1. StarBioTrek
  2. Commit 4cf423d85815d9fb0318d7b418fcc7b961a58067
Browse code

fix

claudiacava authored on 16/10/2017 14:29:48
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DESCRIPTION
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-Package: StarBioTrek
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-Type: Package
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-Title: StarBioTrek
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-Version: 1.3.1
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-Date: 06-05-2017
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-Author: Claudia Cava,
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-    Isabella Castiglioni
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-Maintainer: Claudia Cava <claudia.cava@ibfm.cnr.it>
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-Depends:
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-    R (>= 3.3)
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-Imports:
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-    SpidermiR,
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-	KEGGREST,
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-	org.Hs.eg.db,
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-	AnnotationDbi,
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-	e1071,
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-	ROCR,
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-	grDevices,
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-	igraph
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-Description: This tool StarBioTrek presents some methodologies to measure pathway activity and cross-talk among pathways integrating also the information of network data.
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-License: GPL (>= 3)
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-biocViews: GeneRegulation,
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-    Network,
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-	Pathways,
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-	KEGG
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-Suggests:
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-    BiocStyle,
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-    knitr,
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-    rmarkdown,
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-    testthat,
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-	devtools,
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-	roxygen2,
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-	qgraph,
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-	png,
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-	grid
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-VignetteBuilder: knitr
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-LazyData: true
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-URL: https://github.com/claudiacava/StarBioTrek
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-BugReports: https://github.com/claudiacava/StarBioTrek/issues
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-RoxygenNote: 6.0.1
NAMESPACE
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-# Generated by roxygen2: do not edit by hand
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-
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-export(GE_matrix)
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-export(SelectedSample)
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-export(average)
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-export(ds_score_crtlk)
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-export(euc_dist_crtlk)
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-export(getKEGGdata)
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-export(getNETdata)
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-export(list_path_net)
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-export(matrix_plot)
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-export(path_net)
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-export(plotting_cross_talk)
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-export(proc_path)
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-export(st_dv)
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-export(svm_classification)
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-importFrom(AnnotationDbi,as.list)
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-importFrom(AnnotationDbi,mappedkeys)
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-importFrom(KEGGREST,keggGet)
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-importFrom(KEGGREST,keggList)
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-importFrom(ROCR,performance)
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-importFrom(ROCR,prediction)
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-importFrom(SpidermiR,SpidermiRdownload_net)
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-importFrom(SpidermiR,SpidermiRprepare_NET)
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-importFrom(SpidermiR,SpidermiRquery_spec_networks)
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-importFrom(SpidermiR,SpidermiRquery_species)
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-importFrom(e1071,svm)
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-importFrom(e1071,tune)
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-importFrom(grDevices,rainbow)
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-importFrom(igraph,get.data.frame)
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-importFrom(igraph,graph.data.frame)
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-importFrom(igraph,induced.subgraph)
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-importFrom(org.Hs.eg.db,org.Hs.egSYMBOL2EG)
NEWS
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-  StarBioTrek
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-  FIRST VERSION - FEATURES
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-
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-* getKEGGdata	Searching by KEGG data.
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-* getNETdata	Searching by network data.
R/StarBioTrek.r
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-#' Download data
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-#'
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-#' StarBioTrek allows you to Download data of samples from StarBioTrek
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-#'
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-#' The functions you're likely to need from \pkg{StarBioTrek} is
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-#' \code{path_star}
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-#'Otherwise refer to the vignettes to see
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-#' how to format the documentation.
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-#'
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-#' @docType package
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-#' @name StarBioTrek
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-NULL
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-
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-#' Pathway data from KEGG
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-#' @docType data
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-#' @keywords internal
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-#' @name path
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-#' @format A data frame with rows and  variables
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-NULL
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-
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-#' network data
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-#' @docType data
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-#' @keywords internal
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-#' @name netw
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-#' @format A data frame with  rows and variables
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-NULL
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-
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-
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-
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-
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-#' TCGA data
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-#' @docType data
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-#' @keywords internal
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-#' @name Data_CANCER_normUQ_filt
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-#' @format A data frame with rows and variables
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-NULL
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-
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-#' Score Matrix of pairwise pathway using euclidean distance
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-#' @docType data
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-#' @keywords internal
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-#' @name score_euc_dist
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-#' @format A data frame with rows and variables
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-NULL
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-
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-#' TCGA data with normal samples
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-#' @docType data
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-#' @keywords internal
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-#' @name norm
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-#' @format A data frame with rows and variables
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-NULL
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-
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-#' TCGA data with tumour samples
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-#' @docType data
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-#' @keywords internal
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-#' @name tumo
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-#' @format A data frame with rows and variables
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-NULL
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-
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-#' A matrix of gene expression for pathways given by the user.
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-#' @docType data
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-#' @keywords internal
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-#' @name list_path_plot
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-#' @format A data frame with rows and variables
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-NULL
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\ No newline at end of file
R/getdata.R
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-#' @title Get human KEGG pathway data.
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-#' @description getKEGGdata creates a data frame with human KEGG pathway. Columns are the pathways and rows the genes inside those pathway
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-#' @param KEGG_path  variable
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-#' @export
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-#' @importFrom KEGGREST keggList keggGet
