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#------------------ Packages ------------------ library(flexdashboard) library(coronavirus) data(coronavirus) `%>%` <- magrittr::`%>%` #------------------ Parameters ------------------ # Set colors # https://www.w3.org/TR/css-color-3/#svg-color confirmed_color <- "purple" active_color <- "#1f77b4" recovered_color <- "forestgreen" death_color <- "red" #------data----------- df_daily <- coronavirus %>% dplyr::filter(country == "Japan") %>% dplyr::group_by(date, type) %>% dplyr::summarise(total = sum(cases, na.rm = TRUE)) %>% tidyr::pivot_wider( names_from = type, values_from = total ) %>% dplyr::arrange(date) %>% dplyr::ungroup() %>% dplyr::mutate(active = confirmed - death - recovered) %>% #dplyr::mutate(active = confirmed - death) %>% dplyr::mutate( confirmed_cum = cumsum(confirmed), death_cum = cumsum(death), recovered_cum = cumsum(recovered), active_cum = cumsum(active) ) #---------plot data------- plotly::plot_ly(data = df_daily) %>% plotly::add_trace( x = ~date, # y = ~active_cum, y = ~confirmed_cum, type = "scatter", mode = "lines+markers", # name = "Active", name = "Confirmed", line = list(color = confirmed_color), marker = list(color = confirmed_color) ) %>% plotly::add_trace( x = ~date, y = ~death_cum, type = "scatter", mode = "lines+markers", name = "Death", line = list(color = death_color), marker = list(color = death_color) ) %>% plotly::add_trace( x = ~date, y = ~active_cum, type = "scatter", mode = "lines+markers", name = "Active", line = list(color = active_color), marker = list(color = active_color) ) %>% plotly::add_trace( x = ~date, y = ~recovered_cum, type = "scatter", mode = "lines+markers", name = "Recovered", line = list(color = recovered_color), marker = list(color = recovered_color) ) %>% plotly::layout( title = "", yaxis = list(title = "Número acumulado de casos en Japón"), xaxis = list(title = "Fecha"), legend = list(x = 0.1, y = 0.9), hovermode = "compare" )
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#this loads the facebook embeddings then saves each list element as a separate file so as not to clog up the memory if(!(length(list.files(file.path("/home/jonno/setse_1_data/facebook_embeddings", "processed_embeddings")))==7)){ file_paths <- list.files("/home/jonno/setse_1_data/facebook_embeddings/HPC_embeddings", full.names = T) facebook_embeddings_data <- 1:length(file_paths) %>% map(~{ print(.x) file_name <- basename(file_paths)[.x] readRDS(file_paths[.x]) %>% flatten() %>% map(~{ Out <- .x %>% mutate(file_name = str_remove(file_name, ".rds")) return(Out) }) }) %>% transpose() embeddings_names <-names(facebook_embeddings_data) embeddings_names %>% walk(~{ facebook_embeddings_data[[.x]] %>% bind_rows() %>% saveRDS(., file.path("/home/jonno/setse_1_data/facebook_embeddings", "processed_embeddings", paste0("facebook_", .x, ".rds"))) }) rm(embeddings_names) rm(facebook_embeddings_data) rm(file_paths) }
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#=========== #run_model.R #=========== #This script tests the VisionEval staged model with the second half of the model run #Load libraries #-------------- library(visioneval) writeLog('Running Stage 2') #Initialize model #---------------- initializeModel( ModelScriptFile = "run_model.R", ParamDir = "defs", RunParamFile = "run_parameters.json", GeoFile = "geo.csv", ModelParamFile = "model_parameters.json", LoadDatastore = TRUE, DatastoreName = "../Stage-1/Datastore", SaveDatastore = FALSE ) #Run second stage modules #--------------------------------- for(Year in getYears()) { for (i in 1:2) { runModule("CalculateRoadDvmt", "VETravelPerformance", RunFor = "AllYear", RunYear = Year) runModule("CalculateRoadPerformance", "VETravelPerformance", RunFor = "AllYears", RunYear = Year) runModule("CalculateMpgMpkwhAdjustments", "VETravelPerformance", RunFor = "AllYears", RunYear = Year) runModule("AdjustHhVehicleMpgMpkwh", "VETravelPerformance", RunFor = "AllYears", RunYear = Year) runModule("CalculateVehicleOperatingCost", "VETravelPerformance", RunFor = "AllYears", RunYear = Year) runModule("BudgetHouseholdDvmt", "VETravelPerformance", RunFor = "AllYears", RunYear = Year) runModule("BalanceRoadCostsAndRevenues", "VETravelPerformance", RunFor = "AllYears", RunYear = Year) } runModule("CalculateComEnergyAndEmissions", "VETravelPerformance", RunFor = "AllYears", RunYear = Year) runModule("CalculatePtranEnergyAndEmissions", "VETravelPerformance", RunFor = "AllYears", RunYear = Year) } writeLog('Completed Stage 2')
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#' Describe a matrixTable object #' #' @param jobj #' #' #' @examples #' #' @export describe <- function(jobj){ cat(" Global Fields:", "\n", paste0(" ", mt_globals_fields(jobj), "\n"), "Column Fields:", "\n", paste0(" ", mt_col_fields(jobj), "\n"), "Row Fields:", "\n", paste0(" ", mt_row_fields(jobj)[[1]], "\n"), " Info:", "\n", paste0(" ", mt_row_fields(jobj)[[2]], "\n"), "Entry Fields:", "\n", paste0(" ", mt_entry_fields(jobj), "\n"), "Column Key:", mt_col_key(jobj), "\n", "Row Key:", mt_row_key(jobj)) } #' @importFrom sparklyr %>% invoke #' @export mt_globals_fields <- function(jobj){ jobj %>% invoke("globals") %>% invoke("value") %>% invoke("toString") } #' @importFrom sparklyr %>% invoke #' @export mt_str_rows <- function(jobj){ str_row <- jobj %>% invoke("rowKeyStruct") %>% invoke("parsableString") parse_struct(str_row) } #' @importFrom sparklyr %>% invoke #' @export mt_row_fields <- function(jobj){ row_fields <- jobj %>% invoke("rowType") %>% invoke("parsableString") %>% strsplit(",info:") list(fields = parse_struct(row_fields[[1]][1]), info = parse_struct(row_fields[[1]][2])) } #' @importFrom sparklyr %>% invoke #' @export mt_col_fields <- function(jobj){ col_fields <- jobj %>% invoke("colType") %>% invoke("parsableString") parse_struct(col_fields) } #' @importFrom sparklyr %>% invoke #' @export mt_entry_fields <- function(jobj){ entry_fields <- jobj %>% invoke("entryType") %>% invoke("parsableString") parse_struct(entry_fields) } parse_struct <- function(str){ str <- sub("Struct{", "", str, fixed = TRUE) gsub("}", "", str, fixed = TRUE) %>% strsplit( ",") %>% unlist() } parse_arrayseq <- function(str){ str <- sub("ArraySeq(", "", str, fixed = TRUE) sub(")", "", str, fixed = TRUE) %>% strsplit( ",") %>% unlist() } #' @importFrom sparklyr %>% invoke #' @export mt_row_key <- function(jobj){ row_key <- jobj %>% invoke("rowKey") %>% invoke("toString") parse_arrayseq(row_key) } #' @importFrom sparklyr %>% invoke #' @export mt_col_key <- function(jobj){ jobj %>% invoke("colKey") %>% unlist() }
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f_plot_profit_bars_plus_area.Rd
% Generated by roxygen2: do not edit by hand % Please edit documentation in R/f_plot_profit.R \name{f_plot_profit_bars_plus_area} \alias{f_plot_profit_bars_plus_area} \title{plot revenues cost and profit development over time with bars for revenue and costs and an area chart for profit.} \usage{ f_plot_profit_bars_plus_area(data, col_revenue, col_cost, col_time, now = max(data[, col_time]), unit_time = "years", unit_value = "CHF", title = "", alpha_past = 1, alpha_future = 0.5, alpha_past_area = 0.9, alpha_future_area = 0.7) } \arguments{ \item{data}{datafram} \item{col_revenue}{character vector denoting revenue column} \item{col_cost}{character vector denoting cost column} \item{col_time}{character vector denoting time column} \item{now}{integer denoting a time which should be regarded as the breakpoint, Default: max(data[, col_time])} \item{unit_time}{character vector, will label y-axis, Default: 'years'} \item{unit_value}{character vector, will label x-axis, Default: 'CHF'} \item{title}{character vector, will be title label, Default: ''} \item{alpha_past}{double between 0 and 1 will determine alpha value for fill under the curve before the breakpoint, Default: 1} \item{alpha_future}{double between 0 and 1 will determine alpha value for fill under the curve after the breakpoint, Default: 0.5} \item{alpha_past_area}{as alpha_past but for area only, Default: 0.9} \item{alpha_future_area}{as alpha_future but for area only, Default: 0.7#'} } \value{ plot (to some extent plotly compatible) } \description{ the function can graphically devide the chart into two periods e.g. past and future. } \details{ to some extent plotly compatible } \examples{ data = tibble( time = c(0,1,2,3,4,5,6,7,8,9,10,11,12) , revenue = - time^2 + time * 12 , cost = revenue * 0.4 * -1 ) data[1,'cost'] = -10 data print( f_plot_profit_bars_plus_area( data, 'revenue', 'cost', 'time') ) print( f_plot_profit_bars_plus_area( data, 'revenue', 'cost', 'time', now = 5) ) #clv figure for presenation p = f_plot_profit_bars_plus_area( data, 'revenue', 'cost', 'time', now = 5, alpha_past_area = 0) + theme( panel.grid.major = element_blank() , panel.grid.minor = element_blank() , axis.text = element_blank() )+ labs(x = '', y = '') print(p) }
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library(roxygen2) devtools::document() # install package from computer #devtools::install("~/Documents/R/Packages/dataFun") #devtools::install("//Co.ihc.com/sh/User/jgregor1/GitHub/dataFun") #install package from Github devtools::install_github("JasonGregory/dlearn")
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quad_colored_scatter_plot_RINT.R
# #Sanjeev Sariya #06 14 2021 .libPaths(c( "/home/ss5505/libraries_R/R_LIB4.0",.libPaths())) library(dplyr) library(ggplot2) library(ggpubr) df_zf_human_orthologues<-read.table("/mnt/mfs/hgrcgrid/shared/GT_ADMIX/model_organisms/zebra_fish/DEG_files_ZF/human2zebrafish.txt", header=TRUE) load(file = "/mnt/mfs/hgrcgrid/shared/GT_ADMIX/model_organisms/zebra_fish/DEG_files_ZF/dre_AB42vsCTL.rda") dre_AB42vsCTL$ENS_id<-rownames(dre_AB42vsCTL) df_mayo_deg<- read.table("/mnt/mfs/hgrcgrid/shared/GT_ADMIX/model_organisms/zebra_fish/DEG_files_human/STable4_MAYO_SumStats.csv", header=TRUE,sep=",") df_ch_deg<- read.table("/mnt/mfs/hgrcgrid/shared/GT_ADMIX/model_organisms/zebra_fish/DEG_files_human/STable1_CH_SumStats.csv", header=TRUE,sep=",") df_rosmap_deg<- read.table("/mnt/mfs/hgrcgrid/shared/GT_ADMIX/model_organisms/zebra_fish/DEG_files_human/STable3_ROSMAP_SumStats.csv", header=TRUE, sep=",") colnames(df_mayo_deg)<- paste0("mayo_",colnames(df_mayo_deg)) colnames(df_rosmap_deg)<- paste0("rosmap_",colnames(df_rosmap_deg)) colnames(df_ch_deg)<- paste0("CH_",colnames(df_ch_deg)) merge_tstats<-function(temp_df1, temp_df2, col1){ orthol_merged<- merge( temp_df1, df_zf_human_orthologues, by.x = col1, by.y="Gene_humanstable_ID" ) return ( merge(orthol_merged, dre_AB42vsCTL , by.x ="Gene_ZFstable_ID", by.y="ENS_id")) } ##function ends ##merge using the functions ch_mergeded<-merge_tstats(df_ch_deg, dre_AB42vsCTL,"CH_gene" ) mayo_mergeded<-merge_tstats(df_mayo_deg, dre_AB42vsCTL,"mayo_gene" ) rosmap_mergeded<-merge_tstats(df_rosmap_deg, dre_AB42vsCTL,"rosmap_gene" ) mayo_mergeded_filtered<-mayo_mergeded[which( !is.na(mayo_mergeded$stat) & !is.na(mayo_mergeded$mayo_t )),] rosmap_mergeded_filtered<-rosmap_mergeded[which( !is.na(rosmap_mergeded$stat) & !is.na(rosmap_mergeded$rosmap_t )),] ch_mergeded_filtered<-ch_mergeded[which( !is.na(ch_mergeded$stat) & !is.na(ch_mergeded$CH_t)),] ch_mergeded_filtered_pvalue<-ch_mergeded_filtered[which(ch_mergeded_filtered$CH_P.Value <= 0.05),] rosmap_mergeded_filtered_pvalue <-rosmap_mergeded_filtered[which(rosmap_mergeded_filtered$rosmap_P.Value <= 0.05), ] mayo_mergeded_filtered_pvalue<-mayo_mergeded_filtered[which(mayo_mergeded_filtered$mayo_P.Value <=0.05),] cor.test( ch_mergeded_filtered_pvalue$CH_t, ch_mergeded_filtered_pvalue$stat, method="spearman") cor.test( mayo_mergeded_filtered_pvalue$mayo_t, mayo_mergeded_filtered_pvalue$stat, method="spearman") cor.test( rosmap_mergeded_filtered_pvalue$rosmap_t, rosmap_mergeded_filtered_pvalue$stat, method="spearman") ch_mergeded_filtered_pvalue_zf<-ch_mergeded_filtered[which(ch_mergeded_filtered$CH_P.Value <= 0.05 & ch_mergeded_filtered$pvalue <=0.05),] rosmap_mergeded_filtered_pvalue_zf <-rosmap_mergeded_filtered[which(rosmap_mergeded_filtered$rosmap_P.Value <= 0.05 & rosmap_mergeded_filtered$pvalue<=0.05), ] mayo_mergeded_filtered_pvalue_zf<-mayo_mergeded_filtered[which(mayo_mergeded_filtered$mayo_P.Value <=0.05 & mayo_mergeded_filtered$pvalue<=0.05),] cor.test( ch_mergeded_filtered_pvalue_zf$CH_t, ch_mergeded_filtered_pvalue_zf$stat, method="spearman") cor.test( mayo_mergeded_filtered_pvalue_zf$mayo_t, mayo_mergeded_filtered_pvalue_zf$stat, method="spearman") cor.test( rosmap_mergeded_filtered_pvalue_zf$rosmap_t, rosmap_mergeded_filtered_pvalue_zf$stat, method="spearman") ch_mergeded_filtered_pvalue_zf_quad <- ch_mergeded_filtered_pvalue_zf %>% mutate(quadrant = case_when(stat > 0 & CH_t > 0 ~ "Q1", stat< 0 & CH_t < 0 ~ "Q1", stat< 0 & CH_t > 0 ~ "Q4", stat> 0 & CH_t < 0 ~ "Q2" ) ) rosmap_mergeded_filtered_pvalue_zf_quad <- rosmap_mergeded_filtered_pvalue_zf %>% mutate(quadrant = case_when(stat > 0 & rosmap_t > 0 ~ "Q1", stat< 0 & rosmap_t < 0 ~ "Q1", stat< 0 & rosmap_t > 0 ~ "Q4", stat> 0 & rosmap_t < 0 ~ "Q2" ) ) mayo_mergeded_filtered_pvalue_zf_quad <- mayo_mergeded_filtered_pvalue_zf %>% mutate(quadrant = case_when(stat > 0 & mayo_t > 0 ~ "Q1", stat< 0 & mayo_t < 0 ~ "Q1", stat< 0 & mayo_t > 0 ~ "Q4", stat> 0 & mayo_t < 0 ~ "Q2" ) ) bitmap("CH_quad_colored_RINTed.tiff") ggplot(data=ch_mergeded_filtered_pvalue_zf_quad,aes(x = RNOmni::RankNorm( CH_t, k=3/8), y = RNOmni::RankNorm( stat, k=3/8), color = quadrant)) + geom_point() + theme_bw() + theme( plot.title = element_text( size=15, face="bold", hjust = 0.5), legend.background = element_rect(size=0.5,linetype="solid", colour ="black"), legend.text=element_text(size=14),legend.title=element_text(size=16), axis.title.x = element_text(size=20,face="bold"), legend.position = "none", axis.title.y = element_text(size=20,face="bold"), axis.text.x=element_text(size=18),axis.text.y=element_text(size=18) ) +labs(title="" ,y="ZF t-Stat", x = "CH t-Stat" ) dev.off() bitmap("rosmap_quad_colored_RINTed.tiff") ggplot(data=rosmap_mergeded_filtered_pvalue_zf_quad,aes(x = RNOmni::RankNorm( rosmap_t, k=3/8), y = RNOmni::RankNorm( stat, k=3/8), color = quadrant)) + geom_point() + theme_bw() + theme( plot.title = element_text( size=15, face="bold", hjust = 0.5), legend.background = element_rect(size=0.5,linetype="solid", colour ="black"), legend.text=element_text(size=14),legend.title=element_text(size=16), axis.title.x = element_text(size=20,face="bold"), legend.position = "none", axis.title.y = element_text(size=20,face="bold"), axis.text.x=element_text(size=18),axis.text.y=element_text(size=18) ) +labs(title="" ,y="ZF t-Stat", x = "ROSMAP t-Stat" ) dev.off() bitmap("mayo_quad_colored_RINTed.tiff") ggplot(data=mayo_mergeded_filtered_pvalue_zf_quad,aes(x = RNOmni::RankNorm( mayo_t, k=3/8), y = RNOmni::RankNorm( stat, k=3/8), color = quadrant)) + geom_point() + theme_bw() + theme( plot.title = element_text( size=15, face="bold", hjust = 0.5), legend.background = element_rect(size=0.5,linetype="solid", colour ="black"), legend.text=element_text(size=14),legend.title=element_text(size=16), axis.title.x = element_text(size=20,face="bold"), legend.position = "none", axis.title.y = element_text(size=20,face="bold"), axis.text.x=element_text(size=18),axis.text.y=element_text(size=18) ) +labs(title="" ,y="ZF t-Stat", x = "ROSMAP t-Stat" ) dev.off()
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###################################################### # # Title: functions_grw2012.R # Description: Functions of the analyses of the # Grazer Gemeinderatswahlen 2012 # # # Author: Stefan Kasberger # Date: 02.12.2012 # Version: 1.0 # Language: 2.15.2 # Software: RStudio 0.97.311 # License: FreeBSD (2-clause BSD) # ###################################################### # # Extracts the district out of the parish number # # variables # data: the whole dataframe; # colParish: name of the column for the parish # colDistrict: name of the column for the district # ExtractDistrict <- function(data, colParish="numParish", colDistrict="numDistrict") { library(stringr) temp <- data temp[[colParish]] <- NULL data <- as.character(data[[colParish]]) length <- str_length(data) district <- str_sub(data, end = length - 2) data <- data.frame(as.numeric(data), as.numeric(district), temp) names(data)[1] <- colParish names(data)[2] <- colDistrict rm(temp, length, district) data } # # reduce rows into one row per parish and transform the rows with votes per party into columns # # variables # data: the comlete table (dataframe) # colVotes: column name with the votes # colParty: column name with the party acronym # TransformVotes <- function(data, colVotes, colParty, numParties) { # save numbers of parishes and districts tmp <- data[, c("numParish", "numDistrict")] tmp <- tmp[!duplicated(tmp),] # save data <- data[, c("acrParty", "votes")] rows <- length(data[[colVotes]]) / numParties new <- data[[colVotes]] dim(new) <- c(numParties, rows) new <- data.frame(t(new)) colNames <- lapply(data[1:numParties, colParty], paste0, "abs") names(new) <- colNames data <- cbind(tmp, new) } # # DESCRIPTION # # variables # SaveJSON <- function(data) { filename <- paste0(environment[["folderDataJSON"]], "/", names(data), ".json") write(data[[1]],filename) } # # DESCRIPTION # # variables # Boxplot <- function(data, filename, colors, names, title, yaxis, legend=F, output=T, svg=F, pdf=F, png=F) { # output to the console if(output) { boxplot(data, col=colors, names=names, ylab=yaxis) mtext("Datenquelle: Stadt Graz - data.graz.gv.at, CC-by", side=1, line=3, adj=1) if(legend) { legend("topright", names, fill=colors) } title(title) dev.off() } # export png if(png) { png(file=paste0(filename, ".png"), height=400, width=600) boxplot(data, col=colors, names=names, ylab=yaxis) mtext("Datenquelle: Stadt Graz - data.graz.gv.at, CC-by", side=1, line=3, adj=1) if(legend) { legend("topright", names, fill=colors) } title(title) dev.off() } # export svg if(svg) { svg(file=paste0(filename, ".svg"), height=4, width=6, onefile=TRUE) boxplot(data, col=colors, names=names, ylab=yaxis) mtext("Datenquelle: Stadt Graz - data.graz.gv.at, CC-by", side=1, line=3, adj=1) if(legend) { legend("topright", names, fill=city[["partycolors"]]) } title(title) dev.off() } # export pdf if(pdf) { boxplot(data, col=colors, names=names, ylab=yaxis) mtext("Datenquelle: Stadt Graz - data.graz.gv.at, CC-by", side=1, line=3, adj=1) if(legend) { legend("topright", names, fill=colors) } title(title) dev.copy2pdf(file=paste0(filename, ".pdf")) } } # # DESCRIPTION # # variables # VotesColumnChart <- function(data, filename, colors, names, title, yaxis, shift, legend=F, output=T, png=F, svg=F, pdf=F) { # output to the console if(output) { bp <- barplot(data, col=colors, names=names, main=title, ylab=yaxis) text(x = bp, y=data + shift , labels=as.character(round(data, digits=2)), xpd=TRUE) mtext("Datenquelle: Stadt Graz - data.graz.gv.at, CC-by", side=1, line=3, adj=1) if(legend) { legend("topright", names, fill=colors) } title(title) dev.off() } round # export png if(png) { png(file=paste0(filename, ".png"), height=400, width=600) bp <- barplot(data, col=colors, names=names, main=title, ylab=yaxis) text(x = bp, y=data + shift , labels=as.character(round(data, digits=2)), xpd=TRUE) mtext("Datenquelle: Stadt Graz - data.graz.gv.at, CC-by", side=1, line=3, adj=1) if(legend) { legend("topright", names, fill=colors) } title(title) dev.off() } # export svg if(svg) { svg(file=paste0(filename, ".svg"), height=4, width=6, onefile=TRUE) bp <- barplot(data, col=colors, names=names, main=title, ylab=yaxis) text(x = bp, y=data + shift , labels=as.character(round(data, digits=2)), xpd=TRUE) mtext("Datenquelle: Stadt Graz - data.graz.gv.at, CC-by", side=1, line=3, adj=1) if(legend) { legend("topright", names, fill=colors) } title(title) dev.off() } # export pdf if(pdf) { bp <- barplot(data, col=colors, names=names, main=title, ylab=yaxis) text(x = bp, y=data + shift , labels=as.character(round(data, digits=2)), xpd=TRUE) mtext("Datenquelle: Stadt Graz - data.graz.gv.at, CC-by", side=1, line=3, adj=1) if(legend) { legend("topright", names, fill=colors) } title(title) dev.copy2pdf(file=paste0(filename, ".pdf")) } } # # DESCRIPTION # # variables # Histogram <- function(data, filename, colors, title, xaxis, yaxis, output=T, png=F, svg=F, pdf=F) { # output to the console if(output) { hist(data, col=colors, breaks=100, main=title, xlab=xaxis, ylab=yaxis) mtext("Datenquelle: Stadt Graz - data.graz.gv.at, CC-by", side=1, line=4, adj=1) dev.off() } # export png if(png) { png(file=paste0(filename, ".png"), height=400, width=600) hist(data, col=colors, breaks=100, main=title, xlab=xaxis, ylab=yaxis) mtext("Datenquelle: Stadt Graz - data.graz.gv.at, CC-by", side=1, line=4, adj=1) dev.off() } # export svg if(svg) { svg(file=paste0(filename, ".svg"), height=4, width=6, onefile=TRUE) hist(data, col=colors, breaks=100, main=title, xlab=xaxis, ylab=yaxis) mtext("Datenquelle: Stadt Graz - data.graz.gv.at, CC-by", side=1, line=4, adj=1) dev.off() } # export pdf if(pdf) { hist(data, col=colors, breaks=100, main=title, xlab=xaxis, ylab=yaxis) mtext("Datenquelle: Stadt Graz - data.graz.gv.at, CC-by", side=1, line=4, adj=1) dev.copy2pdf(file=paste0(filename, ".pdf")) } } # # DESCRIPTION # # variables # DensityPlot <- function(data, filename, color, title, yaxis, output=T, png=F, svg=F, pdf=F) { # output to the console if(output) { plot(data,lwd=3,col=color, main=title, ylab=yaxis) mtext("Datenquelle: Stadt Graz - data.graz.gv.at, CC-by", side=1, line=4, adj=1) dev.off() } # export png if(png) { png(file=paste0(filename, ".png"), height=400, width=600) plot(data,lwd=3,col=color, main=title, ylab=yaxis) mtext("Datenquelle: Stadt Graz - data.graz.gv.at, CC-by", side=1, line=4, adj=1) dev.off() } # export svg if(svg) { svg(file=paste0(filename, ".svg"), height=4, width=6, onefile=TRUE) plot(data,lwd=3,col=color, main=title, ylab=yaxis) mtext("Datenquelle: Stadt Graz - data.graz.gv.at, CC-by", side=1, line=4, adj=1) dev.off() } # export pdf if(pdf) { plot(data,lwd=3,col=color, main=title, ylab=yaxis) mtext("Datenquelle: Stadt Graz - data.graz.gv.at, CC-by", side=1, line=4, adj=1) dev.copy2pdf(file=paste0(filename, ".pdf")) } } # # DESCRIPTION # # variables # CalculateCorrelation <- function(dataParish, dataDistrict, corrMethod="pearson", folder, colors, namesIT, namesAT, yaxis, legend=F, output=T, png=F, svg=F, pdf=F) { if(dim(dataParish)[2] & length(names) & dim(dataDistrict)[2]) { numParties <- dim(dataParish)[2] corCoefPar <- array(NA, dim=c(numParties, numParties)) corCoefDis <- array(NA, dim=c(numParties, numParties)) for(i in seq_along(1:numParties)) { for(j in seq_along(1:numParties)) { if(i != j ) { corCoefPar[i, j] <- cor(dataParish[, i], dataParish[, j], method=corrMethod) corCoefDis[i, j] <- cor(dataDistrict[, i], dataDistrict[, j], method=corrMethod) } } } for(i in seq_along(1:numParties)) { corCoefDis[i, i] <- 1 corCoefPar[i, i] <- 1 } if(corrMethod == "pearson") { methName <- "Pearson" methAcr <- "Pear" } if(corrMethod == "spearman") { methName <- "Spearman" methAcr <- "Spear" } # plot correlations as barplots for every party for(i in seq_along(1:numParties)) { # parish CorrelationColumnChart(corCoefPar[i,], filename=paste0(folder, "barCorr", namesIT[i], methAcr, "ParAbs"), colors=colors, names=namesAT, title=paste0(methName, " Korrelationen von ", namesAT[i], " nach Sprengel"), legend=legend, output=output, png=png, svg=svg, pdf=pdf) # district CorrelationColumnChart(corCoefDis[i,], filename=paste0(folder, "barCorr", namesIT[i], methAcr, "DisAbs", methAcr), colors=colors, names=namesAT, title=paste0(methName, " Korrelationen von ", namesAT[i], " nach Bezirke"), legend=legend, output=output, png=png, svg=svg, pdf=pdf) } } else { print("Error: Length of names vector is not the same as number of columns in the dataset!") } } # # DESCRIPTION # # variables # CorrelationColumnChart <- function(data, filename, colors, names, title, legend=F, output=T, png=F, svg=F, pdf=F) { colText <- data colText[data<0] <- 0 # output to the console if(output) { bp <- barplot(data, col=colors, names=names, main=title, ylab="Korrelationskoeffizient") abline(h=mean(data), col="gray", lwd=2) text(x = bp, y=colText + 0.05 , labels=as.character(round(data, digits=2)), xpd=TRUE) mtext("Datenquelle: Stadt Graz - data.graz.gv.at, CC-by", side=1, line=3, adj=1) if(legend) { legend("topright", names, fill=colors) } title(title) dev.off() } # export png if(png) { png(file=paste0(filename, ".png"), height=400, width=600) bp <- barplot(data, col=colors, names=names, main=title, ylab="Korrelationskoeffizient") abline(h=mean(data), col="gray", lwd=2) text(x = bp, y=colText + 0.05 , labels=as.character(round(data, digits=2)), xpd=TRUE) mtext("Datenquelle: Stadt Graz - data.graz.gv.at, CC-by", side=1, line=3, adj=1) if(legend) { legend("topright", names, fill=colors) } title(title) dev.off() } # export svg if(svg) { svg(file=paste0(filename, ".svg"), height=4, width=6, onefile=TRUE) bp <- barplot(data, col=colors, names=names, main=title, ylab="Korrelationskoeffizient") abline(h=mean(data), col="gray", lwd=2) text(x = bp, y=colText + 0.05 , labels=as.character(round(data, digits=2)), xpd=TRUE) mtext("Datenquelle: Stadt Graz - data.graz.gv.at, CC-by", side=1, line=3, adj=1) if(legend) { legend("topright", names, fill=colors) } title(title) dev.off() } # export pdf if(pdf) { bp <- barplot(data, col=colors, names=names, main=title, ylab="Korrelationskoeffizient") abline(h=mean(data), col="gray", lwd=2) text(x = bp, y=colText + 0.05 , labels=as.character(round(data, digits=2)), xpd=TRUE) mtext("Datenquelle: Stadt Graz - data.graz.gv.at, CC-by", side=1, line=3, adj=1) if(legend) { legend("topright", names, fill=colors) } title(title) dev.copy2pdf(file=paste0(filename, ".pdf")) } } # # DESCRIPTION # # variables # WriteCSV <- function(data, filename, folder = "QGIS", enc = "UTF-8") { write.csv(data, paste0(folder, "/", filename, "_comma[", enc, "].csv"), fileEncoding = enc) write.csv2(data, paste0(folder, "/", filename, "_semicolon[", enc, "].csv"), fileEncoding = enc) } BoxplotLR <- function(data, colSeg, filename, colors, names, title, yaxis, legend=F, output=T, svg=F, pdf=F, png=F) { # output to the console if(output) { boxplot(data ~ colSeg, col=colors, names=names) mtext("Datenquelle: Stadt Graz - data.graz.gv.at, CC-by", side=1, line=3, adj=1) title(title) dev.off() } # export png if(png) { png(file=paste0(filename, ".png"), height=400, width=600) boxplot(data ~ colSeg, col=colors, names=names) mtext("Datenquelle: Stadt Graz - data.graz.gv.at, CC-by", side=1, line=3, adj=1) if(legend) { legend("topright", names, fill=colors) } title(title) dev.off() } # export svg if(svg) { svg(file=paste0(filename, ".svg"), height=4, width=6, onefile=TRUE) boxplot(data ~ colSeg, col=colors, names=names) mtext("Datenquelle: Stadt Graz - data.graz.gv.at, CC-by", side=1, line=3, adj=1) if(legend) { legend("topright", names, fill=city[["partycolors"]]) } title(title) dev.off() } # export pdf if(pdf) { boxplot(data ~ colSeg, col=colors, names=names) mtext("Datenquelle: Stadt Graz - data.graz.gv.at, CC-by", side=1, line=3, adj=1) if(legend) { legend("topright", names, fill=colors) } title(title) dev.copy2pdf(file=paste0(filename, ".pdf")) } }
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% Generated by roxygen2: do not edit by hand % Please edit documentation in R/API.R \name{add_tags} \alias{add_tags} \title{Add tags to documents} \usage{ add_tags(documents, tags, prefix = "__label__", new_lines = " ") } \arguments{ \item{documents}{texts to learn} \item{tags}{labels provided as a \link{list} or a \link{vector}. There can be 1 or more per document.} \item{prefix}{\link{character} to add in front of tag (\code{fastText} format)} \item{new_lines}{Character that replaces new lines (\code{\\r\\n}), default is space.} } \value{ \link{character} ready to be written in a file } \description{ Add tags in the `fastText`` format. This format is require for the training step. As fastText doesn't support newlines inside documents (as newlines are delimiting documents) this function also ensures that there are absolutely no new lines. By default new lines are replaced by a single space. } \examples{ library(fastrtext) tags <- list(c(1, 5), 0) documents <- c("this is a text", "this is another document") add_tags(documents = documents, tags = tags) }
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library(funrar) ### Name: distinctiveness ### Title: Functional Distinctiveness on site-species matrix ### Aliases: distinctiveness ### ** Examples data("aravo", package = "ade4") # Site-species matrix mat = as.matrix(aravo$spe) # Compute relative abundances mat = make_relative(mat) # Example of trait table tra = aravo$traits[, c("Height", "SLA", "N_mass")] # Distance matrix dist_mat = compute_dist_matrix(tra) di = distinctiveness(pres_matrix = mat, dist_matrix = dist_mat) di[1:5, 1:5] # Compute distinctiveness for all species in the regional pool # i.e., with all the species in all the communities # Here considering each species present evenly in the regional pool reg_pool = matrix(1, ncol = ncol(mat)) colnames(reg_pool) = colnames(mat) row.names(reg_pool) = c("Regional_pool") reg_di = distinctiveness(reg_pool, dist_mat)
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# Formação IA e ML - UDEMY # Reinforcement Learning # instalação e importação do pacote install.packages("ReinforcementLearning") library(ReinforcementLearning) # Criação do ambiente, usando a função gridworldEnvironment, do próprio pacote ambiente <- gridworldEnvironment # Visualização do ambiente print(ambiente) # Criação dos estados e ações que serão tomados no ambiente estados <- c("s1", "s2", "s3", "s4") acoes <- c("up", "down", "left", "right") # Geração de amostras de experiências a partir das funções dados <- sampleExperience(N = 1000, env = ambiente, states = estados, actions = acoes) head(dados) # Geração do modelo de predição # (amostras, estados, amostras, recompensas, novo estado, controle (taxa de aprendizado, fator de desconto, fator de exploração)) modelo <- ReinforcementLearning(dados, s = "State", a = "Action", r = "Reward", s_new = "NextState", control =list(alpha = 0.1, gamma = 0.5, epsilon = 0.1)) # Mostrar o modelo e a melhor politica modelo policy(modelo)
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## File Name: xxirt_ic.R ## File Version: 0.184 #-- information criteria xxirt xxirt_ic <- function( dev, N, par_items, par_Theta, I, par_items_bounds ) { # Information criteria ic <- list( "deviance"=dev, "n"=N, "I"=I ) # ic$np.item <- length(par_items) ic$np.items <- sum(par_items_bounds$active) ic$np.Theta <- length(par_Theta) ic <- xxirt_ic_compute_criteria(ic=ic) return(ic) }
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Gas_Station.R
