---
title: "netdiffuseR showcase: Medical Innovations"
author: "George G. Vega Yon"
date: "February 24, 2016"
output: rmarkdown::html_vignette
header-includes: \usepackage{graphicx}
vignette: >
  %\VignetteIndexEntry{netdiffuseR showcase: Medical Innovations}
  %\VignetteEngine{knitr::rmarkdown}
  %\usepackage[utf8]{inputenc}
---

```{r Setup, echo=FALSE, message=FALSE, warning=FALSE}
library(knitr)
opts_chunk$set(out.width = 600, fig.align = "center", fig.width = 7, fig.height = 7) 
```

# Data preprocessing

Loading the raw dataset from the package[^diffnetdata].

[^diffnetdata]: Note that there is a `diffnet` version of the same dataset in the package, `medInnovationsDiffNet`.

```{r Loading pkgs and reading the data}
library(netdiffuseR)
data(medInnovations)
```

Now that we have the data in R, we can start working with it, in particular, we want to do the following things:

- Create a unique id for each individual in the network.
- Remove unsurveyed individuals (we don't have additional covariates for them).
- Reshaping the data to long format (so we can use it as a panel), and furthermore, as an edgelist.

```{r Preparing data for netdiffuseR}
# Creating unique ids (including for the network data)
othervars <- c("id", "toa", "city")
netvars <- names(medInnovations)[grepl("^net", names(medInnovations))]
for (i in c("id", netvars))
  medInnovations[[i]] <- medInnovations[[i]] + medInnovations$city*1000

# Leaving unsurveyed individuals with NA
surveyed <- medInnovations$id
for (i in netvars)
  medInnovations[[i]][which(!(medInnovations[[i]] %in% surveyed))] <- NA

# Reshaping data (so we have an edgelist)
medInnovations.long <- reshape(
  medInnovations[,c(othervars, netvars)], v.names= "net",
  varying = netvars,
  timevar = "level", idvar="id", direction="long")
```


Once we have the data in long format, we can coerce it into an `diffnet` object. This is done by reading the edgelist, obtaining the times of adoption vector and applying the `as_diffnet` function.

```{r Importing data to netdiffuseR}
# Coersing the edgelist to an adjacency matrix. Here we are assuming that the
# network is constant through time.
graph <- with(
  medInnovations.long,
  edgelist_to_adjmat(cbind(id, net), t=18,undirected=FALSE, keep.isolates = TRUE)
)
```

Notice that we have included `keep.isolates=TRUE`, so, if any element of our edgelist had an `NA`, `NULL` or related value, it would still be included in the adjacency matrix. This is specially important if, for example, there are isolated nodes in the data, as if we had not set `keep.isolates=TRUE` those would had been discarded.

Now we can create our `diffnet` object. Notice that `medInnovations` happens to be sorted in the same way as the elements in the adjacency matrix. You can check this by accessing the `rownames` and sorting `medInnovations` in that order.

```{r}
# Just to be sure. Sorting the data!
orddata <- as.numeric(as.factor(rownames(graph[[1]])))
medInnovations <- medInnovations[orddata,]

# Creating a diffnet object
diffnet <- as_diffnet(graph, medInnovations$toa, 
                      vertex.static.attrs = subset(medInnovations, select=c(-id, -toa)))
```

# Methods

Once a `diffnet` object, we can apply the usual generic R functions:

```{r Checking-the-methods}
plot(diffnet, t=diffnet$meta$nper)
diffnet
summary(diffnet)
```

And the ones included in the package:

```{r graphs}
plot_diffnet(diffnet, slices=c(1,4,8,12,16,18))
plot_threshold(diffnet, undirected = FALSE, vertex.size = 1/5)
plot_adopters(diffnet)
plot_hazard(diffnet)
```

# Statistical test

Now, we want to know if the threshold model fits here. In order to do so we will use the structure dependency test built in the package, `struct_test`. We will apply this both in a aggregated level and by city. First we need to subset the data:

```{r Subsetting}
# Get cities ids so we can subset the vertices and run the test by city.
city <- diffnet$vertex.static.attrs[,"city"]

# Subsetting diffnet, notice that we can use either indices or ids to create a
# "subdiffnet". In this case we are using indices.
diffnet_city1 <- diffnet[which(city==1),]
diffnet_city2 <- diffnet[which(city==2),]
diffnet_city3 <- diffnet[which(city==3),]
diffnet_city4 <- diffnet[which(city==4),]
```