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-#' @importFrom org.Hs.eg.db org.Hs.egSYMBOL2EG
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-#' @importFrom AnnotationDbi mappedkeys as.list
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-#' @return dataframe with human pathway data
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-#' @examples
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-#' path<-getKEGGdata(KEGG_path="Transcript")
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-getKEGGdata<-function(KEGG_path){
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-if (KEGG_path=="Carb_met") {
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-  mer<-select_path_carb(Carbohydrate)
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-  c<-proc_path(mer)
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-  a<-c[[2]]
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-}
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-  if (KEGG_path=="Ener_met") {
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-    mer<-select_path_en(Energy)
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-    c<-proc_path(mer)
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-    a<-c[[2]]
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-  }
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-  if (KEGG_path=="Lip_met") {
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-    mer<-select_path_lip(Lipid)
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-    c<-proc_path(mer)
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-    a<-c[[2]]
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-  }
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-  if (KEGG_path=="Amn_met") {
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-    mer<-select_path_amn(Aminoacid)
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-    c<-proc_path(mer)
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-    a<-c[[2]]
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-  }
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-  if (KEGG_path=="Gly_bio_met") {
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-    mer<-select_path_gly(Glybio_met)
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-    c<-proc_path(mer)
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-    a<-c[[2]]
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-  }
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-  if (KEGG_path=="Cof_vit_met") {
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-    mer<-select_path_cofa(Cofa_vita_met)
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-    c<-proc_path(mer)
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-    a<-c[[2]]
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-  }
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-  if (KEGG_path=="Transcript") {
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-    mer<-select_path_transc(Transcription)
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-    c<-proc_path(mer)
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-    a<-c[[2]]
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-  }
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-  if (KEGG_path=="Transl") {
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-    mer<-select_path_transl(Translation)
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-    c<-proc_path(mer)
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-    a<-c[[2]]
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-  }
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-  if (KEGG_path=="Fold_degr") {
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-    mer<-select_path_fold(Folding_sorting_and_degradation)
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-    c<-proc_path(mer)
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-    a<-c[[2]]
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-  }
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-  if (KEGG_path=="Repl_repair") {
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-    mer<-select_path_repl(Replication_and_repair)
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-    c<-proc_path(mer)
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-    a<-c[[2]]
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-  }
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-  if (KEGG_path=="sign_transd") {
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-    mer<-select_path_sign(Signal_transduction)
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-    c<-proc_path(mer)
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-    a<-c[[2]]
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-  }
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-  if (KEGG_path=="sign_mol_int") {
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-    mer<-select_path_sign_mol(Signaling_molecules_and_interaction)
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-    c<-proc_path(mer)
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-    a<-c[[2]]
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-  }
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-  if (KEGG_path=="Transp_cat") {
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-    mer<-select_path_transp_ca(Transport_and_catabolism)
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-    c<-proc_path(mer)
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-    a<-c[[2]]
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-  }
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-  if (KEGG_path=="cell_grow_d") {
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-    mer<-select_path_cell_grow(Cell_growth_and_death)
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-    c<-proc_path(mer)
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-    a<-c[[2]]
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-  }
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-  if (KEGG_path=="cell_comm") {
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-    mer<-select_path_cell_comm(Cellular_community)
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-    c<-proc_path(mer)
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-    a<-c[[2]]
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-  }
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-  if (KEGG_path=="imm_syst") {
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-    mer<-select_path_imm_syst(Immune_system)
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-    c<-proc_path(mer)
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-    a<-c[[2]]
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-  }
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-  if (KEGG_path=="end_syst") {
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-    mer<-select_path_end_syst(Endocrine_system)
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-    c<-proc_path(mer)
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-    a<-c[[2]]
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-  }
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-  if (KEGG_path=="circ_syst") {
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-    mer<-select_path_circ_syst(Circulatory_system)
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-    c<-proc_path(mer)
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-    a<-c[[2]]
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-  }
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-  if (KEGG_path=="dig_syst") {
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-    mer<-select_path_dig_syst(Digestive_system)
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-    c<-proc_path(mer)
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-    a<-c[[2]]
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-  }
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-  if (KEGG_path=="exc_syst") {
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-    mer<-select_path_exc_syst(Excretory_system)
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-    c<-proc_path(mer)
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-    a<-c[[2]]
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-  }
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-  if (KEGG_path=="nerv_syst") {
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-    mer<-select_path_ner_syst(Nervous_system)
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-    c<-proc_path(mer)
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-    a<-c[[2]]
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-  }
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-  if (KEGG_path=="sens_syst") {
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-    mer<-select_path_sens_syst(Sensory_system)
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-    c<-proc_path(mer)
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-    a<-c[[2]]
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-  }
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-if (KEGG_path=="KEGG_path") {
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-  pathways.list <- keggList("pathway", "hsa")## returns the list of human pathways
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-pathway.codes <- sub("path:", "", names(pathways.list))
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-pathways.list<-list(pathways.list)
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-pathways.list<-pathways.list[lapply(pathways.list,length)!=0]
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-list_pathkeg<-do.call("cbind", pathways.list)
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-c<-list(pathway.codes,list_pathkeg)
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-a<-c[[2]]
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-
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-}
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-pathway.codes<-c[[1]]
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-genes.by.pathway <- sapply(pathway.codes,
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-                           function(pwid){
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-                             pw <- keggGet(pwid)
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-                             pw[[1]]$GENE[c(TRUE, FALSE)]
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-                           })
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-x <- org.Hs.egSYMBOL2EG
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-mapped_genes <- mappedkeys(x)
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-xx <- as.list(x[mapped_genes])
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-top3 <- matrix(0, length(xx), length(genes.by.pathway))
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-rownames(top3) <- names(xx)
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-colnames(top3)<- names(genes.by.pathway)
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-for (j in  1:length(xx)){
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-  for (k in  1:length(genes.by.pathway)){
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-    if (length(intersect(xx[[j]],genes.by.pathway[[k]])!=0)){
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-
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-      top3[j,k]<-names(xx[j])
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-    }
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-  }
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-}
