| Literature DB >> 35524115 |
Magali Hennion1, Bertrand Theulot2,3, Jean-Michel Arbona4, Benjamin Audit5, Olivier Hyrien6.
Abstract
Most genome replication mapping methods profile cell populations, masking cell-to-cell heterogeneity. Here, we describe FORK-seq, a nanopore sequencing method to map replication of single DNA molecules at 200 nucleotide resolution using a nanopore current interpretation tool allowing the quantification of BrdU incorporation. Along pulse-chased replication intermediates from Saccharomyces cerevisiae, we can orient replication tracks and reproduce population-based replication directionality profiles. Additionally, we can map individual initiation and termination events. Thus, FORK-seq reveals the full extent of cell-to-cell heterogeneity in DNA replication.Entities:
Keywords: Convolutional neural network; DNA replication; Nanopore sequencing; Replication fork direction; Replication origins; Single-molecule analysis; Termination sites; Whole-genome
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Year: 2022 PMID: 35524115 DOI: 10.1007/978-1-0716-2257-5_8
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745