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Please use this identifier to cite or link to this item: http://arks.princeton.edu/ark:/88435/dsp01z603r1676
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dc.contributor.advisorTroyanskaya, Olga G
dc.contributor.authorCofer, Evan Mitchell
dc.contributor.otherQuantitative Computational Biology Department
dc.date.accessioned2023-07-06T20:22:26Z-
dc.date.available2024-06-14T12:00:13Z-
dc.date.created2023-01-01
dc.date.issued2023
dc.identifier.urihttp://arks.princeton.edu/ark:/88435/dsp01z603r1676-
dc.description.abstractThe study of transcriptional regulation is critical to furthering our understanding of life and disease. In the last few decades, high-throughput sequencing methods such as RNA-seq, ChIP-seq, and Hi-C have provided us with the means to assay different aspects of transcriptional regulation with relative ease. The availability of such data has given rise to the field of computational regulatory genomics, which seeks to completely understand all phenomena and mechanisms governing transcriptional regulation through the rigorous analysis and integration of such data. In that vein, we conducted an in-depth investigation into the 3D structure of chromatin during Drosophila embryogenesis. We demonstrate that chromatin structures are highly dynamic, and chromatin structuring elements such as boundaries fall into distinct categories associated with unique regulatory factors and distinct dynamic patterns. Because of the scale of the data being analyzed, the computational challenges in regulatory genomics are non-trivial. Therefore, a major goal of this work has been to develop novel computational techniques for modeling various aspects of transcriptional regulation. In specific, we developed DeepArk, a set of deep learning models for model species that is capable of accurately predicting regulatory features (e.g. chromatin accessibility, histone marks, transcription factor binding) directly from genomic sequences. Beyond simply developing cutting-edge methods, we also carefully demonstrate their relevance to both computational and experimental research endeavors (e.g. genome editing) in the study of regulatory genomics. We also developed Selene, a tool to ease the development and application of models like DeepArk, and created AMBIENT, an algorithm for efficiently identifying optimal neural architectures for regulatory feature prediction tasks. In summary, we have uncovered new aspects of chromatin regulation while simultaneously expanding the computational resources available to regulatory genomics researchers.
dc.format.mimetypeapplication/pdf
dc.language.isoen
dc.publisherPrinceton, NJ : Princeton University
dc.subjectcomputational biology
dc.subjectdeep learning
dc.subjectgenomics
dc.subjectmachine learning
dc.subjectregulatory genomics
dc.subject.classificationBioinformatics
dc.subject.classificationComputer science
dc.subject.classificationBiology
dc.titleA Computational Approach to the Study of Regulatory Genomics
dc.typeAcademic dissertations (Ph.D.)
pu.embargo.terms2024-06-14
pu.date.classyear2023
pu.departmentQuantitative Computational Biology
Appears in Collections:Quantitative Computational Biology

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