{"id":{"repo_id":"uiuc","oai_identifier":"oai:www.ideals.illinois.edu:2142/107846"},"canonical_url":"https://search.dev.ndltd.org/etd/uiuc/oai:www.ideals.illinois.edu:2142/107846","repository":{"repo_id":"uiuc","name":"University of Illinois - Urbana-Champaign","base_url":"https://www.ideals.illinois.edu/oai-pmh"},"display":{"title":"Understanding machine learning models of the epigenome with statistics and statistical mechanics","abstract":"Epigenetic changes are chemical and structural modifications of DNA and its associated proteins which do not change DNA sequence. These modifications mark and package DNA in different ways and help to establish cell types, which are distinct and heritable gene expression states. Understanding determinants of epigenetic modifications and how these modifications affect gene expression is a major challenge with important implications in developmental biology and medicine. Meeting this challenge requires methods for predicting biologically relevant events from a large number of degrees of freedom that interact via unknown rules. The nature of this problem along with large amounts of data provided by high-throughput sequencing techniques motivates a machine-learning approach. This work uses artificial neural networks to predict binding of proteins involved in 3-dimensional organization of DNA as well as locations of methylation marks deposited by DNA methyltransferase enzymes. To understand the rules underlying the sequence-based prediction of our models, we apply interpretation methods based on sampling from constrained maximum entropy distributions. We consider biological and biophysical implications of the important sequence patterns revealed by interpretation. In the case of DNA methylation, our statistical methods help understand how methylation affects gene expression as well as how cells in our engineered yeast system response to DNA methylation stress. Finally, we study the diversity of single-cell gene expression across the cell types of the human skin and demonstrate coordination between changes in epigenetically modified loci and changes in expression of transcription factor proteins predicted to bind these loci.","abstract_html":"Epigenetic changes are chemical and structural modifications of DNA and its associated proteins which do not change DNA sequence. These modifications mark and package DNA in different ways and help to establish cell types, which are distinct and heritable gene expression states. Understanding determinants of epigenetic modifications and how these modifications affect gene expression is a major challenge with important implications in developmental biology and medicine. Meeting this challenge requires methods for predicting biologically relevant events from a large number of degrees of freedom that interact via unknown rules. The nature of this problem along with large amounts of data provided by high-throughput sequencing techniques motivates a machine-learning approach. This work uses artificial neural networks to predict binding of proteins involved in 3-dimensional organization of DNA as well as locations of methylation marks deposited by DNA methyltransferase enzymes. To understand the rules underlying the sequence-based prediction of our models, we apply interpretation methods based on sampling from constrained maximum entropy distributions. We consider biological and biophysical implications of the important sequence patterns revealed by interpretation. In the case of DNA methylation, our statistical methods help understand how methylation affects gene expression as well as how cells in our engineered yeast system response to DNA methylation stress. Finally, we study the diversity of single-cell gene expression across the cell types of the human skin and demonstrate coordination between changes in epigenetically modified loci and changes in expression of transcription factor proteins predicted to bind these loci.","abstract_has_math":false,"creators":["Finnegan, Alex I"],"institution":"University of Illinois at Urbana-Champaign","degree_name":"Ph.D.","degree_level":"Dissertation","degree_discipline":"Physics","degree_department":null,"school":null,"contributors":["Song, Jun S","Oono, Yoshitsugu","Aksimentiev, Aleksei","Chemla, Yann"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2020,"date_issued":"2020-08-26T21:53:55Z","date_published":"2020-08-26T21:53:55Z","updated_at":"2026-07-22T22:24:47Z","subjects":["Artificial neural networks","Machine learning","Epigenetics","Maximum entropy"],"languages":["en"],"rights":["© 2020 by Alex I. Finnegan. 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The nature of this problem along with large amounts of data provided by high-throughput sequencing techniques motivates a machine-learning approach. This work uses artificial neural networks to predict binding of proteins involved in 3-dimensional organization of DNA as well as locations of methylation marks deposited by DNA methyltransferase enzymes. To understand the rules underlying the sequence-based prediction of our models, we apply interpretation methods based on sampling from constrained maximum entropy distributions. We consider biological and biophysical implications of the important sequence patterns revealed by interpretation. In the case of DNA methylation, our statistical methods help understand how methylation affects gene expression as well as how cells in our engineered yeast system response to DNA methylation stress. Finally, we study the diversity of single-cell gene expression across the cell types of the human skin and demonstrate coordination between changes in epigenetically modified loci and changes in expression of transcription factor proteins predicted to bind these loci.","Submission original under an indefinite embargo labeled 'Open Access'. The submission was exported from vireo on 2020-08-25 without embargo terms","The student, Alex Finnegan, accepted the attached license on 2020-01-21 at 11:40.","The student, Alex Finnegan, submitted this Dissertation for approval on 2020-01-21 at 11:59.","This Dissertation was approved for publication on 2020-01-21 at 15:42.","DSpace SAF Submission Ingestion Package generated from Vireo submission #14852 on 2020-08-25 at 17:03:09","Made available in DSpace on 2020-08-26T21:53:55Z (GMT). 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These modifications mark and package DNA in different ways and help to establish cell types, which are distinct and heritable gene expression states. Understanding determinants of epigenetic modifications and how these modifications affect gene expression is a major challenge with important implications in developmental biology and medicine. Meeting this challenge requires methods for predicting biologically relevant events from a large number of degrees of freedom that interact via unknown rules. The nature of this problem along with large amounts of data provided by high-throughput sequencing techniques motivates a machine-learning approach. This work uses artificial neural networks to predict binding of proteins involved in 3-dimensional organization of DNA as well as locations of methylation marks deposited by DNA methyltransferase enzymes. To understand the rules underlying the sequence-based prediction of our models, we apply interpretation methods based on sampling from constrained maximum entropy distributions. We consider biological and biophysical implications of the important sequence patterns revealed by interpretation. In the case of DNA methylation, our statistical methods help understand how methylation affects gene expression as well as how cells in our engineered yeast system response to DNA methylation stress. Finally, we study the diversity of single-cell gene expression across the cell types of the human skin and demonstrate coordination between changes in epigenetically modified loci and changes in expression of transcription factor proteins predicted to bind these loci.","Submission original under an indefinite embargo labeled 'Open Access'. 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All rights reserved."],"dc:subject":["Artificial neural networks","Machine learning","Epigenetics","Maximum entropy"],"dc:title":["Understanding machine learning models of the epigenome with statistics and statistical mechanics"],"dc:type":["text","Thesis"],"thesis:degree_discipline":["Physics"],"thesis:degree_level":["Dissertation"],"thesis:degree_name":["Ph.D."],"thesis:institution_name":["University of Illinois at Urbana-Champaign"]},"updated_at":"2026-07-22T22:24:47Z"}