## ----style, echo=FALSE, results="asis", message=FALSE---------------------- BiocStyle::markdown() knitr::opts_chunk$set(tidy = FALSE, warning = FALSE, message = FALSE) ## ----echo=FALSE, results='hide', message=FALSE----------------------------- library(miRSM) ## ---- eval=TRUE, include=TRUE---------------------------------------------- data(BRCASampleData) ## ---- eval=TRUE, include=TRUE---------------------------------------------- modulegenes_WGCNA <- module_WGCNA(ceRExp[, seq_len(80)], mRExp[, seq_len(80)]) modulegenes_WGCNA ## ---- eval=FALSE, include=TRUE--------------------------------------------- # modulegenes_GFA <- module_GFA(ceRExp[seq_len(20), seq_len(15)], # mRExp[seq_len(20), seq_len(15)], # iter.max = 2600) # modulegenes_GFA ## ---- eval=TRUE, include=TRUE---------------------------------------------- modulegenes_igraph <- module_igraph(ceRExp[, seq_len(10)], mRExp[, seq_len(10)]) modulegenes_igraph ## ---- eval=TRUE, include=TRUE---------------------------------------------- modulegenes_ProNet <- module_ProNet(ceRExp[, seq_len(10)], mRExp[, seq_len(10)]) modulegenes_ProNet ## ---- eval=TRUE, include=TRUE---------------------------------------------- # Reimport NMF package to avoid conflicts with DelayedArray package library(NMF) modulegenes_NMF <- module_NMF(ceRExp[, seq_len(10)], mRExp[, seq_len(10)]) modulegenes_NMF ## ---- eval=TRUE, include=TRUE---------------------------------------------- modulegenes_biclust <- module_biclust(ceRExp[, seq_len(30)], mRExp[, seq_len(30)]) modulegenes_biclust ## ---- eval=TRUE, include=TRUE---------------------------------------------- modulegenes_igraph <- module_igraph(ceRExp[, seq_len(10)], mRExp[, seq_len(10)]) # Identify miRNA sponge modules using cannonical correlation (CC) miRSM_igraph_CC <- miRSM(miRExp, ceRExp, mRExp, miRTarget, modulegenes_igraph, nperms = 5, num_shared_miRNAs = 3, pvalue.cutoff = 0.05, method = "CC", CC.cutoff = 0.8) miRSM_igraph_CC ## ---- eval=FALSE, include=TRUE--------------------------------------------- # modulegenes_WGCNA <- module_WGCNA(ceRExp[, seq_len(150)], # mRExp[, seq_len(150)]) # # Identify miRNA sponge modules using cannonical correlation (CC) # miRSM_WGCNA_CC <- miRSM(miRExp, ceRExp, mRExp, miRTarget, # modulegenes_WGCNA, nperms = 5, # method = "CC") # miRSM_WGCNA_CC_genes <- miRSM_WGCNA_CC[[2]] # miRSM_WGCNA_CC_FEA <- module_FA(miRSM_WGCNA_CC_genes, # Analysis.type ="FEA") # miRSM_WGCNA_CC_DEA <- module_FA(miRSM_WGCNA_CC_genes, # Analysis.type = "DEA") ## -------------------------------------------------------------------------- sessionInfo()