Bayesian approach to discriminant problems for count data with application to multilocus short tandem repeat dataset.

IF 0.9 4区 数学 Q3 Mathematics Statistical Applications in Genetics and Molecular Biology Pub Date : 2020-05-04 DOI:10.1515/sagmb-2018-0044
Koji Tsukuda, Shuhei Mano, Toshimichi Yamamoto
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Abstract

Short Tandem Repeats (STRs) are a type of DNA polymorphism. This study considers discriminant analysis to determine the population of test individuals using an STR database containing the lengths of STRs observed at more than one locus. The discriminant method based on the Bayes factor is discussed and an improved method is proposed. The main issues are to develop a method that is relatively robust to sample size imbalance, identify a procedure to select loci, and treat the parameter in the prior distribution. A previous study achieved a classification accuracy of 0.748 for the g-mean (geometric mean of classification accuracies for two populations) and 0.867 for the AUC (area under the receiver operating characteristic curve). We improve the maximum values for the g-mean to 0.830 and the AUC to 0.935. Computer simulations indicate that the previous method is susceptible to sample size imbalance, whereas the proposed method is more robust while achieving almost identical classification accuracy. Furthermore, the results confirm that threshold adjustment is an effective countermeasure to sample size imbalance.

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计数数据判别问题的贝叶斯方法及其在多位点短串联重复数据集上的应用。
短串联重复序列(STRs)是一种DNA多态性。本研究采用判别分析来确定测试个体的总体,使用包含在多个位点观察到的STR长度的STR数据库。讨论了基于贝叶斯因子的判别方法,提出了一种改进方法。主要问题是开发一种对样本量不平衡具有相对鲁棒性的方法,确定一个选择位点的程序,并处理先验分布中的参数。先前的研究中,g-mean(两个种群分类精度的几何平均值)和AUC(接收者工作特征曲线下面积)的分类精度分别为0.748和0.867。我们将g均值的最大值提高到0.830,AUC提高到0.935。计算机模拟表明,之前的方法容易受到样本量不平衡的影响,而提出的方法在获得几乎相同的分类精度的同时具有更强的鲁棒性。进一步验证了阈值调整是解决样本数量失衡的有效对策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.20
自引率
11.10%
发文量
8
审稿时长
6-12 weeks
期刊介绍: Statistical Applications in Genetics and Molecular Biology seeks to publish significant research on the application of statistical ideas to problems arising from computational biology. The focus of the papers should be on the relevant statistical issues but should contain a succinct description of the relevant biological problem being considered. The range of topics is wide and will include topics such as linkage mapping, association studies, gene finding and sequence alignment, protein structure prediction, design and analysis of microarray data, molecular evolution and phylogenetic trees, DNA topology, and data base search strategies. Both original research and review articles will be warmly received.
期刊最新文献
Empirically adjusted fixed-effects meta-analysis methods in genomic studies. A CNN-CBAM-BIGRU model for protein function prediction. A heavy-tailed model for analyzing miRNA-seq raw read counts. Flexible model-based non-negative matrix factorization with application to mutational signatures. Choice of baseline hazards in joint modeling of longitudinal and time-to-event cancer survival data.
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