Reconstructing diploid 3D chromatin structures from single cell Hi-C data with a polymer-based approach

IF 2.8 Q2 MATHEMATICAL & COMPUTATIONAL BIOLOGY
Jan Rothörl, M. Brems, Tim J. Stevens, Peter Virnau
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引用次数: 0

Abstract

Detailed understanding of the 3D structure of chromatin is a key ingredient to investigate a variety of processes inside the cell. Since direct methods to experimentally ascertain these structures lack the desired spatial fidelity, computational inference methods based on single cell Hi-C data have gained significant interest. Here, we develop a progressive simulation protocol to iteratively improve the resolution of predicted interphase structures by maximum-likelihood association of ambiguous Hi-C contacts using lower-resolution predictions. Compared to state-of-the-art methods, our procedure is not limited to haploid cell data and allows us to reach a resolution of up to 5,000 base pairs per bead. High resolution chromatin models grant access to a multitude of structural phenomena. Exemplarily, we verify the formation of chromosome territories and holes near aggregated chromocenters as well as the inversion of the CpG content for rod photoreceptor cells.
用基于聚合物的方法从单细胞 Hi-C 数据中重建二倍体三维染色质结构
详细了解染色质的三维结构是研究细胞内各种过程的关键要素。由于通过实验确定这些结构的直接方法缺乏所需的空间保真度,基于单细胞 Hi-C 数据的计算推断方法受到了广泛关注。在这里,我们开发了一种渐进式模拟协议,通过使用低分辨率预测结果对模棱两可的 Hi-C 接触进行最大似然关联,从而迭代提高预测的间期结构分辨率。与最先进的方法相比,我们的程序并不局限于单倍体细胞数据,而且能使我们达到每个珠子多达 5000 碱基对的分辨率。高分辨率染色质模型能让我们了解多种结构现象。例如,我们验证了染色体区域的形成、聚集染色体中心附近的孔洞以及杆状感光细胞中 CpG 含量的反转。
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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CiteScore
2.60
自引率
0.00%
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