#install.packages('simmer') #install.packages('simmer.plot') #install.packages('xlsx') #install.packages('parallel') library(simmer.plot) library(simmer) library(dplyr) library(tidyr) library(parallel) library(xlsx) ### Setting initial parameters of the model max_wait_time = 15 simulation_time = 60*7 # 7 hours, say friday 5-12 pm mean_service_time = 4 customer_inter_arrival_time = 2/3 # i.e 3 cars coming every 2 minutes no_of_simulations = 500 output_file_name = "Model_C.xlsx" ### Setting up the system (customer trajectory and environment) customer <- trajectory("Customer's path") %>% log_("Here I am") %>% set_attribute("start_time", function() {now(gas)}) %>% renege_in(max_wait_time, out = trajectory("Reneging customer") %>% log_(function() { paste("Waited", now(gas) - get_attribute(gas, "start_time"), "I am off") })) %>% simmer::select(c("counter1", "counter2","counter1"), policy = "shortest-queue") %>% seize_selected() %>% renege_abort() %>% log_(function() {paste("Waited: ", now(gas) - get_attribute(gas, "start_time"))}) %>% timeout(function() {rexp(1,1/mean_service_time)}) %>% release_selected() %>% log_(function() {paste("Finished: ", now(gas))}) #### gas <- simmer("gas") %>% ### Adding resources (counters with respective number of servers) add_resource("counter1",2) %>% ### 2 is for number of servers per queue add_resource("counter2", 2) %>% add_resource("counter3", 1) %>% ## generating customers ## If number of customers follow poisson distribution, then the interarrival time follows a exponential distribution. add_generator("Customer", customer, function() {c(0, rexp(1000, 1/customer_inter_arrival_time), -1)}) ## WSimulating above set up many times envs <- mclapply(1:no_of_simulations, function(i) { gas %>% run(until = simulation_time) %>% wrap() }) #====================================================== ## Estimating Target Parameters # ---- waiting time waiting_time <- function(x) { a = get_mon_arrivals(x) %>% filter(finished == TRUE, activity_time > 0 ) %>% mutate(waiting_time = end_time - start_time - activity_time) return(mean(a$waiting_time)) } x = lapply(envs, waiting_time ) waiting = c('Waiting_time', mean(unlist(x)),mean(unlist(x)) - 1.96*sd(unlist(x)),mean(unlist(x)) + 1.96*sd(unlist(x))) # ----- % customers served customers_served <- function(x) { a = get_mon_arrivals(x) %>% filter(finished == TRUE) y = (length(which(a$activity_time > 0))/nrow(a))*100 return(y) } x = lapply(envs, customers_served ) srvd_cust = c('Percentage_of_customers_served', mean(unlist(x)),mean(unlist(x)) - 1.96*sd(unlist(x)),mean(unlist(x)) + 1.96*sd(unlist(x))) # -------- mean time in system system_time <- function(x) { a = get_mon_arrivals(x) %>% filter(finished == TRUE, activity_time > 0) %>% mutate(sys_time = end_time - start_time) %>% filter(finished == TRUE, activity_time > 0) return(mean(a$sys_time)) } x = lapply(envs, system_time ) system= c('Time_spent_in_system', mean(unlist(x)),mean(unlist(x)) - 1.96*sd(unlist(x)),mean(unlist(x)) + 1.96*sd(unlist(x))) #### -------- Queue Length qu_length <- function(x) { a = get_mon_resources(x) return(mean(a$queue)) } x = lapply(envs, qu_length ) qu = c('Queue_length', mean(unlist(x)),mean(unlist(x)) - 1.96*sd(unlist(x)),mean(unlist(x)) + 1.96*sd(unlist(x))) #### -------- utilisation utilisation <- function(x) { a = get_mon_resources(x) return((sum(a$server)/sum(a$capacity))*100) } x = lapply(envs, utilisation) ifelse for start time, ifelse for end time util_res = c('resource_utilization', mean(unlist(x)),mean(unlist(x)) - 1.96*sd(unlist(x)),min(100, mean(unlist(x)) + 1.96*sd(unlist(x)))) ##### Combining all metrices into a dataframe final = data.frame(rbind(waiting, system,srvd_cust, qu , util_res )) colnames(final) = c('Parameter', 'Expected mean', "95%_CI_lower_bound", "95%_upper_bound") final[,-1] = apply(final[,-1], 2,as.numeric) final[,-1] = round(final[,-1],1) rownames(final) = NULL ##### Writing output to a Excel File customer_arrival_monitor <- envs[1] %>% get_mon_arrivals() customer_arrival_monitor <- customer_arrival_monitor[order(customer_arrival_monitor$start_time),] resource_monitor <- envs[1] %>% get_mon_resources() %>% select(-c(queue_size,limit)) ### Writing monitor data for a single simulation require(openxlsx) list_of_datasets <- list("customer_arrival_monitor" =customer_arrival_monitor, "resource_monitor" = resource_monitor, "summary_post_1000_simulation" = final) write.xlsx(list_of_datasets, file = output_file_name ) ########## Evolution of waiting time plot arrivals <- get_mon_arrivals(envs) plot(arrivals, metric = "waiting_time")+ labs(subtitle="Includes all customers (both served and not served)", y="Waiting Time (mins)", x="Simulation Time (mins)", title="Waiting Time Evolution")
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04_eda.R
#' This document conducts an EDA on census data only, first at the tract level and then at the places level. library(tidyverse) library(sf) library(spdep) library(tidycensus) data_dir = '~/Google Drive/Coding/EJ datasets/CA pesticide/' load_sf = function(rds_file) { rds_file %>% str_c(data_dir, .) %>% read_rds() %>% ## Remove locations w/ total population or total employed 0 filter(total_popE != 0, total_employedE != 0) %>% ## Population proportions mutate(womenP = womenE / total_popE, womenPM = moe_prop(womenE, total_popE, womenM, total_popM), whiteP = whiteE / total_popE, whitePM = moe_prop(whiteE, total_popE, whiteM, total_popM), blackP = blackE / total_popE, blackPM = moe_prop(blackE, total_popE, blackM, total_popM), indigenousP = indigenousE / total_popE, indigenousPM = moe_prop(indigenousE, total_popE, indigenousM, total_popM), asianP = asianE / total_popE, asianPM = moe_prop(asianE, total_popE, asianM, total_popM), hispanicP = hispanicE / total_popE, hispanicPM = moe_prop(hispanicE, total_popE, hispanicM, total_popM), noncitizensP = noncitizensE / total_popE, noncitizensPM = moe_prop(noncitizensE, total_popE, noncitizensM, total_popM), childrenP = childrenE / total_popE, childrenPM = moe_prop(childrenE, total_popE, childrenM, total_popM), poverty_combE = povertyE + extreme_povertyE, poverty_combM = sqrt(povertyM^2 + extreme_povertyM^2), poverty_combP = poverty_combE / total_popE, poverty_combPM = moe_prop(poverty_combE, total_popE, poverty_combM, total_popM), hisp_povertyP = hisp_povertyE / hispanicE, hisp_povertyPM = moe_prop(hisp_povertyE, hispanicE, hisp_povertyM, hispanicM), ag_employedP = ag_employedE / total_employedE, ag_employedPM = moe_prop(ag_employedE, total_employedE, ag_employedM, total_employedM) ) %>% ## Population densities mutate_at(vars(womenE, whiteE, blackE, indigenousE, asianE, hispanicE, noncitizensE, childrenE, poverty_combE, hisp_povertyP, ag_employedP), funs(D = . / units::drop_units(area))) } #' # Tracts # tracts_sf = load_sf('02_tracts_sf.Rds') ## Gives a warning about NaNs; ## but there aren't any in the output # as.data.frame() %>% # select(-geometry) %>% # transmute_all(funs(is.nan)) %>% # summarize_all(sum) glimpse(tracts_sf) ## Distributions of proportions ---- tracts_sf %>% as.data.frame() %>% select(ends_with('P')) %>% gather(key = variable, value) %>% ggplot(aes(value, color = variable, fill = variable)) + geom_density() + geom_rug() + facet_wrap(~ variable, scales = 'free') + scale_x_continuous(labels = scales::percent_format()) #' There are a few tracts with a modest proportion of Asian and Black residents ($> 20\%$); but only a few. Almost no tracts have more than 5% Indigenous residents, and none have more than about 20%. Children are typically ~5-12% of the population. The poverty rate varies dramatically, with a median somewhere around 30% and some values above 50%. Hispanic and White proportions are the most diverse. Very little variation in proportion of women, though there are a few extreme tracks with values < 25% or > 80% tracts_sf %>% mutate(w_plus_h = whiteP + hispanicP) %>% ggplot(aes(w_plus_h)) + geom_density() + geom_rug() #' In most tracts, a supermajority of people are either White or Hispanic. ggplot(tracts_sf, aes(hispanicP, poverty_combP)) + geom_point() + geom_smooth(method = 'lm') #' A greater Hispanic proportion is associated with a greater poverty rate. ## Correlations ---- tracts_sf %>% as_tibble() %>% select(densityE, ends_with('P')) %>% cor() %>% as.data.frame() %>% rownames_to_column(var = 'var1') %>% as_tibble() %>% gather(key = 'var2', value = 'cor', -var1) %>% mutate(cor.print = round(cor, digits = 1)) %>% ggplot(aes(var1, var2, fill = cor, label = cor.print)) + geom_tile() + geom_text() + scale_fill_gradient2() tracts_sf %>% as_tibble() %>% select(densityE, ends_with('P'), -whiteP) %>% cor() %>% as.data.frame() %>% rownames_to_column(var = 'var1') %>% as_tibble() %>% gather(key = 'var2', value = 'cor', -var1) %>% filter(abs(cor) > .4, var1 < var2) %>% arrange(desc(abs(cor))) #' White proportion has moderate to very strong negative corelations with every other variable (except Indigenous). Very strong correlation between Hispanic and noncitizen proportion and between Hispanic and general poverty. Strong correlations between agricultural employment and noncitizens and Hispanic. Moderate correlations between each pair of poverty, children, noncitizens, and Hispanic, and between agricultural employment and poverty. ggplot(tracts_sf, aes((densityE), hispanicP)) + geom_point() + geom_smooth() #' No indication of a relationship between population density and Hispanic, linear or nonlinear. ## White/Hispanic segregation ---- ## Evenness/dissimilarity tracts_sf %>% as.data.frame() %>% mutate(w_h_dissim = abs(hispanicE/sum(hispanicE) - whiteE/sum(whiteE))) %>% summarize(w_h_dissim = .5 * sum(w_h_dissim)) #' Evenness is moderate, at 47% ggplot(tracts_sf, aes(abs(hispanicP - whiteP))) + geom_density() + geom_rug() ## Exposure/interaction tracts_sf %>% as.data.frame() %>% mutate(w_h_exposure = abs(whiteE/sum(whiteE) * hispanicE / total_popE), h_w_exposure = abs(hispanicE/sum(hispanicE) * whiteE/total_popE)) %>% summarize(w_h_exposure = sum(w_h_exposure), h_w_exposure = sum(h_w_exposure)) #' Exposure is moderate-low, at about 30% in both directions ## Correlation ggplot(tracts_sf, aes(hispanicP, whiteP)) + geom_point() with(tracts_sf, cor(hispanicP, whiteP)) #' Very strong negative correlation between the two proportions. But I guess, in this kind of two-group context, we would get a very strong negative correlation even if dissimilarity were low and exposure were high. tracts_sf %>% as.data.frame() %>% as_tibble() %>% summarize_at(vars(whiteE, hispanicE), funs(sum)) %>% mutate(hw_ratio = hispanicE / whiteE) #' About 20% more Hispanics than Whites ## Spatial weights ---- coords_tracts = tracts_sf %>% st_centroid() %>% st_coordinates() ## Contiguity weights_tracts_contig = tracts_sf %>% pull(geometry) %>% as_Spatial() %>% poly2nb() %>% nb2listw(style = 'W') ## KNN weights_tracts_knn = 3:8 %>% set_names() %>% map(~ {knearneigh(coords_tracts, k = .x) %>% knn2nb() %>% nb2listw(style = 'W')}) ## Inverse spatial weights w/in 50 km dnn_tracts = dnearneigh(coords_tracts, d1 = 0, d2 = 50 * 1000) weights_tracts_d = nbdists(dnn_tracts, coords = coords_tracts) %>% map( ~ 1/.) %>% nb2listw(dnn_tracts, glist = ., style = 'W', zero.policy = TRUE) weights_tracts = c(weights_tracts_knn, contiguity = list(weights_tracts_contig), distance = list(weights_tracts_d)) plot(tracts_sf, max.plot = 1) plot(weights_tracts$contiguity, coords = coords_tracts, add = TRUE, col = 'blue') ## Moran's I ---- moran.i = function(vec, weights, ...) { moran.test(vec, weights, ...)$estimate['Moran I statistic'] } ## Moran's I for overall density moran_i_tracts = weights_tracts %>% map_dfr(~moran.i(log10(tracts_sf$densityE), .)) %>% gather(key = 'k', value = 'I') moran_i_tracts #' Moderate population clustering, ~.40-.45 for KNN weights_tracts %>% tibble(weights = ., k = names(.)) %>% crossing(tibble(variable = c('womenE_D', 'whiteE_D', 'blackE_D', 'indigenousE_D', 'asianE_D', 'hispanicE_D', 'noncitizensE_D', 'childrenE_D', 'poverty_combE_D'))) %>% rowwise() %>% mutate(var_value = {tracts_sf %>% as.data.frame() %>% pull(variable) %>% {. + 1} %>% log10() %>% list()}, moran_i = moran.i(var_value, weights)) %>% select(k, variable, moran_i) %>% arrange(desc(moran_i)) %>% mutate(variable = fct_inorder(variable)) %>% ggplot(aes(variable, moran_i, color = k, group = k)) + geom_point() + geom_line() + geom_hline(data = moran_i_tracts, aes(yintercept = I, color = k), linetype = 'dashed') + coord_flip() #' The 6 KNN neighborings all give similar values of Moran's $I$, with slightly lower values as $K$ increases. The dashed lines correspond to the values of $I$ for total population density, calculated above. Distance-based weights have consistently lower values of Moran's $I$, but order the groups in basically the same way. Continuity weights have consistently higher values of I, with almost no difference between different groups. #' #' Asian and black residents have moderate-high clustering. White, Hispanic, and noncitizen residents have moderate clustering. Children and impoverished residents seem to have clustering values the same as or just above the overall population. Indigenous people have weak positive clustering. #' #' # Places # places_sf = load_sf('02_places_sf.Rds') glimpse(places_sf) ## Distributions of proportions ---- places_sf %>% as.data.frame() %>% select(ends_with('P')) %>% gather(key = variable, value) %>% ggplot(aes(value, color = variable, fill = variable)) + geom_density() + geom_rug() + facet_wrap(~ variable, scales = 'free') + scale_x_continuous(labels = scales::percent_format()) #' Slightly higher proportions across the board. But no dramatic differences. places_sf %>% mutate(w_plus_h = whiteP + hispanicP) %>% ggplot(aes(w_plus_h)) + geom_density() + geom_rug() #' Again, white+Hispanic supermajority ggplot(places_sf, aes(hispanicP, poverty_combP)) + geom_point() + geom_smooth(method = 'lm') #' Again, greater Hispanic proportion is associated with a greater poverty rate. ## Correlations ---- places_sf %>% as_tibble() %>% select(densityE, womenP, whiteP, blackP, childrenP, hispanicP, indigenousP, noncitizensP, poverty_combP, whiteP) %>% cor() %>% as.data.frame() %>% rownames_to_column(var = 'var1') %>% as_tibble() %>% gather(key = 'var2', value = 'cor', -var1) %>% mutate(cor.print = round(cor, digits = 1)) %>% ggplot(aes(var1, var2, fill = cor, label = cor.print)) + geom_tile() + geom_text() + scale_fill_gradient2() places_sf %>% as_tibble() %>% select(densityE, ends_with('P'), -whiteP) %>% cor() %>% as.data.frame() %>% rownames_to_column(var = 'var1') %>% as_tibble() %>% gather(key = 'var2', value = 'cor', -var1) %>% filter(abs(cor) > .4, var1 < var2) %>% arrange(desc(abs(cor))) #' White is still anticorrelated with everything except Indigenous. Strong or moderate correlations between noncitizens, poverty, or Hispanic. (Not children.) Moderate correlations between Hispanic and density, and moderate-weak between Hispanic and children and density and noncitizens. ggplot(places_sf, aes((densityE), hispanicP)) + geom_point() + geom_smooth() #' Monotonic nonlinear relationship between density and Hispanic. ## White/Hispanic segregation ---- ## Evenness/dissimilarity places_sf %>% as.data.frame() %>% mutate(w_h_dissim = abs(hispanicE/sum(hispanicE) - whiteE/sum(whiteE))) %>% summarize(w_h_dissim = .5 * sum(w_h_dissim)) #' 36% dissimilarity, lower than with tracts ggplot(places_sf, aes(abs(hispanicP - whiteP))) + geom_density() + geom_rug() ## Exposure/interaction places_sf %>% as.data.frame() %>% mutate(w_h_exposure = abs(whiteE/sum(whiteE) * hispanicE / total_popE), h_w_exposure = abs(hispanicE/sum(hispanicE) * whiteE/total_popE)) %>% summarize(w_h_exposure = sum(w_h_exposure), h_w_exposure = sum(h_w_exposure)) #' Slightly higher White-Hispanic exposure, but still moderate-low ## Correlation ggplot(places_sf, aes(hispanicP, whiteP)) + geom_point() with(tracts_sf, cor(hispanicP, whiteP)) #' Very strong negative correlation between the two proportions. But I guess, in this kind of two-group context, we would get a very strong negative correlation even if dissimilarity were low and exposure were high. places_sf %>% as.data.frame() %>% as_tibble() %>% summarize_at(vars(whiteE, hispanicE), funs(sum)) %>% mutate(hw_ratio = hispanicE / whiteE) #' Hispanic-white ratio slightly higher, at 27% ## Spatial weights ---- library(spdep) coords_places = places_sf %>% st_centroid() %>% st_coordinates() ## Contiguity weights_places_contig = places_sf %>% pull(geometry) %>% as_Spatial() %>% poly2nb() %>% nb2listw(style = 'W', zero.policy = TRUE) ## KNN weights_places_knn = 3:8 %>% set_names() %>% map(~ {knearneigh(coords_places, k = .x) %>% knn2nb() %>% nb2listw(style = 'W')}) ## Inverse spatial weights w/in 50 km dnn_places = dnearneigh(coords_places, d1 = 0, d2 = 50 * 1000) weights_places_d = nbdists(dnn_places, coords = coords_places) %>% map( ~ 1/.) %>% nb2listw(dnn_places, glist = ., style = 'W', zero.policy = TRUE) weights_places = c(weights_places_knn, contiguity = list(weights_places_contig), distance = list(weights_places_d)) plot(places_sf, max.plot = 1) plot(weights_places$contiguity, coords = coords_places, add = TRUE, col = 'blue') ## All systems of neighbors produce an archipelago of tight clusters and longer connections. Neither seems to produce ridiculously extended "neighbor" connections. ## ## Contiguity weights produce large numbers of islands: 246/397 (62%) have no neighbors weights_places$contiguity$neighbours ## Moran's I ---- moran.i = function(vec, weights, ...) { moran.test(vec, weights, ...)$estimate['Moran I statistic'] } ## Moran's I for overall density moran_i_places = weights_places %>% map_dfr(~moran.i(log10(places_sf$densityE), ., zero.policy = TRUE)) %>% gather(key = 'k', value = 'I') moran_i_places #' Higher moderate population clustering, .45-.53. Distance weights are more consistent w/ KNN here. Contiguity weights are much lower. weights_places %>% tibble(weights = ., k = names(.)) %>% crossing(tibble(variable = c('womenE_D', 'whiteE_D', 'blackE_D', 'indigenousE_D', 'asianE_D', 'hispanicE_D', 'noncitizensE_D', 'childrenE_D', 'poverty_combE_D'))) %>% rowwise() %>% mutate(var_value = {places_sf %>% as.data.frame() %>% pull(variable) %>% {. + 1} %>% log10() %>% list()}, moran_i = moran.i(var_value, weights, zero.policy = TRUE)) %>% select(k, variable, moran_i) %>% arrange(desc(moran_i)) %>% mutate(variable = fct_inorder(variable)) %>% ggplot(aes(variable, moran_i, color = k, group = k)) + geom_point() + geom_line() + geom_hline(data = moran_i_places, aes(yintercept = I, color = k), linetype = 'dashed') + coord_flip() #' With places, most groups have low and below-average clustering. Impoverished people, noncitizens, and Hispanics have moderate clustering, and Hispanics and noncitizens are above the overall average. Distance values are generally similar to but a bit lower than the KNN. Contiguity values are generally quite a bit lower.
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/R/tsht.R
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tsht.R
tsht <- function(X, f, theta, cmat, conf.level, alternative, R, args) { bargs <- args XOBS <- as.data.frame(X) estindsum <- function(X, f, cmat, theta) { estsum <- theta(X = X, f = f) SE <- sqrt(estsum$varest) estC <- (cmat %*% estsum$estimate) varC <- (cmat^2) %*% (estsum$varest) teststat <- estC/ sqrt(varC) return( list( teststat = teststat, estC = estC, varC = varC, cmat = cmat ) ) } EST <- estindsum(X = XOBS, f = f, cmat = cmat, theta = theta) teststat.org <- EST$estC / sqrt(EST$varC) OBS <- EST$estC BTeststat <- function(X, i, f, cmat, obs) { XNEW <- as.data.frame(X[i, ]) est <- estindsum(X = XNEW, f = f, cmat = cmat, theta = theta) Teststat <- (est$estC - obs)/ sqrt(est$varC) return(Teststat) } bargs$data <- as.data.frame(X) bargs$statistic <- BTeststat bargs$strata = f bargs$f <- f bargs$cmat <- cmat bargs$obs <- OBS bargs$R <- R if(is.null(bargs$R)) { bargs$R <- 999 } if(is.null(bargs$sim)) { bargs$sim <- "ordinary" } if(is.null(bargs$stype)) { bargs$stype <- "i" } bootout <- do.call("boot", bargs) matraw <- matrix( c( teststat.org, bootout$t ), byrow = TRUE, ncol = ncol( bootout$t ), dimnames = NULL) # teststat<-bootout$t alpha <- 1 - conf.level switch(alternative, "two.sided" = { maxabsT <- apply(X = bootout$t, MARGIN = 1, FUN = function(x){ max(abs(x), na.rm = TRUE) }) count <- sapply( lapply( X = teststat.org, FUN = function( x ){ maxabsT >= abs( x ) }), FUN = sum ) countraw <- apply( apply( X = matraw, MARGIN = 2, FUN = function( x ){ abs( x[2:length( x )] ) >= abs( x[1] ) }), MARGIN = 2, FUN = sum) pval <- count / R pvalraw <- countraw / R quant <- quantile(maxabsT, probs = 1 - alpha, na.rm = TRUE) LOWER <- EST$estC - quant * sqrt(EST$varC) UPPER <- EST$estC + quant * sqrt(EST$varC) }, "less" = { maxT <- apply(X = bootout$t, MARGIN = 1, FUN = function(x){ max(x, na.rm = TRUE) }) count <- sapply( lapply( X = teststat.org, FUN = function( x ){ maxT >= x }), FUN = sum ) countraw <- apply( apply( X = matraw, MARGIN = 2, FUN = function( x ){ x[2:length( x )] >= x[1] }), MARGIN = 2, FUN = sum) pval <- count / R pvalraw <- countraw / R quant <- quantile(maxT, probs = 1-alpha, na.rm = TRUE) LOWER <- NA UPPER <- EST$estC + quant * sqrt(EST$varC) }, "greater" = { minT <- apply(X = bootout$t, MARGIN = 1, FUN = function(x){ min(x, na.rm = TRUE) }) count <- sapply( lapply( X = teststat.org, FUN = function( x ){ minT <= x }), FUN = sum ) countraw <- apply( apply( X = matraw, MARGIN = 2, FUN = function( x ){ x[2:length( x )] <= x[1] }), MARGIN = 2, FUN = sum) pval <- count / R pvalraw <- countraw / R quant <- quantile(minT, probs = alpha, na.rm = TRUE) LOWER <- EST$estC + quant * sqrt(EST$varC) UPPER <- NA }) conf.int <- cbind(EST$estC, LOWER, UPPER) colnames(conf.int) <- cbind("estimate", "lower", "upper") p.value <- matrix(c( pval, pvalraw ), ncol = 2, dimnames = list(dimnames(cmat)[[1]], c("adj. p", "raw p"))) return(list(conf.int = conf.int, p.value = p.value, conf.level = conf.level, alternative = alternative)) }
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getItem.Rd
% Generated by roxygen2: do not edit by hand % Please edit documentation in R/get.R \name{getItem} \alias{getItem} \title{Function getItem} \usage{ getItem(dgeObj, itemName) } \arguments{ \item{dgeObj}{A class DGEobj created by function initDGEobj()} \item{itemName}{Name of item to retrieve} } \value{ The requested data item } \description{ Retrieve an item from a DGEobj by item name. } \examples{ \dontrun{ MyCounts <- getItem(DGEobj, "counts") } } \author{ John Thompson } \keyword{DGEobj} \keyword{RNA-Seq,}
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/bipartite/man/moduleWeb-class.Rd
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biometry/bipartite
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moduleWeb-class.Rd
\encoding{UTF-8} \name{moduleWeb-class} \docType{class} \alias{moduleWeb-class} \title{Class "moduleWeb"} \description{ This class is the output of an application of the function \code{computeModules} to a graph. It consists of the matrix representing the original graph which has been passed to \code{computeModules} in order to compute modules, a matrix representing the same graph but permutated according to the identified modules, two vectors indicating the permutation of row and column indices, respectively, and information about the modules themselves. } \section{Objects from the class}{ Objects from the class should only be created by using the function \code{computeModules}. } \section{Slots}{ \describe{ \item{\code{likelihood}:}{Contains a number with the likelihood-equivalent of the final proposed module structure. This value is the same value as Q (or M), the modularity as given by Newman or Guimerà & Amaral (2005). } \item{\code{originalWeb}:}{Object of class \code{"matrix"} representing the original bipartite graph in which modules have been computed.} \item{\code{moduleWeb}:}{Object of class \code{"matrix"} representing the original bipartite graph but reordered such that plotting modules is possible.} \item{\code{orderA}:}{Object of class \code{"vector"} representing the permutation of the rows of the original graph.} \item{\code{orderB}:}{Object of class \code{"vector"} representing the permutation of the columns of the original graph.} \item{\code{modules}:}{Object of class \code{"matrix"} containing for each module the information about its depth and involved nodes. The first row is just a consecutive number, so of no information; the first two columns can also be ignored. This matrix shows ALL network players (in the sequence of the original matrix, starting with rows), so first rows, then columns. There are as many rows as modules. Each row writes a number if a species is in that module, or a 0 if it isn't. For the modules of Safariland (\code{mod <- computeModules(Safariland); mod@modules[-1, -c(1,2) ]}), the third module are species 3 and 24, i.e. \emph{Schinus patagonicus} (third row) and Ichneumonidae4 (24 - 9 column).} } } \section{Methods}{ Objects of this class are used in following functions: listModuleInformation(moduleWebObject) printoutModuleInformation(moduleWebObject) plotModuleWeb(moduleWebObject, plotModules=TRUE, rank=FALSE, weighted=TRUE, displayAlabels=TRUE, displayBlabels=TRUE, labsize=1, plotsize=12, xlabel="", ylabel="", square.border="white", fromDepth=0, upToDepth=-1) } \author{Rouven Strauss} \examples{ showClass("moduleWeb") } \keyword{classes} \keyword{modules} \keyword{moduleWeb} \keyword{modularity}
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/Code/Data Collection.R
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almutaz12/Honors-calculations
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Data Collection.R
# This file is using the honors_stocks code to download stock data honors_stocks <- function(symbols='F', what=c("prices","daily","weekly", "monthly", "dividends"), start_year=1986,end_year=2016) { if (! require(RCurl)) stop("Must install RCurl package.") if (! require(dplyr)) stop("Must install dplyr package.") what <- match.arg(what) yahooCode <- switch(what, prices = , daily = "d", weekly = "w", monthly = "m", dividends = "v", "unknown") stockURL <- "http://real-chart.finance.yahoo.com/table.csv?s=%s&a=05&b=1&c=%d&d=01&e=25&f=%d&g=%s&ignore=.csv" output <- NULL # for collecting output for (symbol in symbols) { thisURL <- sprintf(stockURL, symbol, start_year, end_year, yahooCode) con <- try(textConnection(getURLContent( thisURL )), silent = TRUE) if (inherits(con, what = "try-error")) { message(paste("Symbol", symbol, "not found in years", start_year, "to", end_year, "on Yahoo finance.")) } else { res <- read.csv(con) res$company <- symbol close(con) output <- rbind(output, res) } } output <- output%>% mutate(date = lubridate::ymd(Date)) %>% select(-Date) if (yahooCode == 'v') { output <- output %>% rename(dividends = Dividends) } else { output <- output %>% rename(open = Open, high=High, low=Low, close=Close, volume = Volume, adj_close = Adj.Close) } output } # Listed Companies in three indexes: # NYSE & NASDAQ source:http://www.nasdaq.com/screening/company-list.aspx # S&P 500 source:http://data.okfn.org/data/core/s-and-p-500-companies#readme ######################################## #NYSE #Companies <- read.csv("NYSE_companylist.csv", stringsAsFactors = FALSE, na.strings = "n/a") #Symbols <- Companies$Symbol[ ! is.na(Companies$Sector)] ######################################## #Data Source: Yahoo Finance # f1 <- honors_stocks(symbols = Symbols[1:100]) #f2 <- honors_stocks(symbols = Symbols[101:200]) #f3 <- honors_stocks(symbols = Symbols[201:600]) #f4 <- honors_stocks(symbols = Symbols[601:1200]) #f5 <- honors_stocks(symbols = Symbols[1201:1900]) #f6 <- honors_stocks(symbols = Symbols[1901:2235]) #NYSE <- rbind(f1, f2,f3,f4,f5,f6) #save(NYSE, file = "NYSE_Stock_Data.Rda") ######################################## #NASDAQ #Companies <- read.csv("NASDAQ_companylist.csv", stringsAsFactors = FALSE, na.strings = "n/a") #Symbols <- Companies$Symbol[ ! is.na(Companies$Sector)] ######################################## #NASDAQ<- honors_stocks(symbols = Symbols[1:2785]) #save(NASDAQ, file = "NASDAQ_Stock_Data.Rda") ######################################## #S&P 500 #Companies <- read.csv("S&P 500_companylist.csv", stringsAsFactors = FALSE, na.strings = "n/a") #Symbols <- Companies$Symbol[ ! is.na(Companies$Sector)] ######################################## #SP_500<- honors_stocks(symbols = Symbols[1:504]) #save(SP_500, file = "SP_500_Stock_Data.Rda") ######################################## #S&P 500 historical companies Symbols=SP_marketCap$company SP_H_Comp<- honors_stocks(symbols = Symbols) save(SP_H_Comp, file = "SP_H_Data.Rda")
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/wordcloud/src/main_wordcloud.R
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main_wordcloud.R
############################################################################### ## Wordcloud generator from tweets ## ############################################################################### # #Copyright Telefonica Digital #Author: User Modelling Analytics Team #Mantainer: Susana Ferreras <susanaf@tid.es> #Version: 1.1 #Date: 28/05/2013 #Purpose of program: generate wordclouds about topics from Twitter data #Dependencies: XML, tm, wordcloud, RColorBrewer, stringr, R.utils, rjson, # ggplot2, reshape packages #Inputs: Text files with tweets in 3rd field (one per row) #Output: PDF file with individual and common wordclouds #Config: in wordcloud.json file #Run: wordcloud.sh or wordcloud.bat to be executed in batch mode # #Configuration args = (commandArgs(TRUE)) if (length(args) == 0) { print("-----------------------------") print(" Error: missing arguments ") print("-----------------------------") q() } else { for (i in 1:length(args)) { eval(parse(text=args[[i]])) } } if (!file.exists(configfile) == 'TRUE') { print("-------------------------------------") print(" Error: missing configuration file ") print("-------------------------------------") q() } #Import libraries library(XML) library(tm) library(wordcloud) library(RColorBrewer) library(stringr) library(R.utils) library(rjson) library(ggplot2) library(reshape) options(warn=-1) #Add wordcloud functions source("../Wordcloud/src/functions_wordcloud.R") #Import parameters in JSON (choose either local file or parameter) #From local file #config <- fromJSON(paste(readLines("wordcloud.json"), collapse="")) #From parameter config <- fromJSON(file=configfile) tit <- config$input$title subt <- config$input$subtitle num.par <- config$input$number path <- config$input$path files <- config$input$files names <- config$input$names pal.ind <- config$layout$palette_ind pal.comp <- config$layout$palette_comp pal.all <- config$layout$palette_all bg.colour <- config$layout$bg_colour tx.colour <- config$layout$tx_colour ti.colour <- config$layout$ti_colour rp.main <- config$layout$report_title tx.main <- config$layout$text_title tx.date <- config$layout$text_date out.name <- config$output$name #Read input data cumm <- data.frame() tweets <- data.frame() for (i in 1:num.par) { wc <- read_input(paste(path, files[i], sep=""), names[i]) tweets[i, 1] <- names[i] tweets[i, 2] <- nrow(wc) tweets[i, 3] <- num.par - i call <- get_words(wc, names[i], filt, ftype, del, lang, stopw) cumm <- rbind(cumm, call) } colnames(tweets) <- c("words", "count", "num") #Create report pdf(file=out.name, width=9, height=6, family="Helvetica-Narrow") par(bg=bg.colour, mar=c(1,1.2,1.2,1.2), col.main=tx.colour, cex.main=1.8) plot(0:10, type='n', bty='n', xaxt='n', yaxt='n', xlab='', ylab='') text(6, 7, tit, font=2, col=ti.colour, cex=3) text(6, 6, subt, font=2, col=ti.colour, cex=3) text(6, 4, tx.date, font=2, col=ti.colour, cex=2) #Summary ggplot(tweets, aes(x=reorder(words, num), y=count, label=count)) + geom_bar(stat="identity", fill=brewer.pal(num.par, pal.comp)[num.par:1], colour=tx.colour) + theme_clean() + coord_flip() + ggtitle(rp.main) + theme(plot.title= element_text(hjust=0.5, face="bold", colour=tx.colour, size=25), plot.background=element_rect(fill=bg.colour), axis.text.x=element_blank(), axis.text.y= element_text(face="bold", size=15, colour=brewer.pal(num.par, pal.comp)[num.par:1]), panel.grid=element_blank(), axis.ticks=element_blank()) + geom_text(size=3.5, hjust=-0.2, colour=tx.colour, fontface=2) #Individual wordclouds for(n in 1:num.par) { wo <- cumm[cumm[, "topic"] == names[n], ] wordcloud(wo$word,wo$freq, scale=c(5,1), min.freq=1, max.words=100, random.order=FALSE, random.color=FALSE, rot.per=0, colors=brewer.pal(7, pal.ind), use.r.layout=FALSE) title(main=paste(tx.main, names[n], tx.date)) par(fig=c(0,1,0,1), new=TRUE) add_legend(brewer.pal(7, pal.ind)) if (n == 1) { leg <- "* Bigger sizes and higher \ncolours in palette show more importance" par(fig=c(0,1,0,1), new=TRUE) plot(0:25, type="n") text(22, 1, leg, col=tx.colour, cex=0.8) } } #Multi wordclouds if (num.par > 1){ mat <- get_matrix(cumm) comparison.cloud(mat,scale=c(5,1),max.words=2000,random.order=FALSE, rot.per=0, use.r.layout=FALSE, title.size=2, colors=brewer.pal(ncol(mat), pal.comp)) title(main=paste('Multi wordcloud', tx.date)) leg <- "* If a word is related \nto some topics,\nit will be associated to the one with \nmore importance (in %)" par(fig=c(0,1,0,1), new=TRUE) plot(0:25, type="n") text(24, 1.2, leg, col=tx.colour, cex=0.8) all <- list() for (i in 1:nrow(mat)) { all[i] <- sum(mat[i, 1:num.par] > 0) } if (any(all == num.par)) { commonality.cloud(mat, comonality.measure=min, scale=c(5,1), random.order=FALSE, random.color=FALSE, rot.per=0, colors=brewer.pal(7, pal.all), use.r.layout=FALSE) title(main=paste('Wordcloud - Words in all topics', tx.date)) par(fig=c(0,1,0,1), new=TRUE) add_legend(brewer.pal(7, pal.all)) } commonality.cloud(mat, comonality.measure=max, scale=c(5,1), random.order=FALSE, random.color=FALSE, rot.per=0, colors=brewer.pal(7, pal.all), use.r.layout=FALSE) title(main=paste('Wordcloud - Most important words', tx.date)) par(fig=c(0,1,0,1), new=TRUE) add_legend(brewer.pal(7, pal.all)) } dev.off() rm(list=ls())
