型在法医学遗传学中应用的研究进展。
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Evaluation of the microhaplotype markers in kinship analysis.微单倍型标记在亲缘关系分析中的评估。
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本文引用的文献

2
Pairwise kinship testing with a combination of STR and SNP loci.采用 STR 和 SNP 位点的组合进行亲缘关系检验。
Forensic Sci Int Genet. 2020 May;46:102265. doi: 10.1016/j.fsigen.2020.102265. Epub 2020 Feb 25.
6
Development of a new 32-plex InDels panel for forensic purpose.开发一种新的用于法医目的的 32 plex InDels 面板。
Forensic Sci Int Genet. 2020 Jan;44:102171. doi: 10.1016/j.fsigen.2019.102171. Epub 2019 Oct 2.

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