We can explore the model’s primary functions using a test dataset that is available with the package. Load the `Bird.parasites`

dataset, which contains binary occurrences of four avian blood parasites in New Caledonian *Zosterops* species (available in its original form at Dryad; Clark *et al* 2016). A single continuous covariate is also included (`scale.prop.zos`

), which reflects the relative abundance of *Zosterops* species (compared to other avian species) among different sample sites

```
library(MRFcov)
data("Bird.parasites")
```

The `Bird.parasites`

dataset is already in the appropriate structure for running `MRFcov`

models; however, it is useful to understand how this was done. Using the raw dataset (downloaded from `Dryad`

at the above link), we created a scaled continuous covariate to represent *Zosterops* spp. proportional captures in each sample site (as an estimate of relative abundance)

```
#Not run
#install.packages(dplyr)
data.paras = data.frame(data.paras) %>%
dplyr::group_by(Capturesession,Genus) %>%
dplyr::summarise(count = dlyr::n()) %>%
dplyr::mutate(prop.zos = count / sum(count)) %>%
dplyr::left_join(data.paras) %>%
dplyr::ungroup() %>% dplyr::filter(Genus == 'Zosterops') %>%
dplyr::mutate(scale.prop.zos = as.vector(scale(prop.zos)))
data.paras <- data.paras[, c(12:15, 23)]
```

You can visualise the dataset to see how analysis data needs to be structured. In short, for (`family = "binomial"`

) models, node variable (i.e. species) occurrences should be included as binary variables (`1`

s and `0`

s) as the `n_nodes`

left-most variables in `data`

. Note that Gaussian continuous variables (`family = "gaussian"`

) and Poisson non-negative counts (`family = "poisson"`

) are also supported in `MRFcov`

. Any covariates can be included as the right-most variables. It is recommended that these covariates all be on a similar scale, ideally using the `scale`

function for continuous covariates (or similar) so that covariates have roughly `mean = 0`

and `sd = 1`

, as this makes LASSO variable selection and comparisons of effect sizes very straightforward

```
help("Bird.parasites")
View(Bird.parasites)
```

We first test for interactions using a Markov Random Fields (MRF) model without covariates. We set `n_nodes`

as the number of species to be represented in the graphical model (`4`

). We also need to specify the family for the model (`binomial`

in this case). We do not specify the level of penalisation used by the LASSO algorithm. Instead, this is optimised separately for each species through cross validation (using function `cv.glmnet`

in the `glmnet`

package). This ensures the log-likelihood of each species is properly maximised before unifying them into an undirected graph. Finally, it is important to note that for MRF model functions, we can specify the number of processing cores to split the job across (i.e. `n_cores`

). In this case we use 3 cores, but higher numbers *may* increase speed (if more cores are available). Check available cores using the `detectCores()`

function in the `parallel`

package

`MRF_fit <- MRFcov(data = Bird.parasites[, c(1:4)], n_nodes = 4, family = 'binomial')`

```
## Leave-one-out cv used for the following low-occurrence (rare) nodes:
## Microfilaria ...
## Fitting MRF models in sequence using 1 core ...
```

Plot the estimated interaction coefficients as a heatmap using `plotMRF_hm`

. Note that we can specify the names of nodes should we want to change them

```
plotMRF_hm(MRF_mod = MRF_fit, main = 'MRF (no covariates)',
node_names = c('H. zosteropis', 'H. killangoi',
'Plasmodium', 'Microfilaria'))
```

We can now run a Conditional Random Fields (CRF) model using the provided continuous covariate (`scale.prop.zos`

). Again, each species’ regression is optimised separately using LASSO regularization. Note that any columns in `data`

to the right of column `n_nodes`

will be presumed to represent covariates if we don’t specify an `n_covariates`

argument

`MRF_mod <- MRFcov(data = Bird.parasites, n_nodes = 4, family = 'binomial')`

```
## Leave-one-out cv used for the following low-occurrence (rare) nodes:
## Microfilaria ...
## Fitting MRF models in sequence using 1 core ...
```

Visualise the estimated species interaction coefficients as a heatmap. These represent predicted interactions when the covariate is set to its mean (i.e. in this case, when `scale.prop.zos = 0`

). If we had included other covariates, then this graph would represent interactions predicted when *all* covariates were set at their means

`plotMRF_hm(MRF_mod = MRF_mod)`

Regression coefficients and their relative importances can be accessed as well. This call returns a matrix of the raw coefficient, as well as standardised coefficients (standardised by the `sd`

of the covariate). Standardisation in this way helps to compare the relative influences of each parameter on the target species’ occurrence probability, but in general the two coefficients will be identical (unless users have not pre-scaled their covariates). The list also contains contains each variable’s relative importance (calculated using the formula `B^2 / sum(B^2)`