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subfunctie_df_gebied.R
subgebied <- function(df_gebied, gebiedskolom, ci_level, n_vraag_afkapwaarde, data, var_df, survey_design){ # Initialiseer regelnummer op 1, voor het wegschrijven van de uitgerekende data regelnummer <- 1 for (gebied in unique(data[[gebiedskolom]])) { # survey_design_sub <- subset(survey_design, cbs == gemeente) geeft hele rare output, doordat gemeente als R variabele wordt ingevoerd ipv tekst. # Subset geeft geen foutmelding, maar wordt gedaan op verkeerde gemeente. Onderstaande werkt wel tekst <- paste0("subset(survey_design, ", gebiedskolom, " == {gebied})") survey_design_sub <- eval(parse(text = glue(tekst))) data_sub <- data[data[[gebiedskolom]] == gebied & !is.na(data[[gebiedskolom]]),] # Ook hier geen subset() gebruiken, geeft verkeerde data terug for (varcode in var_df$V1){ if (!all(is.na(data[[varcode]]))){ varlabels <- attr(data[[varcode]], "labels") # value labels. # value labels. Gebruik data ipv data_sub, omdat je anders labels mist als een bepaald antwoord niet voorkomt bij de eerste gemeente # loopen met survey package wil niet op normale manier. Daarom methode met glue en eval om tb en betrouwbaarheidsintervallen te krijgen. # tb <- svytable(formula = ~data_sub[[varcode]] , design = survey_design_sub) # Hiermee mis ik de antwoordopties die niemand heeft gekozen string_tb <- paste0("svytable(formula = ~data[['{varcode}']], design = survey_design)") # Deze bevat populatieaantallen. Prima als je tb alleen voor labels gebruikt en niet de gewogen n per gemeente wil weten expr_tb <- glue(string_tb) tb <- eval(parse(text = expr_tb)) # tb <- svytable(formula = ~data[[varcode]] , design = survey_design) for (j in 1:length(tb)){ # Voor het aantal niet-missing antwoordopties uit de vraag val <- names(tb)[j] # val is de numerieke code van de huidige antwoordoptie ## bereken betrouwbaarheidsintervallen string <- paste0("svyciprop(~I({varcode}=={val}), survey_design_sub, method='xlogit', na.rm=TRUE, level = ", ci_level, ")") expr <- glue(string) ci <- eval(parse(text = expr)) # confidence intervals # Schrijf info weg naar dataframe temp_varcode <- varcode # variabelenaam temp_waarde <- names(tb)[j] # numerieke waarde van huidige antwoordoptie temp_label <- names(varlabels)[varlabels == as.numeric(names(tb)[j])] # tekstlabel van huidige antwoordoptie # Als variable label ontbreekt, zet dan naar lege string if (length(temp_label) == 0) { temp_label = "" } # temp_n <- round(tb_regio[[j]]) # Populatie n / gewogen n <= is populatie van hele regio, niet van subset. temp_percentage <- ci[[1]] * 100 # Estimate/percentage temp_CIlower <- attr(ci, "ci")[1] * 100 # CI lower temp_CIupper <- attr(ci, "ci")[2] * 100 # CI upper temp_n_unweighted <- sum(survey_design_sub[["variables"]][varcode] == as.integer(names(tb)[j]), na.rm = TRUE) # sample n / ongewogen n temp_gebied <- gebied # Schrijf data weg naar dataframe df_gebied[regelnummer,] <- c(temp_varcode, temp_waarde, temp_label, temp_percentage, temp_CIlower, temp_CIupper, temp_n_unweighted, temp_gebied) # Print huidige regelnummer om idee te krijgen hoe lang script nog zal runnen print(paste0(regelnummer, " van ", aantal_verwachte_rijen)) # Hoog regelnummer met 1 op om de volgende regel in de dataframe te vullen met de volgende indicator/antwoordoptie regelnummer <- regelnummer + 1 } } } } # Zet naar numeric df_gebied$waarde <- as.numeric(df_gebied$waarde) df_gebied$percentage <- as.numeric(df_gebied$percentage) df_gebied$CIlower <- as.numeric(df_gebied$CIlower) df_gebied$CIupper <- as.numeric(df_gebied$CIupper) df_gebied$n_unweighted <- as.numeric(df_gebied$n_unweighted) # Tel aantal geldige antwoorden per vraag op. df_gebied <- df_gebied %>% group_by(varcode, gebied) %>% mutate(n_vraag = sum(n_unweighted)) %>% ungroup() df_gebied$percentage[df_gebied$n_vraag < n_vraag_afkapwaarde] <- NA df_gebied$CIlower[df_gebied$n_vraag < n_vraag_afkapwaarde] <- NA df_gebied$CIupper[df_gebied$n_vraag < n_vraag_afkapwaarde] <- NA # Maak combi van variable en value aan df_gebied$varval <- paste0(df_gebied$varcode, df_gebied$waarde) # Maak koppelkolom aan df_gebied$gebied_varval <- paste0(df_gebied$gebied, df_gebied$varval) beep(sound = 3) return(df_gebied) }
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library(testthat) library(DynamicStrategies) test_check("DynamicStrategies")
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plot_data.R
# load package, paths and variable sets from global.R -------------------------- source("inst/extdata/scripts/global.R") # MAIN 0: histogram of static water level measurements and data origin --------- if (FALSE) { # plot histogram plot_histogram <- function(df) { ggplot2::ggplot(df, ggplot2::aes( x = W_static, fill = forcats::fct_rev(W_static.origin), alpha = full_data_set)) + ggplot2::geom_histogram(position = "stack", boundary = 0) + ggplot2::scale_fill_manual(values = RColorBrewer::brewer.pal(3, "Set2")) + ggplot2::scale_alpha_manual(values = c(0.4, 1.0)) + sema.berlin.utils::my_theme() + ggplot2::labs(fill = "Type", alpha = "Data complete?", x = "static water level") } plot_histogram(df_Q_W_new) ggplot2::ggsave("W_static_interpolation_m20k1_f15k8_i64k2.png", dpi = 600, width = 5, height = 3) # histogram of Qs_rel vs. n_rehab ---------------------------------------------- ggplot(df, aes(x = Qs_rel, fill = factor(n_rehab))) + geom_histogram(position = "fill", boundary = 0, binwidth = 0.1) + #scale_x_continuous(limit = c(-0.5, 3)) + scale_x_continuous(limit = c(0, 1), labels = scales::percent, breaks = scales::pretty_breaks()) + scale_y_continuous(labels = scales::percent, breaks = scales::pretty_breaks()) + #ggplot2::scale_fill_manual(values = RColorBrewer::brewer.pal(8, "Set2")) + sema.berlin.utils::my_theme() + labs(fill = "n_rehab:") ggsave("plot_Qs_rel_vs_n_rehabs.png", dpi = 600, width = 5, height = 3) } # MAIN 1: plots of data distribution ------------------------------------------- if (FALSE) { # Version 1: plot distribution of well characteristics --- if (TRUE) { load(file.path(paths$data_prep_out, "well_feature_data.RData"), verbose = TRUE) df_well_features <- Data %>% dplyr::filter(well_function == "Betriebsbrunnen") %>% dplyr::select(-well_function) # or select wells represented in model data if (FALSE) { load(file.path(paths$data_prep_out, "well_feature_data.RData"), verbose = TRUE) df_well_features <- Data load(file.path(paths$data_prep_out, "model_data.RData"), verbose = TRUE) df <- Data df_well_features <- df_well_features %>% dplyr::filter(well_id %in% df$well_id) } nums <- unlist(lapply(df_well_features, is.numeric)) df_well_features_num <- df_well_features[, nums] %>% dplyr::select(- c(well_id, well_id_replaced, operational_start.year)) df_well_features_cat <- df_well_features[, !nums] %>% dplyr::select(-c("well_name", tidyr::ends_with("date"))) well_features_num <- model_features_with_plot_names[names(df_well_features_num)] well_features_cat <- model_features_with_plot_names[names(df_well_features_cat)] plots_cat <- lapply(names(well_features_cat), function(x) { plot_frequencies(df_well_features, x, well_features_cat[x], 0.1) }) names(plots_cat) <- names(well_features_cat) # prepare plots for numerical variables if (FALSE) { # simple version with only title plots_num <- lapply(names(well_features_num), function(x) { plot_distribution(df_well_features, x, title = well_features_num[x], vertical_x_axis_labels = FALSE) }) } # plot with xaxis label plots_num <- lapply(names(well_features_num), function(x) { split_label <- unlist(stringr::str_split(well_features_num[x], "\\[")) title_label <- split_label[1] xaxis_label <- ifelse(is.na(split_label[2]), "", paste0("[", split_label[2])) plot_distribution(df_well_features, x, title = title_label, vertical_x_axis_labels = FALSE) + labs(x = xaxis_label) }) names(plots_num) <- names(well_features_num) # combine plots in desired order plot_list_tmp <- c(plots_num, plots_cat) plot_list <- vector("list", length = length(plot_list_tmp)) names(plot_list) <- well_features[well_features %in% names(plot_list_tmp)] for (var in names(plot_list)) { plot_list[[var]] <- plot_list_tmp[[var]] } # cowplot plots <- cowplot::plot_grid(plotlist = plot_list, nrow = 6, ncol = 7, align = "hv", axis = "tblr", scale = 0.9) # save overview plot ggplot2::ggsave("well_characteristics_distribution_Betriebsbrunnen_with_xlabels.png", plot = plots, width = 28, height = 25, dpi = 600) } # Version 2: plot distribution of model features, including Qs_rel --- if (TRUE) { # load data #load(file.path(paths$data_prep_out, "model_data.RData"), verbose = TRUE) df <- model_data # select variables df_well_features <- df %>% select(Qs_rel, all_of(model_features)) nums <- unlist(lapply(df_well_features, is.numeric)) df_well_features_num <- df_well_features[, nums] df_well_features_cat <- df_well_features[, !nums] # prepare named list of model features, add target variable Qs_rel well_features_num <- model_features_with_plot_names[names(df_well_features_num)] well_features_num[[1]] <- "Specific capacity [%]" names(well_features_num)[[1]] <- "Qs_rel" well_features_cat <- model_features_with_plot_names[names(df_well_features_cat)] # prepare plots for categorical variables plots_cat <- lapply(names(well_features_cat), function(x) { plot_frequencies(df_well_features, x, well_features_cat[x]) }) names(plots_cat) <- names(well_features_cat) # prepare plots for numerical variables if (FALSE) { # simple version with only title plots_num <- lapply(names(well_features_num), function(x) { plot_distribution(df_well_features, x, title = well_features_num[x], vertical_x_axis_labels = FALSE) }) } # plot with xaxis label plots_num <- lapply(names(well_features_num), function(x) { split_label <- unlist(stringr::str_split(well_features_num[x], "\\[")) title_label <- split_label[1] xaxis_label <- ifelse(is.na(split_label[2]), "", paste0("[", split_label[2])) plot_distribution(df_well_features, x, title = title_label, vertical_x_axis_labels = FALSE) + labs(x = xaxis_label) }) names(plots_num) <- names(well_features_num) # combine plots in desired order plot_list_tmp <- c(plots_num, plots_cat) plot_list <- vector("list", length = length(plot_list_tmp)) names(plot_list) <- c("Qs_rel", model_features) for (var in names(plot_list)) { plot_list[[var]] <- plot_list_tmp[[var]] } # adapt colour of Qs_rel plot plot_list[[1]] <- plot_list[[1]] + ggplot2::geom_histogram(fill = "orange2", boundary = 0, binwidth = NULL) # cowplot plots <- cowplot::plot_grid(plotlist = plot_list, align = "hv", axis = "tblr", nrow = 6, ncol = 7, scale = 0.9) # save overview plot ggplot2::ggsave("model_feature_distribution.png", plot = plots, width = 28, height = 25, dpi = 600) } } # MAIN 2: correlation of Qs vs. other variables plots -------------------------- if (FALSE) { df <- model_data correlation_plots <- lapply(model_features, function(x) { split_label <- unlist(stringr::str_split(model_features_with_plot_names[x], "\\[")) title_label <- split_label[1] xaxis_label <- ifelse(is.na(split_label[2]), "", paste0("[", split_label[2])) correlation_plot(df = df, x = x, title = title_label) + labs(x = xaxis_label) #correlation_plot(df = df, x = x, title = model_features_with_plot_names[x]) }) multiplots <- cowplot::plot_grid(plotlist = correlation_plots, nrow = 6, ncol = 6, axis = "tblr", align = "hv", scale = 0.9) ggplot2::ggsave("correlation_plots_with_xlabels.png", multiplots, dpi = 600, width = 25, height = 25) # save individual plots lapply(correlation_plots, function(x) { ggplot2::ggsave(filename = paste0(gsub("\\.", "_", names(x$labels$title)), ".png"), plot = x, dpi = 600, width = 6, height = 4) }) } # MAIN 3: Plots zu Qs per well over time --------------------------------------- if (FALSE) { # filter --- df2 <- df %>% dplyr::filter(key2 == "pump tests") %>% dplyr::mutate(key2 = forcats::fct_drop(key2)) length(unique(df2$site_id)) df$key2 <- "pump tests" df$facet_lab <- paste0("well id: ", df$well_id, " (year: ", df$construction_year, ifelse(!is.na(df$well_id_replaced), paste0(", old well id: ", df$well_id_replaced), ""), ")") pdf("Qsrel_over_time_pump_tests.pdf", 16, 9) pdf("Qsrel_over_time_all.pdf", 16, 9) pdf("Qsrel_over_time_with_old_well_info.pdf", 16, 9) for (i in seq(1, length(unique(df$well_id)), 12)) { print(plot_Qs_over_time(df[df$well_id %in% unique(df$well_id)[i:(i + 11)], ]) + facet_wrap(~ facet_lab, scales = "free", ncol = 4) #facet_wrap(~ well_id, scales = "free", labeller = label_both, ncol = 4) ) print(paste("pdf page", (i+11) / 12, "printed.")) } dev.off() # plots for selected well ids plot_Qs_over_time(df[df$well_id %in% c(1081, 3258, 1084, 3259), ], xmax = 15) + facet_wrap(~ facet_lab, scales = "free_x", ncol = 2, dir = "v") + ggplot2::theme(strip.text.x = ggplot2::element_text(size = 9)) ggsave("example_replaced_wells.png", dpi = 600, width = 8, height = 6) old_well_ids <- unique(df$well_id_replaced) old_well_ids[old_well_ids %in% df$well_id] a <- df[, c("well_id", "construction_year", "well_id_replaced", "Qs_rel")] # plot two wells in comparison --- library(dplyr) library(dwc.wells) site_ids <- c(4060070, 11020030) well_ids <- c(1161, 5837) df2 <- df %>% dplyr::filter(site_id %in% site_ids) %>% droplevels() df$n_rehab <- as.factor(df$n_rehab) plot_Qs_over_time(df2, xmax = 40, legend_position = "right") + facet_wrap(~well_id, scales = "free", labeller = label_both, nrow = 1) ggsave("Qs_over_time_two_example_wells_v2.png", dpi = 600, width = 8, height = 3) } # MAIN 4: plot Qs-data for all wells as heatmap -------------------------------- if (FALSE) { # parameters group_var <- "waterworks" n_wells_per_page <- 20 date_limits <- c("1960-01-01", "2021-12-31") file_name <- "Qsrel_over_time_heatmap_per_waterworks.pdf" # select data df <- model_data %>% select(well_id, well_name, date, Qs_rel, waterworks, well_gallery) # interpolate data df_interpol <- interpolate_Qs(df, 1) # group wells well_ids_per_group <- df %>% group_by(group = .data[[group_var]]) %>% summarise(well_id = as.character(unique(well_id))) colours <- sema.berlin.utils::get_bwb_colours()[c(2,3,5)] dummy_labels <- unlist(lapply((1:n_wells_per_page) - 1, strrep, x = " ")) pdf(file_name, width = 9, height = 5) # loop 1: go through well groups for (well_group in unique(well_ids_per_group$group)) { well_ids <- well_ids_per_group %>% filter(group == well_group) %>% pull(well_id) # loop 2: for each well group, go trough wells for (i in seq(1, length(well_ids), n_wells_per_page)) { well_ids_to_plot <- well_ids[i:(i + n_wells_per_page - 1)] plot_data <- df_interpol %>% filter(well_id %in% well_ids_to_plot) print(Qs_heatmap_plot(plot_data, colours, dummy_labels, date_limits, title = well_group, n_wells_per_page)) print(sprintf("Data for %d well(s) of %s '%s' plotted.", i + length(well_ids_to_plot) - 1, group_var, well_group)) } } dev.off() ggsave("example_plot_Qs_over_time_heatmap.png", width = 10, height = 5, dpi = 600) ggsave("example_plot_Qs_over_time_heatmap_v2.png", width = 8, height = 5, dpi = 600) } # MAIN 5: plots for Qmom-Qzul relation ----------------------------------------- if (FALSE) { # required data set: df_Q_monitoring # distribution p1 <- ggplot2::ggplot(df_Q_monitoring, ggplot2::aes(x = ratio_Q_admissible_discharge, y = stat(count) / sum(stat(count)))) + ggplot2::geom_histogram(binwidth = 0.1, fill = "grey", col = "white", boundary = 1) + ggplot2::scale_x_continuous(limits = c(0, 2)) + ggplot2::scale_y_continuous(name = "Percentage", breaks = scales::pretty_breaks(), labels = scales::percent_format(accuracy = 1)) + sema.berlin.utils::my_theme() plotly::ggplotly(p1) # cumulative distribution l <- lapply(seq(0, 2, 0.1), function(x) table(df_Q_monitoring$ratio_Q_admissible_discharge > x)) names(l) <- sprintf("%3.1f", seq(0, 2, 0.1)) df <- data.frame(do.call("rbind", l)) colnames(df) <- c("valid", "invalid") df$threshold <- rownames(df) df <- tidyr::pivot_longer(data = df, cols = c("valid", "invalid")) #df$name <- factor(df$name, levels = c("valid", "invalid")) df$name <- factor(df$name, levels = c("invalid", "valid")) p2 <- ggplot2::ggplot(df, ggplot2::aes(x = threshold, y = value, fill = name)) + ggplot2::geom_bar(stat = "identity", position = "fill") + sema.berlin.utils::my_theme(legend.position = "top", axis.text.x = ggplot2::element_text(angle = 90, vjust = 0.5, hjust = 1)) + ggplot2::scale_fill_manual(values = c("coral", "darkseagreen3")) + ggplot2::scale_x_discrete(expand = c(0.05, 0.05)) + ggplot2::scale_y_continuous(labels = scales::percent_format(), breaks = scales::pretty_breaks()) + ggplot2::labs(x = 'Threshold "Qmom/Qzul"', y = "Percentage", fill = "") p2 ggplot2::ggsave("Qmom_Qzul_threshold.png", p2, dpi = 600, height = 4, width = 6) p2 cowplot::plot_grid(p1, p2) # plot median Q_mom per well --------------------------------------------------- # aggregate data df_Q_agg <- dplyr::filter(df_Q_monitoring, Q < 1000) %>% dplyr::group_by(well_id) %>% dplyr::summarise(Q_median = median(Q, na.rm = TRUE), Q_stddev = sd(Q, na.rm = TRUE), number = dplyr::n()) %>% tidyr::drop_na() # plot Q measurements ggplot2::ggplot(df_Q_agg, ggplot2::aes(x = Q_median)) + ggplot2::geom_histogram(fill = "lightblue", binwidth = 5) + sema.berlin.utils::my_theme() + ggplot2::scale_y_continuous(breaks = scales::pretty_breaks()) + ggplot2::scale_x_continuous(breaks = scales::pretty_breaks()) + ggplot2::labs(x = "Q_obs_median [m³/h]", y = "Frequency [-]") summary(df_Q_agg) ggplot2::ggsave("histogram_Ergiebigkeit_Q_obs.png", width = 4, height = 2.5, dpi = 600) # plots of quality measurements ------------------------------------------------ # requires df_quality_agg_long ggplot2::ggplot(df_quality_agg_long, ggplot2::aes(x = "", y = Wert)) + ggplot2::geom_boxplot(width = 0.3) + ggplot2::facet_wrap(~paste0(Parameter, "\n", "[", Einheit, "]"), scales = "free_y", nrow = 1) + ggplot2::labs(x = "", y = "Werte") + sema.berlin.utils::my_theme() + ggplot2::theme(strip.text.x = ggplot2::element_text(size = 11, hjust = 0.5), axis.ticks.x = ggplot2::element_blank()) ggplot2::ggplot(df_quality, ggplot2::aes(x = "", y = Wert)) + ggplot2::geom_boxplot(width = 0.3) + ggplot2::facet_wrap(id_Brunnen~paste0(Parameter, "\n", "[", Einheit, "]"), scales = "free_y", nrow = 1) + ggplot2::labs(x = "", y = "Werte") + sema.berlin.utils::my_theme() + ggplot2::theme(strip.text.x = ggplot2::element_text(size = 11, hjust = 0.5), axis.ticks.x = ggplot2::element_blank()) ggplot2::ggsave("plot_quality_all_wells.png", width = 15, height = 5000, dpi = 600) getwd() }
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% Generated by roxygen2: do not edit by hand % Please edit documentation in R/pairs2.R \name{pairs_lower} \alias{pairs_lower} \title{lower panel for stats::pairs} \usage{ pairs_lower(x, y) } \description{ correlation coefficients }
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cerealsClustering.R
#install.packages("clustertend") library(cluster) library(ggplot2) library(factoextra) #A. Calificación de clientes de cereales para el desayuno dataCereales<-read.csv("RFiles/Cereals.csv",header = TRUE, sep = ",") #---Exploración inicial de los datos str(dataCereales) View(dataCereales) summary(dataCereales) #----Preprocesamiento de los datos sum(is.na(dataCereales)) dataCereales <- dataCereales[complete.cases(dataCereales),] sum(is.na(dataCereales)) rownames(dataCereales) <- dataCereales$name #Conversion de nombres de cereales a las dataCereales <- dataCereales[, -c(colnames(dataCereales) %in% ("name"))] #filas para mejor visualización de clusters. View(dataCereales) dataCereales <- dataCereales[, -c(1:2)] View(dataCereales) dataCereales <- scale(dataCereales) #---Evaluación de tendencia library(clustertend) set.seed(124) hopkins(dataCereales,n=nrow(dataCereales)-1) #si es cercano a 0 el dataset es agrupable #---Calcular estabilidad de los datos muestra<- dataCereales[sample(nrow(dataCereales), nrow(dataCereales)*0.95), ] muestra hopkins(muestra,n=nrow(muestra)-1) #---Calculo distancia Euclidiana dist <- dist(dataCereales, method = "euclidean") #---Agrupamiento jerarquico hc_simple <- hclust(dist, method = "single") #enlace unico 5 hc_simple plot(hc_simple) fviz_dend(hc_simple, cex =0.5) hc_complete <- hclust(dist, method = "complete") #enlace completo 6 hc_complete plot(hc_complete) fviz_dend(hc_complete, cex =0.5) #---Comparamos los dendogramas de ambos metodos #install.packages("dendextend") library(dendextend) dend1<-as.dendrogram(hc_simple) dend2<-as.dendrogram(hc_complete) dend_list<-dendlist(dend1,dend2) #Se crea la lista de dendogramas. #tanglegram(dend1,dend2) tanglegram(dend1,dend2, highlight_distinct_edges=FALSE, common_subtrees_color_lines=FALSE, common_subtrees_color_branches=TRUE, main=paste("entanglement=", round(entanglement(dend_list),2)) ) #---Determinamos si los dendogramas son similares o no cor.dendlist(dend_list,method="cophenetic") #Si su relación es más cercana a 0 que a 1 significa que no son estadisticamente similares. #En este caso son medianamente similares #---Comparamos los dos metodos dend_list<-dendlist("Single"=dend1,"Complete"=dend2) cors<-cor.dendlist(dend_list) round(cors,2) #install.packages("corrplot") library(corrplot) corrplot(cors,"pie","lower") #---Calcular las distancias cofenéticas para checar que #arbol es mejor >.75 son buenos coph_simple <- cophenetic(hc_simple) cor(dist,coph_simple) #calcular corelación de distancias coph_complete <- cophenetic(hc_complete) cor(dist,coph_complete) hc_average <- hclust(dist, method = "average") #cluster con enlcae average es el mejor en este caso coph_ave <- cophenetic(hc_average) cor(dist,coph_ave) #----Calcular k #install.packages("NbClust") library("NbClust") fviz_nbclust(dataCereales,hcut,method = "silhouette") #NbClust(dataCereales,distance="euclidean",min.nc=2,max.nc=10, method="ward.D") #--Cortar el arbor observar centroides grp_simple <- cutree(hc_simple, k = 10) table(grp_simple) rownames(dataCereales)[grp_simple=1] #Obtener los nombres para los miembros del cluster 1 fviz_dend(hc_simple, k=10, cex = 0.5, k_colors = c("#D81159", "#8F2D56","#218380","#FBB13C", "#73D2DE","#5F1F30", "#9C0D38","#BE7C4D","#82A7A6", "#F06543"), color_labels_by_k = TRUE, rect = TRUE) grp_complete <- cutree(hc_average, k = 10) table(grp_complete) rownames(dataCereales)[grp_complete=1] fviz_dend(hc_average, k=10, cex = 0.5, k_colors = c("#D81159", "#8F2D56","#218380","#FBB13C", "#73D2DE","#5F1F30", "#9C0D38","#BE7C4D","#82A7A6", "#F06543"), color_labels_by_k = TRUE, rect = TRUE) #---observar centroides cluster_Simple<-as.matrix(grp_simple) aggregate(dataCereales,by=list(cluster_Simple),median) dataCereales_simple <- cbind(dataCereales, cluster = cluster_Simple) head(dataCereales_simple) cluster_Complete<-as.matrix(grp_complete) aggregate(dataCereales,by=list(cluster_Complete),median) dataCereales_complete <- cbind(dataCereales, cluster = cluster_Complete) head(dataCereales_complete) fviz_cluster(list(data = dataCereales, cluster = grp_simple)) fviz_cluster(list(data = dataCereales, cluster = grp_complete)) #---Visualuzar estadisticas por grupo View(dataCereales_simple) dataCereales_simple <- as.data.frame(dataCereales_simple) summary(dataCereales_simple[dataCereales_simple$V14==1,]) summary(dataCereales_simple[dataCereales_simple$V14==2,]) summary(dataCereales_simple[dataCereales_simple$V14==3,]) summary(dataCereales_simple[dataCereales_simple$V14==4,]) summary(dataCereales_simple[dataCereales_simple$V14==5,]) summary(dataCereales_simple[dataCereales_simple$V14==6,]) summary(dataCereales_simple[dataCereales_simple$V14==7,]) summary(dataCereales_simple[dataCereales_simple$V14==8,]) summary(dataCereales_simple[dataCereales_simple$V14==9,]) summary(dataCereales_simple[dataCereales_simple$V14==10,]) #---Visualizar conjunto dataCereales_simple[dataCereales_simple$V14==1,] dataCereales_simple[dataCereales_simple$V14==2,]
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/merge-fasta.R
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DanielleQuinn/skate-code
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refs/heads/master
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merge-fasta.R
# Load Packages library(tidyr) library(seqinr) library(dplyr) # Read in Working Data data<-read.delim("data-working.txt") data$finclip<-as.character(data$finclip) data$species_confirmed<-as.character(data$species_confirmed) # Read in Fasta File ffile<-data.frame(id=names(read.fasta("data-genetics.fasta"))) fdata<-separate(ffile, id, sep="_",into=c("tissue_id", "plate","sample","genus","species")) fdata<-fdata%>%filter(!sample=="control" & !genus=="Unclear") # Populate species_confirmed with species names data$species_confirmed[data$finclip %in% unique(fdata$tissue_id[fdata$species=="ocellata"])]<-"winter skate" data$species_confirmed[data$finclip %in% unique(fdata$tissue_id[fdata$species=="erinacea"])]<-"little skate" data$species_confirmed[data$finclip %in% unique(fdata$tissue_id[fdata$species=="radiata"])]<-"thorny skate"
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#!/usr/bin/env Rscript suppressPackageStartupMessages(library(optparse)) suppressPackageStartupMessages(library(magrittr)) ################## #Argument parsing. ################## usage = "%prog SPECIES_DATA_INPUT_FILE FOCAL_OUTPUT_FILE DATA_TYPE RESPONSE_OUTPUT_FILE DESIGN_OUTPUT_FILE SPECIES_DATA_OUTPUT_FILE MIN_OBS_OUTPUT_FILE" description = "Takes the neigh_list data from the cxr package, and reshapes it into the three files desired by the C++ code. Namely, the 0-indexed numerical focal species vector, the response variable vector, and the species density design matrix. All are output as tab-separated matrices, without column headers, with vectors in the form column vectors. DATA_TYPE must be 'indv', for individual response data." option_list <- list( make_option( c("-m", "--minobs"), dest = "bare_min_obs", type = "integer", default = 2, help = "The minimum number of replicate observations required for each species pair" ) ) parser <- OptionParser(usage = usage, description=description, option_list=option_list) arguments <- parse_args(parser, positional_arguments = 6) data_type <- arguments$args[1] focal_outfile <- arguments$args[2] response_outfile <- arguments$args[3] design_outfile <- arguments$args[4] species_data_outfile <- arguments$args[5] min_obs_outfile <- arguments$args[6] attach(arguments$options) if(data_type != "indv") { stop("Invalid data type requested.") } other_name <- "Other" other_code <- "OTHR" ############### #Load the data. ############### data(neigh_list, package = "cxr") data(species_rates, package = "cxr") #With names of each species. ############################## #Filter to the maximal clique. ############################## species <- names(neigh_list) #A function to get a maximum-size clique such that all pairs have at least min_obs observations. get_max_clique <- function(min_obs) { adj_mat <- sapply(species, function(i) { sapply(species, function(j) { sum(neigh_list[[i]][[j]] > 0) >= min_obs && sum(neigh_list[[j]][[i]] > 0) >= min_obs }) }) dist_mat <- as.dist(1 - adj_mat) cliques <- optpart::clique(dist_mat, 0)$member clique_sizes <- sapply(cliques, length) return(cliques[[which.max(clique_sizes)]]) } #We want to find the highest value of min_obs such that the largest clique #still has the same size as at the bare minimum value of min_obs we will accept. max_clique_size <- length(get_max_clique(bare_min_obs)) min_obs <- bare_min_obs while(length(get_max_clique(min_obs + 1)) == max_clique_size) { min_obs <- min_obs + 1 } included_species <- species[get_max_clique(min_obs)] excluded_species <- species[!species %in% included_species] #Append all data in one data frame. #Only including cases where the included species are the focals. #Adding a "focal" column. #And adding one to the focal density, to include the individual itself. data <- data.frame() for(sp in included_species) { neigh_list[[sp]]$focal <- sp neigh_list[[sp]][[sp]] <- neigh_list[[sp]][[sp]] + 1 #TODO: Check this. data <- rbind(data, neigh_list[[sp]]) } #Collapse all excluded species into an "other" column. data[[other_code]] <- rowSums(data[,excluded_species]) data <- data[,!names(data) %in% excluded_species] species_codes <- c(included_species, other_code) ################################# #Extract the relevant components. ################################# focal_output <- data[["focal"]] %>% match(species_codes) focal_output <- focal_output - 1 #Make it 0-indexed. response_output <- data[["fitness"]] design_output <- data[,species_codes] ############################################## #Turn the outputs into matrices, and finalise. ############################################## focal_output %<>% matrix(ncol=1) response_output %<>% matrix(ncol=1) design_output %<>% as.matrix() ################################ #Create the species data output. ################################ species_data <- data.frame( name = species_rates$species, code = species_rates$code, germination_rate = species_rates$germination.rate, seed_survival = species_rates$seed.survival ) species_data$name <- sub("([[:alpha:]])([[:alpha:]]+)_([[:alpha:]]*)", "\\U\\1\\E\\2 \\3", species_data$name, perl = TRUE) #Format binomial names properly. species_data <- species_data[species_data$code %in% included_species,] species_data <- rbind(species_data, list( name = other_name, code = other_code, germination_rate = NA, seed_survival = NA )) ################### #Print the outputs. ################### print_table <- function(table, outfile) { write.table(table, outfile, row.names=FALSE, col.names=FALSE, quote=FALSE, sep="\t") } print_table(focal_output, focal_outfile) print_table(response_output, response_outfile) print_table(design_output, design_outfile) write.csv(species_data, species_data_outfile, row.names = FALSE) print_table(data.frame(min_obs), min_obs_outfile) #Outputs the single number to a file by itself.