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-top3[top3 == 0] <- " "
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-#a<-data.frame(pathways.list)
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-#i <- sapply(a, is.factor)
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-#a[i] <- lapply(a[i], as.character)
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-rownames(a)<-sub("path:","",rownames(a))
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-PROVA<-top3
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-for( i in 1:ncol(PROVA)) {
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-  if (colnames(PROVA)[i]==rownames(a)[i]){
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-    colnames(PROVA)[i]<-a[i]
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-}
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-}
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-return(PROVA)
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-}
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-
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-
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-#' @title Get network data.
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-#' @description getNETdata creates a data frame with network data.
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-#' Network category can be filtered among: physical interactions, co-localization, genetic interactions and shared protein domain.
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-#' @param network  variable. The user can use the following parameters
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-#' based on the network types to be used. PHint for Physical_interactions,
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-#' COloc for Co-localization, GENint for Genetic_interactions and
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-#' SHpd for Shared_protein_domains
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-#' @param organism organism==NULL default value is homo sapiens
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-#' @export
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-#' @importFrom SpidermiR SpidermiRquery_species SpidermiRquery_spec_networks SpidermiRdownload_net SpidermiRprepare_NET
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-#' @return dataframe with gene-gene (or protein-protein interactions)
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-#' @examples
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-#' organism="Saccharomyces_cerevisiae"
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-#' netw<-getNETdata(network="SHpd",organism)
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-getNETdata<-function(network,organism=NULL){
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-  org_shar_pro<-SpidermiRquery_species(species)
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-  if (is.null(organism)) {
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-  net_shar_prot<-SpidermiRquery_spec_networks(organismID = org_shar_pro[6,],network)
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-  out_net_shar_pro<-SpidermiRdownload_net(net_shar_prot)
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-  geneSymb_net_shar_pro<-SpidermiRprepare_NET(organismID = org_shar_pro[6,],data = out_net_shar_pro)
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-  }
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-  if( !is.null(organism) ){
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-    net_shar_prot<-SpidermiRquery_spec_networks(organismID = org_shar_pro[9,],network)
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-    out_net_shar_pro<-SpidermiRdownload_net(net_shar_prot)
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-    geneSymb_net_shar_pro<-SpidermiRprepare_NET(organismID = org_shar_pro[9,],data = out_net_shar_pro)
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-}
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-  ds_shar_pro<-do.call("rbind", geneSymb_net_shar_pro)
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-  data_shar_pro<-as.data.frame(ds_shar_pro[!duplicated(ds_shar_pro), ])
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-  sdc_shar_pro<-unlist(data_shar_pro$gene_symbolA,data_shar_pro$gene_symbolB)
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-  m_shar_pro<-c(data_shar_pro$gene_symbolA)
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-  m2_shar_pro<-c(data_shar_pro$gene_symbolB)
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-  ss_shar_pro<-cbind(m_shar_pro,m2_shar_pro)
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-  data_pr_shar_pro<-as.data.frame(ss_shar_pro[!duplicated(ss_shar_pro), ])
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-  colnames(data_pr_shar_pro) <- c("m_shar_pro", "m2_shar_pro")
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-return(data_pr_shar_pro)
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-}
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-
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-
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-
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-
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-
R/internal.R
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-
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-
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-
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-select_path_carb<-function(Carbohydrate){
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-species<-c("- Homo sapiens (human)")
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-a<-paste("Glycolysis / Gluconeogenesis", species)
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-b<-paste("Citrate cycle (TCA cycle)", species)
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-c<-paste("Pentose phosphate pathway", species)
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-d<-paste("Pentose and glucuronate interconversions", species)
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-e<-paste("Fructose and mannose metabolism", species)
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-f<-paste("Galactose metabolism", species)
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-g<-paste("Ascorbate and aldarate metabolism", species)
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-h<-paste("Starch and sucrose metabolism", species)
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-i<-paste("Amino sugar and nucleotide sugar metabolism", species)
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-l<-paste("Pyruvate metabolism", species)
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-m<-paste("Glyoxylate and dicarboxylate metabolism", species)
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-n<-paste("Propanoate metabolism", species)
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-o<-paste("Butanoate metabolism", species)
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-p<-paste("C5-Branched dibasic acid metabolism", species)
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-q<-paste("Inositol phosphate metabolism", species)
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-r<-paste("Enzymes", species)
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-s<-paste("Compounds with biological roles",species)
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-mer<-c(a,b,c,d,e,f,g,h,i,l,m,n,o,p,q,r,s)
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-return(mer)
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-}
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-
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-select_path_en<-function(Energy){
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-  species<-c("- Homo sapiens (human)")
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-  r<-paste("Oxidative phosphorylation", species)
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-  s<-paste("Photosynthesis", species)
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-  t<-paste("Photosynthesis - antenna proteins", species)
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-  v<-paste("Carbon fixation in photosynthetic organisms", species)
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-  u<-paste("Carbon fixation pathways in prokaryotes", species)
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-  z<-paste("Methane metabolism", species)
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-  aa<-paste("Nitrogen metabolism", species)
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-  ab<-paste("Sulfur metabolism", species)
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-  mer<-c(r,s,t,v,u,z,aa,ab)
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-  return(mer)
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-}
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-
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-
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-select_path_lip<-function(Lipid){
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-  species<-c("- Homo sapiens (human)")
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-ac<-paste("Fatty acid biosynthesis", species)
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-ad<-paste("Fatty acid elongation", species)
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-ae<-paste("Fatty acid degradation", species)
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-af<-paste("Synthesis and degradation of ketone bodies", species)
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-ag<-paste("Cutin, suberine and wax biosynthesis", species)
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-ah<-paste("Steroid biosynthesis", species)
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-ai<-paste("Primary bile acid biosynthesis", species)
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-al<-paste("Secondary bile acid biosynthesis", species)
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-am<-paste("Steroid hormone biosynthesis", species)
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-an<-paste("Glycerolipid metabolism", species)
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-ao<-paste("Glycerophospholipid metabolism", species)
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-ap<-paste("Ether lipid metabolism", species)
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-aq<-paste("Sphingolipid metabolism", species)
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-ar<-paste("Arachidonic acid metabolism", species)
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-as<-paste("Linoleic acid metabolism", species)
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-at<-paste("alpha-Linolenic acid metabolism", species)
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-av<-paste("Biosynthesis of unsaturated fatty acids", species)
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-
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-mer<-c(ac,ad,ae,af,ag,ah,ai,al,am,an,ao,ap,aq,ar,as,at,av)
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-return(mer)
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-}
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-
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-
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-
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-
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-select_path_amn<-function(Aminoacid){
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-  species<-c("- Homo sapiens (human)")
