dc.contributor.advisor | Ernest Fraenkel. | en_US |
dc.contributor.author | Kedaigle, Amanda Joy | en_US |
dc.contributor.other | Massachusetts Institute of Technology. Computational and Systems Biology Program. | en_US |
dc.date.accessioned | 2018-11-15T15:51:34Z | |
dc.date.available | 2018-11-15T15:51:34Z | |
dc.date.copyright | 2018 | en_US |
dc.date.issued | 2018 | en_US |
dc.identifier.uri | http://hdl.handle.net/1721.1/119026 | |
dc.description | Thesis: Ph. D., Massachusetts Institute of Technology, Computational and Systems Biology Program, 2018. | en_US |
dc.description | This electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections. | en_US |
dc.description | Cataloged from student-submitted PDF version of thesis. | en_US |
dc.description | Includes bibliographical references. | en_US |
dc.description.abstract | High-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.statementofresponsibility | by Amanda Joy Kedaigle. | en_US |
dc.format.extent | 315 pages | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Massachusetts Institute of Technology | en_US |
dc.rights | MIT 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.uri | http://dspace.mit.edu/handle/1721.1/7582 | en_US |
dc.subject | Computational and Systems Biology Program. | en_US |
dc.title | Integrating Omics data : a new software tool and its use in implicating therapeutic targets in Huntington's disease | en_US |
dc.type | Thesis | en_US |
dc.description.degree | Ph. D. | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Computational and Systems Biology Program | |
dc.identifier.oclc | 1057726996 | en_US |