squire enables users to simulate models of SARS-CoV-2 epidemics. This is done using an age-structured SEIR model that also explicitly considers healthcare capacity and disease severity.
:warning: This code is released with no support. Please submit any questions or bugs as issues and we will try to address them as quickly as possible.
:warning: This model is in active development and so parameter name and behaviours, and output file formats will change without notice.
:warning: The model is stochastic. Multiple runs with different seeds should be undertaken to see average behaviour.
:warning: As with any mathematical model, it is easy to misconfigure
inputs and therefore get meaningless outputs. Please contact the authors
if you intend to publish results using squire
.
squire is a package enabling users to quickly and easily generate calibrated estimates of SARS-CoV-2 epidemic trajectories under different control scenarios. It consists of the following:
If you are new to squire, the best place to start is below, where we detail how to install the package, how to set up the model, and how to run it with and without control interventions.
squire uses an age-structured SEIR model, with the infectious class
divided into different stages reflecting progression through different
disease severity pathways. These compartments are:
* S = Susceptibles
* E = Exposed (Latent Infection)
* IMild = Mild Infections (Not Requiring Hospitalisation)
* ICase = Infections Requiring Hospitalisation
* IHospital = Hospitalised (Requires Hospital Bed)
* IICU = ICU (Requires ICU Bed)
* IRec = Recovering from ICU Stay (Requires Hospital Bed)
* R = Recovered
* D =
Dead
Given initial inputs of hospital/ICU bed capacity and the average time cases spend in hospital, the model dynamically tracks available hospital and ICU beds over time.
Individuals newly requiring hospitalisation (either a hospital or ICU bed) are then assigned to either receive care (if the relevant bed is available) or not (if maximum capacity would be exceeded otherwise). Whether or not an individual receives the required care modifies their probability of dying.
squire utilises the package odin to generate the model. odin implements a high-level language for implementing mathematical models and can be installed by running the following command:
install.packages("odin")
The model generated using odin is written in C and so you will require a compiler to install dependencies for the package and to build any models with odin. Windows users should install Rtools. See the relevant section in R-admin for advice. Be sure to select the “edit PATH” checkbox during installation or the tools will not be found.
The function odin::can_compile()
will check if it is able to compile
things, but by the time you install the package that will probably have
been satisfied.
After installation of odin, ensure you have the devtools package installed by running the following:
install.packages("devtools")
Then install the squire package directly from GitHub by running:
devtools::install_github("mrc-ide/squire")
If you have any problems installing then please raise an issue on the
squire GitHub
.
If everything has installed correctly, we then need to load the package:
library(squire)
The full model is referred to as the explicit_SEEIR model, with hospital pathways explicitly exploring whether individuals will require a general hospital bed providing oxygen or an ICU bed that provides ventilation.
To run the model we need to provide at least one of the following arguments:
country
population
and contact_matrix_set
If the country
is provided, the population
and contact_matrix_set
will be generated (if not also specified) using the demographics and
matrices specified in the global
report.
To run the model by providing the country
we use
run_explicit_SEEIR_model()
:
r <- run_explicit_SEEIR_model(country = "Afghanistan")
The returned object is a squire_simulation
object, which is a list of
two ojects:
output
- model outputparameters
- model parameterssquire_simulation
objects can be plotted as follows:
plot(r)
This plot will plot each of the compartments of the model output. We can
also plot specific compartments using the var_select
argument that can
be passed to plot()
. Arguments passed to var_select
must be one of
the variables in the plot
above.
plot(r, var_select = c("E", "IMild"))
Or, you can specify one of deaths
, infections
, hospital_occupancy
,
ICU_occupancy
, hospital_demand
or ICU_demand
, and plot these
summary metrics that represent the combination of a number of different
compartment
e.g:
plot(r, var_select = "deaths")
All of the plotting above makes uses of the squire
function
format_output
which provides you with a means of manipulating and
managing the output from a run_explicit_SEEIR_model
call. Using it you
can specify the model outputs (e.g. compartments) you want, as well as
whether you want that output aggregated over age or not. Here we extract
the latent compartment (E). The data columns correspond to the
compartment name (compartment
), timestep (t
), model run number
(replicate
) and the model output (y
).
output <- format_output(r, var_select = "E")
head(output)
#> # A tibble: 6 x 4
#> replicate compartment t y
#> <dbl> <chr> <dbl> <dbl>
#> 1 1 E 0.1 20
#> 2 1 E 0.2 20
#> 3 1 E 0.3 20
#> 4 1 E 0.4 20
#> 5 1 E 0.5 20
#> 6 1 E 0.6 20
If we wanted age-disaggregated data, we could set reduce_age
to
FALSE
which will generate the same dataframe as before, but with an
additional column indicating the age-group.