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/R/cptSlopeplot.R
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BhaktiDwivedi/GISPA
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cptSlopeplot.R
#'@name cptSlopeplot #'@aliases cptSlopeplot #'@title Scatterplot representation of identified change points gene set slopes #'@description This function will plot the average slopes estimated over all gene sets within each change point by data types #'@usage cptSlopeplot(gispa.output,feature,type,cpt) #'@param gispa.output : A data matrix of between gene feature profile statistics for each feature with corrosponding identified changepoints. The row names should corrospond to genes or names to be displayed on y-axis #'@param feature : Analysis type i.e., one ('1'), two ('2') or three ('3') dimensional feature analysis. #'@param type : Type of data, e.g., EXP (default) for expression, VAR of variants, CNV for copy number change. #'@param cpt : Change point cutoff to be highlighted. The default is 1 #'@details This function expects the output from GISPA function of GISPA package, and highlights the gene set slope profile in the selected changepoints #'@return Scatterplot illustrating the average slopes by change point to access the best gene set profile #'@author Bhakti Dwivedi & Jeanne Kowalski #'@import scatterplot3d #'@importFrom data.table data.table #'@importFrom graphics plot #'@importFrom graphics par #'@importFrom graphics text #'@importFrom stats lm #'@examples #'id <- 200 ## number of rows #'s <- 3 ## number of columns #'dm <- matrix(runif(id*s,0,10), nrow=id, ncol=s, #' dimnames=list(paste("gene", 1:id, sep=""), #' paste("sample", 1:s, sep=""))) #'changepoints <- sort(sample(1:2, id, replace=TRUE)) #'dm <- cbind(dm,changepoints) #'cptSlopeplot(gispa.output=dm,feature=1,type="EXP",cpt=1) #'@export cptSlopeplot <- function(gispa.output, feature=1, type="EXP", cpt=1){ changepoints <- NULL # Setting the variables to NULL first ##select for the changepoint of interest gispa.output <- gispa.output[gispa.output[,ncol(gispa.output)]!=1000,] if(feature==1){ #data type 1 subset_data <- gispa.output[,c(1:3,ncol(gispa.output))] #considering we only have three groups lm.r <- lm (t(subset_data[, 1:3]) ~ I(1:3) ) #to get the slope estimates slope <- t(t(lm.r$coeff[2,])) colnames(slope) <- "slope" intercept <- t(t(lm.r$coeff[2,])) colnames(intercept) <- "intercept" subset_data <- cbind(subset_data,intercept,slope) #take average slope for each changepoint dt_data <- data.table(subset_data) avg_slope <- dt_data[,mean(slope),by=changepoints] avg_slope$cptcolor[as.numeric(avg_slope$changepoints) <= cpt] <- "orange" avg_slope$cptcolor[as.numeric(avg_slope$changepoints) > cpt] <- "grey" x <- as.numeric(avg_slope$changepoints) y <- as.numeric(avg_slope$V1) par(bg = "white") slopePlot <- plot(x, y, xlim=c(1,max(x)+1), ylim=c(min(y),max(y)), xlab="", ylab=paste("Mean Slope", " (", type[1], ")", sep=""), cex.lab =1.5, pch=16, cex=5, col=avg_slope$cptcolor) text(avg_slope$V1, labels=avg_slope$changepoints,cex=1.5,pos=4,offset=0.2) } if(feature==2){ #data type 1 subset_data <- gispa.output[,c(1:3,ncol(gispa.output))] #considering we only have three groups lm.r <- lm (t(subset_data[, 1:3]) ~ I(1:3) ) #to get the slope estimates slope <- t(t(lm.r$coeff[2,])) colnames(slope) <- "slope" intercept <- t(t(lm.r$coeff[2,])) colnames(intercept) <- "intercept" subset_data <- cbind(subset_data,intercept,slope) #take average slope for each changepoint dt_data <- data.table(subset_data) avg_slope_type_1 <- dt_data[,mean(slope),by=changepoints] #data type 2 subset_data <- gispa.output[,c(4:6,ncol(gispa.output))] #considering we only have three groups lm.r <- lm (t(subset_data[, 1:3]) ~ I(1:3) ) #to get the slope estimates slope <- t(t(lm.r$coeff[2,])) colnames(slope) <- "slope" intercept <- t(t(lm.r$coeff[2,])) colnames(intercept) <- "intercept" subset_data <- cbind(subset_data,intercept,slope) #take average slope for each changepoint dt_data <- data.table(subset_data) avg_slope_type_2 <- dt_data[,mean(slope),by=changepoints] #Merge the data #### avg_slope <- merge(avg_slope_type_1, avg_slope_type_2, by=c("changepoints")) #plot the data avg_slope$cptcolor[as.numeric(avg_slope$changepoints) <= cpt] <- "orange" avg_slope$cptcolor[as.numeric(avg_slope$changepoints) > cpt] <- "grey" x <- as.numeric(avg_slope$V1.x) y <- as.numeric(avg_slope$V1.y) par(bg = "white") slopePlot <- plot(x, y, xlim=c(min(x),max(x)+1), ylim=c(min(y),max(y)+1), xlab=paste("Mean Slope", " (", type[1], ")", sep=""), ylab=paste("Mean Slope", " (", type[2], ")", sep=""), cex.lab =1.5, pch=16, cex=5, col=avg_slope$cptcolor) text(avg_slope$V1.x, avg_slope$V1.y, labels=avg_slope$changepoints, cex=1.5,pos=4,offset=1.2) } if(feature==3){ #data type 1 subset_data <- gispa.output[,c(1:3,ncol(gispa.output))] #considering we only have three groups lm.r <- lm (t(subset_data[, 1:3]) ~ I(1:3) ) #to get the slope estimates slope <- t(t(lm.r$coeff[2,])) colnames(slope) <- "slope" intercept <- t(t(lm.r$coeff[2,])) colnames(intercept) <- "intercept" subset_data <- cbind(subset_data,intercept,slope) #take average slope for each changepoint dt_data <- data.table(subset_data) avg_slope_type_1 <- dt_data[,mean(slope),by=changepoints] #data type 2 subset_data <- gispa.output[,c(4:6,ncol(gispa.output))] #considering we only have three groups lm.r <- lm (t(subset_data[, 1:3]) ~ I(1:3) ) #to get the slope estimates slope <- t(t(lm.r$coeff[2,])) intercept <- t(t(lm.r$coeff[2,])) subset_data[,c("intercept","slope")]<-rbind(intercept,slope) #take average slope for each changepoint dt_data <- data.table(subset_data) avg_slope_type_2 <- dt_data[,mean(slope),by=changepoints] #data type 3 subset_data <- gispa.output[,c(7:9,ncol(gispa.output))] #considering we only have three groups lm.r <- lm (t(subset_data[, 1:3]) ~ I(1:3) ) #to get the slope estimates slope <- t(t(lm.r$coeff[2,])) colnames(slope) <- "slope" intercept <- t(t(lm.r$coeff[2,])) colnames(intercept) <- "intercept" subset_data <- cbind(subset_data,intercept,slope) #take average slope for each changepoint dt_data <- data.table(subset_data) avg_slope_type_3 <- dt_data[,mean(slope),by=changepoints] #Merge the data #### avg_slope_1_2 <- merge(avg_slope_type_1, avg_slope_type_2, by=c("changepoints")) avg_slope <- merge(avg_slope_1_2, avg_slope_type_3, by=c("changepoints")) #plot the data avg_slope$cptcolor[as.numeric(avg_slope$changepoints) <= cpt] <- "orange" avg_slope$cptcolor[as.numeric(avg_slope$changepoints) > cpt] <- "grey" x <- as.numeric(avg_slope$V1.x) y <- as.numeric(avg_slope$V1.y) z <- as.numeric(avg_slope$V1) par(bg = "white") slopePlot <- scatterplot3d(x, y, z, xlim=c(min(x),max(x)+1), ylim=c(min(y),max(y)+1), zlim=c(min(z),max(z)+1), xlab=paste("Mean Slope"," (",type[1],")",sep=""), ylab=paste("Mean Slope"," (",type[2],")",sep=""), zlab=paste("Mean Slope"," (",type[3],")",sep=""), cex.lab =1.5, pch=19, cex.symbols = 5, type="h", color=avg_slope$cptcolor) # convert 3D coords to 2D projection slopePlot.coords <- slopePlot$xyz.convert(x, y, z) text(slopePlot.coords$x, slopePlot.coords$y, labels=avg_slope$changepoints, cex=1.5, pos=4, offset=1.2) } return (slopePlot) }
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/R/dataset_documentation.R
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dataset_documentation.R
#' Common Packages #' #' Names of basic packages that should always be loaded. #' #' @format Character vector #' @author Malte Thodberg #' @details #' The list of packages includes: #' #' Data manipulation: magrittr, readr, tidyr, dplyr #' #' Special data formats: stringr, lubridate #' #' Plotting: grid, gridExtra, ggplot2, GGally, ggthemes, ggExtra, ggrepel, RColorBrewer, VennDiagram, pheatmap, wesanderson #' #' Performance: matrixStats, parallel "core_packages" #' Bioconductor Packages #' #' Names of biconductor packages that should always be loaded. #' #' @format Character vector #' @author Malte Thodberg #' @details #' The list of packages includes: #' #' Installer: BiocInstaller #' #' Genomic Arithmetic: Biostrings, IRanges, GenomicRanges, rtracklayer #' #' Differential Expression: limma, edgeR, DESeq2 "bioc_packages" #' Development Packages #' #' Names of biconductor packages, which should be loaded when developing. #' #' @format Character vector #' @author Malte Thodberg #' @details #' The list of packages includes: #' #' Development: Rccp, devtools, roxygen2, pryr, profr #' #' RStudio: rstudioapi, manipulate #' #' Terminal: setwidth, colorout "code_packages"
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/Code/R/Likelihood_Function.R
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saulmoore1/MSc_CMEE
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refs/heads/master
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Likelihood_Function.R
#!/usr/bin/env R binomial.likelihood <- function(p){ choose(10,7)*p^7*(1-p)^3 } binomial.likelihood(p=0.1) # Reutrns: 8.748e-06 p <- seq(0,1,0.01) likelihood.values <- binomial.likelihood(p) plot(p, likelihood.values, type="l") abline(h=max(likelihood.values), lty=4) abline(v=p[likelihood.values==max(likelihood.values)[1]], lty=4) grid(nx = NULL, ny = NA) log.binomial.likelihood <- function(p) { log(binomial.likelihood(p=p)) } p <- seq(0,1,0.01) log.likelihood.values <- log.binomial.likelihood(p) plot(p, log.likelihood.values, type="l") abline(h=max(log.likelihood.values), lty=4) abline(v=p[log.likelihood.values==max(log.likelihood.values)[1]], lty=4) grid(nx = NULL, ny = NA) max(log.likelihood.values) # Point at which the function is maximised remains the same (p = ~0.7) optimize(binomial.likelihood, interval = c(0,1), maximum = TRUE) # Maximum = x at max y (0.6999843), Objective=max(likelihood.values) (0.2668279) # Not exactly 0.7 because of rounding errors - theoretical = 0.7 recapture.data <- read.csv("../Data/recapture.csv", header=T) plot(recapture.data$day, recapture.data$length_diff, xlab="Day", ylab="Difference in length", pch=4) # THE LOG-LIKELIHOOD FOR THE LINEAR REGRESSION # PARAMETERS HAVE TO BE INPUT AS A VECTOR regression.log.likelihood<-function(parm, dat) { # DEFINE THE PARAMETERS parm # WE HAVE THREE PARAMETERS: a, b, sigma. BE CAREFUL OF THE ORDER a <- parm[1] # Slope b <- parm[2] # Intercept sigma <- parm[3] # Variance of the errors # DEFINE THE DATA dat # FIRST COLUMN IS x, SECOND COLUMN IS y x <- dat[,1] y <- dat[,2] # DEFINE THE ERROR TERM error.term <- (y-a-b*x) # REMEMBER THE NORMAL pdf? density <- dnorm(error.term, mean=0, sd=sigma, log=T) # log=T for LogLikelihood # THE LOG-LIKELIHOOD IS THE SUM OF INDIVIDUAL LOG-DENSITY return(sum(density)) } # JUST TO SEE WHAT THE LOG-LIKELIHOOD VALUE IS WHEN a=1, b=1, and sigma=1 # YOU MAY TRY ANY DIFFERENT VALUES regression.log.likelihood(c(1,1,1), dat=recapture.data) # -452.6903 # TO OPIMISE THE LOG-LIKELIHOOD FUNCTION IN R - to find peak # optimize() IS ONE-DIMENSIONAL, # optim() GENERALISES TO MULTI-DIMENSIONAL CASES optim(par=c(1,1,1), regression.log.likelihood, method='L-BFGS-B', lower=c(-1000,-1000,0.0001), upper=c(1000,1000,10000), control=list(fnscale=-1), dat=recapture.data, hessian=T) # sigma cannot be negative - lowest value = 0.0001 # par=c(1,1,1) - Initial values for the parameters # log.likelihood.regression - The function you wish to be optimised # method=‘L-BFGS-B’ - Optimisation algorithm # lower=c(-1000,-1000,0.0001) - Lower bound of your parameter space # upper=c(1000,1000,10000) - Upper bound of your parameter space # control=list((fnscale=-1)) - fnscale=-1 means to maximise # REGRESSION WITH THE BUILT-IN lm() m<-lm(length_diff~day, data=recapture.data) summary(m) n<-nrow(recapture.data) sqrt(var(m$residual)*(n-1)/n) # You always need to provide an initial parameter vector by par= # Choice of method can be tricky for advanced users: See R help for details. If you use L-BFGS-B as your method, then you need to specify the upper and lower bound of the parameter values for searching for the maximum. No need to specify if you use Nelder-Mead # If you wish to maximise a function, put fnscale=-1 in your control list, default is to minimise. You can put multiple control parameters in the control list. # Precision can be adjusted by tolerance or maximum number of iterations, say maxit or abstol within control # The Hessian matrix provide information about the variance-covariance # structure of your parameter estimates # Try multiple sets of initial parameters and ensure they all converge to the same estimates # “Stumble around” the parameter space towards the best parameters, just like a drunkard trying to stumble home (the best place). # Not every step is in the right direction, and it takes some time to go home. # Ideal if the drunkard find his place. But also he may get stuck at the local maximum. # THE LOG-LIKELIHOOD FUNCTION FOR M1 WITHOUT AN INTERCEPT regression.no.intercept.log.likelihood<-function(parm, dat) { # DEFINE THE PARAMETERS # NO INTERCEPT THIS TIME b <- parm[1] sigma <- parm[2] # DEFINE THE DATA # SAME AS BEFORE x<-dat[,1] y<-dat[,2] # DEFINE THE ERROR TERM, NO INTERCEPT HERE error.term <- (y-b*x) # REMEMBER THE NORMAL pdf? density<-dnorm(error.term, mean=0, sd=sigma, log=T) # LOG-LIKELIHOOD IS THE SUM OF DENSITIES return(sum(density)) } regression.no.intercept.log.likelihood(c(1,1), dat=recapture.data) # PERFORMING LIKELIHOOD-RATIO TEST M1<-optim(par=c(1,1), regression.no.intercept.log.likelihood, dat=recapture.data, method='L-BFGS-B', lower=c(-1000,0.0001), upper=c(1000,10000), control=list(fnscale=-1), hessian=T) M2<-optim(par=c(1,1,1), regression.log.likelihood, dat=recapture.data, method='L-BFGS-B', lower=c(-1000,-1000,0.0001), upper=c(1000,1000,10000), control=list(fnscale=-1), hessian=T) # THE TEST STATISTIC D D<-2*(M2$value-M1$value) D # Likelihood-ratio test statistic = 3.047676 # CRITICAL VALUE qchisq(0.95, df=1) # df=3-2 => 3.841459 # So we accept the hypothesis that the intercept is zero at α = 0.05 (Same conclusion is drawn from lm() using anova table) # rchisq = rnorm family => generate random numbers from chisq distribution # dchisq = dnorm/dbinom family => density # qchisq = quantile, eg. value at 0.95 (95% CI) regression.non.constant.var.log.likelihood<-function(parm, dat) { b<-parm[1] sigma<-parm[2] x<-dat[,1] y<-dat[,2] error.term<-(y-b*x) density<-dnorm(error.term, mean=0, sd=x*sigma, log=T) # REMEMBER THE NORMAL pdf - Look up BOX-COX transformation??? return(sum(density)) } regression.non.constant.var.log.likelihood(c(1,1), dat=recapture.data) # MAXIMISE THE LOG-LIKELIHOOD # HOW ABOUT CALLING IT M4? M4<-optim(par=c(1,1), regression.non.constant.var.log.likelihood, dat=recapture.data, method='L-BFGS-B', lower=c(-1000,0.0001), upper=c(1000,10000), control=list(fnscale=-1)) M4 # Confidence interval # DEFINE THE RANGE OF PARAMETERS TO BE PLOTTED b<-seq(2, 4, 0.1) sigma<-seq(2, 5, 0.1) # THE LOG-LIKELIHOOD VALUE IS STORED IN A MATRIX log.likelihood.value<-matrix(nr=length(b), nc=length(sigma)) # COMPUTE THE LOG-LIKELIHOOD VALUE FOR EACH PAIR OF PARAMETERS for (i in 1:length(b)) { for (j in 1:length(sigma)) { log.likelihood.value[i,j]<- regression.no.intercept.log.likelihood(parm=c(b[i],sigma[j]), dat=recapture.data) } } # WE ARE INTERESTED IN KNOWING THE LOG-LIKELIHOOD VALUE # RELATIVE TO THE MAXIMA log.likelihood.value<-log.likelihood.value-M1$value # FUNCTION FOR 3D PLOT persp(b, sigma, log.likelihood.value, theta=30, phi=20, xlab='b', ylab='sigma', zlab='log.likelihood.value', col='blue') # CONTOUR PLOT - ie. as viewed from above contour(b, sigma, log.likelihood.value, xlab='b', ylab='sigma', xlim=c(2.5, 3.9), ylim=c(2.0, 4.3), levels=c(-1:-5, -10), cex=2) # DRAW A CROSS TO INDICATE THE MAXIMUM points(M1$par[1], M1$par[2], pch=3) contour.line1<-contourLines(b, sigma, log.likelihood.value, levels=-1.92)[[1]] # Rule of thumb is -1.92 lines(contour.line1$x, contour.line1$y, col='red', lty=2, lwd=2) grid(nx = NULL, ny = NA) grid(nx = NA, ny = NULL) # 95% CI for sigma is [2.23, 3.74] # 95% CI for b is [2.75, 3.57] # 95% CI for 1 parameter = 0.5*chisq1 = 1.92 abline(h=max(contour.line1$x, contour.line1$y), lty=4, col="red") abline(h=min(contour.line1$x, contour.line1$y), lty=4, col="red") print(paste("CI for parameter sigma is:",max(contour.line1$x, contour.line1$y),",",min(contour.line1$x, contour.line1$y))) abline(v=max(contour.line1$x), lty=4, col="red") abline(v=min(contour.line1$x), lty=4, col="red") print(paste("CI for parameter b is:",max(contour.line1$x),",",min(contour.line1$x))) # 3.737046 # 2.23367 # 3.577263 # 2.749373 # But we do not know the joint confident region for both (b,sigma) # 95% CI for 2 joint parameters = 0.5*chisq2 = 2.99 contour.line2<-contourLines(b, sigma, log.likelihood.value, levels=-2.99)[[1]] # Rule of thumb is -1.92 lines(contour.line2$x, contour.line2$y, col='blue', lty=2, lwd=2) # The joint confidence region is wider than the confidence interval for 1 parameter alone, this is because of 'multiple comparison' # Point [3.5, 2.3] lies outside of the joint 95% CI for both parameters (b given sigma), despite lying within the bounds of the 95% CI when considering each individual parameter in turn. ie. when both parameters are considered together (variance-covariance), the confidence interval is constrained such that the point actually lies outside of the true 95% CI for both parameters. points(3.5,2.3, pch=4) # This point lies actually outside of the confidence region when both parameters are considered together. abline(h=max(contour.line2$x, contour.line2$y), lty=4, col="blue") abline(h=min(contour.line2$x, contour.line2$y), lty=4, col="blue") abline(v=max(contour.line2$x), lty=4, col="blue") abline(v=min(contour.line2$x), lty=4, col="blue") max(contour.line2$x, contour.line2$y) # 4.041608 min(contour.line2$x, contour.line2$y) # 2.116497 max(contour.line2$x) # 3.691743 min(contour.line2$x) # 2.635445 # optim() GENERALISES TO MULTI-DIMENSIONAL CASES # WITH HESSIAN MATRIX result<-optim(par=c(1,1), regression.no.intercept.log.likelihood, method='L-BFGS-B', lower=c(-1000,0.0001), upper=c(1000,10000), control=list(fnscale=-1), dat=recapture.data, hessian=T) # Hessian = TRUE returns the Hessian matrix # GET BACK THE HESSIAN MATRIX result$hessian # THE VARIANCE-COVARIANCE MATRIX IS THE NEGATIVE OF # THE INVERSE OF THE HESSIAN MATRIX. # BY solve() FUNCTION variance.matrix<-(-1)*solve(result$hessian) # Return inverse Hessian matrix - all second order partial derivatives variance.matrix # Q3 (iii) coin.log.likelihood <- function(p,n,y){ # p is the parameter # n is the number of trials # y is the number of heads return(lchoose(n,y) + y*log(p) + (n-y)*log(1-p)) } H0 <- coin.log.likelihood(p=0.5, n=50, y=35) H0 # Log likelihood value of -6.215 H1 <- coin.log.likelihood(p=0.7, n=50, y=35) H1 # As expected, a higher log likelihood value of -2.1 D <- 2*(H1-H0) D # D-statistic is 8.228 # Df = H1-H0 = 1-0 = 1 qchisq(0.95, df=1) # 8.228 > 3.841, therefore we can reject H0 and accept H1, that the coin is unfair (loaded) # This demonstrates the effect of sample size! p <- seq(0,1,0.01) coin.log.likelihood.value <- sapply(p, coin.log.likelihood, n=50, y=35) # Sapply works with vectors coin.log.likelihood.value <- coin.log.likelihood.value - max(coin.log.likelihood.value) # Zero stanardise the plot plot(p, coin.log.likelihood.value, type="l", lwd=2) abline(h=max(coin.log.likelihood.value), lty=4) abline(v=p[coin.log.likelihood.value==max(coin.log.likelihood.value)[1]], lty=4) grid(nx = NULL, ny = NA) grid(nx = NA, ny = NULL) plot(p, coin.log.likelihood.value, type="l", lwd=2, xlim=c(0.4, 0.9), ylim=c(-3,0)) abline(h=-1.92, col="red", lty=4) # Lower 95% CI uniroot(function(p){ coin.log.likelihood(p=p, n=50, y=35) - coin.log.likelihood(p=0.7, n=50, y=35) + 1.92}, interval = c(0.01, 0.7) ) # 0.5652006 # Upper 95% CI uniroot(function(p){ coin.log.likelihood(p=p, n=50, y=35) - coin.log.likelihood(p=0.7, n=50, y=35) + 1.92}, interval = c(0.7, 1) ) # 0.8148278 # Question 4 flowering <- read.table("../Data/flowering.txt", header = TRUE) flowering names(flowering) par(mfrow=c(1,2)) plot(flowering$Flowers, flowering$State) plot(flowering$Root, flowering$State) # TWO ARGUMENTS: parm IS A VECTOR OF PARAMETERS, # dat IS THE INPUT DATASET logistic.log.likelihood<-function(parm, dat) { # DEFINE PARAMETERS a<-parm[1] b<-parm[2] c<-parm[3] # DEFINE RESPONSE VARIABLE, WHICH IS THE FIRST COLUMN OF dat State<-dat[,1] # SIMILARLY DEFINE OUR EXPLANATORY VARIABLES Flowers<-dat[,2] Root<-dat[,3] # MODEL OUR SUCCESS PROBABILITY p<-exp(a+b*Flowers+c*Root)/(1+exp(a+b*Flowers+c*Root)) # THE LOG-LIKELIHOOD FUNCTION log.like<-sum(State*log(p)+(1-State)*log(1-p)) return(log.like) } # TRY logistic.log.likelihood(c(0,0,0), dat=flowering) M1 <- optim(par=c(0,0,0), logistic.log.likelihood, dat=flowering, method='L-BFGS-B', lower=c(-1000,-4,-1000), upper=c(1000,1000,1000), control=list(fnscale=-1), hessian = FALSE) M1 # Parameters: a = 0.9614547, b = -0.1064155, c = 6.6003380 # Associated log-likelihood value: -27.03405 logistic.log.likelihood.int<-function(parm, dat) { # DEFINE PARAMETERS a<-parm[1] b<-parm[2] c<-parm[3] d<-parm[4] # DEFINE RESPONSE VARIABLE, WHICH IS THE FIRST COLUMN OF dat State<-dat[,1] # SIMILARLY DEFINE OUR EXPLANATORY VARIABLES Flowers<-dat[,2] Root<-dat[,3] # MODEL OUR SUCCESS PROBABILITY p<-exp(a+b*Flowers+c*Root+d*Flowers*Root)/(1+exp(a+b*Flowers+c*Root+d*Flowers*Root)) # THE LOG-LIKELIHOOD FUNCTION log.like<-sum(State*log(p)+(1-State)*log(1-p)) return(log.like) } logistic.log.likelihood.int(c(0,0,0,0), dat=flowering) # -40.89568 M2 <- optim(par=c(0,0,0,0), logistic.log.likelihood.int, dat=flowering, method='L-BFGS-B', lower=c(-1000,-4,-1000,-Inf), upper=c(1000,1000,1000,1000), control=list(fnscale=-1), hessian = FALSE) M2 # Parameters: a = -2.95495534, b = -0.07888641, c = 25.11688994, d = -0.20865900 # Associated log-likelihood value: -18.56412 M2[2][[1]] M1[2][[1]] # Likelihood ratio test D <- 2*(M2[2][[1]]-M1[2][[1]]) D # 16.93986 # Df = 4 - 3 qchisq(0.95, df=1) # 3.841459 # D-statistic > chisq value, therefore the interaction is significant
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GeoDistPSU.R
GeoDistPSU <- function(lat, ## Latitude variable. Must be in decimal long, ## Longitude variable. Must be in decimal dist.sw, ## Distance: miles or kilometers (kms) max.dist, ## Maximum distance within PSU Input.ID = NULL ## ID variable from input file ) { ## Confirm latitude and longitude are numeric and have no missing values if(is.numeric(lat) == FALSE) stop("Latitude must be numeric.\n") if(any(is.na(lat)) == TRUE) stop("Latitude has missing values, which are not allowed.\n") if(is.numeric(long) == FALSE) stop("Longiitude must be numeric.\n") if(any(is.na(long)) == TRUE) stop("Longitude has missing values, which are not allowed.\n") ## Confirm distance switch is "miles" or "kms" if(dist.sw != "miles" & dist.sw != "kms") stop("Distance switch must be miles or kms (kilometers).\n") ## Confirm distance is numeric and positive if(is.numeric(max.dist) == FALSE) stop("Maximum distance must be numeric.\n") if((max.dist > 0) == FALSE) stop("Maximum distance must be greater than zero.\n") ## Create distance matrix from latitude and longitude geodf <- data.frame(long, lat) ## Create "As the crow flies" distance with lat and long d <- geosphere::distm(geodf, fun = geosphere::distHaversine) ## Distance of d is in meters ## There are 1609.344 meters per mile d <- if(dist.sw == "miles") d/1609.344 else d/1000 ## Convert d to distance matrix dist <- as.dist(d) ## Perform hierarchical clustering using maximum distance between two cluster objects hc <- hclust(dist, method = "complete") ## Cut dendogram by maximum distance for PSU assignment psuID <- cutree(hc, h = max.dist) ## Create plot of PSU centers PSU.Mean.Latitude <- tapply(lat, psuID, mean) PSU.Mean.Longitude <- tapply(long, psuID, mean) ## Calculate maximum distance between units within cluster PSU.Max.Dist <- NULL for(i in 1:length(unique(psuID))){ PSU.Max.Dist[i] <- max(geosphere::distm(geodf[psuID == i, ], fun = geosphere::distHaversine))} PSU.Max.Dist <- if(dist.sw == "miles") PSU.Max.Dist/1609.344 else PSU.Max.Dist/1000 ## Calculate number of SSUs in each PSU Number.SSUs <- table(psuID) ## Carry Input.ID through Input.file.ID <- if(is.null(Input.ID)) seq(1, length(psuID)) else Input.ID ## Create data frame with Input file ID and PSU Cluster ID PSU.ID <- cbind(Input.file.ID, psuID) PSU.ID <- as.data.frame(PSU.ID) ## Create data frame with PSU Centroids, Number of SSUs, and Maximum Cluster Distance PSU.Info <- cbind(Number.SSUs, PSU.Mean.Latitude, PSU.Mean.Longitude, PSU.Max.Dist) PSU.Info <- as.data.frame(PSU.Info) ## Output PSU ID and PSU Information data frames out <- list(PSU.ID, PSU.Info) ## Name data frames in list names(out) <- c("PSU.ID", "PSU.Info") ## Return output return(out) }
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/R/phase.R
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phase.R
#' @name phase #' @title PHASE #' @description Run PHASE to estimate the phase of loci in diploid data. #' #' @param g a \linkS4class{gtypes} object. #' @param loci vector or data.frame of loci in 'g' that are to be phased. If a #' data.frame, it should have columns named #' \code{locus} (name of locus in 'g'), #' \code{group} (number identifying loci in same linkage group), and #' \code{position} (integer identifying location of each locus in a #' linkage group). #' @param positions position along chromosome of each locus. #' @param type type of each locus. #' @param num.iter number of PHASE MCMC iterations. #' @param thinning number of PHASE MCMC iterations to thin by. #' @param burnin number of PHASE MCMC iterations for burnin. #' @param model PHASE model type. #' @param ran.seed PHASE random number seed. #' @param final.run.factor optional. #' @param save.posterior logical. Save posterior sample in output list? #' @param in.file name to use for PHASE input file. #' @param out.file name to use for PHASE output files. #' @param delete.files logical. Delete PHASE input and output files when done? #' @param ph.res result from \code{phase.run}. #' @param thresh minimum probability for a genotype to be selected (0.5 - 1). #' @param keep.missing logical. T = keep missing data from original data set. #' F = Use estimated genotypes from PHASE. #' #' @note PHASE is not included with \code{strataG} and must be downloaded #' separately. Additionally, it must be installed such that it can be run from #' the command line in the current working directory. See the vignette #' for \code{external.programs} for installation instructions. #' #' @details #' \tabular{ll}{ #' \code{phase} \tab runs PHASE assuming that the executable is installed #' properly and available on the command line.\cr #' \code{phaseWrite} \tab writes a PHASE formatted file.\cr #' \code{phaseReadPair} \tab reads the '_pair' output file.\cr #' \code{phaseReadSample} \tab reads the '_sample' output file.\cr #' \code{phaseFilter} \tab filters the result from \code{phase.run} to #' extract one genotype for each sample.\cr #' \code{phasePosterior} \tab create a data.frame of all genotypes for each #' posterior sample.\cr #' } #' #' @return #' \describe{ #' \item{phase}{a list containing: #' \tabular{ll}{ #' \code{locus.name} \tab new locus name, which is a combination of loci #' in group.\cr #' \code{gtype.probs} \tab a data.frame listing the estimated genotype #' for every sample along with probability.\cr #' \code{orig.gtypes} \tab the original gtypes object for the #' composite loci.\cr #' \code{posterior} \tab a list of \code{num.iter} data.frames #' representing posterior sample of genotypes for each sample.\cr #' }} #' \item{phaseWrite}{a list with the input filename and the #' \linkS4class{gtypes} object used.} #' \item{phaseReadPair}{a data.frame of genotype probabilities.} #' \item{phaseReadSample}{a list of data.frames representing the #' posterior sample of genotypes for one set of loci for each sample.} #' \item{phaseFilter}{a matrix of genotypes for each sample.} #' \item{phasePosterior}{a list of data.frames representing the posterior #' sample of all genotypes for each sample.} #' } #' #' @references Stephens, M., and Donnelly, P. (2003). A comparison of Bayesian #' methods for haplotype reconstruction from population genotype data. #' American Journal of Human Genetics 73:1162-1169. Available at: #' \url{http://stephenslab.uchicago.edu/software.html#phase} #' #' @author Eric Archer \email{eric.archer@@noaa.gov} #' #' @examples \dontrun{ #' data(bowhead.snps) #' data(bowhead.snp.position) #' snps <- df2gtypes(bowhead.snps, ploidy = 2, description = "Bowhead SNPS") #' summary(snps) #' #' # Run PHASE on all data #' phase.results <- phase(snps, bowhead.snp.position, num.iter = 100, #' save.posterior = FALSE) #' #' # Filter phase results #' filtered.results <- phaseFilter(phase.results, thresh = 0.5) #' #' # Convert phased genotypes to gtypes #' ids <- rownames(filtered.results) #' strata <- bowhead.snps$Stock[match(ids, bowhead.snps$LABID)] #' filtered.df <- cbind(id = ids, strata = strata, filtered.results) #' phased.snps <- df2gtypes(filtered.df, ploidy = 2, description = "Bowhead phased SNPs") #' summary(phased.snps) #' } #' #' @export #' phase <- function(g, loci, positions = NULL, type = NULL, num.iter = 100000, thinning = 100, burnin = 100000, model = "new", ran.seed = NULL, final.run.factor = NULL, save.posterior = FALSE, in.file = "phase_in", out.file = "phase_out", delete.files = TRUE) { if(getPloidy(g) != 2) stop("'g' must be diploid") # check loci format if(!is.data.frame(loci)) { if(!(is.character(loci) & is.vector(loci))) { stop("'loci' must be a data.frame or character vector") } if(is.null(positions)) positions <- rep(1, getNumLoci(g)) if(length(positions) != length(loci)) { stop("'positions' must be same length as 'loci'") } loci <- data.frame(locus = loci, position = positions, group = 1) } loci$group <- as.character(loci$group) loci$position <- as.numeric(loci$position) if(is.null(type)) type <- rep("S", length(unique(loci$group))) if(length(type) != length(unique(loci$group))) { stop("'type' must be same length as number of locus groups") } names(type) <- unique(loci$group) result <- lapply(unique(loci$group), function(grp) { lets <- paste(sample(c(0:9, letters), 10, replace = TRUE), collapse = "") in.file <- paste("phase_in_", lets, sep = "") out.file <- paste("phase_out_", lets, sep = "") # Write input file group.df <- loci[loci$group == grp, ] locus.type <- rep(type[grp], nrow(group.df)) in.file.data <- phaseWrite( g, loci = group.df$locus, positions = group.df$position, type = locus.type, in.file ) # Set parameters M.opt <- switch(model, new = "-MR", old = "-MS", hybrid = "-MQ", "") S.opt <- ifelse(is.null(ran.seed), "", paste("-S", ran.seed, sep = "")) X.opt <- ifelse( is.null(final.run.factor), "", paste("-X", final.run.factor, sep = "") ) s.opt <- ifelse(save.posterior, "-s", "") in.file.opt <- paste("\"", in.file, "\"", sep = "") out.file.opt <- paste("\"", out.file, "\"", sep = "") iter.params <- paste(trunc(num.iter), trunc(thinning), trunc(burnin)) phase.cmd <- paste( "PHASE", M.opt, S.opt, X.opt, s.opt, in.file.opt, out.file.opt, iter.params ) # Run Phase err.code <- system(phase.cmd) if(err.code == 127) { stop("You do not have PHASE installed.") } else if(!err.code == 0) { stop(paste("Error running PHASE. Error code", err.code, "returned.")) cat("\n") } # Read output opts <- options(warn = -1) gtype.probs <- phaseReadPair(paste(out.file, "_pairs", sep = "")) if(is.null(gtype.probs)) { alleles <- rep(NA, nrow(g$genotypes)) gtype.probs <- data.frame( id = getIndNames(g), a1 = alleles, a2 = alleles, pr = rep(1, getNumInd(g)) ) } new.locus.name <- paste(group.df$locus, collapse = "_") alleles <- paste(new.locus.name, 1:2, sep = ".") colnames(gtype.probs)[1:3] <- c("id", alleles) rownames(gtype.probs) <- NULL options(opts) locus.result <- list( locus.name = new.locus.name, gtype.probs = gtype.probs, orig.gtypes = in.file.data$gtypes ) if(save.posterior) { file <- paste(out.file, "_sample", sep = "") l.type <- paste(locus.type, collapse = "") locus.result$posterior <- phaseReadSample(file, l.type) for(i in 1:length(locus.result$posterior)) { colnames(locus.result$posterior[[i]]) <- c("id", alleles) } } if(delete.files) { file.remove(c(dir(pattern = in.file), dir(pattern = out.file))) } locus.result }) names(result) <- lapply(result, function(x) x$locus.name) class(result) <- c("phase.result", class(result)) result } #' @rdname phase #' @export #' phaseReadSample <- function(out.file, type) { if(!file.exists(out.file)) return(NULL) post.file <- scan(file = out.file, what = "character", sep = "\n", quiet = TRUE) iter.start <- grep(type, post.file) + 1 lapply(iter.start, function(start) { num.samples <- as.integer(post.file[start - 3]) end <- start + (num.samples * 3) - 3 as.data.frame(t(sapply(seq(start, end, by = 3), function(i) { id <- strsplit(post.file[i], " ")[[1]][2] hap1 <- gsub(" ", "", post.file[i + 1]) hap2 <- gsub(" ", "", post.file[i + 2]) c(id, hap1, hap2) })), stringsAsFactors = FALSE) }) } #' @rdname phase #' @export #' phaseReadPair <- function(out.file) { if(!file.exists(out.file)) return(NULL) pair.file <- scan(file = out.file, what = "character", sep = "\n", quiet = TRUE) id.start <- grep("IND:", pair.file) gtype.probs <- lapply(1:length(id.start), function(i) { id.end <- ifelse(i == length(id.start), length(pair.file), id.start[i + 1] - 1) id <- sub("IND: ", "", pair.file[id.start[i]]) t(sapply((id.start[i] + 1):id.end, function(j) { line.split <- unlist(strsplit(pair.file[j], " , ")) names(line.split) <- c("hap1", "hap2", "pr") c(id = id, line.split) })) }) gtype.probs <- as.data.frame(do.call(rbind, gtype.probs), stringsAsFactors = FALSE) gtype.probs$pr <- as.numeric(as.character(gtype.probs$pr)) gtype.probs } #' @rdname phase #' @export #' phaseWrite <- function(g, loci, positions = NULL, type = rep("S", length(loci)), in.file = "phase_in") { if(getPloidy(g) != 2) stop("'g' must be diploid") # Make sure locus.names and locus.positions are sorted properly if(is.null(positions)) positions <- rep(1, length(getNumLoci(g))) asc.order <- order(positions) loci <- loci[asc.order] positions <- positions[asc.order] sub.g <- g[, loci, ] write(c( getNumInd(sub.g), length(loci), paste("P", paste(positions, collapse = " ")), paste(type, collapse = ""), "" ), file = in.file) g.mat <- as.matrix(sub.g, ids = TRUE, strata = FALSE) ids <- g.mat[, "id"] g.mat <- g.mat[, -1] g.mat[is.na(g.mat)] <- "?" for(i in 1:nrow(g.mat)) { write(c( ids[i], paste(g.mat[i, seq(1, ncol(g.mat) - 1, 2)], collapse = " "), paste(g.mat[i, seq(2, ncol(g.mat), 2)], collapse = " ") ), file = in.file, append = TRUE) } invisible(list(filename = in.file, gtypes = sub.g)) } #' @rdname phase #' @export #' phasePosterior <- function(ph.res, keep.missing = TRUE) { if(!"phase.result" %in% class(ph.res)) { stop("'ph.res' is not a result from 'phase.run'.") } num.iter <- length(ph.res[[1]]$posterior) lapply(1:num.iter, function(iter) { do.call(cbind, lapply(1:length(ph.res), function(locus) { ph.res <- ph.res[[locus]] post.df <- ph.res$posterior[[iter]] if(keep.missing) { for(i in 1:nrow(post.df)) { ids <- which(getIndNames(ph.res$orig.gtypes) == post.df[i, 1]) if(any(is.na(as.array(ph.res$orig.gtypes, ids = ids)))) { post.df[i, 2:3] <- NA } } } cols <- if(locus == 1) {1:3} else {2:3} post.df[, cols] })) }) } #' @rdname phase #' @export #' phaseFilter <- function(ph.res, thresh = 0.5, keep.missing = TRUE) { if(!"phase.result" %in% class(ph.res)) { stop("'ph.res' is not a result from 'phase.run'.") } filtered <- lapply(ph.res, function(x) { gtype.probs <- x$gtype.probs pr.vec <- unique(gtype.probs[, 1]) locus.filtered <- do.call(rbind, lapply(pr.vec, function(i) { this.id <- gtype.probs[gtype.probs[, 1] == i, ] max.index <- which.max(this.id$pr) if(length(max.index) == 0) return(this.id[1, ]) kept.line <- this.id[max.index, ] if(as.numeric(kept.line$pr) < thresh) kept.line[, 2:3] <- c(NA, NA) kept.line })) rownames(locus.filtered) <- NULL if(keep.missing) { for(i in 1:nrow(locus.filtered)) { ids <- setdiff(getIndNames(x$orig.gtypes), locus.filtered[i, 1]) id.mat <- as.matrix(x$orig.gtypes, strata = FALSE) id.mat <- id.mat[id.mat[, "id"] %in% ids, , drop = FALSE] if(any(is.na(id.mat))) locus.filtered[i, 2:3] <- NA } } locus.filtered }) ids <- data.frame( id = sort(unique(unlist(lapply(filtered, function(x) x$id)))) ) filtered <- as.matrix(do.call(cbind, lapply(filtered, function(x) { merge(ids, x, by = "id", all.x = TRUE)[, 2:3] }))) rownames(filtered) <- ids$id colnames(filtered) <- paste(rep(names(ph.res), each = 2), ".", 1:2, sep = "") filtered }
