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3D Chromosome Modeling with Semi-Definite Programming and Hi-C Data

机译:具有半定编程和Hi-C数据的3D染色体建模

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摘要

For a long period of time, scientists studied genomes while assuming they are linear. Recently, chromosome conformation capture (3C)-based technologies, such as Hi-C, have been developed that provide the loci contact frequencies among loci pairs in a genome-wide scale. The technology unveiled that two far-apart loci can interact in the tested genome. It indicated that the tested genome forms a three-dimensional (3D) chromosomal structure within the nucleus. With the available Hi-C data, our next challenge is to model the 3D chromosomal structure from the 3C-derived data computationally. This article presents a deterministic method called ChromSDE, which applies semi-definite programming techniques to find the best structure fitting the observed data and uses golden section search to find the correct parameter for converting the contact frequency to spatial distance. Further, we develop a measure called consensus index to indicate if the Hi-C data corresponds to a single structure or a mixture of structures. To the best of our knowledge, ChromSDE is the only method that can guarantee recovering the correct structure in the noise-free case. In addition, we prove that the parameter of conversion from contact frequency to spatial distance will change under different resolutions theoretically and empirically. Using simulation data and real Hi-C data, we showed that ChromSDE is much more accurate and robust than existing methods. Finally, we demonstrated that interesting biological findings can be uncovered from our predicted 3D structure.
机译:长期以来,科学家在假设基因组呈线性的同时对其进行了研究。最近,已经开发了基于染色体构象捕获(3C)的技术,例如Hi-C,该技术可在全基因组范围内提供基因座对之间的基因座接触频率。该技术揭示了两个遥远的基因座可以在测试的基因组中相互作用。它表明测试的基因组在细胞核内形成三维(3D)染色体结构。利用可用的Hi-C数据,我们的下一个挑战是从3C衍生的数据中计算3D染色体结构的模型。本文介绍了一种确定性方法,称为ChromSDE,该方法采用半确定性编程技术来找到适合观测数据的最佳结构,并使用黄金分割搜索来找到将接触频率转换为空间距离的正确参数。此外,我们开发了一种称为共识索引的度量,以指示Hi-C数据是对应于单个结构还是结构的混合物。据我们所知,ChromSDE是唯一可以确保在无噪声情况下恢复正确结构的方法。另外,我们证明了从接触频率到空间距离的转换参数将在理论和经验上在不同分辨率下发生变化。使用仿真数据和实际Hi-C数据,我们证明ChromSDE比现有方法更准确,更可靠。最后,我们证明了可以从我们预测的3D结构中发现有趣的生物学发现。

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