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Proposing a novel community detection approach to identify co-interacting genomic regions

机译:提出一种识别共同互动基因组区域的新型社区检测方法

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摘要

Modern next generation sequencing technologies produce huge amounts of genome-wide data that allow researchers to have a deeper understanding of genomics of organisms. Despite these huge amounts of data, our understanding of the transcriptional regulatory networks is still incomplete. Conformation dependent chromosome interaction maps technologies (Hi-C) have enabled us to detect elements in the genome which interact with each other and regulate the genes. Summarizing these interactions as a data network leads to investigation of the most important properties of the 3D genome structure such as gene co-expression networks. In this work, a Pareto-Based Multi-Objective Optimization algorithm is proposed to detect the co-expressed genomic regions in Hi-C interactions. The proposed method uses fixed sized genomic regions as the vertices of the graph. Number of read between two interacting genomic regions indicate the weight of each edge. The performance of our proposed algorithm was compared to the Multi-Objective PSO algorithm on five networks derived from cis genomic interactions in three Hi-C datasets (GM12878, CD34+ and ESCs). The experimental results show that our proposed algorithm outperforms Multi-Objective PSO technique in the identification of co-interacting genomic regions.
机译:现代下一代测序技术产生大量的基因组数据,使研究人员更深入地了解生物的基因组学。尽管有这些巨额数据,但我们对转录监管网络的理解仍然不完整。构象依赖性染色体相互作用图技术(HI-C)使我们能够检测到彼此相互作用并调节基因组中的基因组中的元素。将这些相互作用总结为数据网络导致研究3D基因组结构的最重要特性,例如基因共表达网络。在这项工作中,提出了一种基于帕累托的多目标优化算法来检测Hi-C相互作用中的共同表达的基因组区域。所提出的方法使用固定大小的基因组区域作为图的顶点。两个相互作用基因组区域之间的读数表示每个边缘的重量。将所提出的算法的性能与来自三个高C数据集(GM12878,CD34 +和ESC)的CIS基因组交互的五个网络进行了比较了多目标PSO算法。实验结果表明,我们所提出的算法在共同交互基因组区域鉴定中优于多目标PSO技术。

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