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dc.contributor.advisorErnest Fraenkel.en_US
dc.contributor.authorKedaigle, Amanda Joyen_US
dc.contributor.otherMassachusetts Institute of Technology. Computational and Systems Biology Program.en_US
dc.date.accessioned2018-11-15T15:51:34Z
dc.date.available2018-11-15T15:51:34Z
dc.date.copyright2018en_US
dc.date.issued2018en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/119026
dc.descriptionThesis: Ph. D., Massachusetts Institute of Technology, Computational and Systems Biology Program, 2018.en_US
dc.descriptionThis electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections.en_US
dc.descriptionCataloged from student-submitted PDF version of thesis.en_US
dc.descriptionIncludes bibliographical references.en_US
dc.description.abstractHigh-throughput "omics" data are becoming commonplace in biological research and can provide important translational insights, but there is a need for well-crafted user-friendly tools for integrating and analyzing these data. In this thesis, I present versions 1 and 2 of Omics Integrator, a software tool designed to take advantage of the Prize-Collecting Steiner Forest algorithm from graph theory to provide users with high-confidence biological networks informed by their omics results. I show the results of using this flexible tool in several studies of Huntington's disease (HD), a fatal neurodegenerative disorder with no cure. By leveraging Omics Integrator on omics datasets from induced pluripotent stem cell (iPSC) derived models of HD, I discovered and highlighted several pathways that are altered in these cell line models, including neurodevelopment and glycolytic metabolism, which may lead to important therapeutic targets in the disease. Finally, I compare omics data derived from three iPSC-derived models differentiated towards a striatal neuron cell type using different protocols, and show that by performing this large comparative analysis I can implicate functions and pathways common to several models of HD. Future integrative and comparative studies like these will be made easier by the Omics Integrator tool.en_US
dc.description.statementofresponsibilityby Amanda Joy Kedaigle.en_US
dc.format.extent315 pagesen_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsMIT theses are protected by copyright. They may be viewed, downloaded, or printed from this source but further reproduction or distribution in any format is prohibited without written permission.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582en_US
dc.subjectComputational and Systems Biology Program.en_US
dc.titleIntegrating Omics data : a new software tool and its use in implicating therapeutic targets in Huntington's diseaseen_US
dc.typeThesisen_US
dc.description.degreePh. D.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Computational and Systems Biology Program
dc.identifier.oclc1057726996en_US


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