Identification of Individuals in a DNA Mixture Using SNP Markers

Abdulwasiu Ibrahim
{"title":"Identification of Individuals in a DNA Mixture Using SNP Markers","authors":"Abdulwasiu Ibrahim","doi":"10.11648/J.IJGG.20170503.11","DOIUrl":null,"url":null,"abstract":"This article focuses mainly on DNA mixture from two contributors, a victim and an unknown culprit. There are two areas I believe will be of interest to forensic scientists, police and a Jury. These areas are identification of an individual in a DNA mixture and familial DNA database searching of a culprit through a relative. In this article, I looked at identification of individuals in a mixture using Single Nucleotide Polymorphisms (SNPs) markers. SNPs are starting to be used for forensic identification; I employed them as they produce incredible results for identification in a two-person mixture. The conservative method I employed here is the random man not excluded probability – P (RMNE) approach, an inclusion probability method generally considered as a frequentist approach. It was found that an optimum allele frequency of 0.2 is required to produce almost certain identification with much distortion in identifying an individual even when inbreeding is up to 50% in a population. Another interesting thing is that relatives of a suspect whom are actual contributors to the DNA mixture can also be identified. In a case where there are relatives in the mixture it was found that twice the number of SNP panels is required to identify an individual than in a case where no relative is involved. And lastly, typing more SNP panels helps to improve identification and therefore produce forensically useful results.","PeriodicalId":88902,"journal":{"name":"International journal of genetics and molecular biology","volume":"12 1","pages":"27"},"PeriodicalIF":0.0000,"publicationDate":"2017-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International journal of genetics and molecular biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.11648/J.IJGG.20170503.11","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

This article focuses mainly on DNA mixture from two contributors, a victim and an unknown culprit. There are two areas I believe will be of interest to forensic scientists, police and a Jury. These areas are identification of an individual in a DNA mixture and familial DNA database searching of a culprit through a relative. In this article, I looked at identification of individuals in a mixture using Single Nucleotide Polymorphisms (SNPs) markers. SNPs are starting to be used for forensic identification; I employed them as they produce incredible results for identification in a two-person mixture. The conservative method I employed here is the random man not excluded probability – P (RMNE) approach, an inclusion probability method generally considered as a frequentist approach. It was found that an optimum allele frequency of 0.2 is required to produce almost certain identification with much distortion in identifying an individual even when inbreeding is up to 50% in a population. Another interesting thing is that relatives of a suspect whom are actual contributors to the DNA mixture can also be identified. In a case where there are relatives in the mixture it was found that twice the number of SNP panels is required to identify an individual than in a case where no relative is involved. And lastly, typing more SNP panels helps to improve identification and therefore produce forensically useful results.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
利用SNP标记在DNA混合物中鉴定个体
这篇文章主要集中在两个贡献者的DNA混合,一个受害者和一个未知的罪犯。我相信法医科学家、警察和陪审团会对这两个领域感兴趣。这些领域是在DNA混合物中识别个体和通过亲属查找罪犯的家族DNA数据库。在这篇文章中,我研究了使用单核苷酸多态性(snp)标记在混合物中识别个体。snp开始被用于法医鉴定;我之所以使用它们,是因为它们在两个人的混合物中产生了令人难以置信的结果。我在这里采用的保守方法是随机人不排除概率- P (RMNE)方法,这是一种通常被认为是频率论方法的包含概率方法。结果发现,即使种群中近亲繁殖率高达50%,当等位基因频率达到0.2时,对个体的识别也会产生很大的失真。另一件有趣的事情是,嫌疑人的亲属也可以被识别出来,他们是DNA混合物的实际贡献者。在混合物中有亲属的情况下,发现识别个体所需的SNP面板数量是没有亲属的情况下的两倍。最后,输入更多的SNP面板有助于提高鉴定,从而产生法医有用的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Genetic variability, heritability and genetic advance among yield and yield related traits of advanced Tef [Eragrostis tef (Zucc.) Trotter] breeding lines Sequencing of S5 gene in autotetraploid rice japonica and indica to overcome F1 hybrids embryo sac sterility In silico analysis of mutations associated with genetic variability of the strain African cassava mosaic virus (ACMV) in three departments of Cte dIvoire Contribution of cytogenetic and molecular biology in disorders of sex development diagnosis: About 55 cases The Impact of Sequencing Human Genome on Genomic Food & Medicine
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1