output <- format_output(r, var_select = "E", reduce_age = FALSE)
head(output)
#> # A tibble: 6 x 5
#> replicate age_group compartment t y
#> <dbl> <int> <chr> <dbl> <dbl>
#> 1 1 1 E 0.1 0
#> 2 1 1 E 0.2 0
#> 3 1 1 E 0.3 0
#> 4 1 1 E 0.4 0
#> 5 1 1 E 0.5 0
#> 6 1 1 E 0.6 0
The model has a number of parameters for setting the R0, demography, contact matrices, the durations of each compartment and the health care outcomes and healthcare availability. In addition, the initial state of the population can be changed as well as simulation parameters, such as the number of replicates, length of simulation and the timestep. For a full list of model inputs, please see the function documentation
For example, changing the initial R0 (default = 3), number of replicates ( default = 10), simulation length (default = 365 days) and time step (default = 0.5 days), as well as setting the population and contact matrix manually:
# Get the population
pop <- get_population("United Kingdom")
population <- pop$n
# Get the mixing matrix
contact_matrix <- get_mixing_matrix("United Kingdom")
# run the model
r <- run_explicit_SEEIR_model(population = population,
contact_matrix_set = contact_matrix,
R0 = 2.5,
time_period = 200,
dt = 0.1,
replicates = 5)
plot(r)
#> Warning in plot.squire_simulation(r): Summary statistic estimated from <10
#> replicates
#> Warning in plot.squire_simulation(r): Confidence bounds estimated from <10
#> replicates
We can also change the R0 and contact matrix at set time points, to reflect changing behaviour resulting from interventions. For example to set an 80% reduction in the contact matrix after 100 days :
# run the model
r <- run_explicit_SEEIR_model(population = population,
tt_contact_matrix = c(0, 100),
contact_matrix_set = list(contact_matrix,
contact_matrix*0.2),
R0 = 2.5,
time_period = 200,
dt = 0.1,
replicates = 5)
plot(r, var_select = "infections")
#> Warning in plot.squire_simulation(r, var_select = "infections"): Summary
#> statistic estimated from <10 replicates
#> Warning in plot.squire_simulation(r, var_select = "infections"): Confidence
#> bounds estimated from <10 replicates
where n_E2_I
is the daily number of new infections.
To show an 80% reduction after 80 days but only maintained for 40 days :
# run the model
r <- run_explicit_SEEIR_model(population = population,
tt_contact_matrix = c(0, 80, 120),
contact_matrix_set = list(contact_matrix,
contact_matrix*0.2,
contact_matrix),
R0 = 2.5,
time_period = 220,
dt = 0.1,
replicates = 5)
plot(r, var_select = "infections")
#> Warning in plot.squire_simulation(r, var_select = "infections"): Summary
#> statistic estimated from <10 replicates
#> Warning in plot.squire_simulation(r, var_select = "infections"): Confidence
#> bounds estimated from <10 replicates
Alternatively, we could set a changing R0, which falls below 1 after 80 days:
# run the model
r <- run_explicit_SEEIR_model(population = population,
contact_matrix_set = contact_matrix,
tt_R0 = c(0, 80),
R0 = c(2.5, 0.9),
time_period = 200,
dt = 0.1,
replicates = 5)
plot(r, var_select = "infections")
#> Warning in plot.squire_simulation(r, var_select = "infections"): Summary
#> statistic estimated from <10 replicates
#> Warning in plot.squire_simulation(r, var_select = "infections"): Confidence
#> bounds estimated from <10 replicates
The model in squire also allows you to alter healthcare capacity.
Default values for the arguments hosp_bed_capacity
and ICU_capacity
are taken from the World Bank and a systematic review of the literature.
However, you can also specify your own:
library(patchwork)
r <- run_explicit_SEEIR_model(population = population,
contact_matrix_set = contact_matrix,
R0 = 2.5,
time_period = 200,
dt = 0.1,
replicates = 15,
hosp_bed_capacity = 1000,
ICU_bed_capacity = 100)
c <- plot(r, var_select = "hospital_occupancy")
d <- plot(r, var_select = "ICU_occupancy")
c / d
Whilst the above provides quick and easy ways to plot relevant outputs,
we recognise users might want to play around with the data themselves.