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DF0_COUNTY_DATA <- function(matching_key){ # This function depends on the matching key, for this test application # specifically the healthauthority_county_key. # This function creates a dataframe, with the first 3 columns equal to # the three columns of the matching key. The rest of the dataframe is filled # with zeros. # Each observation is one county. # The varialbles for each county can be seen from the list of colnames below. # The created dataframe is used later on to be updated with data from the # sormas_persons on the the county level values for each variable # listed below. ############################################################################# df0 <- data.frame(matrix(0, ncol = 23, nrow = nrow(matching_key))) colnames(df0) <- c("state", "county", "health_authority", "population", "case_category_confirmed", "case_category_none", "case_category_suspected", "hospitalized_FALSE", "hospitalized_NA", "hospitalized_TRUE", "died_FALSE", "died_NA", "died_TRUE", "new_case_category_confirmed", "new_case_category_none", "new_case_category_suspected", "new_hospitalized_FALSE", "new_hospitalized_NA", "new_hospitalized_TRUE", "new_died_FALSE", "new_died_NA", "new_died_TRUE", "n") df0$county <- matching_key$county df0$state <- matching_key$state df0$health_authority <- matching_key$health_authority return(df0) }
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#Code for Plot 2 plot(subdata$datetime, subdata$Global_active_power, type="l", ylab = "Global Active Power (kilowatts)", xlab=NA) dev.copy(png,'plot2.png') dev.off()
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% Generated by roxygen2: do not edit by hand % Please edit documentation in R/geom_bernie.R \name{bernieGrob} \alias{bernieGrob} \title{bernie grob} \usage{ bernieGrob(x, y, size, theme) } \description{ bernie grob }
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prepare_ecologist_r_code.R
#' Rewrite the dataset into a usable format. #' #' \code{PrepareDataset} rewrites the dataset to make it useable for the #' Sampling function of this package. The function comibines the different #' columns and creates a new dataset. If there are now data fro a column the #' Column will be filled with zeros. #' #' @param data The input dataset. #' @param plot #' @param num.of.individuals #' @param species #' @param x.coord #' @param y.coord #' @param visit.year #' #' @export Dataset in which the columns in the right order. #' PrepareDataset <- function(data, plot, num.of.individuals, species, x.coord, y.coord, visit.year, visit.month, visit.day) { column.plot <- ifelse (plot > 0, data[plot], rep(0, length(data[, 1]))) column.num.of.individuals <- ifelse (num.of.individuals > 0, data[num.of.individuals], rep(0, length(data[, 1]))) column.species <- ifelse (species > 0, data[species], rep(0, length(data[, 1]))) column.x.coord <- ifelse (x.coord > 0, data[x.coord], rep(0, length(data[, 1]))) column.y.coord <- ifelse (y.coord > 0, data[y.coord], rep(0, length(data[, 1]))) column.visit.year <- ifelse (visit.year > 0, data[visit.year], rep(0, length(data[, 1]))) column.visit.month <- ifelse (visit.month > 0,data[visit.month], rep(0, length(data[, 1]))) column.visit.day <- ifelse (visit.day > 0, data[visit.day], rep(0, length(data[, 1]))) data <- data.frame (column.plot, column.num.of.individuals, column.species, # other name than data column.x.coord, column.y.coord, column.visit.year, column.visit.month, column.visit.day) colnames (data) <- c("plot", "num.of.individuals", "species", "x.coord", "y.coord", "year", "month", "day") return (data) } #' Creates a vector with the behaviour of an ecologist. #' #' \code{CreateEcologist} creates a vector with characteristics of the behaviour #' of an ecologist in the field. The characteristics are: The sampled area of a #' plot, the detection probability, the identification error, the probability #' of missed vistis and the costs. The first four characteristics are expected #' to be in percent. #' #' @param sampling.area A number in percent. #' @param detection.probability A number in percent. #' @param identification.error A number in percent. #' @param propability.missed.visits A number in percent. #' @param costs A number in monetary units. #' #' @export A vector with the five characteristics of an ecologist. CreateEcologist <- function (sampling.area, detection.probability, identification.error, probability.missed.visits, costs) { ecologist <- c(sampling.area, detection.probability, identification.error, probability.missed.visits, costs) return (ecologist) }
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s2_analysis.R
## Last edited 19/10/21 AXL ## This script analyzes data from replication adult and child participants. ## ESS added analysis on post-tests 1/24/2020. library(tidyverse) library(ggthemes) library(ggplot2) library(ggpubr) library(here) library(effsize) data_sum <- read_csv(here("data_tidy", "study2_data_sum.csv")) age_info<-read_csv(here("data_tidy","study2_ageinfo.csv")) data_sum<-merge(data_sum,age_info, by.x="subjID") #-------------------------------------------------------------------------------------# ## Analysis for switching and explore* and stars #### ## *Note that explore is called 'non-maximizing' in the paper ## #-------------------------------------------------------------------------------------# library(BayesFactor) data_sum = data_sum[data_sum$group %in% c("child", "adult"),] data_sum$group = factor(data_sum$group) ################################ Switching ################################ plot(switch ~ group, data = data_sum, main = "% switching choices") #* reported: paper*# switchBF = ttestBF(formula = switch ~ group, data = data_sum) switchBF ## [1]Alt., r=0.707 : 7.620799e+36 ±0% switchChains= posterior(ttestBF(formula = switch ~ group, data = data_sum),iterations=1000) mean(switchChains[,2]) # mean difference -0.6184066 quantile(switchChains[,2],probs=c(0.025,0.975)) # mean difference CI -0.6846195 -0.5512568 mean(switchChains[,4])# effect size estimite -3.021579 quantile(switchChains[,4],probs=c(0.025,0.975)) # effect size CI -3.479296 -2.565163 ############################# 'Explore' choices ############################# plot(explore ~ group, data = data_sum, main = "% 'explore' choices") exploreBF = ttestBF(formula = explore ~ group, data = data_sum) exploreBF ## 2.588539e+37 ±0% exploreChains= posterior(ttestBF(formula = explore ~ group, data = data_sum),iterations=1000) mean(exploreChains[,2]) # mean difference -0.492433 quantile(exploreChains[,2],probs=c(0.025,0.975)) # mean difference CI -0.5479371 -0.4349280 mean(exploreChains[,4])# effect size estimite -3.033899 quantile(exploreChains[,4], probs=c(0.025,0.975)) # effect size CI -3.508251 -2.563191 ################################ Stars Won ################################ aggregate(data = data_sum, totalEarn~group, FUN = "mean") rewardBF = ttestBF(formula = totalEarn ~ group, data = data_sum) rewardBF ## [1] Alt., r=0.707 : 8.857099e+32 ±0% starChains= posterior(ttestBF(formula = totalEarn ~ group, data = data_sum),iterations=1000) mean(starChains[,2]) # mean difference 116.0546 quantile(starChains[,2],probs=c(0.025,0.975)) # mean difference CI 101.9744 131.4045 mean(starChains[,4])# effect size estimite 2.746324 quantile(starChains[,4],probs=c(0.025,0.975)) # effect size CI 2.301249 3.208194 ######################################################################################### ################ Between-group comparisons for post-test performance ################## ######################################################################################### ### 8-star #### # Preliminary glimpse at diff in proportion of correctly identifying 8-star option between # adult and child groups # % of participants child vs adult who correctly ID'ed 8-star monster dataDynamic <- data_sum %>% filter(condition == "dynamic") dataStatic <- data_sum %>% filter(condition == "static") dataDynamic %>% #* reported: paper*# group_by(group) %>% summarise(mean(correct_8)) %>% ungroup() # group `mean(correct_8)` # <fct> <dbl> # 1 adult 0.349 # 2 child 0.771 dynamic <- xtabs( ~ correct_8 + group, dataDynamic ) #* reported: paper*# contingencyTableBF(dynamic,sampleType = "poisson") # Non-indep. (a=1) : 585.2952 ±0% ### Overall #### # mean prop overall correct in posttest, broken up by condition and age group aggregate(data = data_sum, correct~ condition + group, FUN = "mean") #* reported: paper*# # across both conditions subset(data_sum, group == "child")$correct %>% mean() #* reported: paper*# 0.864 subset(data_sum, group == "adult")$correct %>% mean() #* reported: paper*# 0.7756522 # mean for study 2, dynamic, adults, EXCLUDING 8-star question study2post <- read_csv(here("data_tidy","study2_posttest.csv"))[-1] study2post_long <- study2post %>% rename(correctProp = correct) %>% pivot_longer( cols = c(6:10), names_to = "question", names_prefix = "correct_", values_to = "correct" ) study2post_long$question <- ifelse(study2post_long$question == "1", paste0(study2post_long$question, " star"), # if "1" then "1 star" paste0(study2post_long$question, " stars")) # if not "1" then "X stars" (e.g., "8 stars") tmp <- subset(study2post_long, question != "8 stars" & group == "adult" & condition == "dynamic") %>% group_by(subjID) %>% summarise(correctProp = mean(correct)) %>% ungroup() tmp$correctProp %>% mean() # 0.7209302 ################################## ##### LINEAR MODELS #### ################################## dataDynamic$group<-as.factor(dataDynamic$group) groupBF<-lmBF(correct_8~group, dataDynamic) #* reported: paper*# group : 100.4961 ±0% groupBF switchBF<-lmBF(correct_8~switch, dataDynamic) # reported switch: 13216616 ±0.01% switchBF exploreBF<-lmBF(correct_8~explore, dataDynamic) # reported explore : 1632918 ±0.01% exploreBF switchgroupBF<-lmBF(correct_8~switch+group, dataDynamic) exploregroupBF<-lmBF(correct_8~explore+group, dataDynamic) segBF<-lmBF(correct_8~switch+explore+group, dataDynamic) allBF<-c(switchBF,exploreBF,groupBF,switchgroupBF,exploregroupBF,segBF) allBF[1]/allBF[3] # How much better switch is than group [1] switch : 70239.28 ±0.01% allBF[2]/allBF[3] # How much better explore is than group [1] explore : 8678.091 ±0.01% # Comparing the child-only model to one that also includes switching allBF[4]/allBF[3] # switch+group vs group-only. # Check for relationship between age and exploration within children dataChild<- data_sum %>% filter(group == "child") plot(dataChild$AgeYear,dataChild$explore) plot(dataChild$AgeYear,dataChild$switch) switchAgeBF<-lmBF(switch~AgeYear, dataChild) switchAgeBF # AgeYear : 0.4546462 ±0% exploreAgeBF<-lmBF(explore~AgeYear, dataChild) # [1] AgeYear : 0.3908611 ±0% #################################################################### ##### DATA VIZ FOR PAPER #### #################################################################### labels <- c(dynamic = "Dynamic condition", static = "Static condition") theme_custom <- theme(strip.text.x = element_text(size = 28), axis.title.y = element_text(size = 28, angle = 90), axis.title.x = element_text(size = 28), axis.text.x = element_text(size=24), axis.text.y = element_text(size=24) ) ##### EARNINGS ###### earn2<-ggplot(data_sum, aes(x=group,y=totalEarn,fill=group))+ geom_dotplot(binaxis='y', stackdir='center', dotsize=.5, alpha=.3)+ geom_boxplot(alpha=.5)+ theme_bw()+ scale_fill_manual(values = c("#f4d221", "#e5263a"))+ ylab("Stars won")+ xlab(" ")+ theme(legend.position="none")+ stat_summary(fun.y=mean, geom="point", shape=23, size=4)+ facet_grid(~condition, labeller=labeller(condition = labels))+ ylim(0,500)+ scale_x_discrete(labels = c("Adults", "Children"))+ theme_custom earn2 # ggsave(here("plots","exp2_Stars.png"), width = 9.15, height = 5.66) #### EXPLORE CHOICES #### explore2<-ggplot(data_sum, aes(x=group,y=explore,fill=group))+ #geom_jitter(size = 3, alpha = 0.3, width = 0.15, aes(fill=group)) + geom_dotplot(binaxis='y', stackdir='center', dotsize=.5, alpha=.3)+ geom_boxplot(alpha=.5)+ scale_x_discrete(labels = c("Adults", "Children"))+ theme_bw()+ scale_fill_manual(values = c("#f4d221", "#e5263a"))+ ylab("Proportion of \n non-maximizing choices")+ xlab(" ")+ theme(legend.position="none")+ stat_summary(fun.y=mean, geom="point", shape=23, size=4)+ facet_grid(~condition, labeller=labeller(condition = labels))+ theme_custom + ylim(0,1) explore2 # ggsave(here("plots","exp2_Explore.png"), width = 9.15, height = 5.66) ### SWITCH CHOICES ### switch2<-ggplot(data_sum, aes(x=group,y=switch,fill=group))+ geom_dotplot(binaxis='y', stackdir='center', dotsize=.5, alpha=.3)+ scale_x_discrete(labels = c("Adults", "Children"))+ #geom_jitter(size = 3, alpha = 0.3, width = 0.15) + geom_boxplot(alpha=.5)+ theme_bw()+ scale_fill_manual(values = c("#f4d221", "#e5263a"))+ ylab("Proportion of switch choices")+ xlab(" ")+ theme(legend.position="none")+ stat_summary(fun.y=mean, geom="point", shape=23, size=4)+ facet_grid(~condition, labeller=labeller(condition = labels))+ theme_custom switch2 # ggsave(here("plots","exp2_Switch.png"), width = 9.15, height = 5.66) #### Post test ### eight2<- ggplot(data_sum, aes(x = group, y = correct_8, fill=group)) + stat_summary(fun.y=mean, geom="bar",alpha=.6, colour="black") + theme_bw() + # stat_summary(fun.data="mean_cl_boot", geom="errorbar", aes(width=0.1)) + scale_fill_manual(values = c("#f4d221", "#e5263a"))+ ylab("Proportion of participants \n correct about 8-star monster")+ xlab(" ")+ scale_x_discrete(labels = c("Adults", "Children"))+ theme(legend.position="none") + facet_grid(~condition, labeller=labeller(condition = labels))+ theme_custom + ylim(0,1) eight2 # ggsave(here("plots", "exp2_8Star.png"), width = 9.15, height = 5.66) # # Final Plot for paper # # library(patchwork) (switch1|switch2)/(explore1|explore2)/(earn1|earn2)/(eight1|eight2) ########################################################## # Within-condition analysis for the figures #### ########################################################## dataDynamic <- data_sum %>% filter(condition == "dynamic") dataStatic <- data_sum %>% filter(condition == "static") ### Switching Dynamic ### switchBF = ttestBF(formula = switch ~ group, data = dataDynamic) switchBF ## [1] Alt., r=0.707 : 2.803773e+13 ±0% switchChains= posterior(ttestBF(formula = switch ~ group, data = dataDynamic),iterations=1000) mean(switchChains[,2]) # mean difference -0.579253 quantile(switchChains[,2],probs=c(0.025,0.975)) # mean difference CI mean(switchChains[,4])# effect size estimite -2.341969 quantile(switchChains[,4]) # effect size CI ### Switching Static ### switchBF = ttestBF(formula = switch ~ group, data = dataStatic) switchBF ## [1] Alt., r=0.707 : 1.426302e+20 ±0% switchChains= posterior(ttestBF(formula = switch ~ group, data = dataStatic),iterations=1000) mean(switchChains[,2]) # mean difference -0.6092656 quantile(switchChains[,2],probs=c(0.025,0.975)) # mean difference CI mean(switchChains[,4])# effect size estimite -3.860834 quantile(switchChains[,4]) # effect size CI ### Non-max Dynamic ### exploreBF = ttestBF(formula = explore ~ group, data = dataDynamic) exploreBF ## [1] Alt., r=0.707 : 1.067564e+14 ±0% exploreChains= posterior(ttestBF(formula = explore ~ group, data = dataDynamic),iterations=1000) mean(exploreChains[,2]) # mean difference -0.4729586 quantile(exploreChains[,2],probs=c(0.025,0.975)) # mean difference CI mean(exploreChains[,4])# effect size estimite -2.416524 quantile(exploreChains[,4]) # effect size CI ### Non-max Static ### exploreBF = ttestBF(formula = explore ~ group, data = dataStatic) exploreBF ## [1] Alt., r=0.707 : 6.424851e+19 ±0% exploreChains= posterior(ttestBF(formula = explore ~ group, data = dataStatic),iterations=1000) mean(exploreChains[,2]) # mean difference -0.4687977 quantile(exploreChains[,2],probs=c(0.025,0.975)) # mean difference CI mean(exploreChains[,4])# effect size estimite-3.812591 quantile(exploreChains[,4]) # effect size CI ### Reward dynamic ### rewardBF = ttestBF(formula = totalEarn ~ group, data = dataDynamic) rewardBF ## [1] Alt., r=0.707 : 1.080903e+14 ±0% starChains= posterior(ttestBF(formula = totalEarn ~ group, data = dataDynamic),iterations=1000) mean(starChains[,2]) # mean difference 105.374 quantile(starChains[,2],probs=c(0.025,0.975)) # mean difference CI mean(starChains[,4])# effect size estimite 2.396081 quantile(starChains[,4]) # effect size CI ### Reward static ### rewardBF = ttestBF(formula = totalEarn ~ group, data = dataStatic) rewardBF ## [1] Alt., r=0.707 : 4.486329e+18 ±0% starChains= posterior(ttestBF(formula = totalEarn ~ group, data = dataStatic),iterations=1000) mean(starChains[,2]) # mean difference 98.46568 quantile(starChains[,2],probs=c(0.025,0.975)) # mean difference CI mean(starChains[,4])# effect size estimite 141.9224 quantile(starChains[,4]) # effect size CI
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ml.est <- function (y, x=NULL, model = "LN", lambda=3, w=0.05, lambda.fix=FALSE, w.fix=FALSE, eps=1e-7, max.iter=500, t.outl=0.5, graph=FALSE) { #------------------------------------------------------------------------------ # Individuazione degli outlier basata su un modello mistura di 2 gaussiane #------------------------------------------------------------------------------ # PARAMETRI # y = matrice ( o data.frame) - Variabili dipendenti (con possibili errori) # x = matrice ( o data.frame) - Variabili indipendenti (dati esatti. P.e. da archivio amministrativo) # model = Indica se i dati osservati hanno distribuzione log-normale (LN) o normale (N). # w = proporzione dei dati contaminati (peso a priori) # max.iter = numero massimo di iterazioni per la convergenza EM # eps = soglia di accettazione # lambda = fattore di inflazione della varianza # graph = visualizzazione dei grafici durante l'elaborazione #------------------------------------------------------------------------------ ris<-list( ypred = NA, B=NA, sigma=NA, lambda=Inf, w=NA, tau=NA, outlier = NA, n.outlier =0, pattern= NA, is.conv = NA, n.iter =NA, sing=NA, bic.aic = NA, msg="", model=model ) #------------------------------------------------------------------------------ # Copio i dati di input su aree di appoggio #------------------------------------------------------------------------------ memo.y <- y <- as.matrix(y) memo.x <- x #------------------------------------------------------------------------------ # CONTROLLI SUI PARAMETRI # Eliminazione dei record contenenti missing per la stima dei parametri #------------------------------------------------------------------------------ ind.NA<- which(rowSums(is.na(y)) >0) #------------------------------------------------------------------------------ if (length(ind.NA) > 0 ) { warning(paste("Input matrix y contains", length(ind.NA), " (%",length(ind.NA)*100/nrow(y) , ") rows with missing values not included in parameter's estimation\n" )) y <- y[-ind.NA,,drop=FALSE] if (!is.null(x)) { x <-as.matrix(x) x <- x[-ind.NA,,drop=FALSE] } } #------------------------------------------------------------------------------ # CONTROLLI SUI PARAMETRI #------------------------------------------------------------------------------ vars <- check.vars(y,x,model,parent="ml.est") if (vars$ret == -9) { stop(vars$msg.err) } if (vars$ret != 0) { warning(vars$msg.err) } y <- as.matrix(vars$y) x <- as.matrix(vars$x) #y <- as.matrix(y, dimnames = NULL) p <- ncol(y) n <- nrow(y) omega <- rep(1,n) # x <- as.matrix(cbind (rep(1,n),x)) q <- ncol(x) #------------------------------------------------------------------------------ #--------------------- DEFINIZIONE VARIABILI --------------------- conv <- FALSE continua <- TRUE lik<-NA lik0 <- 10 oldlik <- 0 iter <- 0 sing <- FALSE if (ncol(x)+ ncol(y) < 3) # INSERIRE BOXPLOT graph=FALSE if (graph ) { lambda_all <- lambda if (ncol(y) >= 2) { lab <- names(y)[1:2] Var <- y[,1:2] } else if (ncol(y) == 1 & ncol(x) > 1) { lab <- c(names(x)[2],names(y)[1]) Var <- cbind(x[,2],y[,1]) } par(mfrow=c(2,1)) } # B ha q (ncol(x)) righe e p (ncol(y)) variabili B <- solve((t(x) %*% x) + (10e-8* diag(rep(1,q)))) %*% t(x) %*% y # B <- try(solve(t(x) %*% x) %*% t(x) %*% y, TRUE) B0 <- B sigma <- (t(y - x%*%B) %*% (y - x%*%B)) / (n-1) sigma <- sigma + (10e-8* diag(rep(1,p))) sigma0 <- sigma sigma2 <- (1 + lambda) * sigma w1 <- 1-w #------------------------------------------------------------------------------ # CALCOLO DEL BIC per il modello normale da usare per i confronti #------------------------------------------------------------------------------ # N. parametri per il modello normale k1 <- ncol(x) * p + (p*(p+1))/2 # p=ncol(y) # N. parametri per il modello di contaminazione k2 <- k1 + 2 - w.fix - lambda.fix if (n < k2) { warning(paste("Input data are fewer than the number of model parameters\n" )) } #------------------------------------------------------------------------------ # Calcolo della verisimiglianza normale #------------------------------------------------------------------------------ dati<-cbind(x,y) norm.mv<-function(u){dmvnorm(u[q+1:p], t(B0)%*%u[1:q], sigma0, log=TRUE)} lik.n <- sum(apply(dati,1,norm.mv)) BIC.n <- -2*lik.n + k1*log(n) #************************ INIZIO CICLO EM ************************************ while (iter < max.iter & continua == TRUE) { iter <- iter + 1 # print(paste("E-step",iter)) #*********************** E - STEP ************************************ tau1 <- post.prob(y, x, B, sigma, w1, lambda) tau2 <- 1 - tau1 #*********************** M - STEP ************************************ # print(paste("M-step",iter)) #*********************** calcolo dei pesi ********************************** if (!w.fix) w1 <- sum(tau1)/n; #*********************** omega ********************************** omega <- as.vector(tau1 + tau2 / (1+lambda)) #*********************** B ********************************** appo <- t(x) %*% (omega * x) appo <- solve(appo) B <- appo %*% t(x) %*% (omega * y) #*********************** sigma ********************************** dif <- y - x%*%B sigma <- (t(dif) %*% (omega * dif)) / n if (det(sigma) < 10e-10) { ris$sing <- TRUE ris$is.conv <- FALSE ris$msg <- "Covariance matrix quasi singular: essentially perfect fit" warning(ris$msg) } s1 <- solve(sigma) #*********************** lambda ********************************** # q1 <- matrix(diag(dif %*% solve(sigma1) %*% t(dif)),n,1) ## DIM n,1 # q2 <- matrix(diag(dif %*% solve(sigma2) %*% t(dif)),n,1) ## DIM n,1 if (!lambda.fix) { appo <- t(dif) %*% (as.vector(tau2) * dif) %*% s1 lambda <- sum(diag(as.matrix(appo))) / (p * sum(tau2)) -1 # if (lambda > 1e+06) { # sing <- TRUE # continua <- conv <- FALSE # warning (paste("lambda =" ,lambda,": iterations stopped because of essentially perfect fit", sep="")) # break # } if (lambda < 0.5) { continua <- conv <- FALSE warning (paste("lambda parameter lower than 0.5. Possible lack of model identification.", sep="")) break } } #*********************** CONVERGENZA ********************************** s2 <- s1 / (1 + lambda) sigma2 <- (1+lambda)* sigma q1 <- matrix(tensorizza (dif, s1),n,1) q2 <- matrix(tensorizza (dif, s2),n,1) rm (s1,s2) q1 <- -0.5*q1 q2 <- -0.5*q2 ll <- w1 * exp(q1) / sqrt(2*pi*det(sigma)) + (1-w1) * (exp(q2)) / sqrt(2*pi*det(sigma2)) lik <- sum(log(ll)) if (graph) { plot(Var, col = "lightgrey", main= "EM IN ACTION...\n Identifying outliers", xlab=lab[1], ylab=lab[2] ) points(Var[tau2 > t.outl, ],pch=21,col="blue",bg=paste("cyan",sample(1:4,1),sep="")) lambda_all <- c (lambda_all, lambda) plot( lambda_all, xlab="n. iterations", ylab="lambda") } BIC.mix <- -2*lik + k2*log(n) continua <- (abs(lik-oldlik) > eps*abs(lik-lik0) ) conv <- !continua if (iter > round(max.iter/5) & BIC.n < BIC.mix ) { continua <- conv <- FALSE warning (paste("EM stopped because BIC value " ,BIC.mix,"for the contamination model is greater than BIC value", BIC.n, " for the Gaussian model", sep="")) break } #alpha <- sqrt((lambda+1) ) oldlik <- lik if (iter == 1) lik0 <- lik } #************************ FINE CICLO EM ************************************ if (iter >= max.iter) conv <- FALSE # CALCOLO DEI VALORI PREVISTI yprev <- pred.y(y=memo.y, x=memo.x, B, sigma, lambda, w=1-w1, model = model, t.outl=t.outl) ############### calcolo di BIC e AIC per i due modelli ############# BIC.n <- -2*lik.n + k1*log(n) BIC.mix <- -2*lik + k2*log(n) AIC.n <- 2*k1 - lik.n AIC.mix <- 2*k2 - lik ris$ypred <- as.matrix(yprev[,1:(ncol(yprev)-3)]) ris$B <- B ris$sigma <- sigma ris$lambda <- lambda ris$w <- 1-w1 ris$tau <- yprev$tau ris$outlier <- yprev$outlier ris$n.outlier <- sum(yprev$outlier) ris$pattern <- yprev$pattern ris$is.conv <- conv ris$n.iter <- iter ris$sing <- sing ris$bic.aic <- c(BIC.norm=BIC.n, BIC.mix=BIC.mix, AIC.norm=AIC.n, AIC.mix=AIC.mix) class(ris) <- c(class(ris), "mlest" ) if (conv == FALSE) warning (paste("EM algorithm failed to converge: stop after", iter, "iterations")) ris }
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# Simple normal mean model in LaplacesDemon # Generate two samples of body mass measurements of male peregrines y1000 <- rnorm(n = 1000, mean = 100, sd = 10) # Sample of 1000 birds ###========================================================== mean(y1000) ###========================================================== lm0 <- lm(y1000~1) sd(y1000) summary(lm0) ###========================================================= population.sd <- 1 for(i in 1:10){ mu <- 1:3000 la00 <- sapply(mu,function(xx)sum(dnorm(y1000, xx, population.sd, log=TRUE))) mu <- mu[which.max(la00)] population.sd <- 1:100 d01 <- sapply(population.sd,function(xx)sum(dnorm(y1000, mu, xx, log=TRUE))) population.sd <- population.sd[which.max(d01)] } c(mean=mu,sd=population.sd) plot(la00) plot(d01) ###=============================================================== ### Random walk MCMC for binomial proportion ############################################ # Parameters parm <- c(1,10) population.mean <- parm[1] population.sd <- parm[2] # Prior density population.mean.prior <- dunif(population.mean, 0, 5000) population.sd.prior <- dunif(population.sd, 0, 100) # Log-Likelihood LL <- sum(dnorm(y1000, population.mean, population.sd, log=TRUE)) # Log-Posterior LP <- LL + population.mean.prior + population.sd.prior Modelout <- list(LP=LP, Dev=-2*LL, Monitor=c(LP), yhat=rnorm(length(y1000), population.mean, population.sd), parm=c(rnorm(1,600), runif(1, 1, 30)) ) ###=============================================================== # Load library library(LaplacesDemon) # Model specification Model <- function(parm, Data) { # Parameters population.mean <- parm[1] population.sd <- parm[2] # Prior density population.mean.prior <- dunif(population.mean, 0, 5000) population.sd.prior <- dunif(population.sd, 0, 100) # Log-Likelihood mu <- population.mean LL <- sum(dnorm(Data$mass, mu, population.sd, log=TRUE)) # Log-Posterior LP <- LL + population.mean.prior + population.sd.prior Modelout <- list(LP=LP, Dev=-2*LL, Monitor=c(LP), yhat=rnorm(Data$N, mu, population.sd), parm=parm) return(Modelout) } # Prepare the data parm.names <- c("population.mean", "population.sd") Data <- list(mass=y1000, N=length(y1000), mon.names=c("LP"), parm.names=parm.names) # Initial values Initial.Values <- c( rnorm(1,600), # population.mean runif(1, 1, 30) # population.sd ) # MCMC settings ni <- 50000 # Number of draws from posterior (for each chain) st <- 1000 # Steps when status message should be given nt <- 50 # Thinning rate # Run LaplacesDemon out <- LaplacesDemon(Model, Data=Data, Initial.Values, Iterations=ni, Status=st, Thinning=nt) # Have a look at some summary statistics out # Plotting output plot(out, BurnIn=100, Data, PDF=T, Parms=c("population.mean", "population.sd"))
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% Generated by roxygen2: do not edit by hand % Please edit documentation in R/analysed.R \name{gcol} \alias{gcol} \title{Centre gravite de colonnes} \usage{ gcol(data) } \arguments{ \item{data:}{valeur d'origine} } \value{ un vector de centre de gravite } \description{ Le centre de gravite de profils-lignes affect¨¦s avec des poids(frequences) }
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# 90% positive of 10 ratings o1 <- 9 o0 <- 1 M <- 100 N <- 100000 m <- sapply(0:M/M,function(prob)rbinom(N,o1+o0,prob)) v <- colSums(m==o1) df_sim1 <- data.frame(p=rep(0:M/M,v)) df_beta1 <- data.frame(p=0:M/M, y=dbeta(0:M/M,o1+1,o0+1)) # 80% positive of 500 ratings o1 <- 400 o0 <- 100 M <- 100 N <- 100000 m <- sapply(0:M/M,function(prob)rbinom(N,o1+o0,prob)) v <- colSums(m==o1) df_sim2 <- data.frame(p=rep(0:M/M,v)) df_beta2 <- data.frame(p=0:M/M, y=dbeta(0:M/M,o1+1,o0+1)) ggplot(data=df_sim1,aes(p)) + scale_x_continuous(breaks=0:10/10) + geom_histogram(aes(y=..density..,fill=..density..), binwidth=0.01, origin=-.005, colour=I("gray")) + geom_line(data=df_beta1 ,aes(p,y),colour=I("red"),size=2,alpha=.5) + geom_histogram(data=df_sim2, aes(y=..density..,fill=..density..), binwidth=0.01, origin=-.005, colour=I("gray")) + geom_line(data=df_beta2,aes(p,y),colour=I("orange"),size=2,alpha=.5)
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% Generated by roxygen2: do not edit by hand % Please edit documentation in R/errorGen.R \name{errorGen} \alias{errorGen} \title{Generate interpolation error stats from validation datasets} \usage{ errorGen( finalraster, validation.sf_ob, validation.data, plot = FALSE, title = "" ) } \arguments{ \item{finalraster}{RasterLayer object} \item{validation.sf_ob}{sf object with points geometry} \item{validation.data}{data.frame} \item{plot}{logical. Plot comparison?} \item{title}{Plot labels} } \value{ List of error statistics } \description{ Generate error statistics from validation point datasets overlaid on a raster surface } \examples{ library(sf) validation.data <- data.frame(rnorm(10, mean = 0.2, sd = 1)) names(validation.data) <- c("validation") validation.sf_ob <- validation.data validation.data <- as.numeric(unlist(validation.data)) xy <- data.frame(x = c(0:9), y = rep(1, 10)) validation.sf_ob <- st_as_sf(cbind(validation.sf_ob, xy), coords = c("x", "y")) m <- matrix(NA, 1, 10) out.ras <- raster(m, xmn = 0, xmx = ncol(m), ymn = 0, ymx = nrow(m)) out.ras[] <- validation.data + rnorm(ncell(out.ras), mean = 0.01, sd = 0.2) valid.stats <- errorGen(out.ras, validation.sf_ob, validation.data, plot = TRUE, title = "Validation Plot") valid.stats }
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cran/idealstan
6aeffb800be1490c1f2f969313e3f79d57eb5c5d
daa29ce7e203c63fbba916aa258d53b48ea430b2
refs/heads/master
2021-05-02T03:26:00.009381
2019-07-10T14:00:03
2019-07-10T14:00:03
