diff --git a/inst/scripts/match-package-to-data-hub.R b/inst/scripts/match-package-to-data-hub.R index 1c7d701..9ad1ff2 100644 --- a/inst/scripts/match-package-to-data-hub.R +++ b/inst/scripts/match-package-to-data-hub.R @@ -1,9 +1,9 @@ #!/bin/R # Nicole Gay # 1/11/23 +# Updated 3/1/23 -library(MotrpacRatTraining6mo) -library(MotrpacRatTraining6moData) +library(MotrpacRatTraining6mo) # also attaches MotrpacRatTraining6moData library(data.table) secret = "it's a secret" secret2 = "it's also a secret" @@ -323,21 +323,79 @@ colors = rbindlist(color_list) colors[hex_colour == "white", hex_colour := "#FFFFFF"] write.table(colors, "~/Desktop/pass1b-06_color_codes.txt", col.names = TRUE, row.names = FALSE, quote = FALSE, sep="\t") -####### I LEFT OFF HERE -# TODO +#### Write text files for lists #### -# custom handling for lists/nested lists # "GENE_UNIVERSES" names(GENE_UNIVERSES) names(GENE_UNIVERSES$gene_symbol) names(GENE_UNIVERSES$gene_symbol$IMMUNO) +# for each ID type, one column per tissue and ome +for (id_type in names(GENE_UNIVERSES)){ + cols = list() # names: ome_tissue + row_ome = c() + row_tissue = c() + longest = 0 + for(ome in names(GENE_UNIVERSES[[id_type]])){ + for(tissue in names(GENE_UNIVERSES[[id_type]][[ome]])){ + label = sprintf("%s_%s", ome, tissue) + genes = GENE_UNIVERSES[[id_type]][[ome]][[tissue]] + genes = genes[order(genes)] + longest = max(longest, length(genes)) + row_ome = c(row_ome, ome) + row_tissue = c(row_tissue, tissue) + cols[[label]] = as.character(genes) + } + } + # now extend each list to longest + cols_filled = lapply(cols, function(x){ + c(x, rep(NA_character_, times=(longest-length(x)))) + }) + # now make it a data.table + dt = data.table::copy(cols_filled) + setDT(dt) + # add column headers + header = data.table(V1 = row_ome, V2 = row_tissue) + header = data.table(t(header)) + dt = rbindlist(list(header, dt), use.names=FALSE) + + write.table(dt, file=sprintf("~/Desktop/GENE_UNIVERSES_by_%s.txt",id_type), col.names=FALSE, row.names=FALSE, quote=FALSE, sep='\t') +} # "PATHWAY_PARENTS" - +head(names(PATHWAY_PARENTS)) +dt = data.table(PATHWAY_ID = names(PATHWAY_PARENTS), + PATHWAY_PARENTS = unname(unlist(PATHWAY_PARENTS))) +write.table(dt, file=sprintf("~/Desktop/PATHWAY_PARENTS.txt"), col.names=TRUE, row.names=FALSE, quote=FALSE, sep='\t') # "REPFDR_INPUTS" - +names(REPFDR_INPUTS) +for(f in names(REPFDR_INPUTS)){ + df = as.data.frame(REPFDR_INPUTS[[f]]) + if(!is.null(rownames(df)) & !'feature' %in% colnames(df)){ + df = cbind(feature=rownames(df), df) + } + write.table(df, file=sprintf("~/Desktop/REPFDR_INPUTS_%s.txt",f), col.names=TRUE, row.names=FALSE, quote=FALSE, sep='\t') +} # "REPFDR_RES" - +names(REPFDR_RES) +# repfdr_em_res +dt = data.table(cbind(data.table(feature=rownames(REPFDR_RES$repfdr_em_res$mat)), + REPFDR_RES$repfdr_em_res$mat)) +write.table(dt, file=sprintf("~/Desktop/REPFDR_RES_repfdr_em_res_matrix.txt"), col.names=TRUE, row.names=FALSE, quote=FALSE, sep='\t') + +dt = data.table(cbind(data.table(state=rownames(REPFDR_RES$repfdr_em_res$Pi)), + REPFDR_RES$repfdr_em_res$Pi)) +write.table(dt, file=sprintf("~/Desktop/REPFDR_RES_repfdr_em_res_Pi.txt"), col.names=TRUE, row.names=FALSE, quote=FALSE, sep='\t') + +# repfdr_clusters +dt = data.table(cbind(data.table(rowname=rownames(REPFDR_RES$repfdr_clusters)), + REPFDR_RES$repfdr_clusters)) +write.table(dt, file=sprintf("~/Desktop/REPFDR_RES_repfdr_clusters.txt"), col.names=TRUE, row.names=FALSE, quote=FALSE, sep='\t') + +# repfdr_clusters_str +# repfdr_clusters_pi +dt = data.table(cluster = names(REPFDR_RES$repfdr_clusters_pi), + pi = REPFDR_RES$repfdr_clusters_pi) +write.table(dt, file=sprintf("~/Desktop/REPFDR_RES_repfdr_clusters_pi.txt"), col.names=TRUE, row.names=FALSE, quote=FALSE, sep='\t')