Show simple item record

dc.contributor.advisorPop, Mihaien_US
dc.contributor.authorMendelowitz, Lee M.en_US
dc.date.accessioned2016-02-06T06:32:57Z
dc.date.available2016-02-06T06:32:57Z
dc.date.issued2015en_US
dc.identifierdoi:10.13016/M2JD95
dc.identifier.urihttp://hdl.handle.net/1903/17218
dc.description.abstractOptical mapping and nanocoding are single molecule restriction mapping systems for interrogating genomic structure at a scale that cannot currently be achieved using DNA sequencing methods. In these mapping experiments, large DNA molecules approximately 500 kb are stretched, immobilized or confined, and then digested with a restriction endonuclease that cuts or nicks the DNA at its cognate sequence. The cut/nick sites are then observed through fluorescent microscopy and machine vision is used to estimate the length of the DNA fragments between consecutive sites. This produces, for each molecule, a barcode-like pattern comprising the ordered list of restriction fragment lengths Despite the promise of the optical mapping and nanocoding systems, there are few open source tools for working with the data generated by these platforms. Most analyses rely on custom in-house software pipelines using proprietary software. In this dissertation we present open source software tools for the alignment and vizualization of restriction mapping data. In this work we first present a review of the optical mapping and nanocoding systems and provide an overview of the current methods for aligning and assembling consensus restriction maps and their related applications. Next, we present the Maligner software for the alignment of a query restriction pattern to a reference pattern. Alignment is a fundamental problem which is the first step in many downstream analyses, such as consensus map assembly or structural variant calling. The Maligner software features both a sensitive dynamic programming implementation and a faster but less sensitive index based mode of alignment. We compare the Maligner software to other available tools for the task of aligning a sequence contig assembly to a reference optical map and for aligning single molecule maps to a reference. Next, we present a portable data visualization web application for visualizing pairwise alignments of restriction maps. Finally, we present updates to the Maligner software to support partial alignments of single molecule maps, allowing for the clustering of compatible split map alignments to identify structural variants.en_US
dc.language.isoenen_US
dc.titleALGORITHMS FOR THE ALIGNMENT AND VISUALIZATION OF GENOME MAPPING DATA WITH APPLICATIONS TO STRUCTURAL VARIANT DETECTIONen_US
dc.typeDissertationen_US
dc.contributor.publisherDigital Repository at the University of Marylanden_US
dc.contributor.publisherUniversity of Maryland (College Park, Md.)en_US
dc.contributor.departmentApplied Mathematics and Scientific Computationen_US
dc.subject.pqcontrolledBioinformaticsen_US
dc.subject.pquncontrolleden_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record