Hi-C, a genome-wide chromosome conformation capture assay, is a powerful tool used to study three-dimensional genome organization by converting physical pairwise interactions into counts of pairwise interactions. To study the many temporally regulated facets of meiotic recombination in S. cerevisiae, the Hi-C assay must be robust such that fine- and wide-scale comparisons between genetic datasets can be made. Here we describe an updated protocol for Hi-C (Hi-C2B) that generates reproducible libraries of interaction data with low noise and for a relatively low cost.
Keywords: Chromosome conformation capture; Genome stability; Hi-C; Meiosis; Paired-end sequencing.
© 2024. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.