{"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.
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。