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-ac<-paste("Alanine, aspartate and glutamate metabolism", species)
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-ad<-paste("Glycine, serine and threonine metabolism", species)
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-ae<-paste("Cysteine and methionine metabolism", species)
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-af<-paste("Valine, leucine and isoleucine degradation", species)
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-ag<-paste("Valine, leucine and isoleucine biosynthesis", species)
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-ah<-paste("Lysine biosynthesis", species)
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-ai<-paste("Lysine degradation", species)
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-al<-paste("Arginine biosynthesis", species)
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-am<-paste("Arginine and proline metabolism", species)
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-an<-paste("Histidine metabolism", species)
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-ao<-paste("Tyrosine metabolism", species)
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-ap<-paste("Phenylalanine metabolism", species)
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-aq<-paste("Tryptophan metabolism", species)
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-ar<-paste("Phenylalanine, tyrosine and tryptophan biosynthesis", species)
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-as<-paste("beta-Alanine metabolism", species)
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-at<-paste("Taurine and hypotaurine metabolism", species)
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-av<-paste("Phosphonate and phosphinate metabolism", species)
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-au<-paste("Selenocompound metabolism", species)
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-az<-paste("Cyanoamino acid metabolism", species)
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-a<-paste("D-Glutamine and D-glutamate metabolism", species)
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-b<-paste("D-Arginine and D-ornithine metabolism", species)
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-c<-paste("D-Alanine metabolism", species)
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-d<-paste("Glutathione metabolism", species)
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-
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-mer<-c(ac,ad,ae,af,ag,ah,ai,al,am,an,ao,ap,aq,ar,as,at,av,au,az,a,b,c,d)
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-return(mer)
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-}
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-
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-select_path_gly<-function(Glybio_met){
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-  species<-c("- Homo sapiens (human)")
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-ac<-paste("N-Glycan biosynthesis", species)
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-ad<-paste("Various types of N-glycan biosynthesis", species)
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-ae<-paste("Mucin type O-Glycan biosynthesis", species)
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-af<-paste("Other types of O-glycan biosynthesis", species)
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-ag<-paste("Glycosaminoglycan biosynthesis - CS/DS", species)
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-ah<-paste("Glycosaminoglycan biosynthesis - HS/Hep", species)
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-ai<-paste("Glycosaminoglycan biosynthesis - KS", species)
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-al<-paste("Glycosaminoglycan degradation", species)
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-am<-paste("Glycosylphosphatidylinositol(GPI)-anchor biosynthesis", species)
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-an<-paste("Glycosphingolipid biosynthesis - lacto and neolacto series", species)
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-ao<-paste("Glycosphingolipid biosynthesis - globo series", species)
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-ap<-paste("Glycosphingolipid biosynthesis - ganglio series", species)
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-aq<-paste("Lipopolysaccharide biosynthesis", species)
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-ar<-paste("Peptidoglycan biosynthesis", species)
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-as<-paste("Other glycan degradation", species)
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-mer<-c(ac,ad,ae,af,ag,ah,ai,al,am,an,ao,ap,aq,ar,as)
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-return(mer)
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-}
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-
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-
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-
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-select_path_cofa<-function(Cofa_vita_met){
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-  species<-c("- Homo sapiens (human)")
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-ac<-paste("Thiamine metabolism", species)
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-ad<-paste("Riboflavin metabolism", species)
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-ae<-paste("Vitamin B6 metabolism", species)
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-af<-paste("Nicotinate and nicotinamide metabolism", species)
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-ag<-paste("Pantothenate and CoA biosynthesis", species)
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-ah<-paste("Biotin metabolism", species)
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-ai<-paste("Lipoic acid metabolism", species)
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-al<-paste("Folate biosynthesis", species)
132 
-am<-paste("One carbon pool by folate", species)
133 
-an<-paste("Retinol metabolism", species)
134 
-ao<-paste("Porphyrin and chlorophyll metabolism", species)
135 
-ap<-paste("Ubiquinone and other terpenoid-quinone biosynthesis", species)
136 
-mer<-c(ac,ad,ae,af,ag,ah,ai,al,am,an,ao,ap)
137 
-return(mer)
138 
-}
139 
-
140 
-select_path_transc<-function(Transcription){
141 
-  species<-c("- Homo sapiens (human)")
142 
-ac<-paste("RNA polymerase", species)
143 
-ad<-paste("Basal transcription factors", species)
144 
-ae<-paste("Spliceosome", species)
145 
-af<-paste("Transcription factors", species)
146 
-ag<-paste("Transcription machinery", species)
147 
-mer<-c(ac,ad,ae,af,ag)
148 
-return(mer)
149 
-}
150 
-
151 
-
152 
-
153 
-select_path_transl<-function(Translation){
154 
-  species<-c("- Homo sapiens (human)")
155 
-ac<-paste("Ribosome", species)
156 
-ad<-paste("Aminoacyl-tRNA biosynthesis", species)
157 
-ae<-paste("RNA transport", species)
158 
-af<-paste("mRNA surveillance pathway", species)
159 
-ag<-paste("Ribosome biogenesis in eukaryotes", species)
160 
-ah<-paste("Ribosomal proteins", species)
161 
-ai<-paste("Ribosome biogenesis", species)
162 
-al<-paste("Transfer RNA biogenesis", species)
163 
-am<-paste("Translation factors", species)
164 
-mer<-c(ac,ad,ae,af,ag,ah,ai,al,am)
165 
-return(mer)
166 
-}
167 
-
168 
-select_path_fold<-function(Folding_sorting_and_degradation){
169 
-  species<-c("- Homo sapiens (human)")
170 
-ac<-paste("Protein export", species)
171 
-ad<-paste("Protein processing in endoplasmic reticulum", species)
172 
-ae<-paste("SNARE interactions in vesicular transport", species)
173 
-af<-paste("Ubiquitin mediated proteolysis", species)
174 
-ag<-paste("Sulfur relay system", species)
175 
-ah<-paste("RNA degradation", species)
176 
-ai<-paste("Chaperones and folding catalysts", species)
177 
-al<-paste("SNAREs", species)
178 
-am<-paste("Ubiquitin system", species)
179 
-an<-paste("Proteasome", species)
180 
-mer<-c(ac,ad,ae,af,ag,ah,ai,al,am,an)
181 
-return(mer)
182 
-}
183 
-
184 
-
185 
-
186 
-
187 
-select_path_repl<-function(Replication_and_repair){
188 
-  species<-c("- Homo sapiens (human)")
189 
-ac<-paste("DNA replication", species)
190 
-ad<-paste("Base excision repair", species)
191 
-ae<-paste("Nucleotide excision repair", species)
192 
-af<-paste("Mismatch repair", species)
193 
-ag<-paste("Homologous recombination", species)
194 
-ah<-paste("Non-homologous end-joining", species)
195 
-ai<-paste("Fanconi anemia pathway", species)
196 
-al<-paste("DNA replication proteins", species)
197 
-am<-paste("Chromosome", species)
198 
-an<-paste("DNA repair and recombination", species)
199 
-ao<-paste("proteins", species)
200 
-mer<-c(ac,ad,ae,af,ag,ah,ai,al,am,an,ao)
201 
-return(mer)
202 
-}
203 
-
204 
-
205 
-
206 
-select_path_sign<-function(Signal_transduction){
207 
-  species<-c("- Homo sapiens (human)")
208 
-a<-paste("Ras signaling pathway", species)
209 
-b<-paste("Rap1 signaling pathway", species)
210 
-c<-paste("MAPK signaling pathway", species)
211 
-d<-paste("ErbB signaling pathway", species)
212 
-e<-paste("Wnt signaling pathway", species)
213 
-f<-paste("Notch signaling pathway", species)
214 
-g<-paste("Hedgehog signaling pathway", species)
215 
-h<-paste("TGF-beta signaling pathway", species)
216 
-i<-paste("Hippo signaling pathway", species)
217 
-l<-paste("VEGF signaling pathway", species)
218 
-m<-paste("Jak-STAT signaling pathway", species)
219 
-n<-paste("NF-kappa B signaling pathway", species)
220 
-o<-paste("TNF signaling pathway", species)
221 
-p<-paste("HIF-1 signaling pathway", species)
222 
-q<-paste("FoxO signaling pathway", species)
223 
-r<-paste("Calcium signaling pathway", species)
224 
-s<-paste("Phosphatidylinositol signaling system", species)
225 
-t<-paste("Phospholipase D signaling pathway", species)
226 
-v<-paste("Sphingolipid signaling pathway", species)
227 
-u<-paste("cAMP signaling pathway", species)
228 
-z<-paste("cGMP-PKG signaling pathway", species)
229 
-ab<-paste("PI3K-Akt signaling pathway", species)
230 
-ac<-paste("AMPK signaling pathway", species)
231 
-ad<-paste("mTOR signaling pathway", species)
232 
-mer<-c(a,b,c,d,e,f,g,h,i,l,m,n,o,p,q,r,s,t,v,u,z,ab,ac,ad)
233 
-return(mer)
234 
-}
235 
-
236 
-
237 
-select_path_sign_mol<-function(Signaling_molecules_and_interaction){
238 
-  species<-c("- Homo sapiens (human)")
239 
-a<-paste("Neuroactive ligand-receptor interaction", species)
240 
-b<-paste("Cytokine-cytokine receptor interaction", species)
241 
-c<-paste("ECM-receptor interaction", species)
242 
-d<-paste("Cell adhesion molecules (CAMs)", species)
243 
-mer<-c(a,b,c,d)
244 
-return(mer)
245 
-}
246 
-
247 
-
248 
-select_path_transp_ca<-function(Transport_and_catabolism){
249 
-  species<-c("- Homo sapiens (human)")
250 
-a<-paste("Endocytosis", species)
251 
-b<-paste("Phagosome", species)
252 
-c<-paste("Lysosome", species)
253 
-d<-paste("Peroxisome", species)
254 
-e<-paste("Regulation of autophagy", species)
255 
-mer<-c(a,b,c,d,e)
256 
-return(mer)
257 
-}
258 
-
259 
-select_path_cell_grow<-function(Cell_growth_and_death){
260 
-  species<-c("- Homo sapiens (human)")
261 
-  a<-paste("Cell cycle", species)
262 
-b<-paste("Apoptosis", species)
263 
-c<-paste("p53 signaling pathway", species)
264 
-mer<-c(a,b,c)
265 
-return(mer)
266 
-}
267 
-
268 
-
269 
-select_path_cell_comm<-function(Cellular_community){
270 
-  species<-c("- Homo sapiens (human)")
271 
-  a<-paste("Focal adhesion", species)
272 
-b<-paste("Adherens junction", species)
273 
-c<-paste("Tight junction", species)
274 
