Key DNA profiling markers for identification: A mini review

N. Su, Momoh Sm, Nwokolo Cc, Ojo Og, Ajayi Jo, Irabor Im, Oboh Bo
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Abstract

DNA Profiling also referred to as DNA fingerprinting, is a sequence of tests and methodology employed to examine and identify the genetic information contained within an individual’s cell, and within the context of forensics, it is considered as the comparison of genetic information or profile of a person to a profile of biological evidence found at the scene of crime, or profile stored in the DNA database for the sole purpose of administration of justice. Remarkably, a core base for DNA profiling is the fact that, about 99.9% sequence of DNA is found to be common among humans, and the other 0.1% is unique and vary from person to person, and the likelihood of two individual having exactly the same DNA profile is about 1 in 594.1 trillion individuals. Therefore, the present study elucidated key molecular markers for DNA profiling including short tandem repeat, variable number tandem repeat, and restriction fragment length polymorphism. In conducting this study, a comprehensive electronic literature search using PubMed, ScienceDirect, Google Scholar, and Google search for similar and related works were used, and all works meeting the subject matter were considered, including; reviews, meta-analyses, retrospective studies, observational studies, organization recommendations, and original articles. Going forward, the stated molecular markers have been demonstrated to be used for identification purpose, however, the validated technology of short tandem repeat and also its abundance in the human genome makes it a better option for forensic DN profiling and it is currently the gold standard for analysis and storage of DNA profiles in the DNA databases around the world.
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鉴定的关键DNA分析标记:一个小回顾
DNA侧写,也称为DNA指纹,是用来检查和识别个人细胞内的遗传信息的一系列测试和方法,在法医方面,它被认为是将一个人的遗传信息或侧写与在犯罪现场发现的生物证据的侧写或存储在DNA数据库中的侧写进行比较,其唯一目的是为了司法。值得注意的是,DNA分析的核心基础是,大约99.9%的DNA序列在人类中是共同的,另外0.1%的DNA序列是独特的,因人而异,两个个体拥有完全相同DNA谱的可能性约为594.1万亿个人中的1个。因此,本研究阐明了DNA分析的关键分子标记,包括短串联重复序列、可变数目串联重复序列和限制性片段长度多态性。在进行本研究时,使用PubMed、ScienceDirect、Google Scholar和Google search对类似和相关作品进行了全面的电子文献检索,并考虑了所有符合主题的作品,包括;综述、荟萃分析、回顾性研究、观察性研究、组织推荐和原创文章。展望未来,所述分子标记已被证明用于鉴定目的,然而,经过验证的短串联重复技术及其在人类基因组中的丰富程度使其成为法医DN分析的更好选择,并且它目前是世界各地DNA数据库中分析和存储DNA图谱的黄金标准。
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