4.7 Article

Assessing relationships between chromatin interactions and regulatory genomic activities using the self-organizing map

Journal

METHODS
Volume 189, Issue -, Pages 12-21

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ymeth.2020.07.002

Keywords

Hi-C; Self-Organizing Map; Gene regulation

Funding

  1. National Science Foundation under ABI Innovation [DBI1564466]
  2. Erickson Discovery Grant from Penn State University
  3. Edward B Nelson Undergraduate Research Fund from Penn State University

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Existing methods struggle to visualize relationships between genomic activities and Hi-C data, but projecting high-dimensional Hi-C data onto three-dimensional structures allows for exploration of these relationships.
Few existing methods enable the visualization of relationships between regulatory genomic activities and genome organization as captured by Hi-C experimental data. Genome-wide Hi-C datasets are often displayed using ?heatmap? matrices, but it is difficult to intuit from these heatmaps which biochemical activities are compartmentalized together. High-dimensional Hi-C data vectors can alternatively be projected onto threedimensional space using dimensionality reduction techniques. The resulting three-dimensional structures can serve as scaffolds for projecting other forms of genomic information, thereby enabling the exploration of relationships between genome organization and various genome annotations. However, while three-dimensional models are contextually appropriate for chromatin interaction data, some analyses and visualizations may be more intuitively and conveniently performed in two-dimensional space. We present a novel approach to the visualization and analysis of chromatin organization based on the SelfOrganizing Map (SOM). The SOM algorithm provides a two-dimensional manifold which adapts to represent the high dimensional chromatin interaction space. The resulting data structure can then be used to assess relationships between regulatory genomic activities and chromatin interactions. For example, given a set of genomic coordinates corresponding to a given biochemical activity, the degree to which this activity is segregated or compartmentalized in chromatin interaction space can be intuitively visualized on the 2D SOM grid and quantified using Lorenz curve analysis. We demonstrate our approach for exploratory analysis of genome compartmentalization in a high-resolution Hi-C dataset from the human GM12878 cell line. Our SOM-based approach provides an intuitive visualization of the large-scale structure of Hi-C data and serves as a platform for integrative analyses of the relationships between various genomic activities and genome organization.

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