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The multiDEGGs package performs multi-omic differential network analysis by showing differential interactions between molecular entities (genes, proteins, miRNAs, or other biomolecules) across the omic datasets provided.

For each omic dataset, a differential network is constructed, where links represent statistically significant differential interactions between entities. These networks are then integrated into a comprehensive visualization using distinct colors to distinguish interactions from different omic layers.

This unified visualization allows interactive exploration of cross-omic patterns (e.g., differential interactions present at both transcript and protein level). For each link, users can access differential statistical significance metrics (p-values or adjusted p-values, calculated via robust or traditional linear regression with interaction term), and differential regression plots.

Installation

multiDEGGs can be installed from GitHub using devtools:

devtools::install_github("elisabettasciacca/multiDEGGs")

Getting Started

Let’s start by loading the package and sample data:

library(multiDEGGs)
data("synthetic_metadata")
data("synthetic_rnaseqData")
data("synthetic_proteomicData")
data("synthetic_OlinkData")

Generate Differential Networks

assayData_list <- list("RNAseq" = synthetic_rnaseqData,
                       "Proteomics" = synthetic_proteomicData,
                       "Olink" = synthetic_OlinkData)

deggs_object <- get_diffNetworks(assayData = assayData_list,
                                 metadata = synthetic_metadata,
                                 category_variable = "response",
                                 regression_method = "lm",
                                 padj_method = "bonferroni",
                                 verbose = FALSE,
                                 show_progressBar = FALSE,
                                 cores = 2)

Key Parameters of get_diffNetworks

It’s worth explaining some of the important parameters of get_diffNetworks:

  • assayData: accepts either a single normalized matrix/data frame (for single omic differential analysis), or a list of matrices/data frames (for multi-omic scenarios). For multi-omic analysis, it’s highly recommended to use a named list of data. If unnamed, sequential names (assayData1, assayData2, etc.) will be assigned to identify each matrix or data frame.

  • metadata: can also be a named factor vector, with names matching the patient IDs in column names of the assay data matrices/data frames. In that case, the category_variable can remain unset (NULL by default).

  • category_subset: this parameter can restrict the analysis to a certain subset of categories available in the metadata/category vector.

  • regression_method: set to "lm" by default because it is faster and highly recommended in machine learning scenarios, where the function might be repeatedly called many times. For basic differential analyses, "rlm" can also be used and may perform better in some cases.

  • percentile_vector: by default, molecular targets (genes, proteins, etc.) whose expression level is below the 35th percentile of the entire data matrix are excluded from the analysis. This threshold can be modified by specifying the percentile vector that is internally used for the percolation analysis. For example, to remove only targets below the 25th percentile, set percentile_vector = seq(0.25, 0.98, by = 0.05).

  • padj_method: the default method is Bonferroni. Storey’s q values often give more generous results but the qvalue package needs to be installed first.

NOTE: Not all patient IDs need to be present across datasets. Different numbers of samples per omic are acceptable. Only IDs whose data is available in the colnames of the assayData will be included in the analysis. Missing IDs will be listed in a message similar to:

The following samples IDs are missing in Proteomics: PT001, PT005, PT0030

Visualization

The deggs_object now contains the differential networks for each omic data in assayData_list. These networks can be integrated into a comprehensive visualization where different colors distinguish links from different omic layers.

View_diffNetworks(deggs_object)

This visualization interface allows you to:

  1. Navigate the networks associated with each patient category
  2. Filter by link significance
  3. Search for specific genes inside the network

 

 

Thicker links correspond to higher significant p-values.
The direction of the arrows shows the relationship direction reported in literature, not derived from the data.

The user can visualize differential regression plots by clicking on a link:

 

 

Single node differential expressions can also be visualized by clicking on the nodes:

 

 

NOTE: For multi-omic scenarios, the data from the first matrix in the list passed to assayData will be used for this boxplot.