Notice that by subsetting the set of vertices we have created 4 new `diffnet` objects, so all the methods and functions work for each one of these, for example, threshold levels in each city

```{r Multithreshold}
oldpar <- par(no.readonly = TRUE)
par(mfrow=c(2,2))
plot_threshold(diffnet_city1, vertex.label = "", main="Threshold and ToA\nin City 1")
plot_threshold(diffnet_city2, vertex.label = "", main="Threshold and ToA\nin City 2")
plot_threshold(diffnet_city3, vertex.label = "", main="Threshold and ToA\nin City 3")
plot_threshold(diffnet_city4, vertex.label = "", main="Threshold and ToA\nin City 4")
par(oldpar)
```

```{r}
plot_infectsuscep(diffnet_city1, K=5, logscale = TRUE, bins=30)
```


Now we run the test for each city. Observe that we can use the __parallel__ package to speedup the test as we will do in the first two cities using two cores (this is done thanks to the __boot__ package).

```{r Stat-test}
# Defining the statistic
avgthr <- function(x) mean(threshold(x), na.rm = TRUE)

# Running the test by city
test1   <- struct_test(diffnet_city1, avgthr, 500, ncpus=2, parallel="multicore")
test2   <- struct_test(diffnet_city2, avgthr, 500, ncpus=2, parallel="multicore")
test3   <- struct_test(diffnet_city3, avgthr, 500)
test4   <- struct_test(diffnet_city4, avgthr, 500)

# Running the test aggregated
testall <- struct_test(diffnet, avgthr, 500, ncpus=2, parallel="multicore")

# Printing the outcomes
test1
test2
test3
test4
testall
```

This shows in no City threshold seems to be struture dependent, as after simulating 1,000 networks by rewiring each one of these preserving the degree sequence (using `algorithm = "swap"` by default in the `rewire.args`) the null can't be rejected. Now we can make an histogram of the outcomes by city:

```{r Histograms}
# To make it nicer, we change the parameters in using par
# (see ?par)
oldpar <- par(no.readonly = TRUE)
par(mfrow=c(2,2))

# Now we use the hist method for the -diffnet_boot- class
hist(test1, main="Distribution of Statistic on rewired\nnetwork (City 1)", ask = FALSE)
hist(test2, main="Distribution of Statistic on rewired\nnetwork (City 2)", ask = FALSE)
hist(test3, main="Distribution of Statistic on rewired\nnetwork (City 3)", ask = FALSE)
hist(test4, main="Distribution of Statistic on rewired\nnetwork (City 4)", ask = FALSE)

# Returning to the previous graphical parameters
par(oldpar)
```

# Retrieving the data to create a panel/envent history/longitudinal data

To use the data for statistical models we can retrieve the data stored in the `diffnet` object and coerce it as a `data.frame`. First, we will compute __lagged__ exposure at each time period and add it as a dynamic vertex attribute, including a dummy variable called `adopted` equal to 1 if the individual adopted at that time point.

```{r Computing-exposure}
# Calculating lagged exposure
expo <- exposure(diffnet, lags = 1L)
head(expo)

# Netdiffuser automatically identifies whether the input is dynamic or not.
diffnet[["lagged_expo"]] <- expo
diffnet[["adopted"]]  <- toa_mat(diffnet)$cumadopt
```

Now we can create a data frame from our `diffnet` object

```{r Creating the diffnet model}
# Getting the data
mydata <- as.data.frame(diffnet)
```

The following model illustrates how can we use netdiffuseR to run a lagged exposure model. In this (toy) model we are including fixed effects for time (`per`), `city`, belief in science (`belief`) and age, and only including observations prior to the adoption of the behavior, and excluding observations from the last time point.


```{r Running the model}
# Running a model
summary(
  glm(adopted ~ lagged_expo + factor(per) + factor(city) + belief + 
        proage + I(proage^2),
      dat    = mydata, 
      subset = (per <= toa) & per < 18,
      family = binomial(link="logit"))
)
```

As shown, we find no lagged exposure effects and the adoption was mainly drive by belief in science and age of the MD.



