Statistical Challenges in Analyzing Methylation and Long-Range Chromosomal Interaction Data

被引:4
|
作者
Qin Z. [1 ]
Li B. [1 ]
Conneely K.N. [2 ]
Wu H. [1 ]
Hu M. [2 ]
Ayyala D. [4 ]
Park Y. [5 ]
Jin V.X. [6 ]
Zhang F. [7 ]
Zhang H. [4 ]
Li L. [1 ]
Lin S. [1 ]
机构
[1] Department of Biostatistics and Bioinformatics, Rollins School of Public Health, Emory University, Atlanta, 30322, GA
[2] Department of Human Genetics, Emory University School of Medicine, Atlanta, 30322, GA
[3] Division of Biostatistics, Department of Population Health, New York University School of Medicine, New York, 10016, NY
[4] Department of Statistics, The Ohio State University, Columbus, 43210, OH
[5] Department of Biostatistics, University of Pittsburgh, Pittsburgh, 15261, PA
[6] Department of Molecular Medicine, The University of Texas Health Science Center at San Antonio, San Antonio, 78229, TX
[7] Department of Mathematics & Statistics, Texas Tech University, Lubbock, 79409, TX
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
Methylation Level; Bisulfite Treatment; Chromatin Interaction; Cell Type Proportion; Differentially Methylated Locus;
D O I
10.1007/s12561-016-9145-0
中图分类号
学科分类号
摘要
With the rapid development of high-throughput technologies such as array and next generation sequencing, genome-wide, nucleotide-resolution epigenomic data are increasingly available. In recent years, there has been particular interest in data on DNA methylation and 3-dimensional (3D) chromosomal organization, which are believed to hold keys to understand biological mechanisms, such as transcription regulation, that are closely linked to human health and diseases. However, small sample size, complicated correlation structure, substantial noise, biases, and uncertainties, all present difficulties for performing statistical inference. In this review, we present an overview of the new technologies that are frequently utilized in studying DNA methylation and 3D chromosomal organization. We focus on reviewing recent developments in statistical methodologies designed for better interrogating epigenomic data, pointing out statistical challenges facing the field whenever appropriate. © 2016, International Chinese Statistical Association.
引用
收藏
页码:284 / 309
页数:25
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