List All Differential Interactions

Outside of the interactive environment, the get_multiOmics_diffNetworks() function can be used to get a table of all differential interactions, ordered by p-value or adjusted p-value:

get_multiOmics_diffNetworks(deggs_object, sig_threshold = 0.05)
#> $`Non-responder`
#>                  from       to      p.value        p.adj      layer
#> TNF-TNFRSF1A      TNF TNFRSF1A 3.325023e-04 1.330009e-03     RNAseq
#> IL1B-IL1R2       IL1B    IL1R2 5.389195e-04 2.155678e-03     RNAseq
#> TGFB3-TGFBR1    TGFB3   TGFBR1 5.329071e-15 2.131628e-14     RNAseq
#> AKT2-MTOR        AKT2     MTOR 4.347083e-04 1.738833e-03     RNAseq
#> FANCD2-FAN1    FANCD2     FAN1 4.440892e-16 3.552714e-15 Proteomics
#> GNG12-RASA2     GNG12    RASA2 0.000000e+00 0.000000e+00 Proteomics
#> RASGRP3-RRAS  RASGRP3     RRAS 2.202344e-04 1.761875e-03 Proteomics
#> TNF-TNFRSF1A1     TNF TNFRSF1A 0.000000e+00 0.000000e+00 Proteomics
#> RASGRP1-RAP1A RASGRP1    RAP1A 2.840564e-03 2.272452e-02 Proteomics
#> 
#> $Responder
#>                from    to      p.value        p.adj  layer
#> FANCD2-FAN1  FANCD2  FAN1 0.000000e+00 0.000000e+00 RNAseq
#> FASLG-FAS     FASLG   FAS 6.947839e-07 2.084352e-06 RNAseq
#> MAP2K2-MAPK3 MAP2K2 MAPK3 1.153300e-12 3.459899e-12 RNAseq

For single omic scenarios, use the get_sig_deggs() function:

deggs_object_oneOmic <- get_diffNetworks(assayData = synthetic_rnaseqData,
                                 metadata = synthetic_metadata,
                                 category_variable = "response",
                                 regression_method = "lm",
                                 padj_method = "bonferroni",
                                 verbose = FALSE,
                                 show_progressBar = FALSE,
                                 cores = 2)

get_sig_deggs(deggs_object_oneOmic, sig_threshold = 0.05)
#>                              from       to      p.value        p.adj
#> Non-responder.TNF-TNFRSF1A    TNF TNFRSF1A 3.325023e-04 1.330009e-03
#> Non-responder.IL1B-IL1R2     IL1B    IL1R2 5.389195e-04 2.155678e-03
#> Non-responder.TGFB3-TGFBR1  TGFB3   TGFBR1 5.329071e-15 2.131628e-14
#> Non-responder.AKT2-MTOR      AKT2     MTOR 4.347083e-04 1.738833e-03
#> Responder.FANCD2-FAN1      FANCD2     FAN1 0.000000e+00 0.000000e+00
#> Responder.FASLG-FAS         FASLG      FAS 6.947839e-07 2.084352e-06
#> Responder.MAP2K2-MAPK3     MAP2K2    MAPK3 1.153300e-12 3.459899e-12

Differential Regression Plots

To plot the differential regression fits outside of the interactive environment, use plot_regressions() specifying the omic data to be used and the two targets:

plot_regressions(deggs_object,
                 assayDataName = "RNAseq",
                 gene_A = "MTOR", 
                 gene_B = "AKT2",
                 legend_position = "bottomright")

In single omic analyses, the assayDataName parameter can remain unset.

Differential Network Analysis with More Than Two Groups

It’s possible to compare differential interactions among more than two categorical groups. All steps described above stay the same;
the dropdown menu of the interactive environment will show all available categories:

while regressions and boxplots will show all categories:

The statistical significance of the interaction term is calculated via one-way ANOVA in this case.
We highly recommend to have at least 4 or 5 observations per group.

Using multiDEGGs for Feature Selection in Machine Learning with nestedCV

Detecting differentially expressed interactions is useful for gaining insights into molecular dysregulations affecting certain conditions. This information can also be leveraged to train predictive models for the category of interest.

While some models, such as glmnet, allow for sparsity and have built-in variable selection, many models fail to fit when given massive numbers of predictors, or perform poorly due to overfitting. In medicine, one of the common goals of predictive modeling is the development of diagnostic or biomarker tests, for which reducing the number of predictors is typically a practical necessity.
The differential molecular interactions found with multiDEGGs can be used to filter down the number of predictors.

