We present analytic methods for extracting a class of bulk geometries given information of certain physical quantities in the boundary CFT. More specifically we look at singular correlators and entanglement entropy in the CFT to provide information of null and spacelike geodesics repectively in the bulk. We show that static spherically symmetric, asymptotically AdS spacetimes which do not admit null circular orbits can be fully recovered, and that any spacetime can be recovered up to the local maximum of the potential. We provide analytical and numerical examples to verify the methods used.
Motivated by the holographic principle, within the context of the AdS/CFT Correspondence in the large t'Hooft limit, we investigate how the geometry of certain highly symmetric bulk spacetimes can be recovered given information of physical quantities in the dual boundary CFT. In particular, we use holographic entanglement entropy proposal (relating the entanglement entropy of certain subsystems on the boundary to the area of static minimal surfaces) to recover the bulk metric using higher dimensional minimal surface probes within a class of static, planar symmetric, asymptotically AdS spacetimes. We find analytic and perturbative expressions for the metric function in terms of the entanglement entropy of straight belt and circular disk subsystems of the boundary theory respectively. Finally, we discuss how such extractions can be generalised.
Infectious diseases exert a large and in many contexts growing burden on human health, but violate most of the assumptions of classical epidemiological statistics and hence require a mathematically sophisticated approach. Viral shedding data are collected during human studies—either where volunteers are infected with a disease or where existing cases are recruited—in which the levels of live virus produced over time are measured. These have traditionally been difficult to analyse due to strong, complex correlations between parameters. Here, we show how a Bayesian approach to the inverse problem together with modern Markov chain Monte Carlo algorithms based on information geometry can overcome these difficulties and yield insights into the disease dynamics of two of the most prevalent human pathogens—influenza and norovirus—as well as Ebola virus disease.
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