This can be done with the format_output
function.
library(ggplot2)
library(patchwork)
library(dplyr)
#>
#> Attaching package: 'dplyr'
#> The following objects are masked from 'package:stats':
#>
#> filter, lag
#> The following objects are masked from 'package:base':
#>
#> intersect, setdiff, setequal, union
x <- run_explicit_SEEIR_model(country = "Afghanistan", hosp_bed_capacity = 500, ICU_bed_capacity = 200)
deaths <- format_output(x = x, var_select = "deaths") %>%
mutate(replicate = factor(replicate))
a <- ggplot(deaths, aes(x = t, y = y, col = replicate)) +
geom_line() + ylab("Daily Deaths")
infections <- format_output(x = x, var_select = "infections") %>%
mutate(replicate = factor(replicate))
b <- ggplot(infections, aes(x = t, y = y, col = replicate)) +
geom_line() + ylab("Daily Infections")
hosp_bed <- format_output(x = x, var_select = "hospital_occupancy") %>%
mutate(replicate = factor(replicate))
c <- ggplot(hosp_bed, aes(x = t, y = y, col = replicate)) +
geom_line() + ylab("Hospital Bed Occupancy")
ICU_bed <- format_output(x = x, var_select = "ICU_occupancy") %>%
mutate(replicate = factor(replicate))
d <- ggplot(ICU_bed, aes(x = t, y = y, col = replicate)) +
geom_line() + ylab("ICU Bed Occupancy")
z <- a + b + c + d +
plot_layout(guides = 'collect')
z
Hospital bed occupancy fluctuates very slightly above the user-specified number of hospital beds available (+1 in the above example). This is due to individuals being discharged from ICU beds into general hospital beds when general hospital bed occupancy is already at maximum capacity.
We assume that these individuals newly discharged from the ICU would in reality be prioritised to receive general hospital beds and so give them a general hospital bed. Whilst this is now shown in the above panel of hospital bed occupancy, this means that less-sick individuals in general hospital beds would be discharged slightly early to make space. We assume that for these small number of the healthiest individuals in hospital, there is no excess mortality associated with this early discharge.
Future work will explore a range of bed-prioritisation structures to consider how results might be shaped by who gets a bed and when.
The model can be simply calibrated to time series of deaths reported in
settings. This can be done using the calibrate
function. For example,
let’s use the time series of deaths in Algeria up to the 22nd April
2020:
df <- read.csv(squire:::squire_file("extdata/example_DZA.csv"), stringsAsFactors = FALSE)
head(df)
#> X date deaths cases
#> 1 1 2020-02-26T00:00:00Z 0 1
#> 2 2 2020-03-01T00:00:00Z 0 2
#> 3 3 2020-03-04T00:00:00Z 0 2
#> 4 4 2020-03-05T00:00:00Z 0 7
#> 5 5 2020-03-06T00:00:00Z 0 5
#> 6 6 2020-03-09T00:00:00Z 0 3
We can calibrate the model to this data. This calibration will infer the
most likely start date of the epidemic and the R0 at the start of the
epidemic. Calibration occurs by scanning across a range of possible R0
values and start dates. Fitting works using a particle filter, which can
be parallelised using future::plan(future::multiprocess())
before
running calibrate
.
# set up for parallelisation
future::plan(future::multiprocess())
# Fit model
out <- calibrate(
data = df,
R0_min = 2,
R0_max = 4,
R0_step = 0.5,
first_start_date = "2020-02-10",
last_start_date = "2020-02-22",
day_step = 4,
replicates = 10,
n_particles = 20,
country = "Algeria"
)
#> Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ─────────────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ─────────────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100%
#>
#> Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100%
calibrate
returns the same output as run_explicit_SEEIR_model
, with
the first three elements in out
being the simulation outputs, the
model and model parameters. Note that simulation replicates are aligned
to the maximum date in the data provided, and as a result we can use the
same plotting functions as before:
plot(out, "deaths", date_0 = max(df$date), x_var = "date")
With default parameters, calibrate
will simulate up to the maximum date
in the data provided. The fit to this data can be shown using the
plotting function and specifying particle_fit
to be TRUE
plot(out, particle_fit = TRUE)
We can see that this is not the best fit, capturing only the beginning
of the data points. We can also diagnose the fitting further by looking
at the scan_results
of the grid search.
plot(out$scan_results)
This grid shows the negative log likeihood for each parameter pair. We can also plot the related probability for each pair as follows:
plot(out$scan_results, what = "probability")
The reason for the poor fits to the data shown earlier is because
Algeria has implemented interventions prior to today. These can also be
incorporated into calibrate
. For example, we can grab the assumed
changes to transmission based on government intervention for
Algeria.
