DNA甲基化
相关性
焦测序
CpG站点
选择(遗传算法)
标准差
生物
统计
集合(抽象数据类型)
甲基化
遗传学
计算生物学
计算机科学
数学
DNA
生物信息学
进化生物学
人工智能
基因
基因表达
程序设计语言
几何学
作者
Renata Zbieć-Piekarska,Magdalena Spólnicka,Tomasz Kupiec,Agnieszka Parys-Proszek,Żanetta Makowska,Anna Pałeczka,Krzysztof Kucharczyk,Rafał Płoski,Wojciech Branicki
标识
DOI:10.1016/j.fsigen.2015.05.001
摘要
Forensic DNA phenotyping needs to be supplemented with age prediction to become a relevant source of information on human appearance. Recent progress in analysis of the human methylome has enabled selection of multiple candidate loci showing linear correlation with chronological age. Practical application in forensic science depends on successful validation of these potential age predictors. In this study, eight DNA methylation candidate loci were analysed using convenient and reliable pyrosequencing technology. A total number of 41 CpG sites was investigated in 420 samples collected from men and women aged from 2 to 75 years. The study confirmed correlation of all the investigated markers with human age. The five most significantly correlated CpG sites in ELOVL2 on 6p24.2, C1orf132 on 1q32.2, TRIM59 on 3q25.33, KLF14 on 7q32.3 and FHL2 on 2q12.2 were chosen to build a prediction model. This restriction allowed the technical analysis to be simplified without lowering the prediction accuracy significantly. Model parameters for a discovery set of 300 samples were R(2)=0.94 and the standard error of the estimate=4.5 years. An independent set of 120 samples was used to test the model performance. Mean absolute deviation for this testing set was 3.9 years. The number of correct predictions ±5 years achieved a very high level of 86.7% in the age category 2-19 and gradually decreased to 50% in the age category 60-75. The prediction model was deterministic for individuals belonging to these two extreme age categories. The developed method was implemented in a freely available online age prediction calculator.
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