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dc.contributor.advisorNick Rhind
dc.contributor.authorLiu, Victor
dc.date2022-08-11T08:08:46.000
dc.date.accessioned2022-08-23T16:07:57Z
dc.date.available2022-08-23T16:07:57Z
dc.date.issued2017-12-26
dc.date.submitted2018-04-10
dc.identifier.doi10.13028/M2097W
dc.identifier.urihttp://hdl.handle.net/20.500.14038/32351
dc.description.abstractDNA replication is a fundamental process that is primarily regulated at the initiation step. In higher eukaryotes, the location and properties of replication origins are not well understood. Existing genome-wide approaches to map origins—such as nascent strand abundance mapping, Okazaki fragment mapping, or chromatin immunoprecipitation-based assays—average the behavior of a population of cells. However, due to cell-to-cell variability in origin usage, single molecule techniques are necessary to investigate the actual behavior of a cell. Here, I investigate the feasibility of using three single molecule, genome-wide technologies to map origins of replication. The Pacific Biosciences Single Molecule Real-Time (SMRT) sequencing technology, the BioNano Genomics Irys optical mapping technology, and the Oxford Nanopore Technologies MinION nanopore sequencing technology are promising approaches that can advance our understanding of DNA replication in higher eukaryotes.
dc.language.isoen_US
dc.rightsCopyright is held by the author, with all rights reserved.
dc.subjectDNA replication origins
dc.subjectBiochemistry, Biophysics, and Structural Biology
dc.subjectGenetics and Genomics
dc.titleSingle Molecule Approaches to Mapping DNA Replication Origins
dc.typeMaster's Thesis
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=1970&context=gsbs_diss&unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_diss/965
dc.legacy.embargo2019-09-12T00:00:00-07:00
dc.identifier.contextkey11942468
refterms.dateFOA2022-08-30T15:13:04Z
html.description.abstract<p>DNA replication is a fundamental process that is primarily regulated at the initiation step. In higher eukaryotes, the location and properties of replication origins are not well understood. Existing genome-wide approaches to map origins—such as nascent strand abundance mapping, Okazaki fragment mapping, or chromatin immunoprecipitation-based assays—average the behavior of a population of cells. However, due to cell-to-cell variability in origin usage, single molecule techniques are necessary to investigate the actual behavior of a cell. Here, I investigate the feasibility of using three single molecule, genome-wide technologies to map origins of replication. The Pacific Biosciences Single Molecule Real-Time (SMRT) sequencing technology, the BioNano Genomics Irys optical mapping technology, and the Oxford Nanopore Technologies MinION nanopore sequencing technology are promising approaches that can advance our understanding of DNA replication in higher eukaryotes.</p>
dc.identifier.submissionpathgsbs_diss/965
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.description.thesisprogramMD/PhD
dc.identifier.orcid0000-0003-0667-6573


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