However, filtering predictors on the whole dataset creates information leakage about the test set, leading to overly optimistic performance assessments (Vabalas et al., 2019).
Feature selection should be considered an integral part of a model, with selection performed only on training data. Then the selected features and accompanying model can be tested on hold-out test data without bias.

While most machine learning pipelines involve splitting data into training and testing cohorts (typically 2/3 and 1/3 respectively), medical datasets may be too small for this approach, resulting in accuracy determination problems, due to small test sets. Nested cross-validation (CV) provides a way to address this by maximizing use of the whole dataset for testing overall accuracy, while maintaining the split between training and testing.

As mentioned earlier, it is important that any filtering of predictors is performed within the CV loops to prevent test data information leakage. For this reason, we demonstrate how to use multiDEGGs in combination with the nestedCV package, where filtering can be applied to each outer CV training fold (see also the nestedCV vignette).

Modification of Predictors

The core idea behind multiDEGGs is that the interaction between two molecular entities can provide additional information beyond the expression of individual molecular entities. In machine learning terms, this suggests that combinations of certain predictors may carry more information than individual predictor data.

Therefore, we propose using multiDEGGs not only to select predictors involved in differential interactions but also to create new predictors based on combinations of the original ones. These relationships can be modeled by adding new predictors as combinations of pairs of original predictors (e.g., multiplication, ratio, etc.).

To evaluate the performance of the resulting trained model, these combined predictors must also be added to the test set. The nestedCV package allows integration of predictor modification into the CV loop, enabling modification of both training and test sets separately, avoiding data leakage.

The first step is to define a custom filtering function that extracts the differential nodes and links from the selected fold:

# Convert metadata into a named factor vector containing only the labels to 
# predict (to ensure compatibility with the nestedCV functions)
metadata_vector <- as.factor(synthetic_metadata[, "response"])

# Make sure the assay data you want to use for prediction is a matrix and
# transpose it, so features are in columns 
# (standard format for machine learning)
assayData <- as.matrix(t(synthetic_rnaseqData))

# NOTE: Make sure your vector is ALIGNED with assayData. 
# The order of the annotations in the metadata_vector must match the 
# samples in the rows of assayData

# Remove zero variance columns from data
assayData <- assayData[,apply(assayData, 2, var, na.rm=TRUE) != 0] 

# define a filtering function that extracts differential nodes and links
# using multiDEGGs:
DEGGs_modxy <- function(metadata, assayData, ...) {
  counts <- t(assayData)
  names(metadata_vector) <- rownames(assayData)
  
  deggs_object <- multiDEGGs::get_diffNetworks(
    assayData = counts,
    metadata = metadata_vector,
    percentile_vector = seq(0.25, 0.98, by = 0.05),
    use_qvalues = TRUE, 
    show_progressBar = FALSE,
    verbose = FALSE,
    cores = 1
  )
  
  pairs <- multiDEGGs::get_sig_deggs(deggs_object, 1, 0.05)
  
  # Take genes 2 by 2 from top pairs to lower ones
  keep_DEGGs <- unique(unlist(lapply(1:nrow(pairs), function(i) {
    row_n = c(pairs[i,1], pairs[i,2])
  })))
  
  # The following could be added if you want to set a maximum number of 
  # predictors to be selected: 
  # if (length(keep_DEGGs) > 50) {    # take only top 50 predictors 
  #   keep_DEGGs <- keep_DEGGs[1:50]
  #   pairs <- pairs[which(pairs$var1 %in% keep_DEGGs & 
  #                        pairs$var2 %in% keep_DEGGs), ]
  # }
  
  out <- list(keep_DEGGs = keep_DEGGs, pairs = pairs)
  class(out) <- "DEGGs_modxy"
  return(out)
}

Next, define a predict function that specifies how to modify the train and test set predictors based on the filtering:

