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Updated: Apr 25, 2026

Hi-C: A Method to Study the Three-dimensional Architecture of Genomes.
Published on: May 6, 2010
Two-dimensional segmentation for analyzing Hi-C data
Celine Lévy-Leduc1, M Delattre1, T Mary-Huard2
1AgroParisTech/INRA MIA 518, 75005 Paris and UMR de Génétique Végétale, INRA/Univ. Paris-Sud/CNRS, 91190 Gif-sur-Yvette, France.
Motivation:
The spatial conformation of the chromosome has a deep influence on gene regulation and expression. Hi-C technology allows the evaluation of the spatial proximity between any pair of loci along the genome. It results in a data matrix where blocks corresponding to (self-)interacting regions appear. The delimitation of such blocks is critical to better understand the spatial organization of the chromatin. From a computational point of view, it results in a 2D segmentation problem.
Results:
We focus on the detection of cis-interacting regions, which appear to be prominent in observed data. We define a block-wise segmentation model for the detection of such regions. We prove that the maximization of the likelihood with respect to the block boundaries can be rephrased in terms of a 1D segmentation problem, for which the standard dynamic programming applies. The performance of the proposed methods is assessed by a simulation study on both synthetic and resampled data. A comparative study on public data shows good concordance with biologically confirmed regions.
Availability And Implementation:
The HiCseg R package is available from the Comprehensive R Archive Network and from the Web page of the corresponding author.