-d<-paste("Gap junction", species)
275 
-e<-paste("Signaling pathways regulating pluripotency of stem cells ", species)
276 
-mer<-c(a,b,c,d,e)
277 
-return(mer)
278 
-}
279 
-
280 
-
281 
-select_path_imm_syst<-function(Immune_system){
282 
-  species<-c("- Homo sapiens (human)")
283 
-a<-paste("Hematopoietic cell lineage", species)
284 
-b<-paste("Complement and coagulation cascades", species)
285 
-c<-paste("Platelet activation", species)
286 
-d<-paste("Toll-like receptor signaling pathway", species)
287 
-e<-paste("Toll and Imd signaling pathway", species)
288 
-f<-paste("NOD-like receptor signaling pathway", species)
289 
-g<-paste("RIG-I-like receptor signaling pathway", species)
290 
-h<-paste("Cytosolic DNA-sensing pathway", species)
291 
-i<-paste("Natural killer cell mediated cytotoxicity", species)
292 
-l<-paste("Antigen processing and presentation", species)
293 
-m<-paste("T cell receptor signaling pathway", species)
294 
-n<-paste("B cell receptor signaling pathway", species)
295 
-o<-paste("Fc epsilon RI signaling pathway", species)
296 
-p<-paste("Fc gamma R-mediated phagocytosis", species)
297 
-q<-paste("Leukocyte transendothelial migration", species)
298 
-r<-paste("Intestinal immune network for IgA production", species)
299 
-s<-paste("Chemokine signaling pathway", species)
300 
-
301 
-mer<-c(a,b,c,d,e,f,g,h,i,l,m,n,o,p,q,r,s)
302 
-return(mer)
303 
-}
304 
-
305 
-
306 
-
307 
-
308 
-select_path_end_syst<-function(Endocrine_system){
309 
-  species<-c("- Homo sapiens (human)")
310 
-a<-paste("Insulin secretion", species)
311 
-b<-paste("Insulin signaling pathway", species)
312 
-c<-paste("Glucagon signaling pathway", species)
313 
-d<-paste("Regulation of lipolysis in adipocytes", species)
314 
-e<-paste("Adipocytokine signaling pathway", species)
315 
-f<-paste("PPAR signaling pathway", species)
316 
-g<-paste("GnRH signaling pathway", species)
317 
-h<-paste("Ovarian steroidogenesis", species)
318 
-i<-paste("Estrogen signaling pathway", species)
319 
-l<-paste("Progesterone-mediated oocyte maturation", species)
320 
-m<-paste("Prolactin signaling pathway", species)
321 
-n<-paste("Oxytocin signaling pathway", species)
322 
-o<-paste("Thyroid hormone synthesis", species)
323 
-p<-paste("Thyroid hormone signaling pathway", species)
324 
-q<-paste("Melanogenesis", species)
325 
-r<-paste("Renin secretion", species)
326 
-s<-paste("Renin-angiotensin system", species)
327 
-t<-paste("Aldosterone synthesis and secretion", species)
328 
-
329 
-
330 
-mer<-c(a,b,c,d,e,f,g,h,i,l,m,n,o,p,q,r,s,t)
331 
-return(mer)
332 
-}
333 
-
334 
-
335 
-select_path_circ_syst<-function(Circulatory_system){
336 
-  species<-c("- Homo sapiens (human)")
337 
-  a<-paste("Cardiac muscle contraction", species)
338 
-b<-paste("Adrenergic signaling in cardiomyocytes", species)
339 
-c<-paste("Vascular smooth muscle contraction", species)
340 
-mer<-c(a,b,c)
341 
-return(mer)
342 
-}
343 
-
344 
-
345 
-select_path_dig_syst<-function(Digestive_system){
346 
-  species<-c("- Homo sapiens (human)")
347 
-  a<-paste("Salivary secretion", species)
348 
-b<-paste("Gastric acid secretion", species)
349 
-c<-paste("Pancreatic secretion", species)
350 
-d<-paste("Bile secretion", species)
351 
-e<-paste("Carbohydrate digestion and absorption", species)
352 
-f<-paste("Protein digestion and absorption", species)
353 
-g<-paste("Fat digestion and absorption", species)
354 
-h<-paste("Vitamin digestion and absorption", species)
355 
-i<-paste("Mineral absorption", species)
356 
-
357 
-mer<-c(a,b,c,d,e,f,g,h,i)
358 
-return(mer)
359 
-}
360 
-
361 
-
362 
-
363 
-select_path_exc_syst<-function(Excretory_system){
364 
-  species<-c("- Homo sapiens (human)")
365 
-  a<-paste("Vasopressin-regulated water reabsorption", species)
366 
-b<-paste("Aldosterone-regulated sodium reabsorption", species)
367 
-c<-paste("Endocrine and other factor-regulated calcium reabsorption", species)
368 
-d<-paste("Proximal tubule bicarbonate reclamation", species)
369 
-e<-paste("Collecting duct acid secretion", species)
370 
-
371 
-
372 
-mer<-c(a,b,c,d,e)
373 
-return(mer)
374 
-}
375 
-
376 
-
377 
-select_path_ner_syst<-function(Nervous_system){
378 
-  species<-c("- Homo sapiens (human)")
379 
-a<-paste("Glutamatergic synapse", species)
380 
-b<-paste("GABAergic synapse", species)
381 
-c<-paste("Cholinergic synapse", species)
382 
-d<-paste("Dopaminergic synapse", species)
383 
-e<-paste("Serotonergic synapse", species)
384 
-f<-paste("Long-term potentiation", species)
385 
-g<-paste("Long-term depression", species)
386 
-h<-paste("Retrograde endocannabinoid signaling", species)
387 
-i<-paste("Synaptic vesicle cycle", species)
388 
-l<-paste("Neurotrophin signaling pathway", species)
389 
-
390 
-mer<-c(a,b,c,d,e,f,g,h,i,l)
391 
-return(mer)
392 
-}
393 
-
394 
-
395 
-select_path_sens_syst<-function(Sensory_system){
396 
-  species<-c("- Homo sapiens (human)")
397 
-  a<-paste("Phototransduction", species)
398 
-b<-paste("Olfactory transduction", species)
399 
-c<-paste("Taste transduction", species)
400 
-d<-paste("Inflammatory mediator regulation of TRP channels", species)
401 
-mer<-c(a,b,c,d)
402 
-return(mer)
403 
-}
404 
-
405 
-
406 
-
407 
-#' @title Select the class of TCGA data
408 
-#' @description select two labels from ID barcode
409 
-#' @param Dataset gene expression matrix
410 
-#' @param typesample the labels of the samples (e.g. tumor,normal)
411 
-#' @export
412 
-#' @return a gene expression matrix of the samples with specified label
413 
-#' @examples
414 
-#' tumo<-SelectedSample(Dataset=Data_CANCER_normUQ_filt,typesample="tumor")[,2]
415 
-SelectedSample <- function(Dataset,typesample){
416 
-  if( typesample =="tumor"){
417 
-    Dataset <- Dataset[,which( as.numeric(substr(colnames(Dataset), 14, 15)) == 01) ]
418 
-  }
419 
-
420 
-  if( typesample =="normal"){
421 
-    Dataset <- Dataset[,which( as.numeric(substr(colnames(Dataset), 14, 15)) >= 10) ]
422 
-  }
423 
-
424 
-  return(Dataset)
425 
-
426 
-}
427 
-
428 
-
429 
-#' @title Select the class of TCGA data
430 
-#' @description select two labels from ID barcode
431 
-#' @param cutoff cut-off for AUC value
432 
-#' @param auc.df list of AUC value
433 
-#' @return a gene expression matrix with only pairwise pathway with a particular cut-off
434 
-select_class<-function(auc.df,cutoff){
435 
-ds<-do.call("rbind", auc.df)
436 
-tmp_ordered <- as.data.frame(ds[order(ds,decreasing=TRUE),])
437 
-colnames(tmp_ordered)<-'pathway'
438 
-er<-as.data.frame(tmp_ordered$pathway>cutoff)
439 
-ase<-tmp_ordered[tmp_ordered$pathway>cutoff,]
440 
-rownames(er)<-rownames(tmp_ordered)
441 
-er[,2]<-tmp_ordered$pathway
442 
-lipid_metabolism<-er[1:length(ase),]
443 
-return(lipid_metabolism)
444 
-}
445 
-
446 
-
447 
-
448 
-
449 
-#' @title Process matrix TCGA data after the selection of pairwise pathway
450 
-#' @description processing gene expression matrix
451 
-#' @param measure matrix with measure of cross-talk among pathways
452 
-#' @param list_perf output of the function select_class
453 
-#' @return a gene expression matrix for case study 1
454 
-process_matrix<-function(measure,list_perf){
455 
-scoreMatrix <- as.data.frame(measure[,3:ncol(measure)])
456 
-for( i in 1: ncol(scoreMatrix)){
457 
-  scoreMatrix[,i] <- as.numeric(as.character(scoreMatrix[,i]))
458 
-}
459 
-measure[,1] <- gsub(" ", "_", measure[,1])
460 
-d<-sub('_-_Homo_sapiens_*', '', measure[,1])
461 
-d_pr<- gsub("(human)", "", d, fixed="TRUE")
462 
-d_pr <- gsub("_", "", d_pr)
463 
-d_pr <- gsub("-", "", d_pr)
464 
-measure[,2] <- gsub(" ", "_", measure[,2])
465 
-d2<-sub('_-_Homo_sapiens_(human)*', '', measure[,2])
466 
-d_pr2<- gsub("(human)", "", d2, fixed="TRUE")
467 
-d_pr2 <- gsub("_", "", d_pr2)
468 
-d_pr2 <- gsub("-", "", d_pr2)
469 
-PathwaysPair <- paste( as.matrix(d_pr), as.matrix(d_pr2),sep="_" )
470 
-rownames(scoreMatrix) <-PathwaysPair
471 
-intera<-intersect(rownames(scoreMatrix),rownames(list_perf))
472 
-path_bestlipd<-scoreMatrix[intera,]
473 
-return(path_bestlipd)
474 
-}
475 
-
476 
-
477 
-
478 
-process_matrix_cell_process<-function(measure_cell_process){
479 
-score__cell_grow_d <- as.data.frame(measure_cell_process[,3:ncol(measure_cell_process)])
480 
-for( i in 1: ncol(score__cell_grow_d)){
481 
-  score__cell_grow_d[,i] <- as.numeric(as.character(score__cell_grow_d[,i]))
482 
-}
483 
-
484 
-measure_cell_process[,1] <- gsub(" ", "_", measure_cell_process[,1])
485 
-d<-sub('_-_Homo_sapiens_*', '', measure_cell_process[,1])
486 
-
487 
-d_pr<- gsub("(human)", "", d, fixed="TRUE")
488 
-d_pr <- gsub("_", "", d_pr)
489 
-d_pr <- gsub("-", "", d_pr)
490 
-
491 
-measure_cell_process[,2] <- gsub(" ", "_", measure_cell_process[,2])
492 
-d2<-sub('_-_Homo_sapiens_(human)*', '', measure_cell_process[,2])
493 
-d_pr2<- gsub("(human)", "", d2, fixed="TRUE")
494 
-d_pr2 <- gsub("_", "", d_pr2)
495 
-d_pr2 <- gsub("-", "", d_pr2)
496 
-
497 
-PathwaysPair <- paste( as.matrix(d_pr), as.matrix(d_pr2),sep="_" )
498 
-rownames(score__cell_grow_d) <-PathwaysPair
499 
-return(score__cell_grow_d)
500 
-}
501 
-
502 
-
503 
-#' @title Get human KEGG pathway data.
504 
-#' @description getKEGGdata creates a data frame with human KEGG pathway. Columns are the pathways and rows the genes inside those pathway
505 
-#' @param mer  output for example of select_path_carb
506 
-#' @export
507 
-#' @importFrom KEGGREST keggList
508 
-#' @return dataframe with human pathway data
509 
-proc_path<-function(mer){
510 
-pathways.list <- keggList("pathway", "hsa")## returns the list of human pathways
511 
-common<-intersect(pathways.list,mer)
512 
-lo<-list()
513 
-for (i in 1:length(pathways.list)){
514 
-  if (length(intersect(pathways.list[[i]],common)!=0)){
515 
-    lo[[i]]<-pathways.list[[i]]
516 
-    names(lo)[[i]]<-names(pathways.list)[[i]]
517 
-  }
518 
-}
519 
-pathways.list<-lo[lapply(lo,length)!=0]
520 
-pathway.codes <- sub("path:", "", names(pathways.list))
521 
-b<-do.call("rbind", pathways.list)
522 
-list_pathkegg<-list(pathway.codes,b)
523 
-return(list_pathkegg)
524 
-}
525 
-
R/path_star.R
History View file @ 4cf423d
526 0 
deleted file mode 100644
... ... 
@@ -1,500 +0,0 @@
1 
-#' @title Get human KEGG pathway data and network data in order to define the common gene.
2 
-#' @description path_net creates a list of network data for each human pathway. The network data will be generated when interacting genes belong to that pathway.
3 
-#' @param data  network data as provided by getNETdata
4 
-#' @param pathway  pathway data as provided by getKEGGdata
5 
-#' @importFrom igraph graph.data.frame induced.subgraph get.data.frame
6 
-#' @export
7 
-#' @return a list of network data for each pathway (interacting genes belong to that pathway)
8 
-#' @examples
9 
-#' lista_net<-path_net(pathway=path,data=netw)
10 
-path_net<-function(pathway,data){
11 
-  lista_int<-list()
12 
-  for (k in 1:ncol(pathway)){
13 
-    print(colnames(pathway)[k])
14 
-    currentPathway_genes<-pathway[,k]
15 
-    colnames(data) <- c("gene_symbolA", "gene_symbolB")
16 
-    i <- sapply(data, is.factor)
17 
-    data[i] <- lapply(data[i], as.character)
18 
-    ver<-unlist(data)
19 
-    n<-unique(ver)
20 
-    s<-intersect(n,currentPathway_genes)
21 
-    g <- graph.data.frame(data,directed=FALSE)
22 
-    g2 <- induced.subgraph(graph=g,vids=s)
23 
-    aaa<-get.data.frame(g2)
24 
-    colnames(aaa)[1] <- 'V1'
25 
-    colnames(aaa)[2] <- 'V2'
26 
-    lista_int[[k]]<-aaa
27 
-    names(lista_int)[k]<-colnames(pathway)[k]
28 
-  }
29 
-  return(lista_int)
30 
-}
31 
-
32 
-
33 
-
34 
-
35 
-#' @title Get human KEGG pathway data and output of path_net in order to define the common genes.
