Simulating data is a good way to test an experimental design prior to running a costly experiment. The isotracer package provides some basic functionality to simulate data for a network model in which the true parameter values are given by the user.
In this vignette, you will learn:
By repeating those basic steps, one can test different assumptions on the real system under study and different experimental designs to decide on the most cost-effective approach for the real experiment to be run.
In this vignette, we will use the same example as in the Including Fixed Effects of Covariates tutorial. The modelled foodweb has three compartments:
NH4
),
which is enriched in 15N at
the beginning of the experimentalgae
)The experiment is done in two aquariums, with one aquarium exposed to light while the other is kept in the dark.
The first step is to build the network model structure. This is done in exactly the same way as in the previous vignettes: we have to specify the network topology, some initial values, and potentially some covariates.
Let’s start with the topology:
## Using default distribution family for proportions ("gamma_cv").
## (eta is the coefficient of variation of gamma distributions.)
## Using default distribution family for sizes ("normal_cv").
## (zeta is the coefficient of variation of normal distributions.)
We prepare a table of initial values which could be used in the real-life experiment we want to prepare:
inits <- tibble::tribble(
~comps, ~sizes, ~props, ~treatment,
"NH4", 0.2, 0.8, "light",
"algae", 1, 0.004, "light",
"daphnia", 2, 0.004, "light",
"NH4", 0.5, 0.8, "dark",
"algae", 1.2, 0.004, "dark",
"daphnia", 1.3, 0.004, "dark")
We had the initial values to the model, and we indicate that we want
to group initial values by "treatment"
:
mod <- set_init(mod, inits, comp = "comps", size = "sizes",
prop = "props", group_by = "treatment")
mod
## # A tibble: 2 × 5
## topology initial observations parameters group
## <list> <list> <list> <list> <list>
## 1 <topology [3 × 3]> <tibble [3 × 3]> <NULL> <tibble [8 × 2]> <chr [1]>
## 2 <topology [3 × 3]> <tibble [3 × 3]> <NULL> <tibble [8 × 2]> <chr [1]>
We have the basic model ready to be given some “true” parameter values. What are the parameters we have to specify?
## # A tibble: 8 × 2
## in_model value
## <chr> <dbl>
## 1 eta NA
## 2 lambda_algae NA
## 3 lambda_daphnia NA
## 4 lambda_NH4 NA
## 5 upsilon_algae_to_daphnia NA
## 6 upsilon_daphnia_to_NH4 NA
## 7 upsilon_NH4_to_algae NA
## 8 zeta NA
Let’s say that we want to simulate an effect of
"treatment"
(light/dark) on the uptake of NH4 by the
algae:
Now we have more parameters to specify:
## # A tibble: 9 × 2
## in_model value
## <chr> <dbl>
## 1 eta NA
## 2 lambda_algae NA
## 3 lambda_daphnia NA
## 4 lambda_NH4 NA
## 5 upsilon_algae_to_daphnia NA
## 6 upsilon_daphnia_to_NH4 NA
## 7 upsilon_NH4_to_algae|dark NA
## 8 upsilon_NH4_to_algae|light NA
## 9 zeta NA
We can set the parameter values with the set_params()
function:
mod <- mod %>%
set_params(c("eta" = 0.2, "lambda_algae" = 0, "lambda_daphnia" = 0,
"lambda_NH4" = 0, "upsilon_NH4_to_algae|light" = 0.3,
"upsilon_NH4_to_algae|dark" = 0.1,
"upsilon_algae_to_daphnia" = 0.13,
"upsilon_daphnia_to_NH4" = 0.045, "zeta" = 0.1))
Once the parameter values are stored in the network model, they are
visible in the parameters
column:
## [[1]]
## # A tibble: 8 × 3
## in_replicate in_model value
## <chr> <chr> <dbl>
## 1 eta eta 0.2
## 2 lambda_algae lambda_algae 0
## 3 lambda_daphnia lambda_daphnia 0
## 4 lambda_NH4 lambda_NH4 0
## 5 upsilon_algae_to_daphnia upsilon_algae_to_daphnia 0.13
## 6 upsilon_daphnia_to_NH4 upsilon_daphnia_to_NH4 0.045
## 7 upsilon_NH4_to_algae upsilon_NH4_to_algae|light 0.3
## 8 zeta zeta 0.1
##
## [[2]]
## # A tibble: 8 × 3
## in_replicate in_model value
## <chr> <chr> <dbl>
## 1 eta eta 0.2
## 2 lambda_algae lambda_algae 0
## 3 lambda_daphnia lambda_daphnia 0
## 4 lambda_NH4 lambda_NH4 0
## 5 upsilon_algae_to_daphnia upsilon_algae_to_daphnia 0.13
## 6 upsilon_daphnia_to_NH4 upsilon_daphnia_to_NH4 0.045
## 7 upsilon_NH4_to_algae upsilon_NH4_to_algae|dark 0.1
## 8 zeta zeta 0.1
The model is now complete and can be used to generate data!
