model_evaluation_optimization will take as input a setting of parameters (data source weights and hyperparameters) and layer-specific networks to construct a ligand-target matrix and evaluate its performance on input validation settings (average performance for both target gene prediction and ligand activity prediction, as measured via the auroc and aupr).
model_evaluation_optimization(x, source_names, algorithm, correct_topology, lr_network, sig_network, gr_network, settings, secondary_targets = FALSE, remove_direct_links = "no",damping_factor = NULL,...)A list containing parameter values for parameter optimization. $source_weights: numeric vector representing the weight for each data source; $lr_sig_hub: hub correction factor for the ligand-signaling network; $gr_hub: hub correction factor for the gene regulatory network; $damping_factor: damping factor in the PPR algorithm if using PPR and optionally $ltf_cutoff: the cutoff on the ligand-tf matrix. For more information about these parameters: see construct_ligand_target_matrix and apply_hub_correction.
Character vector containing the names of the data sources. The order of data source names accords to the order of weights in x$source_weights.
Selection of the algorithm to calculate ligand-tf signaling probability scores. Different options: "PPR" (personalized pagerank), "SPL" (shortest path length) and "direct"(just take weights of ligand-signaling network as ligand-tf weights). Default and recommended: PPR.
This parameter indicates whether the PPR-constructed ligand-target matrix will be subtracted by a PR-constructed target matrix. TRUE or FALSE.
A data frame / tibble containing ligand-receptor interactions (required columns: from, to, source)
A data frame / tibble containing signaling interactions (required columns: from, to, source)
A data frame / tibble containing gene regulatory interactions (required columns: from, to, source)
A list of lists for which each sub-list contains the following elements: .$name: name of the setting; .$from: name(s) of the ligand(s) active in the setting of interest; .$response: named logical vector indicating whether a target is a TRUE target of the possibly active ligand(s) or a FALSE.
Indicate whether a ligand-target matrix should be returned that explicitly includes putative secondary targets of a ligand (by means of an additional matrix multiplication step considering primary targets as possible regulators). Default: FALSE
Indicate whether direct ligand-target and receptor-target links in the gene regulatory network should be kept or not. "no": keep links; "ligand": remove direct ligand-target links; "ligand-receptor": remove both direct ligand-target and receptor-target links. Default: "no"
The value of the damping factor if damping factor is a fixed parameter and will not be optimized and thus not belong to x. Default NULL.
Additional arguments to make_discrete_ligand_target_matrix.
A numeric vector of length 4 containing the average auroc for target gene prediction, average aupr (corrected for TP fraction) for target gene prediction, average auroc for ligand activity prediction and average aupr for ligand activity prediction.
# NOT RUN {
library(dplyr)
nr_datasources = source_weights_df$source %>% unique() %>% length()
test_input = list("source_weights" = rep(0.5, times = nr_datasources), "lr_sig_hub" = 0.5, "gr_hub" = 0.5, "damping_factor" = 0.5)
# }
# NOT RUN {
# }
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