run_clr: Wrapper for CLR method

In dnapath: Differential Network Analysis using Gene Pathways

Wrapper for CLR method

Description

Conducts co-expression analysis using CLR \insertCitefaith07dnapath. Uses the implementation from the minet package \insertCitemeyer08dnapath. Can be used for the network_inference argument in dnapath.

Usage

run_clr(x, weights = NULL, estimator = "spearman", ...)

Arguments

x	A n by p matrix of gene expression data (n samples and p genes).
weights	An optional vector of weights. This is used by dnapath() to apply the probabilistic group labels to each observation when estimating the group-specific network.
estimator	Argument is passed into build.mim.
...	Additional arguments are ignored.

Value

A p by p matrix of association scores.

References

\insertRef

faith07dnapath

\insertRef

meyer08dnapath

See Also

run_aracne, run_bc3net, run_c3net, run_corr, run_dwlasso, run_genie3, run_glasso, run_mrnet, run_pcor, and run_silencer

Examples

data(meso)
data(p53_pathways)

# To create a short example, we subset on two pathways from the p53 pathway list,
# and will only run 5 permutations for significance testing.
pathway_list <- p53_pathways[c(8, 13)]
n_perm <- 5

# Use this method to perform differential network analysis.
# The parameters in run_clr() can be adjusted using the ... argument.
# For example, the 'estimator' paramter can be specified as shown here.
results <- dnapath(x = meso$gene_expression,
                   pathway_list = pathway_list,
                   group_labels = meso$groups,
                   n_perm = n_perm,
                   network_inference = run_clr,
                   estimator = "spearman")
summary(results)

# The group-specific association matrices can be extracted using get_networks().
nw_list <- get_networks(results[[1]]) # Get networks for pathway 1.


# nw_list has length 2 and contains the inferred networks for the two groups.
# The gene names are the Entrezgene IDs from the original expression dataset.
# Renaming the genes in the dnapath results to rename those in the networks.
# NOTE: The temporary directory, tempdir(), is used in this example. In practice,
#       this argument can be removed or changed to an existing directory
results <- rename_genes(results, to = "symbol", species = "human",
                        dir_save = tempdir())
nw_list <- get_networks(results[[1]]) # The genes (columns) will have new names.

# (Optional) Plot the network using SeqNet package (based on igraph plotting).
# First rename entrezgene IDs into gene symbols.
SeqNet::plot_network(nw_list[[1]])

dnapath documentation built on May 9, 2022, 9:05 a.m.