36 
-#' @description list_path_net creates a list of interacting genes for each human pathway.
37 
-#' @param lista_net  output of path_net
38 
-#' @param pathway  pathway data as provided by getKEGGdata
39 
-#' @export
40 
-#' @return a list of genes for each pathway (interacting genes belong to that pathway)
41 
-#' @examples
42 
-#' lista_netw<-path_net(pathway=path,data=netw)
43 
-#' list_path<-list_path_net(lista_net=lista_netw,pathway=path)
44 
-list_path_net<-function(lista_net,pathway){
45 
-v=list()
46 
-bn=list()
47 
-for (j in 1:length(lista_net)){
48 
-  cf<-lista_net[[j]]
49 
-  i <- sapply(cf, is.factor)
50 
-  cf[i] <- lapply(cf[i], as.character)
51 
-  colnames(cf) <- c("m_shar_pro", "m2_shar_pro")
52 
-  m<-c(cf$m_shar_pro)
53 
-  m2<-c(cf$m2_shar_pro)
54 
-  s<-c(m,m2)
55 
-  fr<- unique(s)
56 
-  n<-as.data.frame(fr)
57 
-  if(length(n)==0){
58 
-    v[[j]]<-NULL
59 
-
60 
-  }
61 
-  if(length(n)!=0){
62 
-  i <- sapply(n, is.factor)
63 
-  n[i] <- lapply(n[i], as.character)
64 
-  #for (k in  1:ncol(pathway)){
65 
-  if (length(intersect(n$fr,pathway[,j]))==nrow(n)){
66 
-    print(paste("List of genes interacting in the same pathway:",colnames(pathway)[j]))
67 
-    aa<-intersect(n$fr,pathway[,j])
68 
-    v[[j]]<-aa
69 
-    names(v)[j]<-colnames(pathway)[j]
70 
-  }
71 
-}}
72 
-return(v)}
73 
-
74 
-
75 
-
76 
-
77 
-#' @title Get human KEGG pathway data and a gene expression matrix in order to obtain a matrix with the gene expression for only pathways given in input .
78 
-#' @description GE_matrix creates a matrix of gene expression for pathways given by the user.
79 
-#' @param DataMatrix  gene expression matrix (eg.TCGA data)
80 
-#' @param pathway  pathway data as provided by getKEGGdata
81 
-#' @export
82 
-#' @return a matrix for each pathway ( gene expression level belong to that pathway)
83 
-#' @examples
84 
-#' list_path_gene<-GE_matrix(DataMatrix=tumo[,1:2],pathway=path)
85 
-GE_matrix<-function(DataMatrix,pathway) {
86 
-  path_name<-sub(' ', '_',colnames(pathway))
87 
-d_pr<- gsub(" - Homo sapiens (human)", "", path_name, fixed="TRUE")
88 
-colnames(pathway)<-d_pr
89 
-#zz<-as.data.frame(rowMeans(DataMatrix))
90 
-zz<-as.data.frame(DataMatrix)
91 
-v<-list()
92 
-for ( k in 1: ncol(pathway)){
93 
-  #k=2
94 
-  if (length(intersect(rownames(zz),pathway[,k])!=0)){
95 
-    print(colnames(path)[k])
96 
-  currentPathway_genes_list_common <- intersect(rownames(zz), currentPathway_genes<-pathway[,k])
97 
-  currentPathway_genes_list_commonMatrix <- as.data.frame(zz[currentPathway_genes_list_common,])
98 
-  rownames(currentPathway_genes_list_commonMatrix)<-currentPathway_genes_list_common
99 
-  v[[k]]<- currentPathway_genes_list_commonMatrix
100 
-  names(v)[k]<-colnames(pathway)[k]
101 
-  }
102 
-}
103 
-#PEAmatrix <- matrix( 0,nrow(DataMatrix),ncol(pathway))
104 
-#rownames(PEAmatrix) <- as.factor(rownames(DataMatrix))
105 
-#colnames(PEAmatrix) <-  as.factor(colnames(pathway))
106 
-#for (i in 1:length(v)){
107 
-#PEAmatrix[v[[i]],i]<-zz[v[[i]],]
108 
-#}
109 
-#PEAmatrix<-PEAmatrix[which(rowSums(PEAmatrix) > 0),]
110 
-return(v)
111 
-}
112 
-
113 
-
114 
-
115 
-#' @title Get human KEGG pathway data and a gene expression matrix in order to obtain a matrix with the mean gene expression for only pathways given in input .
116 
-#' @description GE_matrix creates a matrix of mean gene expression for pathways given by the user.
117 
-#' @param DataMatrix  gene expression matrix (eg.TCGA data)
118 
-#' @param pathway  pathway data as provided by getKEGGdata
119 
-#' @export
120 
-#' @return a matrix for each pathway (mean gene expression level belong to that pathway)
121 
-#' @examples
122 
-#' list_path_plot<-matrix_plot(DataMatrix=tumo[,1:2],pathway=path)
123 
-matrix_plot<-function(DataMatrix,pathway) {
124 
-  path_name<-sub(' ', '_',colnames(pathway))
125 
-  d_pr<- gsub(" - Homo sapiens (human)", "", path_name, fixed="TRUE")
126 
-  colnames(pathway)<-d_pr
127 
-  zz<-as.data.frame(rowMeans(DataMatrix))
128 
-  v<-list()
129 
-  for ( k in 1: ncol(pathway)){
130 
-    #k=2
131 
-    if (length(intersect(rownames(zz),pathway[,k])!=0)){
132 
-      print(colnames(path)[k])
133 
-      currentPathway_genes_list_common <- intersect(rownames(zz), currentPathway_genes<-pathway[,k])
134 
-      currentPathway_genes_list_commonMatrix <- as.data.frame(zz[currentPathway_genes_list_common,])
135 
-      rownames(currentPathway_genes_list_commonMatrix)<-currentPathway_genes_list_common
136 
-      v[[k]]<- currentPathway_genes_list_common
137 
-      names(v)[k]<-colnames(pathway)[k]
138 
-    }
139 
-  }
140 
-  PEAmatrix <- matrix( 0,nrow(DataMatrix),ncol(pathway))
141 
-  rownames(PEAmatrix) <- as.factor(rownames(DataMatrix))
142 
-  colnames(PEAmatrix) <-  as.factor(colnames(pathway))
143 
-  for (i in 1:length(v)){
144 
-  PEAmatrix[v[[i]],i]<-zz[v[[i]],]
145 
-  }
146 
-  PEAmatrix<-PEAmatrix[which(rowSums(PEAmatrix) > 0),]
147 
-  return(PEAmatrix)
148 
-}
149 
-
150 
-
151 
-
152 
-
153 
-
154 
-
155 
-
156 
-
157 
-
158 
-
159 
-
160 
-
161 
-
162 
-#' @title Get human KEGG pathway data and a gene expression matrix we obtain a matrix with the gene expression for only pathways given in input .
163 
-#' @description plotting_matrix creates a matrix of gene expression for pathways given by the user.