interventions <- read.csv(squire:::squire_file("extdata/example_DZA_intervention.csv"))
int_unique <- squire:::interventions_unique(interventions)
int_unique
#> $dates_change
#> [1] "2020-03-12" "2020-03-18" "2020-03-22" "2020-03-23"
#>
#> $change
#> [1] 0.900 0.850 0.550 0.225
We can then provide these to calibrate
as the dates (date_R0_change
)
and relative reductions to R0 (R0_change
). We will also specify for
model fits to be continued for 14 days into the future with forceast = 14
:
out <- calibrate(
data = df,
R0_min = 2,
R0_max = 4,
R0_step = 0.5,
first_start_date = "2020-02-10",
last_start_date = "2020-02-22",
day_step = 4,
replicates = 10,
n_particles = 20,
forecast = 14,
R0_change = int_unique$change,
date_R0_change = int_unique$dates_change,
country = "Algeria"
)
#> Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100%
#>
#> Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100%
Let’s see if that is any better.
plot(out, particle_fit = TRUE)
That is a much better fit.
Any parameter that you could provide to run_explicit_SEEIR_model
can
be passed to calibrate
. This includes time varying arguments such as
contact_matrix_set
, ICU_bed_capacity
and hosp_bed_capacity
. To
incorporate these into model fitting correctly, the date at which these
change must be provided (similarly to how date_R0_change
was provided
above) using date_ICU_bed_capacity_change
,
date_ICU_bed_capacity_change
and date_hosp_bed_capacity_change
respectively. In addition, the user must provide a baseline value for
these, i.e. the contact matrix and bed capacity at the beginning of the
epidemic:
out <- calibrate(
data = df,
R0_min = 2,
R0_max = 4,
R0_step = 0.5,
first_start_date = "2020-02-10",
last_start_date = "2020-02-22",
day_step = 4,
replicates = 10,
n_particles = 20,
forecast = 14,
R0_change = int_unique$change,
date_R0_change = int_unique$dates_change,
baseline_contact_matrix = get_mixing_matrix("Algeria"),
contact_matrix_set = list(get_mixing_matrix("Algeria")*0.9),
date_contact_matrix_set_change = "2020-03-16",
baseline_hosp_bed_capacity = squire:::get_hosp_bed_capacity("Algeria"),
hosp_bed_capacity = squire:::get_hosp_bed_capacity("Algeria")*c(1.1,1.2),
date_hosp_bed_capacity_change = c("2020-04-02", "2020-04-08"),
baseline_ICU_bed_capacity = squire:::get_ICU_bed_capacity("Algeria"),
ICU_bed_capacity = squire:::get_ICU_bed_capacity("Algeria")*c(1.05),
date_ICU_bed_capacity_change = c("2020-04-10"),
country = "Algeria"
)
#> Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100%
#>
#> Progress: ──────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100%
(N.B. Given the potentially long running time for the grid search, the
model state is returned at the end of every day rather than every time
step (provided by dt
). As a result model outputs such as n_E2_I
(number of infections in a time step) and delta_D
(number of deaths in
a time step) reflect the outputs in the last time step rather than in
all the time steps in the last day. The plotting functions and
format_output
provided in squire
handle this correctly and work out
the correct number for these in the last day.)
Once you have calibrated the model to death data, it is possible to then
implement mitigation strategies forwards in time from the point of
calibration. This is achieved using the projections
function. For
example, let’s consider a country that as of 28th April 2020 is yet to
experience an epidemic take off but may be about to. Guinea reported its
first COVID-19 death on 16th April 2020 and has reported 7 deaths by the
28th April 2020 according to data from the European
CDC.
