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  <title><![CDATA[BioE PhD Proposal Presentation-  Emi M. Wheelock]]></title>
  <body><![CDATA[<p><strong>Advisor</strong>: Hang Lu, Ph.D. (Chemical and Biomolecular Engineering, Georgia Institute of Technology)</p><p><strong>Committee:</strong></p><p>Gordon Berman, Ph.D. (Biology, Emory University)<br>Matthieu Bloch, Ph.D. (Electrical and Computer Engineering, Georgia Institute of Technology)<br>Anqi Wu, Ph.D. (Computational&nbsp;Science and Engineering, Georgia Institute of Technology)<br>Patrick McGrath, Ph.D. (Biological Sciences, Georgia Institute of Technology)</p><p><strong>Experience-Dependent Reweighting of Conserved Neural Circuit Dynamics in </strong><em><strong>C. elegans</strong></em></p><p>Learning allows animals to use past experience to change how sensory cues guide future behavior, but it remains unclear how this change is implemented in brain-wide neural activity. One possibility is that learning creates a new neural response pattern; another is that learning changes how sensory cues recruit pre-existing patterns already present in the circuit. Distinguishing these possibilities requires treating neural activity as a time-evolving population process, rather than only asking which neurons increase or decrease their activity. <em>C. elegans</em>&nbsp;is well suited for this problem because controlled sensory stimulation, whole-brain calcium imaging, quantitative behavior, and genetic perturbation can be combined in the same animal. This thesis investigates how aversive olfactory learning changes brain-wide neural dynamics in <em>C. elegans</em>, using odors from standard bacterial food (<em>E. coli</em>&nbsp;OP50), pathogenic bacteria (<em>Pseudomonas aeruginosa</em>&nbsp;PA14), and buffer controls. Aim 1 will identify reproducible odor-evoked dynamical features across animals using latent dynamical modeling and invariant summaries. Aim 2 will test whether pathogen training shifts pathogen-evoked dynamics toward food-associated structure or produces a distinct trained-state response. Aim 3 will determine whether learning-sensitive dynamical readouts predict turning behavior and reveal how targeted genetic perturbations disrupt learned sensorimotor computation.</p>]]></body>
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