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PGS:一种用于高维微小RNA表达数据与重复测量关联研究的工具。

PGS: a tool for association study of high-dimensional microRNA expression data with repeated measures.

作者信息

Zheng Yinan, Fei Zhe, Zhang Wei, Starren Justin B, Liu Lei, Baccarelli Andrea A, Li Yi, Hou Lifang

机构信息

Institute for Public Health and Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, Department of Biostatistics, University of Michigan, Ann Arbor, MI 48109, Institute of Human Genetics, University of Illinois at Chicago, Chicago, IL 60612, Division of Health and Biomedical Informatics, Departments of Preventive Medicine and Medical Social Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, Department of Environmental Health, Harvard School of Public Health, Boston, MA 02115 and The Robert H. Lurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.

Institute for Public Health and Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, Department of Biostatistics, University of Michigan, Ann Arbor, MI 48109, Institute of Human Genetics, University of Illinois at Chicago, Chicago, IL 60612, Division of Health and Biomedical Informatics, Departments of Preventive Medicine and Medical Social Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, Department of Environmental Health, Harvard School of Public Health, Boston, MA 02115 and The Robert H. Lurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA Institute for Public Health and Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, Department of Biostatistics, University of Michigan, Ann Arbor, MI 48109, Institute of Human Genetics, University of Illinois at Chicago, Chicago, IL 60612, Division of Health and Biomedical Informatics, Departments of Preventive Medicine and Medical Social Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, Department of Environmental Health, Harvard School of Public Health, Boston, MA 02115 and The Robert H. Lurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.

出版信息

Bioinformatics. 2014 Oct;30(19):2802-7. doi: 10.1093/bioinformatics/btu396. Epub 2014 Jun 19.

Abstract

MOTIVATION

MicroRNAs (miRNAs) are short single-stranded non-coding molecules that usually function as negative regulators to silence or suppress gene expression. Owning to the dynamic nature of miRNA and reduced microarray and sequencing costs, a growing number of researchers are now measuring high-dimensional miRNA expression data using repeated or multiple measures in which each individual has more than one sample collected and measured over time. However, the commonly used univariate association testing or the site-by-site (SBS) testing may underutilize the longitudinal feature of the data, leading to underpowered results and less biologically meaningful results.

RESULTS

We propose a penalized regression model incorporating grid search method (PGS), for analyzing associations of high-dimensional miRNA expression data with repeated measures. The development of this analytical framework was motivated by a real-world miRNA dataset. Comparisons between PGS and the SBS testing revealed that PGS provided smaller phenotype prediction errors and higher enrichment of phenotype-related biological pathways than the SBS testing. Our extensive simulations showed that PGS provided more accurate estimates and higher sensitivity than the SBS testing with comparable specificities.

AVAILABILITY AND IMPLEMENTATION

R source code for PGS algorithm, implementation example and simulation study are available for download at https://github.com/feizhe/PGS.

摘要

动机

微小RNA(miRNA)是短的单链非编码分子,通常作为负调控因子来沉默或抑制基因表达。由于miRNA的动态特性以及微阵列和测序成本的降低,现在越来越多的研究人员正在使用重复或多次测量来测量高维miRNA表达数据,其中每个个体随着时间的推移有多个样本被收集和测量。然而,常用的单变量关联测试或逐位点(SBS)测试可能未充分利用数据的纵向特征,导致功效不足的结果以及生物学意义较小的结果。

结果

我们提出了一种结合网格搜索方法(PGS)的惩罚回归模型,用于分析具有重复测量的高维miRNA表达数据的关联。这个分析框架的开发是受一个实际的miRNA数据集的启发。PGS与SBS测试之间的比较表明,与SBS测试相比,PGS提供了更小的表型预测误差和更高的表型相关生物途径富集度。我们广泛的模拟表明,在具有可比特异性的情况下,PGS比SBS测试提供了更准确的估计和更高的灵敏度。

可用性和实现方式

PGS算法的R源代码、实现示例和模拟研究可在https://github.com/feizhe/PGS上下载。

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