## ----include = FALSE---------------------------------------------------------- knitr::opts_chunk$set( collapse = TRUE, comment = "#>", fig.width = 7, fig.height = 7, fig.align = "center", eval = FALSE ) suppressPackageStartupMessages(library(pathfindR)) ## ----mmu_kegg----------------------------------------------------------------- # gsets_list <- get_gene_sets_list( # source = "KEGG", # org_code = "mmu" # ) ## ----KEGG_save---------------------------------------------------------------- # mmu_kegg_genes <- gsets_list$gene_sets # mmu_kegg_descriptions <- gsets_list$descriptions # # ## Save both as RDS files for later use # saveRDS(mmu_kegg_genes, "mmu_kegg_genes.RDS") # saveRDS(mmu_kegg_descriptions, "mmu_kegg_descriptions.RDS") ## ----KEGG_load---------------------------------------------------------------- # mmu_kegg_genes <- readRDS("mmu_kegg_genes.RDS") # mmu_kegg_descriptions <- readRDS("mmu_kegg_descriptions.RDS") ## ----process_PIN1------------------------------------------------------------- # ## Downloading the STRING PIN file to tempdir # url <- "https://stringdb-static.org/download/protein.links.v11.0/10090.protein.links.v11.0.txt.gz" # path2file <- file.path(tempdir(check = TRUE), "STRING.txt.gz") # download.file(url, path2file) # # ## read STRING pin file # mmu_string_df <- read.table(path2file, header = TRUE) # # ## filter using combined_score cut-off value of 800 # mmu_string_df <- mmu_string_df[mmu_string_df$combined_score >= 800, ] # # ## fix ids # mmu_string_pin <- data.frame( # Interactor_A = sub("^10090\\.", "", mmu_string_df$protein1), # Interactor_B = sub("^10090\\.", "", mmu_string_df$protein2) # ) # head(mmu_string_pin, 2) ## ----process_PIN2, eval=FALSE------------------------------------------------- # # library(biomaRt) # # mmu_ensembl <- useMart("ensembl", dataset = "mmusculus_gene_ensembl") # # converted <- getBM( # attributes = c("ensembl_peptide_id", "mgi_symbol"), # filters = "ensembl_peptide_id", # values = unique(unlist(mmu_string_pin)), # mart = mmu_ensembl # ) # mmu_string_pin$Interactor_A <- converted$mgi_symbol[match(mmu_string_pin$Interactor_A, converted$ensembl_peptide_id)] # mmu_string_pin$Interactor_B <- converted$mgi_symbol[match(mmu_string_pin$Interactor_B, converted$ensembl_peptide_id)] # mmu_string_pin <- mmu_string_pin[!is.na(mmu_string_pin$Interactor_A) & !is.na(mmu_string_pin$Interactor_B), ] # mmu_string_pin <- mmu_string_pin[mmu_string_pin$Interactor_A != "" & mmu_string_pin$Interactor_B != "", ] # # head(mmu_string_pin, 2) ## ----process_PIN3------------------------------------------------------------- # # remove self interactions # self_intr_cond <- mmu_string_pin$Interactor_A == mmu_string_pin$Interactor_B # mmu_string_pin <- mmu_string_pin[!self_intr_cond, ] # # # remove duplicated inteactions (including symmetric ones) # mmu_string_pin <- unique(t(apply(mmu_string_pin, 1, sort))) # this will return a matrix object # # mmu_string_pin <- data.frame( # A = mmu_string_pin[, 1], # pp = "pp", # B = mmu_string_pin[, 2] # ) ## ----process_PIN4------------------------------------------------------------- # path2SIF <- file.path(tempdir(), "mmusculusPIN.sif") # write.table(mmu_string_pin, # file = path2SIF, # col.names = FALSE, # row.names = FALSE, # sep = "\t", # quote = FALSE # ) # path2SIF <- normalizePath(path2SIF) ## ----mmu_input_df, eval=TRUE-------------------------------------------------- knitr::kable(head(example_mmu_input)) ## ----run---------------------------------------------------------------------- # example_mmu_output <- run_pathfindR( # input = example_mmu_input, # convert2alias = FALSE, # gene_sets = "Custom", # custom_genes = mmu_kegg_genes, # custom_descriptions = mmu_kegg_descriptions, # pin_name_path = path2SIF # ) ## ----enr_chart, echo=FALSE, eval=TRUE----------------------------------------- enrichment_chart(example_mmu_output) ## ----output, eval=TRUE-------------------------------------------------------- knitr::kable(example_mmu_output) ## ----run2--------------------------------------------------------------------- # example_mmu_output <- run_pathfindR( # input = example_mmu_input, # convert2alias = FALSE, # gene_sets = "mmu_KEGG", # pin_name_path = "mmu_STRING" # )