An Empirical Bayes approach for the identification of long-range chromosomal interaction from Hi-C data

被引:0
|
作者
Zhang, Qi [1 ]
Xu, Zheng [2 ]
Lai, Yutong [3 ]
机构
[1] Univ New Hampshire, Dept Math & Stat, Durham, NH 03824 USA
[2] Wright State Univ, Dept Math & Stat, Dayton, OH 45435 USA
[3] ClinChoice, Ft Washington, PA 19034 USA
关键词
empirical Bayes; epigenetics; Hi-C; peak identification; RHODOPSIN KINASE GENE; MODEL; NULL; ARCHITECTURE; GENOME; MAP;
D O I
10.1515/sagmb-2020-0026
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hi-C experiments have become very popular for studying the 3D genome structure in recent years. Identification of long-range chromosomal interaction, i.e., peak detection, is crucial for Hi-C data analysis. But it remains a challenging task due to the inherent high dimensionality, sparsity and the over-dispersion of the Hi-C count data matrix. We propose EBHiC, an empirical Bayes approach for peak detection from Hi-C data. The proposed framework provides flexible over-dispersion modeling by explicitly including the "true" interaction intensities as latent variables. To implement the proposed peak identification method (via the empirical Bayes test), we estimate the overall distributions of the observed counts semiparametrically using a Smoothed Expectation Maximization algorithm, and the empirical null based on the zero assumption. We conducted extensive simulations to validate and evaluate the performance of our proposed approach and applied it to real datasets. Our results suggest that EBHiC can identify better peaks in terms of accuracy, biological interpretability, and the consistency across biological replicates. The source code is available on Github (https:// github.com/QiZhangStat/EBHiC).
引用
收藏
页码:1 / 15
页数:15
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