, where the vector of `B`

s represents regression coefficients for predictor variables). Variables with an underscore (`_`

) indicate an interaction between a covariate and another node, suggesting that conditional dependencies of the two nodes vary across environmental gradients. Because of this, it is recommended to avoid using column names with `_`

in them

`MRF_mod$key_coefs$Hzosteropis`

```
## Variable Rel_importance Standardised_coef Raw_coef
## 1 Hkillangoi 0.67848980 -2.4824213 -2.4824213
## 5 scale.prop.zos_Microfilaria 0.12246787 -1.0546659 -1.0546659
## 4 scale.prop.zos 0.09272597 -0.9177080 -0.9177080
## 3 Microfilaria 0.09161539 0.9121958 0.9121958
## 2 Plas 0.01164506 -0.3252181 -0.3252181
```

Finally, a useful capability is to generate some fake data and test predictions. For instance, say we want to know how frequently malaria parasite infections are predicted to occur in sites with high occurrence of microfilaria

```
fake.dat <- Bird.parasites
fake.dat$Microfilaria <- rbinom(nrow(Bird.parasites), 1, 0.8)
fake.preds <- predict_MRF(data = fake.dat, MRF_mod = MRF_mod)
```

The returned object from `predict_MRF`

depends on the family of the model. For `family = "binomial"`

, we get a list including both linear prediction probabilities and binary predictions (where a linear prediction probability `> 0.5`

equates to a binary prediction of `1`

). These binary predictions can be used to estimate parasite prevalence

```
H.zos.pred.prev <- sum(fake.preds$Binary_predictions[, 'Hzosteropis']) / nrow(fake.preds$Binary_predictions)
Plas.pred.prev <- sum(fake.preds$Binary_predictions[, 'Plas']) / nrow(fake.preds$Binary_predictions)
Plas.pred.prev
```

`## [1] 0.3474388`

A key step in the process of model exploration is to determine whether inclusion of covariates actually improves model fit and is warranted when estimating interaction parameters. This is straightforward for binomial models, as we can compare classification accuracy quickly and easily. The `cv_diag`

functions will fit models and then determine their predictive performances against the supplied data. We can also compare MRF and CRF models directly to determine whether covariates are warranted. For this dataset, considering that parasite infections are quite rare, we are primarily interested in maximising model Sensitivity (capacity to successfully predict positive infections)

```
mod_fits <- cv_MRF_diag_rep(data = Bird.parasites, n_nodes = 4,
n_cores = 1, family = 'binomial', plot = F,
compare_null = T,
n_folds = 10)
```

```
## Generating node-optimised Conditional Random Fields model
## Leave-one-out cv used for the following low-occurrence (rare) nodes:
## Microfilaria ...
## Fitting MRF models in sequence using 1 core ...
##
## Generating Markov Random Fields model (no covariates)
## Leave-one-out cv used for the following low-occurrence (rare) nodes:
## Microfilaria ...
## Fitting MRF models in sequence using 1 core ...
##
## Calculating model predictions of the supplied data
## Generating CRF predictions ...
## Generating null MRF predictions ...
##
## Calculating predictive performance across test folds using cross-validation
## Processing cross-validation run 1 of 10 ...
## Processing cross-validation run 2 of 10 ...
## Processing cross-validation run 3 of 10 ...
## Processing cross-validation run 4 of 10 ...
## Processing cross-validation run 5 of 10 ...
## Processing cross-validation run 6 of 10 ...
## Processing cross-validation run 7 of 10 ...
## Processing cross-validation run 8 of 10 ...
## Processing cross-validation run 9 of 10 ...
## Processing cross-validation run 10 of 10 ...
```

```
# CRF (with covariates) model sensitivity
quantile(mod_fits$mean_sensitivity[mod_fits$model == 'CRF'], probs = c(0.05, 0.95))
```

```
## 5% 95%
## 0.1394547 0.4288095
```

```
# MRF (no covariates) model sensitivity
quantile(mod_fits$mean_sensitivity[mod_fits$model != 'CRF'], probs = c(0.05, 0.95))
```

```
## 5% 95%
## 0.03992308 0.25705128
```

We now may want to fit models to bootstrapped subsets of the data to account for parameter uncertainty. Users can change the proportion of observations to include in each bootstrap run with the `sample_prop`

option.

