mtDNA高变区最高突变及其应用核苷酸碱基X - t-n生物统计学通过过渡强度矩阵确定突变的身份

Palit Eiy, Y. Ngili
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引用次数: 1

摘要

人类线粒体DNA (mtDNA)已被广泛应用于通过生物证据对被害人或犯罪嫌疑人进行法医鉴定。单个细胞中mtDNA分子的数量数以万计,这使得分析样品很少或损坏。目前,针对自然灾害、战争、事故等重大灾害受害者的mtDNA鉴定还没有统一的标准方法,导致鉴定过程无法快速进行。本研究在mtDNA序列中发现了C16.223t变异,可用于将数据库分为两组,从而通过数学算法加快鉴定过程。该变异在NCBI数据库中多达142个序列的300个核苷酸(16,024-16,324)沿线的91个多态人类mtDNA HVS1中频率最高(29.7%)。从已在NCBI上发表的巴布亚人MtDNA组数据收集中获得的MtDNA序列。下一个可以在序列的一行中用作分类器的变体是16,311;16304;16189;16270的恒等式为(T→c)。对于矩阵Q是可逆的所以矩阵和可以有相反的对角线。因此,上面的方程可以用对角线法求解,可以写成:U³= U μ רU μ a μ μ 1。这个方程可以计算mtDNA核苷酸序列中发生的转变和翻转取代突变的数量。通过这种分组,可以减少数据库,从而加快样本识别的过程。根据频率最高的变异进行分组的预期方法可以在法医学数据库(如警察)或mtDNA数据库(用于研究人类学和进化生物学)中开发。
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The Highest Mutation in mtDNA Hypervariable Region and Application of Biostatistics with Nucleotide Base X t-n in Determining the Identity of the Mutation through a Transition Intensity Matrix
Human mitochondrial DNA (mtDNA) have been used intensively in the field of forensic identification of victims or suspects of crime through biological evidence. The number of mtDNA molecules in a single cell are in the tens of thousands which enable analysis of samples very little or damaged. Till now there is no standard method for identification using mtDNA in a mass disaster victims such as natural disasters, wars and accidents so that the identification process can not run fast. This study found C16.223t variants in mtDNA sequences that can be used to divide the database into two groups so as to accelerate the process of identification through a mathematical algorithm. This variant has the highest frequency (29.7%) of the 91 polymorphic human mtDNA HVS1 along the 300 nucleotide (16,024-16,324) derived from the NCBI database as much as 142 sequences. MtDNA sequences obtained from data collection Papuan human mtDNA groups that have been published in the NCBI. The next variant that can be used as a classifier in a row in the sequence is 16,311; 16,304; 16,189; and 16,270 with the identity (T→c). For a matrix Q is reversible so the matrix and could have the opposite diagonal. Thus the above equation can be solved by using the diagonal method that can be written: U³ = Uµ רUµ aµ†1 . This equation could count the number of transitions and transversion substitution mutations that occur in a nucleotide sequence of mtDNA. With this grouping, the database can be reduced so as to accelerate the process of identification of samples. Expected method of grouping by the variant with the highest frequency can be developed in the codification database for forensic interest such as the police or the mtDNA database purposes of study anthropology and evolutionary biology.
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