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SUMMARY:PLENARY TALK - Spatial modelling of early-phase COVID-19 epidemic 
 in Norway - Arnoldo Frigessi (University of Oslo)
DTSTART:20200724T110000Z
DTEND:20200724T120000Z
UID:TALK150100@talks.cam.ac.uk
CONTACT:INI IT
DESCRIPTION:We developed a stochastic SEIR model for the COVID-19<br>epide
 mic at a fine spatial scale\, using mobile phone mobility data\, to descri
 be<br>the geographical spread of the virus. The model is developed for the
  very early<br>phase of the epidemic\, when movement of individuals plays 
 a key role. In the<br>beginning\, importation of the virus into the region
  of interest is decisive\,<br>and we estimate the proportion of unknown im
 ported cases. Our model represents<br>non-pharmaceutical interventions to 
 contain the epidemic by means of a<br>regionally varying step function of 
 the effective reproduction numbers. The<br>regionally varying effective re
 production numbers are estimated by sequential<br>Approximate Bayesian Com
 puting\, using hospitalisation data of the infected<br>individuals at regi
 onal level. For prediction\, we develop a way to regularise<br>the mobilit
 y matrices\, to conserve the geographical distribution of the<br>populatio
 n. This allows adequate long term predictions of all quantities of<br>inte
 rest. Uncertainty in the parameters (both the estimated ones and the ones<
 br>learned from the literature) is prolonged into the future by simulation
 . We use<br>our model to describe the history of the first phase of the CO
 VID-19 epidemic<br>in Norway\, during which social distancing and hygienic
  measures have been<br>adopted together with teleworking and school closur
 e and reopening. The result<br>of these measures have reduced the presence
  of the virus in Norway to such a<br>low level\, leading to a relaxation o
 f restrictions\, to resemble the early phase<br>of the epidemic\, making o
 ur model again important. We compare the results of<br>our model to the on
 es obtained by a similar nonregional model. We also<br>developed a version
  of the model which has a time varying reproduction number.<br>In this cas
 e we resort to Sequential Monte Carlo for inference. I will discuss<br>the
  difficulties in making predictions using this model. This is joint work w
 ith Birgitte Freiesleben de Blasio\, Solveig<br>Engebretsen\, Gunnar Isaks
 son R&oslash\;\, Alfonso Diz-Lois Palomares\, Kenth Eng&oslash\;-Monsen\,<
 br>Anja Br&aring\;then Kristoffersen and Geir Storvik.
LOCATION:Seminar Room 1\, Newton Institute
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