Abstract
Hi-C (high throughput chromosome conformation capture) is a powerful tool designed to explore the genome-wide collection of chromosomal contacts within a cell population. However, the highly complex nature of Hi-C libraries often precludes the robust identification of interactions between individual restriction fragments with high resolution and statistical significance. This challenge led to the incorporation of sequence capture technology into Hi-C protocols, giving rise to a Capture Hi-C methodology. In this chapter, we review the general principles of the technique and provide a view emanating from our experience employing this approach to study the dynamics of episomal viral DNA contacts during specific stages of the viral life cycle.
Original language | English (US) |
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Title of host publication | Epigenetics Methods |
Publisher | Elsevier |
Pages | 419-444 |
Number of pages | 26 |
ISBN (Electronic) | 9780128194140 |
DOIs | |
State | Published - Jan 1 2020 |
Keywords
- Chromatin
- Computational analysis
- Episome
- Herpesvirus
- Kaposi’s sarcoma-associated herpesvirus
- Nucleome
- Reactivation
- Sequence capture
- Target enrichment
ASJC Scopus subject areas
- Medicine(all)
- Biochemistry, Genetics and Molecular Biology(all)