# This custom predict function will add new columns to x (can be train or test)
predict.DEGGs_modxy <- function(DEGGs.object, newdata, filter = TRUE, 
                                interaction.type = "ratio",
                                sep = ":", ...) {
  if (length(DEGGs.object$keep) != 0) {
    pairs <- DEGGs.object$pairs
    x2a <- newdata[, pairs[, 1], drop = FALSE]
    x2b <- newdata[, pairs[, 2], drop = FALSE]
    
    if (interaction.type == "ratio") {
      x2 <- x2a/x2b
    } else {
      x2 <- x2a*x2b
    }
    
    colnames(x2) <- paste(colnames(x2a), colnames(x2b), sep = sep)
    
    if (filter) {
      keep <- DEGGs.object$keep[!is.na(DEGGs.object$keep)]
      x1 <- newdata[, keep]
      return(cbind(x1, x2))
    } else {
      return(cbind(newdata, x2))
    }
  }
  return(newdata)
}

Now you’re ready to train your model with glmnet or any other model available in the caret package:

library(nestedCV)

# Train a glmnet model
fitted_model <- nestcv.glmnet(
  y = metadata_vector, 
  x = assayData,
  filterFUN = NULL,
  filter_options = list(nfilter = 20),
  family = "binomial",
  alphaSet = seq(0.7, 1, 0.1),
  min_1se = 0,
  cv.cores = 1,
  modifyX_useY = TRUE,
  verbose = TRUE
)

# Train a random forest model
fitted_model <- nestcv.train(
  y = metadata_vector,
  x = assayData,
  method = "rf",
  n_outer_folds = 8,
  modifyX = "DEGGs_ttest_modxy",
  filter_options = list(nfilter = 20),
  modifyX_useY = TRUE,
  cv.cores = 4, 
  verbose = TRUE
)

The ROC curve can be easily plotted:

plot(fitted_model$roc, col = 'red')

Session Info

sessionInfo()
#> R version 4.4.2 (2024-10-31)
#> Platform: aarch64-apple-darwin20
#> Running under: macOS Sequoia 15.2
#> 
#> Matrix products: default
#> BLAS:   /Library/Frameworks/R.framework/Versions/4.4-arm64/Resources/lib/libRblas.0.dylib 
#> LAPACK: /Library/Frameworks/R.framework/Versions/4.4-arm64/Resources/lib/libRlapack.dylib;  LAPACK version 3.12.0
#> 
#> locale:
#> [1] C/en_US.UTF-8/en_US.UTF-8/C/en_US.UTF-8/en_US.UTF-8
#> 
#> time zone: Europe/Rome
#> tzcode source: internal
#> 
#> attached base packages:
#> [1] stats     graphics  grDevices utils     datasets  methods   base     
#> 
#> other attached packages:
#> [1] multiDEGGs_1.0.0
#> 
#> loaded via a namespace (and not attached):
#>  [1] digest_0.6.37     R6_2.6.1          fastmap_1.2.0     xfun_0.52        
#>  [5] magrittr_2.0.3    cachem_1.1.0      parallel_4.4.2    knitr_1.50       
#>  [9] htmltools_0.5.8.1 rmarkdown_2.29    lifecycle_1.0.4   cli_3.6.5        
#> [13] sfsmisc_1.1-20    sass_0.4.10       jquerylib_0.1.4   compiler_4.4.2   
#> [17] rstudioapi_0.17.1 tools_4.4.2       evaluate_1.0.3    bslib_0.9.0      
#> [21] yaml_2.3.10       rlang_1.1.6       jsonlite_2.0.0    MASS_7.3-65

Citation

citation("multiDEGGs")
#> To cite package 'multiDEGGs' in publications use:
#> 
#>   Sciacca E, et al. (2023). "DEGGs: An R package with shiny app for the
#>   identification of differentially expressed gene-gene interactions in
#>   high-Throughput sequencing data." _Bioinformatics_, *39*, btad192.
#>   doi:10.1093/bioinformatics/btad192
#>   <https://doi.org/10.1093/bioinformatics/btad192>.
#> 
#> A BibTeX entry for LaTeX users is
#> 
#>   @Article{,
#>     title = {DEGGs: An R package with shiny app for the identification of differentially expressed gene-gene interactions in high-Throughput sequencing data},
#>     author = {Elisabetta Sciacca and {et al.}},
#>     journal = {Bioinformatics},
#>     year = {2023},
#>     volume = {39},
#>     pages = {btad192},
#>     doi = {10.1093/bioinformatics/btad192},
#>   }

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They may not be fully stable and should be used with caution. We make no claims about them.
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