%\VignetteIndexEntry{2. Interface tutorial} %\VignetteKeywords{user interface} %\VignettePackage{BioNetStat} %\VignetteEngine{knitr::knitr}

# BioNetStat background

The diversity of interactions that occurs in biological systems from the cells and organelles to the whole biosphere, can be assessed with tools of the networks theory. The dynamic in structure and in the interactions among elements is an inherent trait of those systems. Several tools have been proposed to compare networks, representing the many states assumed by a system. However, until the present, none of them is able to compare structural characteristics among more than two networks simultaneously. Due to the many states that can be assumed by a given biological system, we developed a statistical tool to compare two or more networks and point key variables in a system. BioNetStat is able to compare correlation networks built from gene expression data, metabolites concentrations or any kind of variables that could be statistically correlated, considering a previous data preprocessing. The networks comparison is based on graph spectra (the group of eigenvalues in an adjacency matrix), such as the spectral distribution. This measure is associated with several structural characteristics of networks such as the number of walks, diameter, and clicks. In addition to the spectral distribution, BioNetStat can also compare networks by using spectral entropy, degree distribution, and nodes centralities. Until now the BioNetStat theoretical base is available only in the master dissertation, in Portuguese. The paper is under production and will be posted here as soon as possible.

# BioNetStat user interface tutorial

Being R and BioNetStat installed, as showed in README, you have just open R and run the following commands.

    library(devtools)
    library(shiny)
    library(BioNetStat)
    runBioNetStat()

## First screen

When you start BioNetStat you will see this image.

If you are using Rstudio an alternative window will open, therefore BNS will performs well when is used in browser. So, hit “open in browser” in the upper left of the screen and the BNS will open in browser as the first picture.

## Loading the files

By clicking on the 'Browse ..' icon in section 1 (Load data) a window will open for the table of variables values to be selected.

In this tutorial the file to be selected is bnsDataTest. The file will load and the software will identify the colunms classified as “numeric” by R. A previous view of table is showed on the screen. In addition, a 'Factors' section will recognize which columns are rated as 'factor' by R. In this section you can select the factors that will be used to select the states (treatments, conditions) compared, each state will be a network to be compared. The selection of states can be done in 'Choose the conditions to be compared:'

The tutorial to build your table of variables values is here.

After selecting the variable values table, it is possible to load the file 'variable group' (optional) into 'Variable set database'. In our tutorial the selected file is c2.cp.v5.2.symbols.gmt that sets the groups of variables according to the metabolic pathways which they are associated. If the user does not load any files, the program will compare the networks with all variables loaded in the file 'Variables values data'

The tutorial to build your table of variables groups is here.

## Parameters setting

After load input files, you migth set the parameters to network construction: 1. Lower and higher numbers of variables (nodes) that will be in the networks compared in 'Variable sets size range'. The program returns the number of sets of variables that are between these values (figure above). 2. Dependency measure used to infer the correlation network. 3. Association strength that will be used as the threshold for the formation of an edge between two nodes and which threshold value is used. 4. Type of network to be built, with or without weight on the edges. In the case of nets with weight, which measure of association will be used as edge weight.

1. Networks comparison method. If the spectral or degree distribution were used to compare the networks it is necessary to set the method to set the bandwith (“Silveram” or “Sturges” are aviable).
2. Number of permutations and if a seed will be used on the resampling method also could be used.

## Runnig the differential network analysis

After loading the files and selecting the analysis parameters, click on 'Start analysis' to compare the networks.

## Results

1. While the analysis is performed, this warning is shown:

1. When the analysis is finished the program will show the parameters used to perform the analysis.

1. The final table is shown as in the following figure:

### Node differential analysis

1. It is also possible to compare the importance of nodes. In the 'Further analysis' tab you migth select the groups of variables according to a threshold criteria. The group of variables is chosen and the program will generate the nodes comparison by degree centrality.