First let’s calibrate to this data with no interventions in place (there are likely some interventions in place but nothing major, such as a lockdown, has been implemented by 2020-04-28) and simulate forward for 180 days:
df <- read.csv(squire:::squire_file("extdata/example_GIN.csv"), stringsAsFactors = FALSE)
out <- calibrate(
data = df,
R0_min = 2.5,
R0_max = 4,
R0_step = 0.5,
first_start_date = "2020-03-10",
last_start_date = "2020-03-25",
day_step = 5,
replicates = 10,
n_particles = 20,
forecast = 180,
country = "Guinea"
)
#> Progress: ────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100%
#>
#> Progress: ─────────────────────────────────────────────────────────────── 100% Progress: ──────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100%
Firstly, let’s plot the fit up to the current day
plot(out, particle_fit = TRUE) +
ggplot2::xlim(as.Date(c("2020-04-10","2020-04-28"))) +
ggplot2::ylim(c(0,10))
The fit is good and captures the stuttering chains at the beginning of the epidemic. However, if we plot the forecasted deaths we can see the epidemic is likely to take off:
plot(out, "deaths")
We can now use the output of calibrate
to explore different scenario
projections using projections
. For example, to contast this
unmitigated epidemic against a mitigation scenario with a 50% reduction
in R0 today and a further 30% in 2 weeks time:
# create our projections
p <- projections(r = out, R0_change = c(0.5, 0.2), tt_R0 = c(0, 14))
The output generated from projections
is the same class and structure
as from calibrate
and can be plotted against the unmitigated scenario
using projection_plotting
:
ggproj <- projection_plotting(r_list = list(out,p),
scenarios = c("Unmitigated","Mitigation"),
var_select = c("ICU_occupancy", "ICU_demand"),
add_parms_to_scenarios = TRUE,ci = FALSE,summarise = TRUE)
# and lets add in the ICU capacity
ggproj + ggplot2::geom_hline(yintercept = out$parameters$ICU_bed_capacity)
We can see above that the intervention introduced is nearly sufficient to prevent ICU demand (solid line red) from exceeding the supply, whereas in the unmitigated strategy this did occur.
We can also model changing interventions by changing the contact matrix
over time as well as the availability of ICU and hospital beds. E.g.
decreasing contacts by 75% in a week before relaxing it to 80% in 30
days time, while increasing hospital and ICU beds by 200% in 30 days
time. (N.B. We can turn off the automatic scenario parameter labelling
with add_parms_to_scenarios = FALSE
):
# create our projections
p <- projections(r = out,
contact_matrix_set_change = c(1, 0.25, 0.8),
tt_contact_matrix = c(0, 7, 30),
hosp_bed_capacity_change = c(1, 3),
tt_hosp_beds = c(0, 30),
ICU_bed_capacity_change = c(1, 3),
tt_ICU_beds = c(0,30))
projection_plotting(r_list = list(out, p),
scenarios = c("Unmitigated","Mitigation"),
var_select = c("ICU_occupancy", "ICU_demand","deaths"),
add_parms_to_scenarios = FALSE,
ci = FALSE,summarise = TRUE) +
ggplot2::geom_hline(yintercept = out$parameters$ICU_bed_capacity)
Above we can see that the increase in bed causes the mitigation strategy to plateau at a higher bed occupancy, however, not high enough to meet the demand. However, the impacts to the contact matrix and beds have caused both a shift and a decrease in the daily deaths, which in turn causes a noticable decrease in total deaths:
projection_plotting(r_list = list(out,p),
scenarios = c("Unmitigated","Mitigation"),
var_select = c("D"),
add_parms_to_scenarios = FALSE,
ci = FALSE,summarise = TRUE)
Rather than using relative changes to the interventions, we can provide absolute measures. For example, to change the R0 to 2 today and add 500 ICU beds in 40 days time:
# what is the current capacity
icu <- tail(out$parameters$ICU_bed_capacity,1)
# create our projections
p <- projections(r = out,
R0 = 2,
tt_R0 = 0,
ICU_bed_capacity = c(icu, icu + 500),
tt_ICU_beds = c(0,40))
projection_plotting(r_list = list(out,p),
scenarios = c("Unmitigated","Mitigation"),
var_select = c("ICU_occupancy", "ICU_demand","deaths"),
add_parms_to_scenarios = FALSE,
ci = FALSE,summarise = TRUE)
Lastly, in order to run simulations for longer than the number set in
calibrate(forecast = x)
, we can use the argument time_period
to set
the numbers of days that projections
should simulate for. For example,
we could redo our calibration and have it only run up the current
day:
df <- read.csv(squire:::squire_file("extdata/example_GIN.csv"), stringsAsFactors = FALSE)
out <- calibrate(
data = df,
R0_min = 2.5,
R0_max = 4,
R0_step = 0.5,
first_start_date = "2020-03-10",
last_start_date = "2020-03-25",
day_step = 5,
replicates = 10,
n_particles = 20,
forecast = 0,
country = "Guinea"
)
#> Progress: ────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100%
#>
#> Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ───────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100% Progress: ────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────── 100%
plot(out, particle_fit = TRUE)
We can now use this to project 90 days forwards with the current level of interventions, as well as a projection of 90 days with a 50% reduction in R0:
p_no_change <- projections(out, time_period = 90)
p_change <- projections(out, R0_change = 0.5, tt_R0 = 0, time_period = 90)
projection_plotting(list(p_no_change, p_change),
scenarios = c("No Change", "50% R0"),
add_parms_to_scenarios = FALSE,
var_select = "deaths",
date_0 = max(df$date),
x_var = "date")