120,898,012
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rstan_generics.R
# These functions are implemented for compatibility with the # rstantools package (and rstanarm) #' Generic Method for Obtaining Posterior Predictive Distribution from Stan Objects #' #' This function is a generic that is used to match the functions used with \code{\link[bayesplot]{ppc_bars}} to calculate #' the posterior predictive distribution of the data given the model. #' #' @param object A fitted \code{idealstan} object #' @param ... All other parameters passed on to the underlying function. #' @export #' @return \code{posterior_predict} methods should return a \eqn{D} by \eqn{N} #' matrix, where \eqn{D} is the number of draws from the posterior predictive #' distribution and \eqn{N} is the number of data points being predicted per #' draw. #' @export setGeneric('id_post_pred',signature='object', function(object,...) standardGeneric('id_post_pred')) #' Posterior Prediction for \code{idealstan} objects #' #' This function will draw from the posterior distribution, whether in terms of the outcome (prediction) #' or to produce the log-likelihood values. #' #' This function can also produce either distribution of the #' outcomes (i.e., predictions) or the log-likelihood values of the posterior (set option #' \code{type} to \code{'log_lik'}. #' For more information, see the package vignette How to Evaluate Models. #' #' You can then use functions such as #' \code{\link{id_plot_ppc}} to see how well the model does returning the correct number of categories #' in the score/vote matrix. #' Also see \code{help("posterior_predict", package = "rstanarm")} #' #' @param object A fitted \code{idealstan} object #' @param draws The number of draws to use from the total number of posterior draws (default is 100). #' @param sample_scores In addition to reducing the number of posterior draws used to #' calculate the posterior predictive distribution, which will reduce computational overhead. #' Only available for calculating predictive distributions, not log-likelihood values. #' @param type Whether to produce posterior predictive values (\code{'predict'}, the default), #' or log-likelihood values (\code{'log_lik'}). See the How to Evaluate Models vignette for more info. #' @param output If the model has an unbounded outcome (Poisson, continuous, etc.), then #' specify whether to show the \code{'observed'} data (the default) or the binary #' output \code{'missing'} showing whether an observation was predicted as missing or not #' @param ... Any other arguments passed on to posterior_predict (currently none available) #' #' @export setMethod('id_post_pred',signature(object='idealstan'),function(object,draws=100, output='observed', type='predict', sample_scores=NULL,...) { #all_params <- rstan::extract(object@stan_samples) n_votes <- nrow(object@score_data@score_matrix) if(object@stan_samples@stan_args[[1]]$method != 'variational') { n_iters <- (object@stan_samples@stan_args[[1]]$iter-object@stan_samples@stan_args[[1]]$warmup)*length(object@stan_samples@stan_args) } else { # there is no warmup for VB n_iters <- dim(object@stan_samples)[1] } if(!is.null(sample_scores) && type!='log_lik') { this_sample <- sample(1:n_votes,sample_scores) } else { this_sample <- 1:n_votes } if(type!='log_lik') { these_draws <- sample(1:n_iters,draws) } else { these_draws <- 1:n_iters draws <- n_iters } print(paste0('Processing posterior replications for ',n_votes,' scores using ',draws, ' posterior samples out of a total of ',n_iters, ' samples.')) y <- object@score_data@score_matrix$outcome[this_sample] # check to see if we need to recode missing values from the data if the model_type doesn't handle missing data if(object@model_type %in% c(1,3,5,7,9,11,13) & !is.null(object@score_data@miss_val)) { y <- .na_if(y,object@score_data@miss_val) } if(object@use_groups) { person_points <- as.numeric(object@score_data@score_matrix$group_id)[this_sample] } else { person_points <- as.numeric(object@score_data@score_matrix$person_id)[this_sample] } bill_points <- as.numeric(object@score_data@score_matrix$item_id)[this_sample] time_points <- as.numeric(factor(object@score_data@score_matrix$time_id))[this_sample] remove_nas <- !is.na(y) & !is.na(person_points) & !is.na(bill_points) & !is.na(time_points) y <- y[remove_nas] if(is.factor(y)) { miss_val <- which(levels(y)==object@score_data@miss_val) y <- as.numeric(y) } max_val <- max(y) bill_points <- bill_points[remove_nas] time_points <- time_points[remove_nas] person_points <- person_points[remove_nas] model_type <- object@model_type latent_space <- model_type %in% c(13,14) inflate <- model_type %in% c(2,4,6,8,10,12,14) # we can do the initial processing here # loop over posterior iterations L_tp1 <- .extract_nonp(object@stan_samples,'L_tp1')[[1]] A_int_free <- .extract_nonp(object@stan_samples,'A_int_free')[[1]] B_int_free <- .extract_nonp(object@stan_samples,'B_int_free')[[1]] sigma_abs_free <- .extract_nonp(object@stan_samples,'sigma_abs_free')[[1]] sigma_reg_free <- .extract_nonp(object@stan_samples,'sigma_reg_free')[[1]] pr_absence_iter <- sapply(these_draws, function(d) { if(latent_space) { # use latent-space formulation for likelihood pr_absence <- sapply(1:length(person_points),function(n) { -sqrt((L_tp1[d,time_points[n],person_points[n]] - A_int_free[d,bill_points[n]])^2) }) %>% plogis() } else { # use IRT formulation for likelihood pr_absence <- sapply(1:length(person_points),function(n) { L_tp1[d,time_points[n],person_points[n]]*sigma_abs_free[d,bill_points[n]] - A_int_free[d,bill_points[n]] }) %>% plogis() } return(pr_absence) }) pr_vote_iter <- sapply(these_draws, function(d) { if(latent_space) { if(inflate) { pr_vote <- sapply(1:length(person_points),function(n) { -sqrt((L_tp1[d,time_points[n],person_points[n]] - B_int_free[d,bill_points[n]])^2) }) %>% plogis() } else { # latent space non-inflated formulation is different pr_vote <- sapply(1:length(person_points),function(n) { sigma_reg_free[d,bill_points[n]] + sigma_abs_free[d,bill_points[n]] - sqrt((L_tp1[d,time_points[n],person_points[n]] - B_int_free[d,bill_points[n]])^2) }) %>% plogis() } } else { pr_vote <- sapply(1:length(person_points),function(n) { L_tp1[d,time_points[n],person_points[n]]*sigma_reg_free[d,bill_points[n]] - B_int_free[d,bill_points[n]] }) %>% plogis() } return(pr_vote) }) rep_func <- switch(as.character(model_type), `1`=.binary, `2`=.binary, `3`=.ordinal_ratingscale, `4`=.ordinal_ratingscale, `5`=.ordinal_grm, `6`=.ordinal_grm, `7`=.poisson, `8`=.poisson, `9`=.normal, `10`=.normal, `11`=.lognormal, `12`=.lognormal, `13`=.binary, `14`=.binary) # pass along cutpoints as well if(model_type %in% c(3,4)) { cutpoints <- .extract_nonp(object@stan_samples,'steps_votes')[[1]] cutpoints <- cutpoints[these_draws,] } else if(model_type %in% c(5,6)) { cutpoints <- .extract_nonp(object@stan_samples,'steps_votes_grm')[[1]] cutpoints <- cutpoints[these_draws,,] } else { cutpoints <- 1 } out_predict <- rep_func(pr_absence=pr_absence_iter, pr_vote=pr_vote_iter, N=length(person_points), ordinal_outcomes=length(unique(object@score_data@score_matrix$outcome)), inflate=inflate, latent_space=latent_space, time_points=time_points, item_points=bill_points, max_val=max_val, outcome=y, miss_val=miss_val, person_points=person_points, sigma_sd=.extract_nonp(object@stan_samples,'extra_sd')[[1]][these_draws], cutpoints=cutpoints, type=type, output=output) # set attributes to pass along sample info attr(out_predict,'chain_order') <- attr(L_tp1,'chain_order')[these_draws] attr(out_predict,'this_sample') <- this_sample if(type=='predict') { class(out_predict) <- c('matrix','ppd') } else if(type=='log_lik') { class(out_predict) <- c('matrix','log_lik') } return(out_predict) }) #' Plot Posterior Predictive Distribution for \code{idealstan} Objects #' #' This function is the generic method for generating posterior distributions #' from a fitted \code{idealstan} model. Functions are documented in the #' actual method. #' #' This function is a wrapper around \code{\link[bayesplot]{ppc_bars}}, #' \code{\link[bayesplot]{ppc_dens_overlay}} and #' \code{\link[bayesplot]{ppc_violin_grouped} that plots the posterior predictive distribution #' derived from \code{\link{id_post_pred}} against the original data. You can also subset the #' posterior predictions over #' legislators/persons or #' bills/item sby specifying the ID of each in the original data as a character vector. #' Only persons or items can be specified, #' not both. #' #' If you specify a value for \code{group} that is either a person ID or a group ID #' (depending on whether a person or group-level model was fit), then you can see the #' posterior distributions for those specific persons. Similarly, if an item ID is passed #' to \code{item}, you can see how well the model predictions compare to the true values #' for that specific item. #' #' @param object A fitted \code{idealstan} object #' @param ... Other arguments passed on to \code{\link[bayesplot]{ppc_bars}} #' @export setGeneric('id_plot_ppc',signature='object', function(object,...) standardGeneric('id_plot_ppc')) #' Plot Posterior Predictive Distribution for \code{idealstan} Objects #' #' This function is the actual method for generating posterior distributions #' from a fitted \code{idealstan} model. #' #' This function is a wrapper around \code{\link[bayesplot]{ppc_bars}}, #' \code{\link[bayesplot]{ppc_dens_overlay}} and #' \code{\link[bayesplot]{ppc_violin_grouped} that plots the posterior predictive distribution #' derived from \code{\link{id_post_pred}} against the original data. You can also subset the #' posterior predictions over #' legislators/persons or #' bills/item sby specifying the ID of each in the original data as a character vector. #' Only persons or items can be specified, #' not both. #' #' If you specify a value for \code{group} that is either a person ID or a group ID #' (depending on whether a person or group-level model was fit), then you can see the #' posterior distributions for those specific persons. Similarly, if an item ID is passed #' to \code{item}, you can see how well the model predictions compare to the true values #' for that specific item. #' #' @param object A fitted idealstan object #' @param ppc_pred The output of the \code{\link{id_post_pred}} function on a fitted idealstan object #' @param group A character vector of the person or group IDs #' over which to subset the predictive distribution #' @param item A character vector of item IDs to subset the posterior distribution #' @param ... Other arguments passed on to \code{\link[bayesplot]{ppc_bars}} #' @export setMethod('id_plot_ppc',signature(object='idealstan'),function(object, ppc_pred=NULL, group=NULL, item=NULL,...) { this_sample <- attr(ppc_pred,'this_sample') # create grouping variable if(!is.null(group)) { if(object@use_groups) { group_var <- factor(object@score_data@score_matrix$group_id, levels=group) } else { group_var <- factor(object@score_data@score_matrix$person_id, levels=group) } grouped <- T } else if(!is.null(item)) { group_var <- factor(object@score_data@score_matrix$item_id, levels=item) grouped <- T } else { grouped <- F } y <- object@score_data@score_matrix$outcome[this_sample] # check to see if we need to recode missing values from the data if the model_type doesn't handle missing data if(object@model_type %in% c(1,3,5,7,9,11,13) & !is.null(object@score_data@miss_val)) { y <- .na_if(y,object@score_data@miss_val) } if(object@use_groups) { person_points <- as.numeric(object@score_data@score_matrix$group_id)[this_sample] } else { person_points <- as.numeric(object@score_data@score_matrix$person_id)[this_sample] } bill_points <- as.numeric(object@score_data@score_matrix$item_id)[this_sample] time_points <- as.numeric(object@score_data@score_matrix$time_id)[this_sample] remove_nas <- !is.na(y) & !is.na(person_points) & !is.na(bill_points) & !is.na(time_points) y <- y[remove_nas] bill_points <- bill_points[remove_nas] time_points <- time_points[remove_nas] person_points <- person_points[remove_nas] if(!is.null(group)) { group_var <- group_var[remove_nas] # create a second one for the grouping variable remove_nas_group <- !is.na(group) } if(!is.null(item) && !is.null(group)) stop('Please only specify an index to item or person, not both.') if(attr(ppc_pred,'output')=='all') { y <- as.numeric(y) if(grouped) { bayesplot::ppc_bars_grouped(y=y[remove_nas_group],yrep=ppc_pred[,remove_nas_group], group=group_var[remove_nas_group],...) } else { bayesplot::ppc_bars(y=y,yrep=ppc_pred,...) } } else if(attr(ppc_pred,'output')=='observed') { # only show observed data for yrep y <- .na_if(y,object@score_data@miss_val) to_remove <- !is.na(y) y <- y[to_remove] if(!is.null(group)) { group_var <- group_var[to_remove] remove_nas_group <- !is.na(group_var) } y <- as.numeric(y) if(attr(ppc_pred,'output_type')=='continuous') { ppc_pred <- ppc_pred[,to_remove] #unbounded observed outcomes (i.e., continuous) if(grouped) { bayesplot::ppc_violin_grouped(y=y[remove_nas_group],yrep=ppc_pred[,remove_nas_group], group=group_var[remove_nas_group], ...) } else { bayesplot::ppc_dens_overlay(y=y,yrep=ppc_pred,...) } } else if(attr(ppc_pred,'output_type')=='discrete') { ppc_pred <- ppc_pred[,to_remove] if(grouped) { bayesplot::ppc_bars_grouped(y=y[remove_nas_group],yrep=ppc_pred[,remove_nas_group], group=group_var[remove_nas_group],...) } else { bayesplot::ppc_bars(y=y,yrep=ppc_pred,...) } } } else if(attr(ppc_pred,'output')=='missing') { y <- .na_if(y,object@score_data@miss_val) y <- as.numeric(is.na(y)) if(grouped) { bayesplot::ppc_bars_grouped(y=y[remove_nas_group],yrep=ppc_pred[,remove_nas_group], group=group_var[remove_nas_group],...) } else { bayesplot::ppc_bars(y=y,yrep=ppc_pred,...) } } }) #' Helper Function for `loo` calculation #' #' This function accepts a log-likelihood matrix produced by `id_post_pred` and #' extracts the IDs of the MCMC chains. It is necessary to use this function #' as the second argument to the `loo` function along with an exponentiated #' log-likelihood matrix. See the package vignette How to Evaluate Models #' for more details. #' #' @param ll_matrix A log-likelihood matrix as produced by the \code{\link{id_post_pred}} #' function #' @export derive_chain <- function(ll_matrix=NULL) { attr(ll_matrix,'chain_order') }
d705f7d7ef096c97472fb22981d95fe2eea28e37
030e413aebffc20fe1243ebe264755d7f8d5cee5
/Census NAICS Trade.R
b10203aef90434a0f807b0cb77dd7f85f2866db0
[]
no_license
szmsp/bilateral-trade-in-goods-naics
63e2d79663996620fb319a0ff7c95465a677d4b9
dbad0737fe78c0d77f08c227b2e94f245ad0e4d5
refs/heads/master
2020-04-28T01:44:14.120594
2019-03-24T16:58:22
2019-03-24T16:58:22
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Census NAICS Trade.R
############################################################################################################################### # README # Project: Goods trade by three-digit NAICS code between the US and other countries # Objective: From the Census API, download two years of the US Census Bureau bilateral trade by three-digit NAICS codes # US Census API Setup # Census API Key request here: http://api.census.gov/data/key_signup.html # In the API call: months must be specified as "\d\d" ("01", "02") # The as.yearqtr function converts the underlying date value to the first day-month of the quarter # For help on Census international trade data API # https://www.census.gov/foreign-trade/reference/guides/Guide%20to%20International%20Trade%20Datasets.pdf # To run, replace "[key]" and "[path]" below ############################################################################################################################### # Run before every program to clear your workspace rm(list=ls()) cat("\014") # Root paths folder <- "[path]" analysis <- paste(folder, "Analysis\\", sep = "") # Set dates to download # First date first_year <- "2013" first_month <- "01" # Final date final_year <- "2018" final_month <- "12" ### PATHS AND PARAMETERS ### # Census key, obtained from Census website above census_key <- "[key]" # Set analysis parameters and vars you want to grab. Currently set to Germany # Parameters ctry_code <- 4280 # Vars import_vars <- paste("CTY_CODE","CTY_NAME","NAICS","NAICS_LDESC","GEN_VAL_MO","GEN_VAL_YR", sep=",") export_vars <- paste("CTY_CODE","CTY_NAME","NAICS","NAICS_LDESC","ALL_VAL_MO","ALL_VAL_YR", sep=",") ############################################################################################################################### ### PULL DATA FROM CENSUS API### # Set location Sys.setlocale("LC_ALL","C") # Set working directory setwd(folder) # Load libraries library("tidyverse") library("RJSONIO") library("sqldf") library("ggthemes") library("zoo") library("dplyr") library("tools") library("lubridate") library("reshape2") library("formattable") #### PULL DATA #### # Function to extract imports data getImports <- function(census_key, year_month, import_vars, ctry_code) { imp_resURL <- paste("https://api.census.gov/data/timeseries/intltrade/imports/", "naics?get=",import_vars,"&COMM_LVL=","&COMM_LVL=NA3","&time=",year_month, "&CTY_CODE=",ctry_code,"&key=",census_key,sep="") imp_lJSON <- fromJSON(imp_resURL) # convert JSON content to R objects imp_lJSON <- imp_lJSON[2:length(imp_lJSON)] # keep everything but the 1st element (var names) in lJSON imp_lJSON.cc <- sapply(imp_lJSON,function(x) x[1]) # extract country code imp_lJSON.cn <- sapply(imp_lJSON,function(x) x[2]) # extract country name imp_lJSON.nc <- sapply(imp_lJSON,function(x) x[3]) # extract three-digit NAICS code imp_lJSON.nd <- sapply(imp_lJSON,function(x) x[4]) # extract NAICS description imp_lJSON.avm <- sapply(imp_lJSON,function(x) x[5]) # extract all value month imp_lJSON.avy <- sapply(imp_lJSON,function(x) x[6]) # extract all value year imp_lJSON.t <- sapply(imp_lJSON,function(x) x[8]) # extract time imp_df <- data.frame(as.Date(paste(imp_lJSON.t,"-02", sep=""), format="%Y-%m-%d"), imp_lJSON.cc, as.character(imp_lJSON.cn), imp_lJSON.nc, imp_lJSON.nd, as.numeric(imp_lJSON.avm),as.numeric(imp_lJSON.avy)) # put in dataframe names(imp_df) <- c("year_month", "country_code", "country_name", "naics_code", "naics_desc", "monthly_import_value", "ytd_import_value") # name the vars in the data frame return(imp_df) } # API calls split by year for efficiency date_list <- seq(as.Date(paste(first_year, "/", first_month, "/1", sep = "")), as.Date(paste(final_year, "/", final_month, "/1", sep = "")), "years") year_list <- year(date_list) # Call imports data for (y in year_list){ if((y == first_year)){ month_imports <- getImports(census_key, year_month = (paste("from+", y,"-01+to+", y,"-12", sep = "")), import_vars, ctry_code) } if(exists("month_imports") && (y != first_year) && (y != final_year)){ temp_data <- getImports(census_key, year_month = (paste("from+", y,"-01+to+", y,"-12", sep = "")), import_vars, ctry_code) month_imports <- rbind(month_imports, temp_data) rm(temp_data) } if(exists("month_imports") && (y == final_year)){ temp_data <- getImports(census_key, year_month = (paste("from+", y,"-01+to+", y,"-",final_month, sep = "")), import_vars, ctry_code) month_imports <- rbind(month_imports, temp_data) rm(temp_data) } } View(month_imports) check_imports <- sqldf("select year_month, naics_code, count(country_code) as naics_count from month_imports group by 1, 2") View(check_imports) # Check for one observation per three-digit NAICS code per month stopifnot(check_imports$naics_count == 1) month_imports <- month_imports[order(month_imports$naics_desc, month_imports$year_month),] # Function to extract exports data getExports <- function(census_key, year_month, export_vars, ctry_code) { exp_resURL <- paste("https://api.census.gov/data/timeseries/intltrade/exports/", "naics?get=",export_vars,"&COMM_LVL=","&COMM_LVL=NA3","&time=",year_month, "&CTY_CODE=",ctry_code,"&key=",census_key,sep="") exp_lJSON <- fromJSON(exp_resURL) # convert JSON content to R objects exp_lJSON <- exp_lJSON[2:length(exp_lJSON)] # keep everything but the 1st element (var names) in lJSON exp_lJSON.cc <- sapply(exp_lJSON,function(x) x[1]) # extract country code exp_lJSON.cn <- sapply(exp_lJSON,function(x) x[2]) # extract country name exp_lJSON.nc <- sapply(exp_lJSON,function(x) x[3]) # extract three-digit NAICS code exp_lJSON.nd <- sapply(exp_lJSON,function(x) x[4]) # extract NAICS description exp_lJSON.avm <- sapply(exp_lJSON,function(x) x[5]) # extract all value month exp_lJSON.avy <- sapply(exp_lJSON,function(x) x[6]) # extract all value year exp_lJSON.t <- sapply(exp_lJSON,function(x) x[8]) # extract time exp_df <- data.frame(as.Date(paste(exp_lJSON.t,"-02", sep=""), format="%Y-%m-%d"), exp_lJSON.cc, as.character(exp_lJSON.cn), exp_lJSON.nc, exp_lJSON.nd, as.numeric(exp_lJSON.avm), as.numeric(exp_lJSON.avy)) # put in dataframe names(exp_df) <- c("year_month", "country_code", "country_name", "naics_code", "naics_desc", "monthly_export_value", "ytd_export_value") # name the vars in the data frame return(exp_df) } # Call exports data for (y in year_list){ if(!exists("month_exports") && (y == first_year)){ month_exports <- getExports(census_key, year_month = (paste("from+", y,"-01+to+", y,"-12", sep = "")), export_vars, ctry_code) } if(exists("month_exports") && (y != first_year) && (y != final_year)){ temp_data <- getExports(census_key, year_month = (paste("from+", y,"-01+to+", y,"-12", sep = "")), export_vars, ctry_code) month_exports <- rbind(month_exports, temp_data) rm(temp_data) } if(exists("month_exports") && (y == final_year)){ temp_data <- getExports(census_key, year_month = (paste("from+", y,"-01+to+", y,"-",final_month, sep = "")), export_vars, ctry_code) month_exports <- rbind(month_exports, temp_data) rm(temp_data) } } View(month_exports) check_exports <- sqldf("select year_month, naics_code, count(country_code) as naics_count from month_exports group by 1, 2") View(check_exports) # Check for one observation per three-digit NAICS code per month stopifnot(check_exports$naics_count == 1) month_exports <- month_exports[order(month_exports$naics_desc, month_exports$year_month),] #### CREATE LAGGED VALUES #### # Merge import and export dataset to single dataset to create single set trade_data <- merge(month_imports, month_exports, by = c("year_month", "country_code", "country_name", "naics_code", "naics_desc"), all = TRUE) # Proper case NAICS fields trade_data$naics_desc <- tolower(trade_data$naics_desc) trade_data$naics_desc <- toTitleCase(trade_data$naics_desc) # Create quarterly date-time variable in trade data trade_data$yq <- as.yearqtr(trade_data$year_month, format = "%Y-%m-%d") format(trade_data$yq, format = "%y 0%q") View(trade_data) # Create new dataset to sum trade by quarter-NAICS quarterly_data <- sqldf("select country_name, yq, naics_code, naics_desc, sum(monthly_import_value) as yq_import_value, sum(monthly_export_value) as yq_export_value from trade_data group by 1, 2, 3, 4") # YTD lagged values ytd_data <- sqldf("select naics_code, naics_desc, year_month, ytd_import_value, ytd_export_value from trade_data group by 1, 2, 3") ytd_data <- ytd_data %>% group_by(naics_desc) %>% mutate(lag.ytd_import_value = dplyr::lag(ytd_import_value, n = 12, order_by = naics_desc, default = NA)) ytd_data <- ytd_data %>% group_by(naics_desc) %>% mutate(lag.ytd_export_value = dplyr::lag(ytd_export_value, n = 12, order_by = naics_desc, default = NA)) # Quarterly lagged values quarterly_data <- sqldf("select country_name, naics_code, naics_desc, yq, yq_import_value, yq_export_value from quarterly_data group by 1, 2, 3, 4") quarterly_data <- quarterly_data %>% group_by(naics_desc) %>% mutate(lag.yq_import_value = dplyr::lag(yq_import_value, n = 4, order_by = naics_desc, default = NA)) quarterly_data <- quarterly_data %>% group_by(naics_desc) %>% mutate(lag.yq_export_value = dplyr::lag(yq_export_value, n = 4, order_by = naics_desc, default = NA)) #### FIND YEAR-ON-YEAR CHANGE #### pct_change <- function(new, old) {(new - old)/old} quarterly_data$change_m_yoy <- pct_change(quarterly_data$yq_import_value, quarterly_data$lag.yq_import_value) quarterly_data$change_x_yoy <- pct_change(quarterly_data$yq_export_value, quarterly_data$lag.yq_export_value) ytd_data$change_m_yoy <- pct_change(ytd_data$ytd_import_value, ytd_data$lag.ytd_import_value) ytd_data$change_x_yoy <- pct_change(ytd_data$ytd_export_value, ytd_data$lag.ytd_export_value) #### VIEW CURRENT QUARTER AND YTD SUBSETS #### current_quarter <- as.yearqtr(paste(final_year, "-", final_month, "-02", sep=""), format = "%Y-%m-%d") format(current_quarter, format = "20%y Q%q") current_month <- as.Date(paste(final_year, "-", final_month, "-02", sep=""), format = "%Y-%m-%d") quarter_subset <- subset(quarterly_data, yq == current_quarter) ytd_subset <- subset(ytd_data, year_month == current_month) #### CHART TRENDS BY INDUSTRY #### # Set theme theme_set(theme_bw()) gross_charts <- function(df, output_loc){ # Create list of industries naics_list <- unique(df$naics_desc) # Produce by-industry plots for(i in seq_along(naics_list)){ # Create plots plot <- ggplot(subset(df, naics_desc == naics_list[i]), aes(x = year_month, y = gross_value, color = trade_type)) + geom_line() + xlab("Period") + scale_y_continuous("Value ($)", labels = scales::dollar) + ggtitle(paste("U.S.-Germany Trade in ", naics_list[i], " Products, 1/2013 to 12/2018", sep = "")) + theme(legend.position = "bottom") + theme(legend.title = element_blank()) + theme(legend.spacing.x = unit(0.25, 'cm')) + labs(caption = paste("Source: U.S. Census, U.S. Trade in Goods with Germany.", sep = "")) # Save plots ggsave(filename = paste(naics_list[i], " Gross Chart.pdf", sep = ""), plot, path = output_loc) # Print to screen print(plot) } } # Monthly Gross Charts monthly_gross_trends <- trade_data[, c(1, 3, 5:6, 8)] monthly_gross_trends$ex_less_im <- monthly_gross_trends$monthly_export_value - monthly_gross_trends$monthly_import_value names(monthly_gross_trends) <- c("year_month", "country_name", "naics_desc", "U.S. Monthly Imports", "U.S. Monthly Exports", "U.S. Monthly Exports Less Imports") monthly_gross_trends$year_month <- as.Date(monthly_gross_trends$year_month) monthly_gross_trends2 <- melt(monthly_gross_trends, id.vars = c("year_month", "country_name", "naics_desc"), variable.name = "trade_type", value.name = "gross_value") gross_charts(df = monthly_gross_trends2, output_loc = paste(analysis, "Monthly Charts\\", sep = ""))
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/plot4.R
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ShrutiVij/Coursera_ExploratoryDataAnalysis
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refs/heads/master
2021-01-13T07:57:23.853206
2016-10-23T03:59:26
2016-10-23T03:59:26
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plot4.R
setwd("./Desktop/Coursera/ExploratoryDataAnalysis/Assignment") library(ggplot2) library(dplyr) # Read the RDS Summary and Source Classification code RDS files sData <- readRDS("summarySCC_PM25.rds") scCode <- readRDS("Source_Classification_Code.rds") coalSource <- subset(scCode, EI.Sector %in% c("Fuel Comb - Electric Generation - Coal","Fuel Comb - Industrial Boilers, ICEs - Coal","Fuel Comb - Comm/Institutional - Coal")) allData <- merge(sData,coalSource,by = "SCC") grpData <- allData %>% group_by(year) %>% summarise(Emissions = sum(Emissions)) png("plot4.PNG") qplot(year,Emissions,data=grpData,geom = "line", color = "red")+ ggtitle("Coal combustion Emissions between 1999 to 2008") dev.off()
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/data/genthat_extracted_code/spind/examples/GEE.Rd.R
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surayaaramli/typeRrh
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refs/heads/master
2023-05-05T04:05:31.617869
2019-04-25T22:10:06
2019-04-25T22:10:06
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GEE.Rd.R
library(spind) ### Name: GEE ### Title: GEE (Generalized Estimating Equations) ### Aliases: GEE plot.GEE predict.GEE summary.GEE ### ** Examples data(musdata) coords<- musdata[,4:5] ## Not run: ##D mgee <- GEE(musculus ~ pollution + exposure, ##D family = "poisson", ##D data = musdata, ##D coord = coords, ##D corstr = "fixed", ##D scale.fix = FALSE) ##D ##D summary(mgee, printAutoCorPars = TRUE) ##D ##D pred <- predict(mgee, newdata = musdata) ##D ##D library(ggplot2) ##D ##D plot(mgee) ##D ##D my_gee_plot <- mgee$plot ##D ##D # move the legend to a new position ##D print(my_gee_plot + ggplot2::theme(legend.position = 'top')) ##D ## End(Not run)
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/data/genthat_extracted_code/BosonSampling/examples/permanents.Rd.R
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2023-05-05T04:05:31.617869
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permanents.Rd.R
library(BosonSampling) ### Name: Permanent-functions ### Title: Functions for evaluating matrix permanents ### Aliases: Permanent-functions cxPerm rePerm cxPermMinors ### ** Examples set.seed(7) n <- 20 A <- randomUnitary(n) cxPerm(A) # B <- Re(A) rePerm(B) # C <- A[,-n] v <- cxPermMinors(C) # # Check Laplace expansion by sub-permanents c(cxPerm(A),sum(v*A[,n]))
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/R/ons-ts-collision.R
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mhoehle/naming
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df7a59ceceac1964f66832df5f808bb3b92370db
refs/heads/master
2023-01-29T05:30:27.153488
2017-09-20T22:02:47
2017-09-20T22:02:47
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ons-ts-collision.R
###################################################################### ## Author: Michael Höhle <http://www.math.su.se/~hoehle> ## Date: 2017-04-23, modified 2017-09-20 to include 2016 data. ## ## Description: ## Create bonus material plot containing the time series of the UK baby ## name collision probability. All data files specified in the ## file filenames.txt are ###################################################################### library("readxl") library("dplyr") library("ggplot2") ##devtools::install_github("hoehleatsu/birthdayproblem") library("birthdayproblem") ###################################################################### ## ONS Data files have to be manually downloaded from ## https://www.ons.gov.uk/peoplepopulationandcommunity/birthsdeathsandmarriages/livebirths/datasets/babynamesenglandandwalesbabynamesstatisticsgirls ## and ## https://www.ons.gov.uk/peoplepopulationandcommunity/birthsdeathsandmarriages/livebirths/datasets/babynamesenglandandwalesbabynamesstatisticsboys. Alternatively, ## one can run the following R code: ###################################################################### filenames <- readLines("filenames.txt") for (filename in filenames) { ##Extract year and sex sex <- gsub("^([0-9]{4})(girls|boys).*","\\2",filename) year <- gsub("^([0-9]{4})(girls|boys).*","\\1",filename) ##Download the file if it doesn't exist destfile <- file.path("..","Data",filename) if (!file.exists(destfile)) { download.file(paste0("https://www.ons.gov.uk/file?uri=/peoplepopulationandcommunity/birthsdeathsandmarriages/livebirths/datasets/babynamesenglandandwalesbabynamesstatistics",sex,"/",year,"/",filename),destfile=destfile) } } ##Loop over all available files in the Data2 directory. Some warnings ##are to be expected, because the excel file contains text passages at ##the end informing about special removals etc. names <- NULL for (sex in c("Girls","Boys")) { files <- list.files(file.path("..","Data"), pattern=paste0("[0-9]{4}",tolower(sex))) for (i in seq_len(length(files))) { name <- files[i] filePath <- file.path("..","Data",name) ##Find name of the sheet containing the NAME & COUNT information sheets <- readxl::excel_sheets(path=filePath) sheetName <- grep(paste0(sex," names - E&W"),sheets, value=TRUE) if (length(sheetName) == 0) { sheetName <- tail(grep("Table [0-9]",sheets, value=TRUE),n=1) } ##Read the data from the excel file x <- readxl::read_excel(path=filePath,sheet=sheetName,skip=4) %>% select(Rank, Name, Count) ##Add column containing info about the year and sex x <- x %>% filter(!is.na(Rank)) %>% mutate(year=substr(name,1,4),sex=tolower(sex)) ##Debug information ##cat("Sex = ", sex, "\t file= ",name, "\tncol = ", ncol(x),"\n") ##print(names(x)) names <- rbind(names, x) } } ##Add empirical relative frequencies per year names$Name <- gsub("[ ]+$","",names$Name) names <- names %>% group_by(year) %>% mutate(p = Count/sum(Count)) ###################################################################### ##Compute and visualize the collision probablity ###################################################################### ## Compute collision prob for different group sizes collision <- names %>% group_by(year) %>% do({ n <- 27L p <- sapply(n, function(n) birthdayproblem::pbirthday_up(n=n, .$p ,method="mase1992")$prob) data.frame(n=n, p=p) }) collision <- collision %>% mutate(type=as.character("Names occurring > 2 times")) collision <- bind_rows(collision, data.frame(year=c("2015","2016"),n=27,p=c(0.458,0.429), type="All names")) p <- ggplot(collision, aes(x=as.numeric(year),y=p,colour=type)) + geom_line(size=1.2) + xlab("Year of birth") + ggtitle("Probability of a name clash in a group of 27 kids born in year YYYY in the UK and Wales") + ylab("Probability")+ scale_y_continuous(limits=c(0,1),labels=scales::percent) + scale_colour_discrete(name ="n") + scale_x_continuous(breaks=seq(min(as.numeric(collision$year)),max(as.numeric(collision$year)),2)) p + theme(#axis.text.x = element_text(angle = 45, hjust = 1), legend.direction = "horizontal", legend.position = "bottom") + scale_colour_discrete(name="Data basis: ") ##Store to file. ggsave(filename="timeseries.png", dpi=300, width=8, height=4, bg = "transparent") ###################################################################### ## Word clouds ###################################################################### require("wordcloud") #source("mywordcloud.R") names2015 <- names %>% filter(year==2015) boys2015 <- names %>% filter(year==2015, sex == "boys") girls2015 <- names %>% filter(year==2015, sex == "girls") # set.seed(123) # pdf(file="wordcloud-girls.pdf",width=10,height=10) # par(mar=c(0,0,0,0)) # pal <- brewer.pal(9, "PuRd")[-c(1:2)] # wordcloud(girls2015$Name,girls2015$Count,colors=pal,min.freq=50,random.order=FALSE) # dev.off() # pdf(file="wordcloud-boys.pdf",width=10,height=10) # par(mar=c(0,0,0,0)) # pal <- brewer.pal(9, "Blues")[-c(1:2)] # wordcloud(boys2015$Name,boys2015$Count,colors=pal,min.freq=50,random.order=FALSE) # dev.off() set.seed(123) png(file="wordclouds.png",width=800,height=400,res=72,bg = "transparent") par(mar=c(0,0,0,0), mfcol=c(1,2)) pal <- brewer.pal(9, "PuRd")[-c(1:2)] wordcloud(girls2015$Name,girls2015$Count,colors=pal,min.freq=50,random.order=FALSE) pal <- brewer.pal(9, "Blues")[-c(1:2)] wordcloud(boys2015$Name,boys2015$Count,colors=pal,min.freq=50,random.order=FALSE) dev.off()