164 
-#' @param DataMatrix  gene expression matrix (eg.TCGA data)
165 
-#' @param pathway  pathway data as provided by getKEGGdata
166 
-#' @param path_matrix  output of the function matrix_plot
167 
-#' @export
168 
-#' @return a plot for pathway cross talk
169 
-#' @examples
170 
-#' mt<-plotting_cross_talk(DataMatrix=tumo[,1:2],pathway=path,path_matrix=list_path_plot)
171 
-plotting_cross_talk<-function(DataMatrix,pathway,path_matrix){
172 
-  zz<-as.data.frame(rowMeans(DataMatrix))
173 
-  v<-list()
174 
-  for ( k in 1: ncol(pathway)){
175 
-    path_name<-sub(' ', '_',colnames(pathway))
176 
-    d_pr<- gsub(" - Homo sapiens (human)", "", path_name, fixed="TRUE")
177 
-    colnames(pathway)<-d_pr
178 
-    if (length(intersect(rownames(zz),pathway[,k])!=0)){
179 
-      print(colnames(path)[k])
180 
-      currentPathway_genes_list_common <- intersect(rownames(zz), currentPathway_genes<-pathway[,k])
181 
-      currentPathway_genes_list_commonMatrix <- as.data.frame(zz[currentPathway_genes_list_common,])
182 
-      rownames(currentPathway_genes_list_commonMatrix)<-currentPathway_genes_list_common
183 
-      v[[k]]<- as.factor(currentPathway_genes_list_common)
184 
-      names(v)[k]<-colnames(pathway)[k]
185 
-    }
186 
-  }
187 
-  vv<-list()
188 
-  mi<-t(path_matrix)
189 
-
190 
-  dc<-cor(mi)
191 
-  for ( k in 1: length(v)){
192 
-    currentPathway_genes_list_common <- intersect(rownames(dc), v[[k]])
193 
-    a<-match(currentPathway_genes_list_common,rownames(dc))
194 
-    vv[[k]]<- a
195 
-    names(vv)[k]<-colnames(pathway)[k]
196 
-  }
197 
-  list_plt=list(corr=dc,gruppi=vv)
198 
- #r<-qgraph(list_plt$corr, groups=list_plt$gruppi, mar=c(1,1,1,1),minimum=0.6)
199 
-  return(list_plt)
200 
-}
201 
-
202 
-
203 
-
204 
-
205 
-#' @title For TCGA data get human pathway data and creates a matrix with the average of genes for each pathway.
206 
-#' @description average creates a matrix with a summarized value for each pathway
207 
-#' @param dataFilt TCGA matrix
208 
-#' @param pathway pathway data
209 
-#' @export
210 
-#' @return a matrix value for each pathway
211 
-#' @examples
212 
-#' score_mean<-average(dataFilt=tumo[,1:2],path)
213 
-average<-function(dataFilt,pathway){
214 
-  DataMatrix<-dataFilt
215 
-  #dataFilt[ , "new.col"] <- gsub("\\|.*", "", rownames(dataFilt))
216 
-  #DataMatrix<-dataFilt[which(dataFilt$new.col!="?"),]
217 
-  #DataMatrix <- subset(DataMatrix, !duplicated(DataMatrix$new.col))
218 
-  #rownames(DataMatrix)<-DataMatrix$new.col
219 
-  #DataMatrix$new.col<-NULL
220 
-
221 
-PEAmatrix <- matrix( 0, ncol(pathway),ncol(DataMatrix))
222 
-rownames(PEAmatrix) <- colnames(pathway)
223 
-colnames(PEAmatrix) <-  colnames(DataMatrix)
224 
-listIPA_pathways<-colnames(pathway)
225 
-for ( k in 1: nrow(PEAmatrix)){
226 
-  #k=1
227 
-  currentPathway <- colnames(pathway)[k]
228 
-  currentPathway_genes_list_common <- intersect(rownames(DataMatrix), currentPathway_genes<-pathway[,k])
229 
-  currentPathway_genes_list_commonMatrix <- DataMatrix[currentPathway_genes_list_common,]
230 
-  SumGenes <- colSums(currentPathway_genes_list_commonMatrix)
231 
-  AverageGenes <- SumGenes / length(currentPathway_genes_list_common)
232 
-  PEAmatrix[k,] <- AverageGenes
233 
-}
234 
-return(PEAmatrix)
235 
-}
236 
-
237 
-
238 
-
239 
-
240 
-
241 
-
242 
-
243 
-
244 
-
245 
-
246 
-
247 
-
248 
-#' @title For TCGA data get human pathway data and creates a measure of cross-talk among pathways
249 
-#' @description euc_dist_crtlk creates a matrix with euclidean distance for pairwise pathways
250 
-#' @param dataFilt TCGA matrix
251 
-#' @param pathway pathway data
252 
-#' @export
253 
-#' @return a matrix value for each pathway
254 
-#' @examples
255 
-#' score_euc_dista<-euc_dist_crtlk(dataFilt=tumo[,1:2],path)
256 
-euc_dist_crtlk <- function(dataFilt,pathway){
257 
-  PEAmatrix<-average(dataFilt,pathway)
258 
-  #step 5 distance
259 
-  # EUCLIDEA DISTANCE
260 
-  df=combn(rownames(PEAmatrix),2) # possibili relazioni tra i pathway
261 
-  df=t(df)
262 
-  ma_d<-matrix(0,nrow(df),ncol(PEAmatrix)) # creo matrix che conterr? le distanze
263 
-  colnames(ma_d)<-colnames(PEAmatrix) # colnames conterr? il nome dei pazienti
264 
-  for ( p in 1: ncol(PEAmatrix)){ # per ogni paziente
265 
-    patients <- (PEAmatrix)[,p]
266 
-    distance<-dist(patients) # calcolo distanza EUCLIDEA tra le possibile combinazioni
267 
-    ma_d[,p]<-distance
268 
-  }
269 
-  euc_dist<-cbind(df,ma_d) # inserisco label con le relazioni tra i pathway
270 
-  return(euc_dist)
271 
-}
272 
-
273 
-
274 
-
275 
-
276 
-#' @title For TCGA data get human pathway data and creates a measure of standard deviations among pathways
277 
-#' @description st_dv creates a matrix with standard deviation for pathways
278 
-#' @param DataMatrix TCGA matrix
279 
-#' @param pathway pathway data
280 
-#' @export
281 
-#' @return a matrix value for each pathway
282 
-#' @examples
283 
-#' stand_dev<-st_dv(DataMatrix=tumo[,1:2],pathway=path)
284 
-st_dv<-function(DataMatrix,pathway){
285 
-#DataMatrix<-dataFilt
286 
-
287 
-#dataFilt[ , "new.col"] <- gsub("\\|.*", "", rownames(dataFilt))
288 
-#DataMatrix<-dataFilt[which(dataFilt$new.col!="?"),]
289 
-#DataMatrix <- subset(DataMatrix, !duplicated(DataMatrix$new.col))
290 
-#rownames(DataMatrix)<-DataMatrix$new.col
291 
-#DataMatrix$new.col<-NULL
292 
-
293 
-PEAmatrix_sd <- matrix( 0, ncol(pathway),ncol(DataMatrix))
294 
-rownames(PEAmatrix_sd) <- colnames(pathway)
295 
-colnames(PEAmatrix_sd) <-  colnames(DataMatrix)
296 
-for ( k in 1: nrow(PEAmatrix_sd)){
297 
-  print(colnames(pathway)[k])
298 
-  currentPathway <- colnames(pathway)[k]
299 
-  currentPathway_genes_list_common <- intersect( rownames(DataMatrix), currentPathway_genes<-pathway[,k])
300 
-  currentPathway_genes_list_commonMatrix <- DataMatrix[currentPathway_genes_list_common,]
301 
-  stdev<-apply(currentPathway_genes_list_commonMatrix,2,sd) #deviazione standard dei pathway
302 
-  PEAmatrix_sd[k,] <- stdev
303 
-  }
304 
-return(PEAmatrix_sd)
305 
-}
306 
-
307 
-
308 
-
309 
-
310 
-
311 
-
312 
-#' @title For TCGA data get human pathway data and creates a measure of discriminating score among pathways
313 
-#' @description ds_score_crtlk creates a matrix with  discriminating score for pathways
314 
-#' @param dataFilt TCGA matrix
315 
-#' @param pathway pathway data
316 
-#' @export
317 
-#' @return a matrix value for each pathway
318 
-#' @examples
319 
-#' cross_talk_st_dv<-ds_score_crtlk(dataFilt=tumo[,1:2],pathway=path)
320 
-ds_score_crtlk<-function(dataFilt,pathway){
321 
-  PEAmatrix<-average(dataFilt,pathway)
322 
-  #step 5 distance
