Last updated: 2021-02-22

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Knit directory: uci_covid_modeling2/

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Orange County, CA COVID-19 Situation Report, February 22, 2021

Report period: Jan 13 - Feb 17 (we don’t use the most recent data due to reporting delays)

The goal of this report is to inform interested parties about dynamics of SARS-CoV-2 spread in Orange County, CA and to predict epidemic trajectories. Methodological details are provided below and in the accompanying manuscript. We are also contributing to COVID Trends by UC Irvine project that provides data visualizations of California County trends across time and space.

Summary (statements are made assuming 95% credibility levels)

Note: We previously created a report using a similar model with a different implementation. Archives of the old report can be found here.


Abbreviated technical details (optional)

Our approach is based on fitting a mechanistic model of SARS-CoV-2 spread to multiple sources of surveillance data. A more fleshed out method description is in the manuscript.

Model inputs

Our method takes three time series as input: daily new tests, case counts, and deaths. However, we find daily resolution to be too noisy due to delay in testing reports, weekend effect, etc. So we aggregated/binned the three types of counts in 3 day intervals. These aggregated time series are shown below.

Model structure

We assume that all individuals in Orange County, CA can be split into 6 compartments: S = susceptible individuals, E = infected, but not yet infectious individuals, \(\text{I}_\text{e}\) = individuals at early stages of infection, \(\text{I}_\text{p}\) = individuals at progressed stages of infection (assumed 20% less infectious than individuals at the early infection stage), R = recovered individuals, D = individuals who died due to COVID-19. Possible progressions of an individual through the above compartments are depicted in the diagram below.

Version Author Date
dcffe20 Damon Bayer 2020-12-16

Mathematically, we assume that dynamics of the proportions of individuals in each compartment follow a set of ordinary differential equations corresponding to the above diagram. These equations are controlled by the following parameters:

  • Basic reproductive number (\(R_0\))
  • mean duration of the latent period
  • mean duration of the early infection period
  • mean duration of the progressed infection period
  • probability of transitioning from progressed infection to death, rather than to recovery (i.e., IFR)

We fit this model to data by assuming that case counts are noisy realizations of the actual number of individuals progressing from \(\text{I}_\text{e}\) compartment to \(\text{I}_\text{p}\) compartment. Similarly we assume that observed deaths are noisy realizations of the actual number of individuals progressing from \(\text{I}_\text{p}\) compartment to \(\text{D}\) compartment. A priori, we assume that death counts are significantly less noisy than case counts. We use a Bayesian estimation framework, which means that all estimated quantities receive credible intervals (e.g., 80% or 95% credible intervals). Width of these credible intervals encode the amount of uncertainty that we have in the estimated quantities.

Posterior Predictive Plots


R version 4.0.3 (2020-10-10)
Platform: x86_64-apple-darwin17.0 (64-bit)
Running under: macOS Big Sur 10.16

Matrix products: default
BLAS:   /Library/Frameworks/R.framework/Versions/4.0/Resources/lib/libRblas.dylib
LAPACK: /Library/Frameworks/R.framework/Versions/4.0/Resources/lib/libRlapack.dylib

locale:
[1] en_US.UTF-8/en_US.UTF-8/en_US.UTF-8/C/en_US.UTF-8/en_US.UTF-8

attached base packages:
[1] stats     graphics  grDevices utils     datasets  methods   base     

other attached packages:
 [1] patchwork_1.1.1   coda_0.19-4       cowplot_1.1.1     stemr_0.2.0      
 [5] glue_1.4.2        scales_1.1.1      tidybayes_2.3.1   forcats_0.5.1    
 [9] stringr_1.4.0     dplyr_1.0.4       purrr_0.3.4       readr_1.4.0      
[13] tidyr_1.1.2       tibble_3.0.6      ggplot2_3.3.3     tidyverse_1.3.0  
[17] fs_1.5.0          lubridate_1.7.9.2

loaded via a namespace (and not attached):
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 [4] assertthat_0.2.1     rprojroot_2.0.2      digest_0.6.27       
 [7] plyr_1.8.6           R6_2.5.0             cellranger_1.1.0    
[10] backports_1.2.1      reprex_1.0.0         evaluate_0.14       
[13] highr_0.8            httr_1.4.2           pillar_1.4.7        
[16] rlang_0.4.10         readxl_1.3.1         rstudioapi_0.13     
[19] whisker_0.4          rmarkdown_2.6        labeling_0.4.2      
[22] munsell_0.5.0        broom_0.7.4          compiler_4.0.3      
[25] httpuv_1.5.5         modelr_0.1.8         xfun_0.20           
[28] pkgconfig_2.0.3      htmltools_0.5.1.1    tidyselect_1.1.0    
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[34] dbplyr_2.1.0         withr_2.4.1          later_1.1.0.1       
[37] ggdist_2.4.0         grid_4.0.3           distributional_0.2.2
[40] jsonlite_1.7.2       gtable_0.3.0         lifecycle_0.2.0     
[43] DBI_1.1.1            git2r_0.28.0         magrittr_2.0.1      
[46] cli_2.3.0            stringi_1.5.3        farver_2.0.3        
[49] promises_1.1.1       xml2_1.3.2           ellipsis_0.3.1      
[52] generics_0.1.0       vctrs_0.3.6          RColorBrewer_1.1-2  
[55] tools_4.0.3          svUnit_1.0.3         hms_1.0.0           
[58] yaml_2.2.1           colorspace_2.0-0     rvest_0.3.6         
[61] knitr_1.31           haven_2.3.1