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

IF 0.9 4区 数学 Q3 Mathematics
Qi Zhang, Zheng Xu, Yutong Lai
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引用次数: 0

Abstract

Abstract 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).
从Hi-C数据中鉴定远距离染色体相互作用的经验贝叶斯方法
近年来,Hi-C实验已成为研究三维基因组结构的热门方法。鉴定远距离染色体相互作用,即峰检测,对Hi-C数据分析至关重要。但由于Hi-C计数数据矩阵固有的高维性、稀疏性和过色散性,这仍然是一项具有挑战性的任务。我们提出了EBHiC,一种从Hi-C数据中检测峰的经验贝叶斯方法。所提出的框架通过明确地包括“真实”相互作用强度作为潜在变量,提供了灵活的过分散建模。为了实现所提出的峰值识别方法(通过经验贝叶斯检验),我们使用平滑期望最大化算法估计观测计数的半参数总体分布,并基于零假设估计经验零。我们进行了大量的模拟来验证和评估我们提出的方法的性能,并将其应用于实际数据集。我们的研究结果表明,EBHiC在准确性、生物可解释性和跨生物重复的一致性方面可以识别出更好的峰。源代码可在Github (https://github.com/QiZhangStat/EBHiC)上获得。
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.
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