323 
-  # EUCLIDEA DISTANCE
324 
-  df=combn(rownames(PEAmatrix),2) # possibili relazioni tra i pathway
325 
-  df=t(df)
326 
-  ma_d<-matrix(0,nrow(df),ncol(PEAmatrix)) # creo matrix che conterr? le distanze
327 
-  colnames(ma_d)<-colnames(PEAmatrix) # colnames conterr? il nome dei pazienti
328 
-  for ( p in 1: ncol(PEAmatrix)){ # per ogni paziente
329 
-    patients <- (PEAmatrix)[,p]
330 
-    distance<-dist(patients) # calcolo distanza EUCLIDEA tra le possibile combinazioni
331 
-    ma_d[,p]<-distance
332 
-  }
333 
-  PEAmatrix_sd<-st_dv(dataFilt,pathway)
334 
-  df=combn(rownames(PEAmatrix_sd),2)
335 
-  df=t(df)
336 
-  ma<-matrix(0,nrow(df),ncol(PEAmatrix_sd)) # creo matrix che conterr? le somme delle dev st
337 
-  colnames(ma)<-colnames(PEAmatrix_sd) # colnames conterr? il nome dei pazienti
338 
-  for ( p in 1: ncol(PEAmatrix_sd)){ # per ogni paziente
339 
-    patients <- (PEAmatrix_sd)[,p]
340 
-    out <- apply(df, 1, function(x) sum(patients[x])) # calcolo somma delle dev standard tra le possibili combinazioni
341 
-    ma[,p]<-out
342 
-  }
343 
-  score<-ma_d/ma # discriminating score M1-M2/S1+S2
344 
-  score<- cbind(df,score)
345 
-return(score)
346 
-}
347 
-
348 
-
349 
-
350 
-#' @title SVM classification for each feature
351 
-#' @description svm class creates a list with auc value
352 
-#' @param TCGA_matrix gene expression matrix
353 
-#' @param nfs nfs split data into a training  and test set
354 
-#' @param tumour barcode samples for a class
355 
-#' @param normal barcode samples for another class
356 
-#' @export
357 
-#' @importFrom e1071 tune svm
358 
-#' @importFrom ROCR prediction performance
359 
-#' @importFrom  grDevices rainbow
360 
-#' @return a list with AUC value for pairwise pathway
361 
-#' @examples
362 
-#' nf <- 60
363 
-#' res_class<-svm_classification(TCGA_matrix=score_euc_dist,nfs=nf,
364 
-#' normal=colnames(norm[,1:10]),tumour=colnames(tumo[,1:10]))
365 
-svm_classification<-function(TCGA_matrix,tumour,normal,nfs){
366 
-  #library("e1071")
367 
-  #library(ROCR)
368 
-
369 
-  scoreMatrix <- as.data.frame(TCGA_matrix[,3:ncol(TCGA_matrix)])
370 
-  scoreMatrix <-as.data.frame(scoreMatrix)
371 
-  for( i in 1: ncol(scoreMatrix)){
372 
-    scoreMatrix[,i] <- as.numeric(as.character(scoreMatrix[,i]))
373 
-  }
374 
-
375 
-  TCGA_matrix[,1] <- gsub(" ", "_", TCGA_matrix[,1])
376 
-  d<-sub('_-_Homo_sapiens_*', '', TCGA_matrix[,1])
377 
-  #d_pr<-sub(')*', '', DataMatrix[,1])
378 
-
379 
-  d_pr<- gsub("(human)", "", d, fixed="TRUE")
380 
-  d_pr <- gsub("_", "", d_pr)
381 
-  d_pr <- gsub("-", "", d_pr)
382 
-
383 
-  TCGA_matrix[,2] <- gsub(" ", "_", TCGA_matrix[,2])
384 
-  d2<-sub('_-_Homo_sapiens_(human)*', '', TCGA_matrix[,2])
385 
-  d_pr2<- gsub("(human)", "", d2, fixed="TRUE")
386 
-  d_pr2 <- gsub("_", "", d_pr2)
387 
-  d_pr2 <- gsub("-", "", d_pr2)
388 
-
389 
-  PathwaysPair <- paste( as.matrix(d_pr), as.matrix(d_pr2),sep="_" )
390 
-
391 
-  rownames(scoreMatrix) <-PathwaysPair
392 
-
393 
-
394 
-  tDataMatrix<-as.data.frame(t(scoreMatrix))
395 
-  #tDataMatrix$Target[,1]<-0
396 
-
397 
-  tDataMatrix<-cbind(Target=0,tDataMatrix )
398 
-
399 
-  tum<-intersect(rownames(tDataMatrix),tumour)
400 
-  nor<-intersect(rownames(tDataMatrix),normal)
401 
-  #tDataMatrix$
402 
-
403 
-  Dataset_g1<-tDataMatrix[nor,]
404 
-  Dataset_g3<- tDataMatrix[tum,]
405 
-
406 
-
407 
-#training=read.table('C:/Users/UserInLab05/Desktop/trai.txt',header = TRUE)
408 
-#testset=read.table('C:/Users/UserInLab05/Desktop/test.txt',header = TRUE)
409 
-
410 
-  Dataset_g1$Target <- 0
411 
-  Dataset_g3$Target<-1
412 
-#Dataset_g3 <- Dataset_g3[Dataset_g3$Target <- 1, ]
413 
-
414 
-tab_g1_training <- sample(rownames(Dataset_g1),round(nrow(Dataset_g1) / 100 * nfs ))
415 
-tab_g3_training <- sample(rownames(Dataset_g3),round(nrow(Dataset_g3) / 100 * nfs ))
416 
-tab_g1_testing <- setdiff(rownames(Dataset_g1),tab_g1_training)
417 
-tab_g3_testing <- setdiff(rownames(Dataset_g3),tab_g3_training)
418 
-
419 
-FR<-intersect(rownames(Dataset_g1),tab_g1_training)
420 
-
421 
-#rownames(Dataset_g1)<-Dataset_g1[,1]
422 
-G1<-Dataset_g1[FR,]
423 
-
424 
-FR1<-intersect(rownames(Dataset_g3),tab_g3_training)
425 
-#rownames(Dataset_g3)<-Dataset_g3$ID
426 
-
427 
-G3<-Dataset_g3[FR1,]
428 
-training<-rbind(G1,G3)
429 
-
430 
-inter1<-intersect(rownames(Dataset_g1),tab_g1_testing)
431 
-#rownames(Dataset_g1)<-Dataset_g1$ID
432 
-
433 
-G1_testing<-Dataset_g1[inter1,]
434 
-
435 
-inter2<-intersect(rownames(Dataset_g3),tab_g3_testing)
436 
-#rownames(Dataset_g3)<-Dataset_g3$ID
437 
-G3_testing<-Dataset_g3[inter2,]
438 
-
439 
-testing<-rbind(G1_testing,G3_testing)
440 
-
441 
-x <- subset(training, select=-Target)
442 
-y <- training$Target
443 
-#testing[,2]<-NULL
444 
-z<-subset(testing, select=-Target)
445 
-
446 
-zi<-testing$Target
447 
-
448 
-auc.df<-list()
449 
-svm_model_after_tune_COMPL<-list()
450 
-for( k in 2: ncol(training)){
451 
-  print(colnames(training)[k])
452 
-  svm_tune <- tune(svm, train.x=x, train.y=y,
453 
-                   kernel="radial", ranges=list(cost=10^(-1:2), gamma=c(.5,1,2)),cross=10)
454 
-  #print(svm_tune)
455 
-
456 
-  svm_model_after_tune <- svm(Target ~ ., data=training[,c(1,k)], kernel="radial", cost=svm_tune$best.parameters$cost, gamma=svm_tune$best.parameters$gamma,cross=10,probability = TRUE)
457 
-
458 
-
459 
-  #svm_model_after_tune <- svm(Target ~ ., data=training[,c(1,k)], kernel="radial", cost=svm_tune$best.parameters[1], gamma=svm_tune$best.parameters[2],cross=10,probability = TRUE)
460 
-  #summary(svm_model_after_tune)
461 
-
462 
-  j=k-1
463 
-  z2=z[,j]
464 
-  z3<-as.data.frame(z2)
465 
-  #rownames(z3)<-rownames(z)
466 
-  #colnames(z3)<-as.character(paste("X",j,sep = ""))
467 
-  colnames(z3)<-colnames(z)[j]
468 
-  #classifiersMatrix <- c(classifiersMatrix,svm_model_after_tune)
469 
-  pred <- predict(svm_model_after_tune,z3,decision.values=TRUE,cross=10)
470 
-
471 
-  #a<-table(pred,zi)
472 
-  svm.roc <- prediction(attributes(pred)$decision.values, zi)
473 
-  svm.auc <- performance(svm.roc, 'tpr', 'fpr')
474 
-
475 
-  perf <- performance(svm.roc, "auc")
476 
-  auc<-perf@y.values[[1]]
477 
-
478 
-  auc.df[[j]]<- auc
479 
-  svm_model_after_tune_COMPL[[j]]<-svm_model_after_tune
480 
-
481 
-  palette <- as.matrix(rainbow(ncol(z)))
482 
-  #print(j)
483 
-  if (j >1 & j < 6) {
484 
-    plot(svm.auc,col=palette[j], add=TRUE)
485 
-    legend('bottomright', colnames(z),
486 
-           lty=1, col=palette, bty='n', cex=.90,pch = 20,ncol=1)
487 
-
488 
-
489 
-  }
490 
-  else {
491 
-    plot(svm.auc, col=palette[j])
492 
-
493 
-
494 
-  }
495