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构建和法医遗传特征分析由 22 个三等位插入缺失组成的 11 个常染色体单倍型。

Construction and forensic genetic characterization of 11 autosomal haplotypes consisting of 22 tri-allelic indels.

机构信息

West China School of Basic Medical Sciences and Forensic Medicine, Sichuan University, Chengdu, PR China.

West China School of Basic Medical Sciences and Forensic Medicine, Sichuan University, Chengdu, PR China.

出版信息

Forensic Sci Int Genet. 2018 May;34:71-80. doi: 10.1016/j.fsigen.2018.02.001. Epub 2018 Feb 6.

DOI:10.1016/j.fsigen.2018.02.001
PMID:29428890
Abstract

Insertion/deletion polymorphisms (indels), which combine the advantages of both short tandem repeats and single-nucleotide polymorphisms, are suitable for parentage testing. To overcome the limitations of the low polymorphism of di-allelic indels, we constructed a set of haplotypes with physically linked, multi-allelic indels. Candidate haplotypes were selected from the 1000 Genomes Project database, and were subject to the following criteria for inclusion: (i) each marker must have a minimum allele frequency (MAF) of ≥0.1 in the Han population of China; (ii) markers must exist in a non-coding region; (iii) the physical distance between a pair of candidate indels must be <500 bp; (iv) the allele length variation of each indel from 1 to 20 bp; (v) different haplotypes must be located on different chromosomes or chromosomal arms, or be more than 10 Mb apart if on the same chromosomal arm; and (vi) they must not be located across a recombination hotspot. A multiplex system with 11 haplotype markers, comprising 22 tri-allelic indel loci distributed over 10 chromosomes was developed. To validate the multiplex panel, we investigated the haplotype distribution in sets of two and three-generation pedigrees. The results demonstrated that the haplotypes consisting of multi-allelic indel markers exhibited higher polymorphism than a single indel locus, and thus provide Supplementary information for forensic kinship identification.

摘要

插入/缺失多态性(indels)结合了短串联重复序列和单核苷酸多态性的优点,适合用于亲子鉴定。为了克服双等位基因 indels 多态性低的限制,我们构建了一组具有物理连锁的多等位基因 indels 的单倍型。候选单倍型从 1000 基因组计划数据库中选择,并符合以下纳入标准:(i) 每个标记在中国汉族人群中的最小等位基因频率 (MAF) 必须≥0.1;(ii) 标记必须存在于非编码区;(iii) 候选 indels 对之间的物理距离必须<500 bp;(iv) 每个 indel 的等位基因长度变化为 1 到 20 bp;(v) 不同的单倍型必须位于不同的染色体或染色体臂上,或者如果位于同一染色体臂上,则必须相距 10 Mb 以上;(vi) 它们不能位于重组热点。开发了一种包含 11 个单倍型标记的多重系统,由分布在 10 条染色体上的 22 个三等位基因 indel 位点组成。为了验证多重面板,我们研究了两组和三组世代家系的单倍型分布。结果表明,由多等位基因 indel 标记组成的单倍型表现出比单个 indel 位点更高的多态性,从而为法医亲缘鉴定提供了补充信息。

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引用本文的文献

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Systematic Evaluation of a Novel 6-dye Direct and Multiplex PCR-CE-Based InDel Typing System for Forensic Purposes.用于法医目的的新型基于6染料直接和多重PCR-CE的插入缺失分型系统的系统评价
Front Genet. 2022 Jan 10;12:744645. doi: 10.3389/fgene.2021.744645. eCollection 2021.
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Multi-Indel: A Microhaplotype Marker Can Be Typed Using Capillary Electrophoresis Platforms.多插入缺失:一种微单倍型标记可通过毛细管电泳平台进行分型。
Front Genet. 2020 Oct 23;11:567082. doi: 10.3389/fgene.2020.567082. eCollection 2020.
3
Forensic features and genetic background exploration of a new 47-autosomal InDel panel in five representative Han populations residing in Northern China.
中国北方五个代表性汉族人群中一个新的 47-常染色体 InDel 面板的法医学特征和遗传背景探索。
Mol Genet Genomic Med. 2020 May;8(5):e1224. doi: 10.1002/mgg3.1224. Epub 2020 Mar 10.
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Genetic diversity, structure and forensic characteristics of Hmong-Mien-speaking Miao revealed by autosomal insertion/deletion markers.常染色体插入/缺失标记揭示苗瑶语族的苗族的遗传多样性、结构和法医学特征。
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