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基于二代测序平台的微单倍型位点的分型研究
引用本文:陈肯,武建楠,王欢,庞铂实,周宇荀,肖君华,李凯. 基于二代测序平台的微单倍型位点的分型研究[J]. 中国法医学杂志, 2021, 0(1): 57-60,65
作者姓名:陈肯  武建楠  王欢  庞铂实  周宇荀  肖君华  李凯
作者单位:1.东华大学化学化工与生物工程学院;2.上海农林职业技术学院
基金项目:上海市自然科学基金(19ZR1436500)。
摘    要:目的 建立基于二代测序平台的微单倍型分型方案,调查其在中国南方汉族人群中的多态性,探讨其法医学应用价值.方法 以20个微单倍型位点为研究对象,利用多重PCR构建靶向扩增子文库,以二代测序为检测手段,采用生物信息学方法 构建个体微单倍型,最后进行多态性分析.结果 总体测序量为2.12G,覆盖所有片段,平均覆盖深度为335...

关 键 词:法医遗传学  微单倍型  高通量测序  单核苷酸多态性  多态信息含量

Genotyping of microhaplotypes based on the second generation sequencing platform
Chen Ken,Wu Jiannan,Wang Huan,Pang boshi,Zhou Yuxun,Xiao Junhua,Li Kai. Genotyping of microhaplotypes based on the second generation sequencing platform[J]. Chinese Journal of Forensic Medicine, 2021, 0(1): 57-60,65
Authors:Chen Ken  Wu Jiannan  Wang Huan  Pang boshi  Zhou Yuxun  Xiao Junhua  Li Kai
Affiliation:(College of Chemical Engineering&Biological Engineering Donghua University,Shanghai 201620,China;Shanghai Vocational College of Agriculture and Forestry,Shanghai 201699,China)
Abstract:Objective To investigate the genetic polymorphism of 20 microhaplotypes in Chinese South Han population and assess their value in forensic medicine based on the second generation sequencing.Methods 20 microhaplotype loci were selected as the research objects,and the targeted amplified fragment library was constructed by multiplex PCR.Amplicon and The individual microhaplotypes were constructed by Bioinformatics Method with the second generation sequencing as detection method,and the polymorphism was analyzed.Results A total of 2.12 G original data were obtained,covering all the fragments with average depth of 3353×.The observed heterozygosity of 20 microhaplotypes ranged from 0.198 to 0.837 with an average of 0.726,while that of their SNP ranged from 0.109 to 0.587 with an average of 0.364.Only 1 microhaplotype cannot pass the Hardy-Weinberg equilibrium test.The effective number of alleles values of the remaining 19 microhaplotypes ranged from 3.119 to 7.170 and the polymorphic information content ranged from 0.620 to 0.845 with an average of 0.711.The matching probability of the 19 microhaplotypes ranged from 0.044 to 0.181 and the cumulative matching probability value was 3.132×10-19.Conclusion This study confirmed that the performance of 19 microhaplotype systems for forensic parameters is equivalent to the commonly used 15 STR loci,which can be independently applied to forensic individual identification and the mixed DNA genotyping.
Keywords:Forensic genetics  Microhaplotypes  Next generation sequencing  Single nucleotide polymorphism  Polymorphic information content
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