Aarathi Raghuraman, FNU2023-02-052023-02-052021-08-13vt_gsexam:32165http://hdl.handle.net/10919/113672Influenza is a seasonal viral disease affecting over 1 billion people annually around the globe, as reported by the World Health Organization (WHO). The influenza virus has been around for decades causing multiple pandemics and encouraging researchers to perform extensive analysis of its evolutionary patterns. Current research uses phylogenetic trees as the basis to guide population genetics and other phenotypic characteristics when describing the evolution of the influenza genome. Phylogenetic trees are one form of representing the evolutionary trends of sequenced genomes, but that do not capture the multidimensional complexity of mutational pathways. We suggest representing antigenic drifts within influenza A/H1N1 hemagglutinin (HA) protein as a graph, $G = (V, E)$, where $V$ is the set of vertices representing each possible sequence and $E$ is the set of edges representing single amino acid substitutions. Each transition is characterized by a Malthusian fitness model incorporating the genetic adaptation, vaccine similarity, and historical epidemiological response using mortality as the metric where available. Applying reinforcement learning with the vertices as states, edges as actions, and fitness as the reward, we learn the high likelihood mutational pathways and optimal policy, without exploring the entire space of the graph, $G$. Our average predicted versus actual sequence distance of $3.6 \pm 1.2$ amino acids indicates that our novel approach of using naive Q-learning can assist with influenza strain predictions, thus improving vaccine selection for future disease seasons.ETDIn CopyrightFitnessMutational PathwaysMutational PathsReinforcement LearningQ-LearningThesis