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用于法医学的年龄相关DNA甲基化标记物的鉴定与评估。

Identification and evaluation of age-correlated DNA methylation markers for forensic use.

作者信息

Park Jong-Lyul, Kim Jong Hwan, Seo Eunhye, Bae Dong Hyuck, Kim Seon-Young, Lee Han-Chul, Woo Kwang-Man, Kim Yong Sung

机构信息

Epigenomics Research Center, Genome Institute, Korea Research Institute of Bioscience and Biotechnology, 125 Gwahak-ro, Yuseong-gu, Daejeon, Republic of Korea.

Epigenomics Research Center, Genome Institute, Korea Research Institute of Bioscience and Biotechnology, 125 Gwahak-ro, Yuseong-gu, Daejeon, Republic of Korea; Department of Functional Genomics, University of Science of Technology, 125 Gwahak-ro, Yuseong-gu, Daejeon, Republic of Korea.

出版信息

Forensic Sci Int Genet. 2016 Jul;23:64-70. doi: 10.1016/j.fsigen.2016.03.005. Epub 2016 Mar 17.

Abstract

In forensics, age prediction is useful to narrow down the number of potential suspects because it can provide some general characteristics for predicting appearance. Previous genome-wide studies based on DNA methylation have reported age prediction algorithms using a penalized multivariate regression method known as elastic net and a few dozen to hundreds of CpG sites. Although more CpG sites may provide better accuracy than fewer CpG sites, this approach is not applicable to forensics because the amounts of crime-scene DNA are usually limited. In this study, we selected three age-correlated CpG sites, namely cg16867657 (ELOVL2), which is known to be an excellent age predictor, cg04208403 (ZNF423), and cg19283806 (CCDC102B), from HumanMethylation450 BeadChip datasets of 1415 individuals. Furthermore, we evaluated these markers in a 535-sample training set and a 230-sample validation set from Korean individuals using a pyrosequencing platform. From the training set, an age prediction model using the multiple linear regression method explained 91.44% of age-correlated variation in DNA methylation patterns. The standard error of estimate and mean absolute deviation were 6.320 and 3.156 years, respectively. In the validation set, the standard error of estimate and mean absolute deviation were estimated as 6.853 and 3.346 years, respectively. For the validation set, the model explained 91.08% of the variation in methylation and predicted age (±6years) with accuracy of 77.30% in the <60years age group and 57.30% in the older group (≥60 years). These results suggest that our three DNA methylation markers may be useful for age prediction in samples from Asian populations.

摘要

在法医学中,年龄预测有助于缩小潜在嫌疑人的范围,因为它可以为预测外貌提供一些一般特征。先前基于DNA甲基化的全基因组研究报告了使用一种称为弹性网的惩罚多元回归方法以及几十到数百个CpG位点的年龄预测算法。虽然更多的CpG位点可能比更少的CpG位点提供更高的准确性,但这种方法不适用于法医学,因为犯罪现场的DNA数量通常有限。在本研究中,我们从1415名个体的HumanMethylation450 BeadChip数据集中选择了三个与年龄相关的CpG位点,即已知为优秀年龄预测指标的cg16867657(ELOVL2)、cg04208403(ZNF423)和cg19283806(CCDC102B)。此外,我们使用焦磷酸测序平台在来自韩国个体的535个样本训练集和230个样本验证集中评估了这些标记。在训练集中,使用多元线性回归方法的年龄预测模型解释了DNA甲基化模式中与年龄相关变异的91.44%。估计标准误差和平均绝对偏差分别为6.320岁和3.156岁。在验证集中,估计标准误差和平均绝对偏差分别为6.853岁和3.346岁。对于验证集,该模型解释了甲基化变异的91.08%,并在<60岁年龄组中以77.30%的准确率和≥60岁年龄组中以57.30%的准确率预测年龄(±6岁)。这些结果表明,我们的三个DNA甲基化标记可能有助于亚洲人群样本的年龄预测。

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