Hi-C as a molecular rangefinder to examine genomic rearrangements. (January 2022)

• Record Type: Journal Article
• Authors: Kim, Kyukwang; Kim, Mooyoung; Kim, Yubin; Lee, Dongsung; Jung, Inkyung
• Is Part Of: Seminars in cell & developmental biology. Volume 121(2022)
• Page Start: 161
• Page End: 170
• Publication Date: 2022-01
• Subjects: 3D chromatin structure -- Hi-C -- Structural variations -- Single-cell Hi-C; Cytology -- Periodicals; Developmental biology -- Periodicals; 571.6
• DOI: 10.1016/j.semcdb.2021.04.024
• Languages: English
• ISSNs: 1084-9521

Abstract

Abstract: The mammalian genome is highly packed into the nucleus. Over the past decade, the development of Hi-C has contributed significantly to our understanding of the three-dimensional (3D) chromatin structure, uncovering the principles and functions of higher-order chromatin organizations. Recent studies have repositioned its property in spatial proximity measurement to address challenging problems in genome analyses including genome assembly, haplotype phasing, and the detection of genomic rearrangements. In particular, the power of Hi-C in detecting large-scale structural variations (SVs) in the cancer genome has been demonstrated, which is challenging to be addressed solely with short-read-based whole-genome sequencing analyses. In this review, we first provide a comprehensive view of Hi-C as an intuitive and effective SV detection tool. Then, we introduce recently developed bioinformatics tools utilizing Hi-C to investigate genomic rearrangements. Finally, we discuss the potential application of single-cell Hi-C to address the heterogeneity of genomic rearrangements and sub-population identification in the cancer genome.