One can calculate predicted trajectories with the
project()
function:
Real-life data will incorporate some variability around those
trajectories. To simulate data with variability around expected
compartment size (coefficient of variation "zeta"
) and
around expected proportion of tracer (c.v. "eta"
), one can
use the sample_from()
function:
## # A tibble: 60 × 5
## time comp size prop treatment
## <dbl> <chr> <dbl> <dbl> <chr>
## 1 1 algae 0.958 0.0459 light
## 2 2 algae 0.842 0.0895 light
## 3 3 algae 0.930 0.0783 light
## 4 4 algae 0.875 0.103 light
## 5 5 algae 0.936 0.153 light
## 6 6 algae 0.843 0.116 light
## 7 7 algae 0.677 0.0982 light
## 8 8 algae 0.750 0.0935 light
## 9 9 algae 0.904 0.0775 light
## 10 10 algae 0.888 0.0968 light
## # ℹ 50 more rows
To visualize the simulated data, we can add it to the projected trajectories:
We can use the simulated data in spl
to fit parameters
using MCMC. By using different versions of the dataset, we can compare
different experimental designs. Here, to test how sample size
affects the uncertainty of parameter estimates, we will perform
MCMC runs with either the full spl
dataset (ten time
points) or a reduced dataset with only three time points:
We add the simulated data to the model as we would do for real data:
mod_full <- mod %>%
set_obs(spl, comp = "comp", size = "size", prop = "prop", time = "time",
group = "treatment")
We have to define the priors for our model:
mod_full <- mod_full %>%
set_priors(normal_p(0, 5), "lambda|upsilon") %>%
set_priors(normal_p(0, 2), "eta")
## Prior modified for parameter(s):
## - lambda_algae
## - lambda_daphnia
## - lambda_NH4
## - upsilon_algae_to_daphnia
## - upsilon_daphnia_to_NH4
## - upsilon_NH4_to_algae|dark
## - upsilon_NH4_to_algae|light
## Prior modified for parameter(s):
## - eta
## - zeta
We run the MCMC:
run_full <- run_mcmc(mod_full, iter = 2000)
plot(run_full)
# Note: the figure below only shows a few of the traceplots for vignette concision
and we do a posterior predictive check:
We use the reduced dataset this time:
mod_red <- mod %>%
set_obs(spl_reduced, comp = "comp", size = "size", prop = "prop",
time = "time", group = "treatment")
We set the priors:
mod_red <- mod_red %>%
set_priors(normal_p(0, 5), "lambda|upsilon") %>%
set_priors(normal_p(0, 2), "eta")
## Prior modified for parameter(s):
## - lambda_algae
## - lambda_daphnia
## - lambda_NH4
## - upsilon_algae_to_daphnia
## - upsilon_daphnia_to_NH4
## - upsilon_NH4_to_algae|dark
## - upsilon_NH4_to_algae|light
## Prior modified for parameter(s):
## - eta
## - zeta
We run the MCMC:
run_red <- run_mcmc(mod_red, iter = 2000)
plot(run_red)
# Note: the figure below only shows a few of the traceplots for vignette concision
and we do a posterior predictive check:
Does using ten time points (spl
) instead of three
(spl_reduced
) improve a lot the parameter estimates? Let’s
compare the uncertainty in their posteriors:
## 2.5% 25% 50% 75% 97.5%
## eta 0.180000 0.20000 0.2100 0.2200 0.2500
## lambda_algae 0.000240 0.00190 0.0041 0.0069 0.0140
## lambda_daphnia 0.000046 0.00064 0.0015 0.0028 0.0061
## lambda_NH4 0.000160 0.00170 0.0034 0.0065 0.0140
## upsilon_algae_to_daphnia 0.120000 0.12000 0.1300 0.1300 0.1400
## upsilon_daphnia_to_NH4 0.048000 0.05000 0.0510 0.0530 0.0550
## upsilon_NH4_to_algae|dark 0.088000 0.09400 0.0970 0.1000 0.1100
## upsilon_NH4_to_algae|light 0.280000 0.30000 0.3100 0.3200 0.3400
## zeta 0.070000 0.07800 0.0830 0.0890 0.1000
## 2.5% 25% 50% 75% 97.5%
## eta 0.180000 0.22000 0.2500 0.3000 1.100
## lambda_algae 0.000180 0.00290 0.0066 0.0130 0.030
## lambda_daphnia 0.000071 0.00093 0.0023 0.0046 0.011
## lambda_NH4 0.000350 0.00360 0.0075 0.0140 0.033
## upsilon_algae_to_daphnia 0.110000 0.12000 0.1300 0.1400 4.700
## upsilon_daphnia_to_NH4 0.044000 0.04900 0.0520 0.0560 2.000
## upsilon_NH4_to_algae|dark 0.075000 0.08900 0.0970 0.1100 5.100
## upsilon_NH4_to_algae|light 0.240000 0.27000 0.2900 0.3200 11.000
## zeta 0.070000 0.09100 0.1100 0.1300 0.180
library(bayesplot)
library(cowplot)
plot_grid(nrow = 2,
mcmc_intervals(run_full %>% select("lambda")) + xlim(0, 0.025) +
ggtitle("10 time points"),
mcmc_intervals(run_red %>% select("lambda")) + xlim(0, 0.025) +
ggtitle("3 time points")
)
## Warning: Removed 1 row containing missing values or values outside the scale range
## (`geom_segment()`).
plot_grid(nrow = 2,
mcmc_intervals(run_full %>% select("upsilon")) + xlim(0, 0.35) +
ggtitle("10 time points"),
mcmc_intervals(run_red %>% select("upsilon")) + xlim(0, 0.35) +
ggtitle("3 time points")
)
## Warning: Removed 4 rows containing missing values or values outside the scale range
## (`geom_segment()`).
The experiment with three time points seems quite good at estimating parameters despite the low number of observations, but the uncertainties are definitely reduced when 10 time points are used.
This example only used one simulated dataset. When preparing a real-life experiment, it would make sense to try a range of “true” values for the parameters to be estimated and different initial conditions in addition to different experimental designs (number of replicates, number of samples, timing of sampling).
A convenient way to structure many data simulations is to create a tibble containing the simulation variables (e.g. parameter values, sampling points, alternative models) and store the resulting simulated datasets and their corresponding MCMC fits in list columns to make the analysis of the simulations easier.