1. When the table appear, it is possible to select other structural properties to compare the nodes importance. The diferential node analysis table is shown as in the following figure:

#### Node analysis

### KEGG pathway visualization

1. Another available functionality is to observe the variables in the metabolic pathways of the database KEGG, which allow you to know more in depth the metabolic pathways that the studied variables are related.

you need to insert a table that contains two columns, where the first one must be the names of the variables you are studying and the second one is the respective KEGG code of these variables. The KEGG codes can be found on KEGG's website. In addition to the table with the codes of the variables should be chosen the color used in the draw, if the variables studied are genes/proteins or metabolites. The variables that will appear in the figure are the same ones analyzed in the differential analysis table of the node and they can be filtered or according to the value of the test or the pvalor or the qvalue associated with it. It is necessary to choose which metabolic pathway will be used to produce the visualization and in which Species.

On the map KEGG, you will notice one that the rectangles or the circles are divided into columns, representing the treatments you chose to compare. The intensity of the colors is relative to the values of centralities chosen according to the legend. here is an example of a map constructed with genes from the pathway in cancer (05200) of kegg, for humans (“hsa”).

When clicking the button to save it is necessary to wait for the program to download the map, save it in the “Downloads” directory in a compressed file. The view is inside the compressed file.

### Network visualization

Visualizing networks helps us understand the changing patterns more easily. This visualization can be done in several ways and some of them are available in BioNetStat in the “Network visualization plots” tab. As several states can be compared by the BNS in this section you need to choose only two of them to be viewed and compared each time.

1. The first way to visualize the networks is in the form of heatmaps of the adjacency matrices (matrix representing the network). initially the user can choose the parameters (color, shape and size) for the construction of the figure and then you can view the networks of the selected states.

1. The networks produced can be compared through global structural properties such as network spectral entropy or middle degree centrality:

1. The difference matrix allows to analyze for all pairs of variables how their relation changes between states.

1. The list of associations between the variables does not allow us to have a more precise idea of the differences between the forces of association in the two states.

1. Finally, the network can be exported to the biological integration program S.I.T. (System Integration Tool) where the network can be viewed and manipulated.

### Study the behavior of variables

BioNetStat also provides a study of the behavior of the variables so that the user can have a complete view of their object of study. 1. Initially the variables can be explored through the construction of a heatmap where the parameters of the figure are selected. In the columns are the samples with the colors indicating to which state each sample belongs. It is possible to group both the columns (samples) and the lines (variables) of the heatmap in the section “heatmap cluster options”.

1. In the KEGG database maps, we can also observe gene expressions, protein concentrations and metabolites. In “KEGG pathway visualization” the user must enter the variables code, a table that contains two columns, where in the first should be the names of the variables that you are studying and in the second the respective KEGG code of these variables. These codes can be found on the KEGG website itself. The variables that will appear in the figure are the same ones analyzed in the differential analysis table of the vertex and they can be filtered or according to the value of the test or the pvalor or the value associated with it. In the figure will be shown a value that will represent all the samples of each state, which can be the average, the median, the minimum or the maximum. It is necessary to choose which metabolic pathway will be used to produce the visualization and in which Species.

On the map KEGG, you will notice one that the rectangles or the circles are divided into columns, representing the treatments you chose to compare. The intensity of the colors is relative to the values of centralities chosen according to the legend. here is an example of a map constructed with genes from the pathway in cancer (05200) of kegg, for humans (“hsa”).

When clicking the button to save it is necessary to wait for the program to download the map, save it in the “Downloads” directory in a compressed file. The view is inside the compressed file.

1. BioNetStat provides a statistical test to verify the change in the behavior of the variables between the states (test t, for two states, and ANOVA, for more than two, with the respective non-parametric tests). The results are presented in the table as follows:

1. Finally, the last analysis available in BioNetStat is the visualization of the values of a given variable in a boxplot graph. Where initially the user must choose the parameters of the figure and the variable that will be displayed.