`booted_MRF <- bootstrap_MRF(data = Bird.parasites, n_nodes = 4, family = 'binomial', n_bootstraps = 10, n_cores = 1)`

`## Fitting bootstrap_MRF models in sequence using 1 core...`

Finally, we can explore regression coefficients to get a better understanding of just how important interactions are for predicting species’ occurrence probabilities (in comparison to other covariates). This is perhaps the strongest property of CRFs, as comparing the relative importances of interactions and fixed covariates using competing methods (such as Joint Species Distribution Models) is difficult. The `bootstrap_MRF`

function conveniently returns a matrix of important coefficients for each node in the graph, as well as their relative importances

`booted_MRF$mean_key_coefs$Hzosteropis`

```
## Variable Rel_importance Mean_coef
## 1 Hkillangoi 0.67783974 -2.4782524
## 5 scale.prop.zos_Microfilaria 0.12000013 -1.0427324
## 3 Microfilaria 0.09211903 0.9136013
## 4 scale.prop.zos 0.09031224 -0.9045974
## 2 Plas 0.01253180 -0.3369681
```

`booted_MRF$mean_key_coefs$Hkillangoi`

```
## Variable Rel_importance Mean_coef
## 1 Hzosteropis 0.79433285 -2.4782524
## 2 Microfilaria 0.11960179 -0.9616413
## 3 scale.prop.zos 0.08189808 -0.7957582
```

`booted_MRF$mean_key_coefs$Plas`

```
## Variable Rel_importance Mean_coef
## 2 Microfilaria 0.64679308 1.5817547
## 3 scale.prop.zos 0.26040862 -1.0036543
## 4 scale.prop.zos_Microfilaria 0.05472223 0.4600853
## 1 Hzosteropis 0.02935381 -0.3369681
```

`booted_MRF$mean_key_coefs$Microfilaria`

```
## Variable Rel_importance Mean_coef
## 3 Plas 0.36735946 1.5817547
## 4 scale.prop.zos 0.18357896 -1.1181627
## 5 scale.prop.zos_Hzosteropis 0.15964624 -1.0427324
## 2 Hkillangoi 0.13578105 -0.9616413
## 1 Hzosteropis 0.12255367 0.9136013
## 6 scale.prop.zos_Plas 0.03108062 0.4600853
```

Users can also use the `predict_MRFnetworks`

function to calculate network statistics for each node in each observation or to generate adjacency matrices for each observation. By default, this function generates a list of `igraph`

adjacency matrices, one for each row in `data`

, which can be used to make network plots using a host of other packages. Note, both this function and the `predict_MRF`

function rely on `data`

that has a structure exactly matching to the data that was used to fit the model. In other words, the column names and column order need to be identical. The `cutoff`

argument is important for binary problems, as this specifies the probability threshold for stating whether or not a species should be considered present at a site (and thus, whether their interactions will be present). Here, we state that a predicted occurrence above `0.33`

is sufficient

```
adj_mats <- predict_MRFnetworks(data = Bird.parasites,
MRF_mod = booted_MRF,
metric = 'eigencentrality',
cutoff = 0.33)
colnames(adj_mats) <- colnames(Bird.parasites[, 1:4])
apply(adj_mats, 2, summary)
```

```
## Hzosteropis Hkillangoi Plas Microfilaria
## Min. 0.0000 0.00000 0.0000 0.00000
## 1st Qu. 0.0000 0.00000 0.0000 0.00000
## Median 0.0000 0.00000 0.0000 0.00000
## Mean 0.1826 0.05791 0.2062 0.08909
## 3rd Qu. 0.4774 0.00000 0.1633 0.00000
## Max. 1.0000 1.00000 1.0000 1.00000
```

Lastly, `MRFcov`

has the capability to account for possible spatial autocorrelation when estimating interaction parameters. To do this, we incorporate functions from the `mgcv`

package to include smoothed Gaussian process spatial regression splines in each node-wise regression. The user must supply a two-column `data.frame`

called `coords`

, which will ideally contain Latitude and Longitude values for each row in `data`

. We don’t have these coordinates for the `Bird.parasites`

dataset, so we will instead create some fake coordinates to showcase the model. Note, these commands were not run here, but feel free to move through them as you did for the above examples

```
Latitude <- sample(seq(120, 140, length.out = 100), nrow(Bird.parasites), TRUE)
Longitude <- sample(seq(-19, -22, length.out = 100), nrow(Bird.parasites), TRUE)
coords <- data.frame(Latitude = Latitude, Longitude = Longitude)
```

The syntax for the `MRFcov_spatial`

function is nearly identical to `MRFcov`

, with the exception that `coords`

must be supplied

```
CRFmod_spatial <- MRFcov_spatial(data = Bird.parasites, n_nodes = 4,
family = 'binomial', coords = coords)
```

Interpretation is also identical to `MRFcov`

objects. Here, key coefficients are those that are retained *after* accounting for spatial influences

`CRFmod_spatial$key_coefs$Hzosteropis`

Finally, we can compare fits of spatial and non-spatial models just as we did for MRFs and CRFs above

```
cv_MRF_diag_rep_spatial(data = Bird.parasites, n_nodes = 4,
n_cores = 3, family = 'binomial', plot = T, compare_null = T,
coords = coords)
```