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/ERA5_grib_data_extraction.R
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jihadrashid/UsedRcodeForMyWork
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1b37b9c524464e0fb1b9e87b4a9a4444d494003a
refs/heads/main
2023-01-31T05:57:38.302766
2020-12-15T06:05:05
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ERA5_grib_data_extraction.R
library(rNOMADS) library(ra/ster) x=raster("D:/Downloads/cape.grib") grib=brick("D:/Downloads/cape.grib") shp=shapefile("D:/Downloads/shp.shp") shp=spTransform(shp, CRSobj = "+proj=longlat +a=6367470 +b=6367470 +no_defs") grib=crop(grib,shp) grib_array= as.array(grib) pointCoordinates=read.csv("D:/Downloads/station.csv") coordinates(pointCoordinates)= ~ LONG+ LAT cape=extract(grib, pointCoordinates) combinePointValue=cbind(pointCoordinates,cape) write.table(combinePointValue,file="D:/Downloads/combinedPointValue.csv", append=FALSE, sep= ",", row.names = FALSE, col.names=TRUE) data=data.frame(combinedPointValue) View(data) cape_ts=t.data.frame(data) View(cape_ts) cape_ts=cape_ts[c(1:493), ] cape_ts=as.data.frame(cape_ts) writexl::write_xlsx(cape_ts, "D:/Downloads/cape_data.xlsx")
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/test/inst/shiny_app/server.R
e7adaacdaaa0c70b3feb2fadd40f1e5da9341b86
[]
no_license
sergeitarasov/ontoFAST
2e48156d3196033ae4e8b5e48db6b1cbf04cc9d5
c4e12584fde3ea4ccb4928374066f954a56a65d2
refs/heads/master
2022-09-02T00:54:23.513397
2022-08-04T13:02:00
2022-08-04T13:02:00
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server.R
server <- function(input, output, session) { ########### Network output$network <- renderVisNetwork({ withProgress(message = "Creating Network", value = 0.9, { # minimal example nodes <- data.frame(id = 1:3) edges <- data.frame(from = c(1,2,3), to = c(2,3,1)) visNetwork(nodes, edges, width = "100%", height = "100%", main = "Ontology Network", submain = "Select terms or IDs above to begin visualization") %>% visNodes( size=30, shadow =T) }) }) ##### Selectize updateSelectizeInput(session, "selectize", label = NULL, choices=srch_items, selected = FALSE, options = list(openOnFocus=F, maxOptions=100, placeholder="Search Ontology term or ID and click Expand to visualize" ), server = TRUE ) #### ####### Safe file observeEvent(input$savefile_btn, { print("sdfds") save(shiny_in, file="OntoFAST_annotation_shiny_in.RData") } ) ############ makeRadioButton=function(n=1){fluidRow(column(10, h3(paste(shiny_in$c1[n], shiny_in$c2[n], sep=" "), style='padding-left: 12px;'), #verbatimTextOutput(paste0("ids_selec", n)), textInput(paste0("ids_in", n), label = "", value = "", placeholder="Enter your ID"), actionButton(paste0("add_btn", n), label = "Add", icon = icon("glyphicon glyphicon-download", lib="glyphicon")), checkboxGroupInput(paste0("checkbox",n),label=NA, choices=shiny_in$c5[[shiny_in$c1[n]]], selected=shiny_in$terms_selected[[shiny_in$c1[n]]]), hr() ))} output$WidgetVectorDisplay <-renderUI( withProgress(message = "Creating character statements", value = 0.1, { incProgress(0.3) incProgress(0.9) {lapply(X = 1:nchar, FUN = makeRadioButton)} }) ) ### Show descnedants upon button observeEvent( input$select_descen, { term2show<-input$selectize output$network <- renderVisNetwork({ withProgress(message = "Creating Network", value = 0.1, { #dt=get_part_descen(hao.obo, term2show, is_a=c("is_a"), part_of=c("BFO:0000050")) if (input$des_chk=="descendants"){ dt=get_part_descen(hao.obo, term2show, is_a=links_chk_map[[input$links_chk]][2], #### HAO.obo to ontology index!!!! part_of=links_chk_map[[input$links_chk]][1], all_links=F, incl.top.anc=T, highliht_focus=T) } if (input$des_chk=="ancestors"){ dt=get_part_anc(hao.obo, term2show, is_a=links_chk_map[[input$links_chk]][2], part_of=links_chk_map[[input$links_chk]][1], all_links=F, incl.top.anc=T, highliht_focus=T) } if (input$des_chk=="both"){ #WORK on duplicated terms dt1=get_part_descen(hao.obo, term2show, is_a=links_chk_map[[input$links_chk]][2], #### HAO.obo to ontology index!!!! part_of=links_chk_map[[input$links_chk]][1], all_links=F, incl.top.anc=T, highliht_focus=T) dt2=get_part_anc(hao.obo, term2show, is_a=links_chk_map[[input$links_chk]][2], part_of=links_chk_map[[input$links_chk]][1], all_links=F, incl.top.anc=T, highliht_focus=T) dt<-list(nodes=rbind(dt1$nodes, dt2$nodes), edges=rbind(dt1$edges, dt2$edges)) dt$nodes<-dt$nodes[!duplicated(as.character(dt$nodes$id)),] #select unique nodes } incProgress(0.3) ## Legend data lnodes <- data.frame(label = c("Selected term"), color = c("orange"), id = term2show) ledges <- data.frame(color = c("blue", "red"), label = c("part_of", "is_a"), arrows =c("from", "from")) #### visNetwork(dt$nodes, dt$edges, height = "65vh", width ="100%", main = NULL, submain =NULL) %>% visNodes(borderWidthSelected=4)%>% visOptions(highlightNearest = TRUE, nodesIdSelection = T)%>% visLegend(addEdges = ledges, addNodes = lnodes, useGroups = F, position = "right", width=0.09) %>% #visLayout(randomSeed = 12) %>% visLayout(randomSeed = 12, hierarchical=F) -> visNt # HIERRACHICAL TRUE can be an option!!! incProgress(0.9) visIgraphLayout(visNt, layout="layout_with_gem") }) }) # visNetworkProxy("network") %>% # visFocus(id = input$selectize, scale = 2) } ) ####### ####### Add button actions observe({ lapply(map_btn_check, function(x) { observeEvent( input[[x]], { term_id<-input[[paste0("ids_in", names(map_btn_check)[which(map_btn_check==x)])]] print(term_id) ## Input from Selectize if ((term_id=="") & (input$selectize!="")){ #if term field is empty then use Selectize input that should not be empty too ############## update checkboxes and ontology index term_id<-input$selectize term_name<-shiny_in$c6[which(names(shiny_in$c6)==term_id)] if (length(term_name)==0){ #check if term is found in ontology term_name="TERM NOT FOUND!!!" } term_id_name<-paste(term_name, term_id, sep=", ") CHAR_id<-paste0("CHAR:", names(map_btn_check)[which(map_btn_check==x)]) if (term_id_name %in% shiny_in$c5[[CHAR_id]]){#check for duplication updateTextInput(session, paste0("ids_in", names(map_btn_check)[which(map_btn_check==x)]), label = "You are trying to add the same term twice") } if (!term_id_name %in% shiny_in$c5[[CHAR_id]]){#check for duplication #update terms selected shiny_in$terms_selected[[CHAR_id]] <<- c(shiny_in$terms_selected[[CHAR_id]], term_id_name) #update terms all shiny_in$c5[[CHAR_id]] <<- c(shiny_in$c5[[CHAR_id]], term_id_name) #update checkbox updateCheckboxGroupInput(session, paste0("checkbox", names(map_btn_check)[which(map_btn_check==x)]), label=NA, choices=shiny_in$c5[[CHAR_id]], selected=shiny_in$terms_selected[[CHAR_id]] ) updateTextInput(session, paste0("ids_in", names(map_btn_check)[which(map_btn_check==x)]), value = "", label = "") term_id<-c("") } ########### } ### Manual input ############## update checkboxes and ontology index if (term_id!=""){ # term fiels must be non-empty term_id<-gsub(" ", "", term_id) # remove white spaces term_name<-shiny_in$c6[which(names(shiny_in$c6)==term_id)] if (length(term_name)==0){ #check if term is found in ontology term_name="TERM NOT FOUND!!!" } term_id_name<-paste(term_name, term_id, sep=", ") CHAR_id<-paste0("CHAR:", names(map_btn_check)[which(map_btn_check==x)]) if (term_id_name %in% shiny_in$c5[[CHAR_id]]){#check for duplication updateTextInput(session, paste0("ids_in", names(map_btn_check)[which(map_btn_check==x)]), label = "You are trying to add the same term twice") } if (!term_id_name %in% shiny_in$c5[[CHAR_id]]){#check for duplication #update terms selected shiny_in$terms_selected[[CHAR_id]] <<- c(shiny_in$terms_selected[[CHAR_id]], term_id_name) #update terms all shiny_in$c5[[CHAR_id]] <<- c(shiny_in$c5[[CHAR_id]], term_id_name) #update checkbox updateCheckboxGroupInput(session, paste0("checkbox", names(map_btn_check)[which(map_btn_check==x)]), label=NA, choices=shiny_in$c5[[CHAR_id]], selected=shiny_in$terms_selected[[CHAR_id]] ) updateTextInput(session, paste0("ids_in", names(map_btn_check)[which(map_btn_check==x)]), value = "", label = "") } } ########### } ) }) }) #### ###### Add checkbox actions observe({ lapply(map_checkbox, function(x) { observeEvent( input[[x]], { CHAR_id<-paste0("CHAR:", names(map_checkbox)[which(map_checkbox==x)]) #update terms selected shiny_in$terms_selected[[CHAR_id]] <<- input[[x]] }) }) }) ######## ################ Node selection observeEvent( input$network_selected, { #print(input$network_selected) updateSelectizeInput(session, "selectize", label = NULL, choices=srch_items, selected = input$network_selected, options = list(openOnFocus=F, maxOptions=100, placeholder="Enter term or ID" ), server = TRUE ) }) ########### Selectize change observeEvent( input$selectize, { #print(input$selectize) output$id_txt<-renderText({input$selectize}) output$def_txt<-renderText({ ontology$def[which(names(ontology$def)==input$selectize)]}) output$syn_txt<-renderText({ ontology$parsed_synonyms[which(names(ontology$parsed_synonyms)==input$selectize)]}) }) ##### } ###############################################################################################################################
ee1b44e815b06e3fbc87a8b7211012fb4ef0c5dc
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/man/aggiungiRisultatiModulo.Rd
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[]
no_license
kendomaniac/BBBMGU
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59d19ad075ad4c2d2db6d40163559d2048e0fb68
refs/heads/master
2022-02-26T06:33:08.160285
2022-02-03T05:13:12
2022-02-03T05:13:12
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aggiungiRisultatiModulo.Rd
% Generated by roxygen2: do not edit by hand % Please edit documentation in R/aggiungiRisultatiModulo.R \name{aggiungiRisultatiModulo} \alias{aggiungiRisultatiModulo} \title{Una funzione che aggrega output di aggiornaStudentiVoti.} \usage{ aggiungiRisultatiModulo( excel.esame, input.voti, output.voti, modulo = c("BB", "BM", "GU") ) } \arguments{ \item{excel.esame, }{e' l'excel scaricato per un modulo dalle prove parziali su SS3.} \item{input.voti, }{output di aggiornaStudentiVotiModuli.} \item{output.voti, }{output di aggiornaStudentiVoti per Genetica Umana, update studenti.} \item{modulo, }{selezione del modulo per il quale i voto vanno aggiunti} } \value{ Il file tab delimited vuoto, studenti_voti.txt, ma con l'inserimento di tutti gli studenti indipendentemente dall'anno di corso. } \description{ Una funzione che aggrega output aggiornaStudentiVoti per i tre moduli. } \examples{ \dontrun{ aggiungiRisultatiModulo(excel.esame="basi_biologiche.xls", input.voti="studenti_voti.txt", output.voti="studenti_votiBB.txt", modulo="BB") aggiungiRisultatiModulo(excel.esame="biologia_molecolare.xls", input.voti="studenti_votiBB.txt", output.voti="studenti_votiBBBM.txt", modulo="BM") aggiungiRisultatiModulo(excel.esame="genetica_umana.xls", input.voti="studenti_votiBBBM.txt", output.voti="studenti_votiBBBMGU.txt", modulo="GU") } } \author{ Raffaele Calogero, raffaele.calogero [at] unito [dot] it, University of Torino, Italy }
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/2_comparison_DHvsBL/2.06_FreqFocusHaps_inBL.r
4e4e2896aaddc9914ad895919fb7f3007af2fb10
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DilanSarange/GWAS_DHs_landraces
4896e4acf58604f8a80b8abfb24c049c3f2ff3c1
dc9b765edbcc3c0e1e68e4a5223c2cf6eebc5597
refs/heads/master
2022-12-30T16:41:46.394929
2020-10-15T06:29:41
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2.06_FreqFocusHaps_inBL.r
################################################################### ################################################################### #### #### assess frequencies of focus haplotypes (identified with GWAS in DHs) #### in breeding lines #### Plot frequencies, distinguishing favorable, unfavorable, random haplotypes #### identify favorable haplotypes absent in BL #### identify unfavorable haplotypes with high frequencies in BL #### #### Manfred Mayer (Technical University of Munich, Plant Breeding) #### manfred.mayer@tum.de #### #### date: 17.04.2020 ################################################################### ################################################################### # general settings options(stringsAsFactors=FALSE) options(scipen=99) options(warn = 1) set.seed(212) # packages library(synbreed) # arguments nSNPs <- 10 steps <- 10 p_thresh <- 0.01 FDR <- "15" minCount <- 3 # graphical parameters cex <- 0.6 cex.axis <- 1.6 cex.lab <- 1.6 # functions # function for calculating haplotype similarity (probability of two randomly chosen gametes to show identical haplotypes) HapSim_f <- function(x, exCount = 0) { allele_counts <- table(x) allele_freqs <- allele_counts/sum(allele_counts) expHet <- 1 - sum(allele_freqs^2) HapSim <- 1 - expHet return(HapSim) } # function for calculating Hudson and Kaplan's minimum number of historical recombination events HudsonKaplan_Rec_f <- function(geno, pos, n_min){ fourGamete_pair <- function(x, n_min){ test <- paste(x[1 : floor(length(x)/2)], x[(floor(length(x)/2) + 1) : length(x)], sep = "_") test <- table(test) test <- test[which(test >= n_min)] if(length(test) == 4){ return(1) } else { return(0) } } # first, exclude all monomorphic markers mono <- which(apply(geno, 2, function(x) {sd(x) == 0})) if(length(mono > 0)){ geno <- geno[ , -mono] pos <- pos[-mono] } if(length(pos) > 1){ col_pairs <- cbind(colnames(geno)[sequence(1:ncol(geno))],colnames(geno)[rep(1:ncol(geno),1:ncol(geno))]) col_pairs <- col_pairs[which(!(col_pairs[,1]==col_pairs[,2])),] if(length(col_pairs) > 2){ start_bp <- pos[col_pairs[,1]] end_bp <- pos[col_pairs[,2]] test_mtx <- rbind(geno[, col_pairs[,1]], geno[ , col_pairs[,2]]) D <- apply(test_mtx, 2, fourGamete_pair, n_min = n_min) D_info <- cbind(start_bp, end_bp, D) D_info <- D_info[which(D_info[ , "D"] == 1), ] if(length(D_info) == 3){ n_rec <- 1 } if(length(D_info) < 3){ n_rec <- 0 } if(length(D_info) > 3){ D_info <- D_info[order(D_info[,1], D_info[,2]), ] # first step of the algorithm ex <- NULL for(i in 1:nrow(D_info)){ temp1 <- D_info[i,1] <= D_info[-i,1] temp2 <- D_info[i,2] >= D_info[-i,2] if(any(temp1 & temp2)){ ex <- c(ex, i) } } if(is.null(ex) == FALSE){ D_info <- D_info[-ex, ] } } if(length(D_info) == 3){ n_rec <- 1 } if(length(D_info) > 3){ # second step of the algorithm i <- 0 repeat{ i <- i + 1 ex <- NULL temp1 <- D_info[(i+1):nrow(D_info),1] > D_info[i,1] temp2 <- D_info[(i+1):nrow(D_info),1] < D_info[i,2] if(any(temp1 & temp2)){ ex <- c(ex, (which(temp1 & temp2) + i)) } if(is.null(ex) == FALSE){ D_info <- D_info[-ex, ] i <- 0 } if(length(D_info) == 3){ break } if(i == (nrow(D_info)-1)){ break } } } if(length(D_info) == 3){ n_rec <- 1 } else { n_rec <- nrow(D_info) } } else { test_vec <- c(geno[, col_pairs[1]], geno[ , col_pairs[2]]) D <- fourGamete_pair(test_vec, n_min = n_min) if(D == 1){ n_rec <- 1 } else { n_rec <- 0 } } } else { n_rec <- 0 } return(n_rec) } # function for generating Infolist of the corresponding blocks makeInfolist_genet_f <- function(x, genet_map) { genet_map_noNA <- genet_map[which(is.na(genet_map[,3]) == FALSE), ] x2 <- x[which(x[,2] >= genet_map_noNA[1,2]), ] x2 <- x2[which(x2[,2] <= genet_map_noNA[nrow(genet_map_noNA),2]), ] genet_InfoList <- NULL for(i in 1:nrow(x2)){ # start pos dif <- x2[i,2] - genet_map_noNA[,2] dif <- dif[order(abs(dif))][1:2] phys <- genet_map_noNA[sort(names(dif)),2] genet <- genet_map_noNA[sort(names(dif)),3] genet_start <- genet[1] + (((x2[i,2] - phys[1]) * diff(genet)) / diff(phys)) # end pos dif <- x2[i,3] - genet_map_noNA[,2] dif <- dif[order(abs(dif))][1:2] phys <- genet_map_noNA[sort(names(dif)),2] genet <- genet_map_noNA[sort(names(dif)),3] genet_end <- genet[1] + (((x2[i,3] - phys[1]) * diff(genet)) / diff(phys)) # size genet_size <- genet_end - genet_start genet_InfoList <- rbind(genet_InfoList, c(x2[i,1], genet_start, genet_end, genet_size, x2[i,5])) } colnames(genet_InfoList) <- c("Chr", "Pos_Start_cM", "Pos_End_cM", "Size_cM", "n_Markers") rownames(genet_InfoList) <- rownames(x2) return(list(genet_InfoList = genet_InfoList, phys_InfoList = x2)) } ################################################################### # load data of DHs load(paste("geno_InfoList_DH_m", nSNPs, "s", steps, ".RData", sep = "")) str(InfoList) str(geno) # load genetic map (genetic and physical position for each marker) # according to PH207 x EP1 mapping population # I:\Projekte\MAZE\Science\Genetic_Data_Analyses\GenMapPH207vsEP1_interpolated_600kArray_Positions load("map_chr_phy_gen_PH207vsEP1_SCAMmpiInterpol_B73v4.RData") str(map_chr_phy_gen) # write out each start and end position of each haplotype as genetic as well as physical positions Info_Lists <- list() for(CHR in 1:10){ print(paste("CHR", CHR)) InfoList_chr <- InfoList[which(InfoList[,1] == CHR), ] # only consider first haplotype per window (start and end is the same for each haplotype in a window anyways) InfoList_chr <- InfoList_chr[which(substr(rownames(InfoList_chr), nchar(rownames(InfoList_chr))-1, nchar(rownames(InfoList_chr))) == "_1"), ] genet_map_chr <- map_chr_phy_gen[which(map_chr_phy_gen[,1] == CHR), ] Info_Lists[[CHR]] <- makeInfolist_genet_f(x = InfoList_chr, genet_map = genet_map_chr) } str(Info_Lists) save(Info_Lists, file = "Info_Lists_genet_phys.RData") ################################################################### dir.create("comp_BL_DHs") dir.create("comp_BL_DHs/focusHaps") traits <- c("TILL", "LO", "MF", "FF", "PH_final", "PH_V6", "PH_V4", "EV_V6", "EV_V4" ) traits <- c("EV_V4", "EV_V6", "PH_V4", "PH_V6", "TILL", "LO") for(TRAIT in traits){ infolder_haps <- paste("FavUnfav_Stability/", TRAIT, sep = "") infolder_haps dir.create(paste("comp_BL_DHs/focusHaps/", TRAIT, sep = "")) outFolder <- paste("comp_BL_DHs/focusHaps/", TRAIT, sep = "") outFolder # load defined haplotypes load(paste(infolder_haps, "/haps_all_", TRAIT, ".RData", sep = "")) haps_Fav_info haps_Unfav_info haps_Inter_info all_markers <- c(haps_Fav_info$qtl_i, haps_Unfav_info$qtl_i, haps_Inter_info$qtl_i) all_markers # if in biallelic case, haplotypes were added, we have to do it here also for geno and InfoList if(any(unique(all_markers) %in% colnames(geno) == FALSE)){ temp_x <- unique(all_markers) temp_x <- temp_x[which(temp_x %in% colnames(geno) == FALSE)] for(temp_xi in temp_x){ temp_xix <- geno[ , which(substr(colnames(geno), 1, 13) == substr(temp_xi, 1, 13))] temp_xix[which(temp_xix == 0)] <- 99 temp_xix[which(temp_xix == 2)] <- 0 temp_xix[which(temp_xix == 99)] <- 2 geno <- cbind(geno, temp_xix) colnames(geno)[ncol(geno)] <- temp_xi InfoList_xi <- InfoList[which(substr(rownames(InfoList), 1, 13) == substr(temp_xi, 1, 13)), ] InfoList <- rbind(InfoList, InfoList_xi) rownames(InfoList)[nrow(InfoList)] <- temp_xi print(tail(InfoList, n = 10)) } } ############################################################################################################### ### ### ### compare ferquencies ### ### ### ### search for haplotypes in breeding lines ### # load check genotypic data # SNP data of BL load("gpBL.RData") str(gpBL) # SNP data of LR load(paste("gpDH.RData", sep="")) str(gpDH) # generate elite line haplotype dataset for "favorable" haplotypes geno_BL_fav <- NULL nR_BL_fav <- NULL HH_BL_fav <- NULL cM_BL_fav <- NULL kb_BL_fav <- NULL for(hap_i in haps_Fav_info$qtl_i){ chr_qtl <- InfoList[hap_i, "Chr"] start_qtl <- InfoList[hap_i, "Pos_Start_bp"] end_qtl <- InfoList[hap_i, "Pos_End_bp"] IDs_qtl <- rownames(geno)[which(geno[, hap_i] == 2)] map_i <- gpBL$map[which(gpBL$map$chr == chr_qtl), ] map_i <- map_i[which(map_i$pos >= start_qtl), ] map_i <- map_i[which(map_i$pos <= end_qtl), ] seq_qtl <- gpDH$geno[ , rownames(map_i)] seq_qtl <- apply(seq_qtl, 1, paste0, collapse = "") seq_qtl <- unique(seq_qtl[IDs_qtl]) haps_BL <- gpBL$geno[ , rownames(map_i)] # nR pos_temp <- map_i$pos names(pos_temp) <- rownames(map_i) nR_BL_fav <- c(nR_BL_fav, HudsonKaplan_Rec_f(geno = haps_BL, pos = pos_temp, n_min = 1)) haps_BL <- apply(haps_BL, 1, paste0, collapse = "") # HH HH_BL_fav <- c(HH_BL_fav, 1 - HapSim_f(haps_BL, exCount = 0)) # cM genet_pos <- Info_Lists[[chr_qtl]][[1]] genet_pos <- genet_pos[which(substr(rownames(genet_pos), 1, 13) == substr(hap_i, 1, 13)),] cM_BL_fav <- c(cM_BL_fav, genet_pos["Size_cM"]) # kb phys_pos <- InfoList phys_pos <- phys_pos[which(substr(rownames(phys_pos), 1, 13) == substr(hap_i, 1, 13)),] kb_BL_fav <- c(kb_BL_fav, phys_pos[1 , "Size_bp"] / 1000) haps_BL <- ifelse(haps_BL == seq_qtl, 2, 0) geno_BL_fav <- cbind(geno_BL_fav, haps_BL) } if(is.null(geno_BL_fav) == FALSE){ colnames(geno_BL_fav) <- haps_Fav_info$qtl_i str(geno_BL_fav) names(nR_BL_fav) <- haps_Fav_info$qtl_i names(HH_BL_fav) <- haps_Fav_info$qtl_i names(cM_BL_fav) <- haps_Fav_info$qtl_i names(kb_BL_fav) <- haps_Fav_info$qtl_i print(summary(nR_BL_fav)) print(summary(HH_BL_fav)) print(summary(cM_BL_fav)) print(summary(kb_BL_fav)) save(geno_BL_fav, nR_BL_fav, HH_BL_fav, cM_BL_fav, kb_BL_fav, file = paste(outFolder, "/info_BL_fav_", TRAIT, ".RData", sep = "")) } # generate elite line haplotype dataset for "unfavorable" haplotypes geno_BL_unfav <- NULL nR_BL_unfav <- NULL HH_BL_unfav <- NULL cM_BL_unfav <- NULL kb_BL_unfav <- NULL for(hap_i in haps_Unfav_info$qtl_i){ chr_qtl <- InfoList[hap_i, "Chr"] start_qtl <- InfoList[hap_i, "Pos_Start_bp"] end_qtl <- InfoList[hap_i, "Pos_End_bp"] IDs_qtl <- rownames(geno)[which(geno[, hap_i] == 2)] map_i <- gpBL$map[which(gpBL$map$chr == chr_qtl), ] map_i <- map_i[which(map_i$pos >= start_qtl), ] map_i <- map_i[which(map_i$pos <= end_qtl), ] seq_qtl <- gpDH$geno[ , rownames(map_i)] seq_qtl <- apply(seq_qtl, 1, paste0, collapse = "") seq_qtl <- unique(seq_qtl[IDs_qtl]) haps_BL <- gpBL$geno[ , rownames(map_i)] # nR pos_temp <- map_i$pos names(pos_temp) <- rownames(map_i) nR_BL_unfav <- c(nR_BL_unfav, HudsonKaplan_Rec_f(geno = haps_BL, pos = pos_temp, n_min = 1)) haps_BL <- apply(haps_BL, 1, paste0, collapse = "") # HH HH_BL_unfav <- c(HH_BL_unfav, 1 - HapSim_f(haps_BL, exCount = 0)) # cM genet_pos <- Info_Lists[[chr_qtl]][[1]] genet_pos <- genet_pos[which(substr(rownames(genet_pos), 1, 13) == substr(hap_i, 1, 13)),] cM_BL_unfav <- c(cM_BL_unfav, genet_pos["Size_cM"]) # kb phys_pos <- InfoList phys_pos <- phys_pos[which(substr(rownames(phys_pos), 1, 13) == substr(hap_i, 1, 13)),] kb_BL_unfav <- c(kb_BL_unfav, phys_pos[1 , "Size_bp"] / 1000) haps_BL <- ifelse(haps_BL == seq_qtl, 2, 0) geno_BL_unfav <- cbind(geno_BL_unfav, haps_BL) } if(is.null(geno_BL_unfav) == FALSE){ colnames(geno_BL_unfav) <- haps_Unfav_info$qtl_i str(geno_BL_unfav) names(nR_BL_unfav) <- haps_Unfav_info$qtl_i names(HH_BL_unfav) <- haps_Unfav_info$qtl_i names(cM_BL_unfav) <- haps_Unfav_info$qtl_i names(kb_BL_unfav) <- haps_Unfav_info$qtl_i print(summary(nR_BL_unfav)) print(summary(HH_BL_unfav)) print(summary(cM_BL_unfav)) print(summary(kb_BL_unfav)) save(geno_BL_unfav, nR_BL_unfav, HH_BL_unfav, cM_BL_unfav, kb_BL_unfav, file = paste(outFolder, "/info_BL_unfav_", TRAIT, ".RData", sep = "")) } # generate elite line haplotype dataset for "neutral" haplotypes (in the same window as the significant haplotypes but without significant effect) geno_BL_neut <- NULL nR_BL_neut <- NULL HH_BL_neut <- NULL cM_BL_neut <- NULL kb_BL_neut <- NULL names_haps_neut <- NULL for(hap_ii in c(haps_Fav_info$qtl_i, haps_Unfav_info$qtl_i)){ # don't take the actual qtl, but all the others which are not significant haps_neut_ii <- colnames(geno)[which(substr(colnames(geno), 1, 13) == substr(hap_ii, 1, 13))] haps_neut_ii <- haps_neut_ii[which(haps_neut_ii %in% c(haps_Fav_info$qtl_i, haps_Unfav_info$qtl_i, haps_Inter_info$qtl_i) == FALSE)] for(hap_i in haps_neut_ii){ names_haps_neut <- c(names_haps_neut, hap_i) chr_qtl <- InfoList[hap_i, "Chr"] start_qtl <- InfoList[hap_i, "Pos_Start_bp"] end_qtl <- InfoList[hap_i, "Pos_End_bp"] IDs_qtl <- rownames(geno)[which(geno[, hap_i] == 2)] map_i <- gpBL$map[which(gpBL$map$chr == chr_qtl), ] map_i <- map_i[which(map_i$pos >= start_qtl), ] map_i <- map_i[which(map_i$pos <= end_qtl), ] seq_qtl <- gpDH$geno[ , rownames(map_i)] seq_qtl <- apply(seq_qtl, 1, paste0, collapse = "") seq_qtl <- unique(seq_qtl[IDs_qtl]) haps_BL <- gpBL$geno[ , rownames(map_i)] # nR pos_temp <- map_i$pos names(pos_temp) <- rownames(map_i) nR_BL_neut <- c(nR_BL_neut, HudsonKaplan_Rec_f(geno = haps_BL, pos = pos_temp, n_min = 1)) haps_BL <- apply(haps_BL, 1, paste0, collapse = "") # HH HH_BL_neut <- c(HH_BL_neut, 1 - HapSim_f(haps_BL, exCount = 0)) # cM genet_pos <- Info_Lists[[chr_qtl]][[1]] genet_pos <- genet_pos[which(substr(rownames(genet_pos), 1, 13) == substr(hap_i, 1, 13)),] cM_BL_neut <- c(cM_BL_neut, genet_pos["Size_cM"]) # kb phys_pos <- InfoList phys_pos <- phys_pos[which(substr(rownames(phys_pos), 1, 13) == substr(hap_i, 1, 13)),] kb_BL_neut <- c(kb_BL_neut, phys_pos[1 , "Size_bp"] / 1000) haps_BL <- ifelse(haps_BL == seq_qtl, 2, 0) geno_BL_neut <- cbind(geno_BL_neut, haps_BL) } } if(is.null(geno_BL_neut) == FALSE){ colnames(geno_BL_neut) <- names_haps_neut str(geno_BL_neut) names(nR_BL_neut) <- names_haps_neut names(HH_BL_neut) <- names_haps_neut names(cM_BL_neut) <- names_haps_neut names(kb_BL_neut) <- names_haps_neut print(summary(nR_BL_neut)) print(summary(HH_BL_neut)) print(summary(cM_BL_neut)) print(summary(kb_BL_neut)) save(geno_BL_neut, nR_BL_neut, HH_BL_neut, cM_BL_neut, kb_BL_neut, file = paste(outFolder, "/info_BL_neut_", TRAIT, ".RData", sep = "")) } # generate elite line haplotype dataset for "random" haplotypes set.seed(232) rand_haps <- sample(colnames(geno), size = 500, replace = FALSE) rand_haps <- sort(rand_haps) rand_haps geno_BL_rand <- NULL nR_BL_rand <- NULL HH_BL_rand <- NULL cM_BL_rand <- NULL kb_BL_rand <- NULL for(hap_i in rand_haps){ chr_qtl <- InfoList[hap_i, "Chr"] start_qtl <- InfoList[hap_i, "Pos_Start_bp"] end_qtl <- InfoList[hap_i, "Pos_End_bp"] IDs_qtl <- rownames(geno)[which(geno[, hap_i] == 2)] map_i <- gpBL$map[which(gpBL$map$chr == chr_qtl), ] map_i <- map_i[which(map_i$pos >= start_qtl), ] map_i <- map_i[which(map_i$pos <= end_qtl), ] seq_qtl <- gpDH$geno[ , rownames(map_i)] seq_qtl <- apply(seq_qtl, 1, paste0, collapse = "") seq_qtl <- unique(seq_qtl[IDs_qtl]) haps_BL <- gpBL$geno[ , rownames(map_i)] # nR pos_temp <- map_i$pos names(pos_temp) <- rownames(map_i) nR_BL_rand <- c(nR_BL_rand, HudsonKaplan_Rec_f(geno = haps_BL, pos = pos_temp, n_min = 1)) haps_BL <- apply(haps_BL, 1, paste0, collapse = "") # HH HH_BL_rand <- c(HH_BL_rand, 1 - HapSim_f(haps_BL, exCount = 0)) # cM genet_pos <- Info_Lists[[chr_qtl]][[1]] genet_pos <- genet_pos[which(substr(rownames(genet_pos), 1, 13) == substr(hap_i, 1, 13)),] cM_BL_rand <- c(cM_BL_rand, genet_pos["Size_cM"]) # kb phys_pos <- InfoList phys_pos <- phys_pos[which(substr(rownames(phys_pos), 1, 13) == substr(hap_i, 1, 13)),] if(length(phys_pos) > 5){ kb_BL_rand <- c(kb_BL_rand, phys_pos[1 , "Size_bp"] / 1000) } else { kb_BL_rand <- c(kb_BL_rand, phys_pos["Size_bp"] / 1000) } haps_BL <- ifelse(haps_BL == seq_qtl, 2, 0) geno_BL_rand <- cbind(geno_BL_rand, haps_BL) } colnames(geno_BL_rand) <- rand_haps str(geno_BL_rand) names(nR_BL_rand) <- rand_haps names(HH_BL_rand) <- rand_haps names(cM_BL_rand) <- rand_haps names(kb_BL_rand) <- rand_haps print(summary(nR_BL_rand)) print(summary(HH_BL_rand)) print(summary(cM_BL_rand)) print(summary(kb_BL_rand)) save(geno_BL_rand, nR_BL_rand, HH_BL_rand, cM_BL_rand, kb_BL_rand, file = paste(outFolder, "/info_BL_rand_", TRAIT, ".RData", sep = "")) } ################################################ ### ### summarize all early traits ### ################################################ name_set <- "earlyTraits" dir.create(paste("comp_BL_DHs/focusHaps/", name_set, sep = "")) outFolder <- paste("comp_BL_DHs/focusHaps/", name_set, sep = "") outFolder traits <- c("EV_V4", "EV_V6", "PH_V4", "PH_V6") traits geno_BL_fav_all <- NULL geno_BL_unfav_all <- NULL geno_BL_rand_all <- NULL nR_BL_fav_all <- NULL nR_BL_unfav_all <- NULL nR_BL_rand_all <- NULL HH_BL_fav_all <- NULL HH_BL_unfav_all <- NULL HH_BL_rand_all <- NULL cM_BL_fav_all <- NULL cM_BL_unfav_all <- NULL cM_BL_rand_all <- NULL kb_BL_fav_all <- NULL kb_BL_unfav_all <- NULL kb_BL_rand_all <- NULL for(TRAIT in traits){ infolder <- paste("comp_BL_DHs/focusHaps/", TRAIT, sep = "") load(paste(infolder, "/info_BL_fav_", TRAIT, ".RData", sep = "")) load(paste(infolder, "/info_BL_unfav_", TRAIT, ".RData", sep = "")) load(paste(infolder, "/info_BL_rand_", TRAIT, ".RData", sep = "")) infolder_haps <- paste("FavUnfav_Stability/", TRAIT, sep = "") load(paste(infolder_haps, "/haps_all_", TRAIT, ".RData", sep = "")) all_markers <- c(haps_Fav_info$qtl_i, haps_Unfav_info$qtl_i, haps_Inter_info$qtl_i) # if in biallelic case, haplotypes were added, we have to do it here also for geno and InfoList if(any(unique(all_markers) %in% colnames(geno) == FALSE)){ temp_x <- unique(all_markers) temp_x <- temp_x[which(temp_x %in% colnames(geno) == FALSE)] for(temp_xi in temp_x){ temp_xix <- geno[ , which(substr(colnames(geno), 1, 13) == substr(temp_xi, 1, 13))] temp_xix[which(temp_xix == 0)] <- 99 temp_xix[which(temp_xix == 2)] <- 0 temp_xix[which(temp_xix == 99)] <- 2 geno <- cbind(geno, temp_xix) colnames(geno)[ncol(geno)] <- temp_xi InfoList_xi <- InfoList[which(substr(rownames(InfoList), 1, 13) == substr(temp_xi, 1, 13)), ] InfoList <- rbind(InfoList, InfoList_xi) rownames(InfoList)[nrow(InfoList)] <- temp_xi print(tail(InfoList, n = 10)) } } geno_BL_fav_all <- cbind(geno_BL_fav_all, geno_BL_fav) nR_BL_fav_all <- c(nR_BL_fav_all, nR_BL_fav) HH_BL_fav_all <- c(HH_BL_fav_all, HH_BL_fav) cM_BL_fav_all <- c(cM_BL_fav_all, cM_BL_fav) kb_BL_fav_all <- c(kb_BL_fav_all, kb_BL_fav) geno_BL_unfav_all <- cbind(geno_BL_unfav_all, geno_BL_unfav) nR_BL_unfav_all <- c(nR_BL_unfav_all, nR_BL_unfav) HH_BL_unfav_all <- c(HH_BL_unfav_all, HH_BL_unfav) cM_BL_unfav_all <- c(cM_BL_unfav_all, cM_BL_unfav) kb_BL_unfav_all <- c(kb_BL_unfav_all, kb_BL_unfav) } # random are the same in every run geno_BL_rand_all <- cbind(geno_BL_rand_all, geno_BL_rand) nR_BL_rand_all <- c(nR_BL_rand_all, nR_BL_rand) HH_BL_rand_all <- c(HH_BL_rand_all, HH_BL_rand) cM_BL_rand_all <- c(cM_BL_rand_all, cM_BL_rand) kb_BL_rand_all <- c(kb_BL_rand_all, kb_BL_rand) summary(nR_BL_fav_all) summary(nR_BL_unfav_all) summary(nR_BL_rand_all) summary(HH_BL_fav_all) summary(HH_BL_unfav_all) summary(HH_BL_rand_all) summary(cM_BL_fav_all) summary(cM_BL_unfav_all) summary(cM_BL_rand_all) summary(kb_BL_fav_all) summary(kb_BL_unfav_all) summary(kb_BL_rand_all) haps_fav_all <- colnames(geno_BL_fav_all) head(sort(table(haps_fav_all), decreasing = TRUE), n = 10) length(haps_fav_all) length(unique(haps_fav_all)) haps_unfav_all <- colnames(geno_BL_unfav_all) head(sort(table(haps_unfav_all), decreasing = TRUE), n = 10) length(haps_unfav_all) length(unique(haps_unfav_all)) haps_rand_all <- colnames(geno_BL_rand_all) head(sort(table(haps_rand_all), decreasing = TRUE), n = 10) length(haps_rand_all) length(unique(haps_rand_all)) # filter for non-overlapping haplotypes geno_BL_fav_all <- geno_BL_fav_all[ , unique(colnames(geno_BL_fav_all))] geno_BL_unfav_all <- geno_BL_unfav_all[ , unique(colnames(geno_BL_unfav_all))] geno_BL_rand_all <- geno_BL_rand_all[ , unique(colnames(geno_BL_rand_all))] str(geno_BL_fav_all) str(geno_BL_unfav_all) str(geno_BL_rand_all) # # calculate frequencies # str(geno_BL_fav_all) str(geno_BL_unfav_all) str(geno_BL_rand_all) # # calculate frequencies including # AF_f <- function(x){ y <- sum(length(which(x==2))*2+length(which(x==1)))/(2*(length(x)-length(which(is.na(x))))) return(y) } ### elite freq_fav_elite_all <- apply(geno_BL_fav_all, 2, AF_f) freq_unfav_elite_all <- apply(geno_BL_unfav_all, 2, AF_f) freq_rand_elite_all <- apply(geno_BL_rand_all, 2, AF_f) summary(freq_fav_elite_all) summary(freq_unfav_elite_all) summary(freq_rand_elite_all) ### LR freq_fav_LR_all <- apply(geno[ ,colnames(geno_BL_fav_all)], 2, AF_f) freq_unfav_LR_all <- apply(geno[ ,colnames(geno_BL_unfav_all)], 2, AF_f) freq_rand_LR_all <- apply(geno[ ,colnames(geno_BL_rand_all)], 2, AF_f) summary(freq_fav_LR_all) summary(freq_unfav_LR_all) summary(freq_rand_LR_all) ## ## permutation test for significant differences between fav/unfav/rand in elite panel ## # permut est function (two.sided) permut.test_f <- function(x, y, n = 10000, alternative = "two.sided"){ # remove NAs x <- na.omit(x) y <- na.omit(y) # count entries per vector nx <- length(x) ny <- length(y) # calculate parameter of interest (here difference in means) stat <- mean(x) - mean(y) # generate permuted samples (in columns) perm_matrix <- replicate(n, sample(c(x, y))) stat_f <- function(x, nx){ mean(x[1:nx]) - mean(x[(nx+1):length(x)]) } # apply test to permuted samples to generate null distribution null_distr <- apply(perm_matrix, 2, stat_f, nx = nx) # calculate p-value n_NULL.larger <- length(which(null_distr > stat)) n_NULL.lower <- length(which(null_distr < stat)) n_NULL.equal <- length(which(null_distr == stat)) if (alternative == "two.sided") p_value <- (2 * (min(n_NULL.larger, n_NULL.lower) + 0.5 * n_NULL.equal)) / (n+1) if (alternative == "less") p_value <- (n_NULL.lower + 0.5 * n_NULL.equal) / (n+1) if (alternative == "greater") p_value <- (n_NULL.larger + 0.5 * n_NULL.equal) / (n+1) p_value <- min(p_value, 1) # generate output object perm_out <- list(stat = stat, null_distr = null_distr, p_value = p_value, original_x = x, original_y = y, nx = nx, ny = ny ) return(perm_out) } set.seed(2121) summary(freq_fav_elite_all) summary(freq_unfav_elite_all) summary(freq_rand_elite_all) permTest_favRand <- permut.test_f(x = freq_fav_elite_all, y = freq_rand_elite_all) permTest_favUnfav <- permut.test_f(x = freq_fav_elite_all, y = freq_unfav_elite_all) permTest_unfavRand <- permut.test_f(x = freq_unfav_elite_all, y = freq_rand_elite_all) str(permTest_favRand) str(permTest_favUnfav) str(permTest_unfavRand) save(freq_fav_elite_all, freq_unfav_elite_all, freq_rand_elite_all, file = paste(outFolder, "/info_freqs_", name_set, "_nonDup.RData", sep = "")) ################################################ ### ### plotting ### ################################################ ## ## generate vectors of "independent" haplotypes (dist > 1Mb and/or r2<0.8) ## # # check overlapping regions between traits # traits <- c("PH_V4", "PH_V6", "EV_V4", "EV_V6") traits HAP_list <- list() for (TRAIT in traits){ infolder_haps <- paste("FavUnfav_Stability/", TRAIT, sep = "") load(paste(infolder_haps, "/haps_all_", TRAIT, ".RData", sep = "")) haps_fav_i <- haps_Fav_info$qtl_i haps_unfav_i <- haps_Unfav_info$qtl_i haps_inter_i <- haps_Inter_info$qtl_i haps_all <- c(haps_fav_i, haps_unfav_i, haps_inter_i) haps <- list() haps[["fav"]] <- haps_fav_i haps[["unfav"]] <- haps_unfav_i haps[["inter"]] <- haps_inter_i haps[["all"]] <- haps_all HAP_list[[TRAIT]] <- haps } str(HAP_list) HAP_list_fav <- unlist(lapply(HAP_list, function(x) {x[[1]]})) str(HAP_list_fav) HAP_list_unfav <- unlist(lapply(HAP_list, function(x) {x[[2]]})) str(HAP_list_unfav) HAP_list_fav[which(HAP_list_fav %in% names(freq_fav_elite_all) == FALSE)] HAP_list_unfav[which(HAP_list_unfav %in% names(freq_unfav_elite_all) == FALSE)] names(freq_fav_elite_all)[which(names(freq_fav_elite_all) %in% HAP_list_fav == FALSE)] names(freq_unfav_elite_all)[which(names(freq_unfav_elite_all) %in% HAP_list_unfav == FALSE)] new_favorable_haps <- names(freq_fav_elite_all)[which(freq_fav_elite_all == 0)] new_favorable_haps for(i in names(HAP_list)){ print(i) print(HAP_list[[i]]$fav[which(HAP_list[[i]]$fav %in% new_favorable_haps)]) } common_unfavorable_haps <- names(freq_unfav_elite_all)[which(freq_unfav_elite_all > 0.25)] common_unfavorable_haps for(i in names(HAP_list)){ print(i) print(HAP_list[[i]]$unfav[which(HAP_list[[i]]$unfav %in% common_unfavorable_haps)]) } common_favorable_haps <- names(freq_fav_elite_all)[which(freq_fav_elite_all > 0.25)] common_favorable_haps for(i in names(HAP_list)){ print(i) print(HAP_list[[i]]$fav[which(HAP_list[[i]]$fav %in% common_favorable_haps)]) } # # now load the according associated genomic regions # REG_list <- list() for (TRAIT in traits){ regs <- read.table(paste(TRAIT, "/QTLregs/finalQTL/finalQTLregs_", TRAIT, ".csv", sep = ""), sep = ";", dec = ".", header = TRUE) rownames(regs) <- regs$qtl_i REG_list[[TRAIT]] <- regs } str(REG_list) # # calculate for traits overlapping associations, defined as: # focus haplotypes within 1Mb and with r2 > 0.8 # # # filter for the 899 gphenotyped ones load("pheno_perEnv_list_DHs.RData") phenotyped <- pheno_perEnv_list[[1]]$Geno ID_set <- intersect(rownames(geno), phenotyped) # generate pairs traits_2 <- combn(traits, 2) traits_2 # # for favorables # direction <- "fav" # pairs pairs_overlap_list_fav <- list() for(trait_i in 1:ncol(traits_2)){ TRAIT1 <- traits_2[1,trait_i] TRAIT2 <- traits_2[2,trait_i] print(paste(TRAIT1, "vs", TRAIT2)) info_r2 <- NULL # get positions of focus haplotypes regs1 <- InfoList[HAP_list[[TRAIT1]][[direction]], 1:3] regs2 <- InfoList[HAP_list[[TRAIT2]][[direction]], 1:3] # extend for 0.5 Mb up and downstream regs1_ext1Mb <- regs1 regs1_ext1Mb[, 2] <- regs1_ext1Mb[,2] - 2500000 regs1_ext1Mb[, 3] <- regs1_ext1Mb[,3] + 2500000 regs2_ext1Mb <- regs2 regs2_ext1Mb[, 2] <- regs2_ext1Mb[,2] - 2500000 regs2_ext1Mb[, 3] <- regs2_ext1Mb[,3] + 2500000 # check for pairs within 1Mb distance and in case, calculate r2 for(regs1_i in 1:nrow(regs1_ext1Mb)){ regs2_chr <- rownames(regs2_ext1Mb)[which(regs2_ext1Mb[,1] == regs1_ext1Mb[regs1_i,1])] if(length(regs2_chr) > 0){ haps2 <- regs2_chr[which((regs2_ext1Mb[regs2_chr, 2] < regs1_ext1Mb[regs1_i,3]) & (regs2_ext1Mb[regs2_chr, 3] > regs1_ext1Mb[regs1_i,2]))] if(length(haps2) > 0){ haps1 <- rownames(regs1_ext1Mb)[regs1_i] r2 <- (cor(geno[ID_set, haps1], geno[ID_set, haps2]))^2 info_r2_i <- data.frame(TRAIT1 = rep(haps1, length(haps2)), TRAIT2 = haps2, r2 = t(r2), chr = regs1_ext1Mb[regs1_i,1], start = min(c(regs1[haps1,2], regs2[haps2, 2])), end = max(c(regs1[haps1,3], regs2[haps2, 3])), stringsAsFactors = FALSE) info_r2 <- rbind(info_r2, info_r2_i) } } } if(is.null(info_r2) == FALSE){ colnames(info_r2) <- c(TRAIT1, TRAIT2, "r2", "chr", "start_bp", "end_bp") rownames(info_r2) <- 1:nrow(info_r2) print(info_r2[which(info_r2$r2 > 0.4),]) } pairs_overlap_list_fav[[paste(TRAIT1, TRAIT2, sep = ".")]] <- info_r2 } # # for unfavorables # direction <- "unfav" # pairs pairs_overlap_list_unfav <- list() for(trait_i in 1:ncol(traits_2)){ TRAIT1 <- traits_2[1,trait_i] TRAIT2 <- traits_2[2,trait_i] print(paste(TRAIT1, "vs", TRAIT2)) info_r2 <- NULL # get positions of focus haplotypes regs1 <- InfoList[HAP_list[[TRAIT1]][[direction]], 1:3] regs2 <- InfoList[HAP_list[[TRAIT2]][[direction]], 1:3] # extend for 0.5 Mb up and downstream regs1_ext1Mb <- regs1 regs1_ext1Mb[, 2] <- regs1_ext1Mb[,2] - 2500000 regs1_ext1Mb[, 3] <- regs1_ext1Mb[,3] + 2500000 regs2_ext1Mb <- regs2 regs2_ext1Mb[, 2] <- regs2_ext1Mb[,2] - 2500000 regs2_ext1Mb[, 3] <- regs2_ext1Mb[,3] + 2500000 # check for pairs within 1Mb distance and in case, calculate r2 for(regs1_i in 1:nrow(regs1_ext1Mb)){ regs2_chr <- rownames(regs2_ext1Mb)[which(regs2_ext1Mb[,1] == regs1_ext1Mb[regs1_i,1])] if(length(regs2_chr) > 0){ haps2 <- regs2_chr[which((regs2_ext1Mb[regs2_chr, 2] < regs1_ext1Mb[regs1_i,3]) & (regs2_ext1Mb[regs2_chr, 3] > regs1_ext1Mb[regs1_i,2]))] if(length(haps2) > 0){ haps1 <- rownames(regs1_ext1Mb)[regs1_i] r2 <- (cor(geno[ID_set, haps1], geno[ID_set, haps2]))^2 info_r2_i <- data.frame(TRAIT1 = rep(haps1, length(haps2)), TRAIT2 = haps2, r2 = t(r2), chr = regs1_ext1Mb[regs1_i,1], start = min(c(regs1[haps1,2], regs2[haps2, 2])), end = max(c(regs1[haps1,3], regs2[haps2, 3])), stringsAsFactors = FALSE) info_r2 <- rbind(info_r2, info_r2_i) } } } if(is.null(info_r2) == FALSE){ colnames(info_r2) <- c(TRAIT1, TRAIT2, "r2", "chr", "start_bp", "end_bp") rownames(info_r2) <- 1:nrow(info_r2) print(info_r2[which(info_r2$r2 > 0.4),]) } pairs_overlap_list_unfav[[paste(TRAIT1, TRAIT2, sep = ".")]] <- info_r2 } # # for changing sign # direction <- "inter" # pairs pairs_overlap_list_inter <- list() for(trait_i in 1:ncol(traits_2)){ TRAIT1 <- traits_2[1,trait_i] TRAIT2 <- traits_2[2,trait_i] print(paste(TRAIT1, "vs", TRAIT2)) info_r2 <- NULL # get positions of focus haplotypes regs1 <- InfoList[HAP_list[[TRAIT1]][[direction]], 1:3] regs2 <- InfoList[HAP_list[[TRAIT2]][[direction]], 1:3] # extend for 0.5 Mb up and downstream regs1_ext1Mb <- regs1 regs1_ext1Mb[, 2] <- regs1_ext1Mb[,2] - 2500000 regs1_ext1Mb[, 3] <- regs1_ext1Mb[,3] + 2500000 regs2_ext1Mb <- regs2 regs2_ext1Mb[, 2] <- regs2_ext1Mb[,2] - 2500000 regs2_ext1Mb[, 3] <- regs2_ext1Mb[,3] + 2500000 # check for pairs within 1Mb distance and in case, calculate r2 for(regs1_i in 1:nrow(regs1_ext1Mb)){ regs2_chr <- rownames(regs2_ext1Mb)[which(regs2_ext1Mb[,1] == regs1_ext1Mb[regs1_i,1])] if(length(regs2_chr) > 0){ haps2 <- regs2_chr[which((regs2_ext1Mb[regs2_chr, 2] < regs1_ext1Mb[regs1_i,3]) & (regs2_ext1Mb[regs2_chr, 3] > regs1_ext1Mb[regs1_i,2]))] if(length(haps2) > 0){ haps1 <- rownames(regs1_ext1Mb)[regs1_i] r2 <- (cor(geno[ID_set, haps1], geno[ID_set, haps2]))^2 info_r2_i <- data.frame(TRAIT1 = rep(haps1, length(haps2)), TRAIT2 = haps2, r2 = t(r2), chr = regs1_ext1Mb[regs1_i,1], start = min(c(regs1[haps1,2], regs2[haps2, 2])), end = max(c(regs1[haps1,3], regs2[haps2, 3])), stringsAsFactors = FALSE) info_r2 <- rbind(info_r2, info_r2_i) } } } if(is.null(info_r2) == FALSE){ colnames(info_r2) <- c(TRAIT1, TRAIT2, "r2", "chr", "start_bp", "end_bp") rownames(info_r2) <- 1:nrow(info_r2) print(info_r2[which(info_r2$r2 > 0.4),]) } pairs_overlap_list_inter[[paste(TRAIT1, TRAIT2, sep = ".")]] <- info_r2 } # # for all # direction <- "all" # pairs pairs_overlap_list_all <- list() for(trait_i in 1:ncol(traits_2)){ TRAIT1 <- traits_2[1,trait_i] TRAIT2 <- traits_2[2,trait_i] print(paste(TRAIT1, "vs", TRAIT2)) info_r2 <- NULL # get positions of focus haplotypes regs1 <- InfoList[HAP_list[[TRAIT1]][[direction]], 1:3] regs2 <- InfoList[HAP_list[[TRAIT2]][[direction]], 1:3] # extend for 0.5 Mb up and downstream regs1_ext1Mb <- regs1 regs1_ext1Mb[, 2] <- regs1_ext1Mb[,2] - 2500000 regs1_ext1Mb[, 3] <- regs1_ext1Mb[,3] + 2500000 regs2_ext1Mb <- regs2 regs2_ext1Mb[, 2] <- regs2_ext1Mb[,2] - 2500000 regs2_ext1Mb[, 3] <- regs2_ext1Mb[,3] + 2500000 # check for pairs within 1Mb distance and in case, calculate r2 for(regs1_i in 1:nrow(regs1_ext1Mb)){ regs2_chr <- rownames(regs2_ext1Mb)[which(regs2_ext1Mb[,1] == regs1_ext1Mb[regs1_i,1])] if(length(regs2_chr) > 0){ haps2 <- regs2_chr[which((regs2_ext1Mb[regs2_chr, 2] < regs1_ext1Mb[regs1_i,3]) & (regs2_ext1Mb[regs2_chr, 3] > regs1_ext1Mb[regs1_i,2]))] if(length(haps2) > 0){ haps1 <- rownames(regs1_ext1Mb)[regs1_i] r2 <- (cor(geno[ID_set, haps1], geno[ID_set, haps2]))^2 info_r2_i <- data.frame(TRAIT1 = rep(haps1, length(haps2)), TRAIT2 = haps2, r2 = t(r2), chr = regs1_ext1Mb[regs1_i,1], start = min(c(regs1[haps1,2], regs2[haps2, 2])), end = max(c(regs1[haps1,3], regs2[haps2, 3])), stringsAsFactors = FALSE) info_r2 <- rbind(info_r2, info_r2_i) } } } if(is.null(info_r2) == FALSE){ colnames(info_r2) <- c(TRAIT1, TRAIT2, "r2", "chr", "start_bp", "end_bp") rownames(info_r2) <- 1:nrow(info_r2) print(info_r2[which(info_r2$r2 > 0.4),]) } pairs_overlap_list_all[[paste(TRAIT1, TRAIT2, sep = ".")]] <- info_r2 } # # for all detected pairs, delete randomly one haplotype # how many "unrelated" haplotypes are left # fav_haps_all <- names(freq_fav_elite_all) unfav_haps_all <- names(freq_unfav_elite_all) str(fav_haps_all) str(unfav_haps_all) set.seed(232) r2_thresh_i <- "0.8" haps_pairs <- NULL r2_thresh <- as.numeric(r2_thresh_i) ex <- NULL for(i in 1:ncol(traits_2)){ haps_i <- pairs_overlap_list_fav[[i]] haps_i <- haps_i[which(haps_i[,1] != haps_i[,2]), ] haps_i <- cbind(haps_i[which(haps_i$r2 >= r2_thresh), 1], haps_i[which(haps_i$r2 >= r2_thresh), 2]) if(nrow(haps_i) > 0){ for(ii in 1:nrow(haps_i)){ if(any(haps_i[ii,] %in% ex) == FALSE){ ex <- c(ex, sample(haps_i[ii,], size = 1)) haps_pairs <- rbind(haps_pairs, haps_i[ii,]) } } } } freq_fav_elite_all[haps_pairs] ex fav_haps_indep <- fav_haps_all[which(fav_haps_all %in% ex == FALSE)] haps_pairs <- NULL r2_thresh <- as.numeric(r2_thresh_i) ex <- NULL for(i in 1:ncol(traits_2)){ haps_i <- pairs_overlap_list_unfav[[i]] haps_i <- haps_i[which(haps_i[,1] != haps_i[,2]), ] haps_i <- cbind(haps_i[which(haps_i$r2 >= r2_thresh), 1], haps_i[which(haps_i$r2 >= r2_thresh), 2]) if(nrow(haps_i) > 0){ for(ii in 1:nrow(haps_i)){ if(any(haps_i[ii,] %in% ex) == FALSE){ ex <- c(ex, sample(haps_i[ii,], size = 1)) haps_pairs <- rbind(haps_pairs, haps_i[ii,]) } } } } freq_unfav_elite_all[haps_pairs] ex unfav_haps_indep <- unfav_haps_all[which(unfav_haps_all %in% ex == FALSE)] str(fav_haps_indep) str(unfav_haps_indep) summary(freq_fav_elite_all) summary(freq_unfav_elite_all) summary(freq_fav_elite_all[fav_haps_indep]) summary(freq_unfav_elite_all[unfav_haps_indep]) summary(freq_rand_elite_all) length(which(freq_unfav_elite_all[unfav_haps_indep] > quantile(freq_rand_elite_all, 0.75))) length(which(freq_unfav_elite_all[unfav_haps_indep] > quantile(freq_rand_elite_all, 0.75))) / length(freq_unfav_elite_all[unfav_haps_indep]) length(which(freq_fav_elite_all[fav_haps_indep] == 0)) length(which(freq_fav_elite_all[fav_haps_indep] == 0)) / length(freq_fav_elite_all[fav_haps_indep]) ## ## test difference between distributions ## # Mann-Whitney wilcox.test(x = freq_fav_elite_all[fav_haps_indep], y = freq_rand_elite_all, alternative = "two.sided") wilcox.test(x = freq_unfav_elite_all[unfav_haps_indep], y = freq_rand_elite_all, alternative = "two.sided") wilcox.test(x = freq_fav_elite_all[fav_haps_indep], y = freq_unfav_elite_all[unfav_haps_indep], alternative = "two.sided") ## ## draw frequency plot ## name_set <- "earlyTraits" freq_fav_elite_all_plot <- freq_fav_elite_all[fav_haps_indep] freq_unfav_elite_all_plot <- freq_unfav_elite_all[unfav_haps_indep] pos_vec <- freq_fav_elite_all_plot neg_vec <- freq_unfav_elite_all_plot rand_vec <- freq_rand_elite_all str(rand_vec) str(pos_vec) str(neg_vec) xlim1 <- c(0,1) xlim2 <- c(-0.5,1) d_rand <- density(rand_vec) str(d_rand) d_rand$y <- d_rand$y[which(d_rand$x > 0)] d_rand$x <- d_rand$x[which(d_rand$x > 0)] d_rand$y <- d_rand$y[which(d_rand$x < 1)] d_rand$x <- d_rand$x[which(d_rand$x < 1)] d_rand$x <- c(0, d_rand$x, 1) d_rand$y <- c(0, d_rand$y, 0) d_pos <- density(pos_vec) str(d_pos) d_pos$y <- d_pos$y[which(d_pos$x > 0)] d_pos$x <- d_pos$x[which(d_pos$x > 0)] d_pos$x <- c(0, d_pos$x) d_pos$y <- c(0, d_pos$y) d_neg <- density(neg_vec) str(d_neg) d_neg$y <- d_neg$y[which(d_neg$x > 0)] d_neg$x <- d_neg$x[which(d_neg$x > 0)] d_neg$x <- c(0, d_neg$x) d_neg$y <- c(0, d_neg$y) png(paste(outFolder, "/density_RandFavUnfav_", name_set, "_indep.png", sep =""), width = 2100, height = 1800, res = 300) par(mar = c(4, 4, 0, 0) + 0.1, mgp = c(2.9, 1, 0)) plot(d_rand, col = rgb(0.2, 0.2, 0.2, alpha = 1), xlim = xlim1, lwd = 2, ylim = c(0, max(c(d_rand$y, d_pos$y, d_neg$y), na.rm = TRUE)), main = "", xlab = paste("Haplotype frequency in breeding lines", sep =""), bty = "n", cex.axis = 1.2, cex.lab = 1.5) polygon(d_rand, col = rgb(0.2, 0.2, 0.2, alpha = 0.2), border=NA) points(d_neg, col = "red", xlim = xlim2, lwd = 2, type = "l") polygon(d_neg, col = rgb(1, 0, 0, alpha = 0.15), border=NA) points(d_pos, col = "blue", xlim = xlim2, lwd = 2, type = "l") polygon(d_pos, col = rgb(0, 0, 1, alpha = 0.15), border=NA) legend("center", pch = 22, col = c("blue", "red", rgb(0.2, 0.2, 0.2, alpha = 1)), pt.bg = c(rgb(0, 0, 1, alpha = 0.15), rgb(1, 0, 0, alpha = 0.15), rgb(0.2, 0.2, 0.2, alpha = 0.2)), pt.lwd = 2, pt.cex = 2, text.col = c("blue", "red", rgb(0.2, 0.2, 0.2, alpha = 1)), cex = 1.2, legend = c("Favorable", "Unfavorable", "Random"), bty = "n") dev.off() ### ###################################################################
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% Generated by roxygen2: do not edit by hand % Please edit documentation in R/data.R \docType{data} \name{AllPreds_E} \alias{AllPreds_E} \title{Data: Predicted abundances of 4 ray species generated using gbm.auto} \format{ A data frame with 378570 rows and 7 variables: \describe{ \item{Latitude}{Decimal latitudes in the Irish Sea} \item{Longitude}{Decimal longitudes in the Irish Sea} \item{Cuckoo}{Predicted abundances of cuckoo rays in the Irish Sea, generated using gbm.auto} \item{Thornback}{Predicted abundances of thornback rays in the Irish Sea, generated using gbm.auto} \item{Blonde}{Predicted abundances of blonde rays in the Irish Sea, generated using gbm.auto} \item{Spotted}{Predicted abundances of spotted rays in the Irish Sea, generated using gbm.auto} \item{Effort}{Irish commercial beam trawler effort 2012} } } \usage{ data(AllPreds_E) } \description{ Predicted abundances of 4 ray species generated using gbm.auto, and Irish commercial beam trawler effort 2012. } \author{ Simon Dedman, \email{simondedman@gmail.com} } \keyword{datasets}
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# mark the encoding of character vectors as UTF-8 mark_utf8 <- function(x) { if (is.character(x)) { Encoding(x) <- 'UTF-8' return(x) } if (!is.list(x)) return(x) attrs <- attributes(x) res <- lapply(x, mark_utf8) attributes(res) <- attrs res } #' Compute the depth of a nested list list.depth <- function(this,thisdepth=0, add.vector=FALSE){ #restore.point("list.depth") if(!is.list(this)){ return(thisdepth + add.vector*(length(this)>1)) }else{ depths = unlist(lapply(this,list.depth,thisdepth=thisdepth+1, add.vector=add.vector)) #restore.point("list.depth1") return(max(depths)) } } int.seq = function(from, to) { if (from > to) return(NULL) from:to } examples.splice = function() { v = "searchA" splice(summarise(dt, mean.v=mean(v, na.rm=TRUE)), v=v, eval=FALSE) } display= function (..., collapse = "\n", sep = "") { str = paste(paste(..., collapse = collapse, sep = sep), "\n", sep = "") invisible(cat(str)) } intersect.list <- function(li) { Reduce(intersect, li) } robust.rbindlist = function(li) { restore.point("robust.rbindlist") cols = intersect.list(lapply(li, function(li) names(li))) ili = lapply(li, function(li) li[cols]) rbindlist(ili) } na.as.zero = function(x) { x[is.na(x)] = 0 x } rowProds = function(mat, cols = 1:NCOL(mat), default=NA) { if (length(cols) == 0) return(rep(default,NROW(mat))) if (is.numeric(cols)) { com = paste0("mat[,",cols,"]", collapse="*") } else { com = paste0("mat[,'",cols,"']", collapse="*") } parse.eval(com) } rows_along = function(x) { if (NROW(x)==0) return(integer(0)) return(1:NROW(x)) } #' Like paste0 but returns an empty vector if some string is empty sc = function(..., sep="", collapse=NULL) { str = list(...) restore.point("str.combine") len = sapply(str,length) if (any(len==0)) return(vector("character",0)) paste0(...,sep=sep,collapse=collapse) } any.field = function(li, field, val) { any(sapply(li, function(el) isTRUE(el[[field]] == val))) } all.fields = function(li, field, val) { all(sapply(li, function(el) isTRUE(el[[field]] == val))) } nlist = function (...) { li = list(...) li.names = names(li) names = unlist(as.list(match.call())[-1]) if (!is.null(li.names)) { no.names = li.names == "" names(li)[no.names] = names[no.names] } else { names(li) = names } li } #' Like paste0 but returns an empty vector if some string is empty str.combine = function(..., sep="", collapse=NULL) { str = list(...) restore.point("str.combine") len = sapply(str,length) if (any(len==0)) return(vector("character",0)) paste0(...,sep=sep,collapse=collapse) } remove.list.elements = function(li, remove=NULL) { #restore.point("remove.list.elements") if (length(remove)==0) return(li) if (is.character(remove)) { remove = which(names(li)==remove) } if (length(remove)==0) return(li) return(li[-remove]) } #' Does an environment / list contain the objects named as names contains = function(env,names, inherits=FALSE,...) { if (is.environment(env)) return(sapply(names, exists, where=env, inherits=inherits, ...)) return(names %in% names(env)) } str.ends.with = function(txt,pattern) { substring(txt,nchar(txt)-nchar(pattern)+1,)==pattern } #' Returns a string constisting of times spaces, vectorized over times str.space = function(times, space=" ") { space.str = paste0(rep(space,max(times)),collapse="") substring(space.str,1,last=times) } example.str.space = function() { str.space(0:4) } #' An operator that is true if the string str starts with the substring key str.starts.with = function(str,key) { substring(str,1,nchar(key))==key } is.true = function(val) { if (length(val)==0) return(FALSE) val[is.na(val)] = FALSE return(val) } is.false = function(val) { if (length(val)==0) return(FALSE) val[is.na(val)] = TRUE return(!val) } path.parts = function(path,sep=".") { str.split(path,sep) } common.and.distinct.path.parts = function(opath, npath,sep=".") { restore.point("common.and.distinct.path.parts") op = str.split(opath,sep)[[1]] np = str.split(npath,sep)[[1]] len = length(np) if (len == 0) return(list(common=NULL,distinct=NULL)) op = fill.vec(op,len,"")[1:len] common = op == np if (all(common)) return(list(common=np,distinct=NULL)) ind = which(!common)[1]-1 if (ind==0) return(list(common=NULL,distinct=np)) return(list(common=np[1:ind], distinct=np[(ind+1):len])) } examples.common.and.distinct.path.parts = function() { opath = "a.b.cd.e" npath = "a.b.e.f" common.and.distinct.path.parts(opath,npath) opath = "" npath = ".stages.intensityChoice.actions.intensityA" common.and.distinct.path.parts(opath,npath) } #' Cuts away early stuff from a tree path cut.to.sub.tree.path = function(tree.path, after) { pos = str.locate.first(tree.path, after) substring(tree.path,pos[,2]+1) } #' Index a list tree with a tree path at.tree.path = function(li, tree.path) { restore.point("get.from.tree.path") tree.path = str.replace(tree.path,".","$") code = paste0("list(",paste0("li",tree.path,collapse=","),")") return(eval(parse(text=code,srcfile=NULL))) } intersect.vector.list = function(li, init) { if (missing(init)) return(Reduce(intersect,li)) else return(Reduce(intersect,li,init)) } #' Gets game variants that correspond to a tree path variants.from.tree.path = function(tree.path) { restore.point("variants.from.tree.path") variants = str.extract.all(tree.path,"_if_variant_.*`") variants = lapply(variants, function(str) str.replace(str,"_if_variant_","")) variants = lapply(variants, function(str) str.replace(str,"`","")) variants = lapply(variants, function(str) str.split(str,"_")) variants = lapply(variants, intersect.vector.list) variants } #' Adapts whisker render for different whisker formats custom.whisker.render = function(template,data,...,whiskers=c("<<",">>")) { library(whisker) if (!is.null(whiskers)) { template = str.replace(template,whiskers[1],"{{") template = str.replace(template,whiskers[2],"}}") } whisker.render(template,data,...) } #' Comverts a list of vectors into a matrix, shorter vectors will be filled up vec.list.to.matrix = function(li,fill=NA, transpose=TRUE) { restore.point("vec.list.to.matrix") cols = max(sapply(li,length)) ret = sapply(li, fill.vec, len=cols, fill=fill) if (transpose) return(t(ret)) return(ret) } #' fill a vector up to a specified length with fill fill.vec = function(vec,len=length(vec),fill=NA) { if (len == length(vec)) return(vec) if (len > length(vec)) return(c(vec,rep(fill,len-length(vec)))) return(vec) } #' Returns all variable names in an R expression var.in.expr.str = function(expr.str, envir=baseenv(), union = TRUE) { if (length(expr.str)>1) { vars = lapply(expr.str,var.in.expr.str,envir=envir) if (union) { return(unique(unlist(vars))) } else { return(vars) } } else { return(var.in.expr(expr.str=expr.str, envir = envir)) } } union.of.list = function(li) { unique(unlist(li)) } #' Returns all variable names in an R expression var.in.expr = function(expr,expr.str, envir=baseenv()) { library(codetools) if (!missing(expr.str)) { if (length(expr.str)==0) return(NULL) expr = parse(text=expr.str,srcfile=NULL) } f <- function() {} # a dummy function body(f) <- expr # containing the expression as its body codetools::findGlobals(f,merge=FALSE)$variables } examples.var.in.expr = function() { var.in.expr(quote(x*y+2+sin(z))) var.in.expr(parse(text="x*y+2+sin(z)")) var.in.expr(expr.str = "x*y+2+sin(z)") } #' Names lists are used to recursively store order of columns as.names.list = function(names) { li = vector("list",length(names)) names(li) = names li } #' Names lists are used to recursively store order of columns flatten.names.list = function(li,name="") { if (length(li)==0) return(name) sub.names = sapply(seq_along(li), function(i) flatten.names.list(li[[i]],names(li)[i])) if (nchar(name)>0) { ret.names = paste0(name,"_",sub.names) ret.names[nchar(sub.names)==0] = name } else { ret.names = sub.names } return(unlist(ret.names)) } flatten.names.list.examples = function() { li = list(A=list(B1=list(),B2=list()),C=list(),list(D=list())) flatten.names.list(li) as.names.list(c("A","B","C")) }
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/man/rotation.Rd
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md0u80c9/huxtable
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rotation.Rd
% Generated by roxygen2: do not edit by hand % Please edit documentation in R/properties.R \name{rotation} \alias{rotation} \alias{rotation<-} \alias{set_rotation} \title{Text rotation} \usage{ rotation(ht) rotation(ht) <- value set_rotation(ht, row, col, value, byrow = FALSE) } \arguments{ \item{ht}{A huxtable.} \item{value}{A numeric vector. Anti-clockwise from the x axis, so 0 is left to right, 90 is going up, etc. Set to \code{NA} to reset to the default, which is \code{0}.} \item{row}{A row specifier. See \code{\link{rowspecs}} for details.} \item{col}{An optional column specifier.} \item{byrow}{If \code{TRUE}, fill in values by row rather than by column.} } \value{ For \code{rotation}, the \code{rotation} property. For \code{set_rotation}, the \code{ht} object. } \description{ Functions to get or set the \emph{text rotation} property of huxtable cells. } \details{ You will probably need to set \code{\link[=col_width]{col_width()}} and \code{\link[=row_height]{row_height()}} explicitly to achieve a nice result, in both HTML and LaTeX. } \examples{ ht <- huxtable(a = 1:3, b = 1:3) rotation(ht) <- 90 rotation(ht) ht <- huxtable(a = 1:3, b = 3:1) ht2 <- set_rotation(ht, 90) rotation(ht2) ht3 <- set_rotation(ht, 1:2, 1, 90) rotation(ht3) ht4 <- set_rotation(ht, 1:2, 1:2, c(90, 270), byrow = TRUE) rotation(ht4) ht5 <- set_rotation(ht, where(ht == 1), 90) rotation(ht5) }
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gr95Resid.Rd
\name{gr95Resid} \alias{gr95Resid} \title{Returns the residuals of the Greco 1995 model for a given set of parameters versus concentration data and observed endpoint data.} \usage{ gr95Resid(param, dlist, evec, mpos) } \arguments{ \item{mpos}{A logical variable indicating whether the dose slopes are positive. Usually false.} \item{param}{A list of numeric values, always of the form B, Econ, C50.1, C50.2, m1, m2, alpha.} \item{dlist}{A 2-column matrix of points at which the response surface is to be constructed.} \item{evec}{A vector of observed endpoint values. Should be the same length as nrow(dlist).} } \description{ Returns the residuals of the Greco 1995 model for a given set of parameters versus concentration data and observed endpoint data. } \author{ Paul Lakin }
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/1lesson.R
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Maxim1488/matmod
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t=c(T,TRUE) f=c(F,FALSE) # commentary as numeric log() ?as `logical-class`() ?as logi # tip peremens # func (a,b,c) plot(density(rnorm(1:100)),col="blue") # operator (=) t=25^.5 # log operatory "==" logical oper z==4 z>4=4 z<4=4 z=c(1,4,10) # seqi(from= ) A=c("A","B","C") B=1:5 C=c(T,F) #names func #f
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cran/peakPick
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helperpeak.Rd
% Generated by roxygen2: do not edit by hand % Please edit documentation in R/peakpicking.R \name{helperpeak} \alias{helperpeak} \title{helper function for small peak elimination} \usage{ helperpeak(thepos, vec, nsd, npos) } \arguments{ \item{thepos}{integer position of peak in vector vec} \item{vec}{vector of values for peakdetection} \item{nsd}{numeric minimum number of standard deviations for a peak to rise above the mean of its immediate vicinity in order to be considered for a peak call} \item{npos}{integer value, peak size will be estimated plus/minus npos positions from peak} } \value{ boolean TRUE if the peak at position thepos is to be deleted } \description{ helper function for small peak elimination } \keyword{internal}
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radivot/myelo
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2022-12-15T00:11:22.751773
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rm(list=ls()) library(tidyverse) library(deSolve) library(myelo) (x0=craigIC[c(1,8)]) (parsQ=craigPars[c("Qss","Aqss","tauS","fQ","the2","s2")]) parsQ["kapDel"]=craigPars["kapss"]+craigPars["kapDel"] parsQ attach(as.list(parsQ)) fbeta=function(Q) fQ/(1+(Q/the2)^s2) betaSS=fbeta(Qss) (kapDel=(Aqss-1)*betaSS) detach(as.list(parsQ)) (StrTimes=seq(0,80,14)) (StpTimes=StrTimes+5) nc=length(StpTimes) (events=tibble(var=rep("Aq",2*nc), time=sort(c(StrTimes,StpTimes)), value=rep(c(0.0*parsQ["Aqss"],parsQ["Aqss"]),nc), method=rep("rep",2*nc))) events2=events events2$time=events2$time+150 (eventsdat=as.data.frame(bind_rows(events,events2))) (f=file.path(system.file(paste("libs",Sys.getenv("R_ARCH"),sep=""), package = "myelo"), paste("myelo",.Platform$dynlib.ext,sep=""))) dyn.load(f) (parsQdb=c(tauS=2.8, fQ = 2*betaSS, thresh = 0.1, betaSS = betaSS, kapDel = kapDel)) times <- seq(-20,500,by=0.01) (x05=c( Q = 1.10216835127605, S1 = 0.0330752837276347, S2 = 0.0330752837276349, S3 = 0.0330752837276351, S4 = 0.0330752837276354, Aq = 1.5116)) system.time(yout5 <- dede(x05,times = times, func = "derivsQdb", parms = parsQdb, dllname = "myelo",initfunc = "parmsQdb", events=list(data=eventsdat),method="lsoda", nout = 1, outnames = c("beta")) ) D5=data.frame(yout5) head(D5,2) tail(D5,2) gx=xlab("Days") sbb=theme(strip.background=element_blank()) cc=coord_cartesian(xlim=c(-2,125)) tc=function(sz) theme_classic(base_size=sz) d5=D5%>%select(time,Q,Aq)%>%gather(key="Lab",value="Value",-time) d5%>%ggplot(aes(x=time,y=Value))+facet_grid(Lab~.,scales = "free")+geom_line(size=1)+gx+tc(14)+sbb#+cc ggsave("~/Results/myelo/Qdb2x6.pdf",width=5, height=5) (parsQdb1=c(fQ = 2*betaSS, thresh = 0.1, betaSS = betaSS, kapDel = kapDel)) times <- seq(-20,500,by=0.01) (x0=c( Q = 1.10216835127605, Aq = 1.5116)) system.time(yout <- dede(x0,times = times, func = "derivsQdb1", parms = parsQdb1, dllname = "myelo",initfunc = "parmsQdb1", events=list(data=eventsdat),method="lsoda", nout = 1, outnames = c("beta")) ) D=data.frame(yout) head(D,2) tail(D,2) d=D%>%select(time,Q,Aq)%>%gather(key="Lab",value="Value",-time) d%>%ggplot(aes(x=time,y=Value))+facet_grid(Lab~.,scales = "free")+geom_line(size=1)+gx+tc(14)+sbb#+cc ggsave("~/Results/myelo/Qdb1_2x6.pdf",width=5, height=5) #flat steps => slightly more killing (better) ### Qdb1 is twice as fast # # library(rbenchmark) # benchmark("db" = { # dede(x05,times = times, func = "derivsQdb", parms = parsQdb, # dllname = "myelo",initfunc = "parmsQdb", # events=list(data=eventsdat),method="lsoda", # nout = 1, outnames = c("beta")) # }, # "db1"={ # dede(x0,times = times, func = "derivsQdb1", parms = parsQdb1, # dllname = "myelo",initfunc = "parmsQdb1", # events=list(data=eventsdat),method="lsoda", # nout = 1, outnames = c("beta")) # }, # "db1ode"={ # ode(x0,times = times, func = "derivsQdb1", parms = parsQdb1, # dllname = "myelo",initfunc = "parmsQdb1", # events=list(data=eventsdat),method="lsoda", # nout = 1, outnames = c("beta")) # }, # # replications = 25, # columns = c("test", "replications", "elapsed", # "relative", "user.self", "sys.self") # ) # #
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cran/RSEIS
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2023-08-25T02:13:28.165769
2023-08-19T12:32:32
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Zdate.Rd
\name{Zdate} \alias{Zdate} \alias{dateList} \alias{dateStamp} \title{Date functions} \description{ Make character vector from dates } \usage{ Zdate(info, sel=1, t1=0, sep=':') dateList(datevec) dateStamp(datelist, sep=':') } \arguments{ \item{info}{info structure from trace structure} \item{sel}{selection of which ones to extract, default=1:length(info$jd) } \item{t1}{ time offset, seconds, default=0 } \item{sep}{ character for separating the components in the string, default=":" } \item{datevec}{ vector with yr, jd, mo, day, hr, mi, sec } \item{ datelist}{ output of dateList } } \details{ Format date stamp for plotting and identification. Used for STAMP. } \value{ character strings } \note{ If using Zdate to create a file name, becareful about the separator. A colon in the file name on PC and MAC systems can be confusing for the OS. } \author{Jonathan M. Lees<jonathan.lees.edu>} \seealso{swig, dateStamp, ghstamp, filedatetime} \examples{ data("GH") sel <- which(GH$COMPS == "V") ftime <- Zdate(GH$info, sel[1:5], 1) dvec <- c(2009, 134, 5, 14, 10, 32, 24.5, 0) A <- dateList(dvec) dateStamp(A) dateStamp(A, sep="_") } \keyword{misc}
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syyang93/yangR
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2021-06-14T21:12:42.469432
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make.quartiles.Rd
% Generated by roxygen2: do not edit by hand % Please edit documentation in R/make.quartiles.R \name{make.quartiles} \alias{make.quartiles} \title{Function to make quartiles from a column within a dataframe --> taken from fashaR} \usage{ make.quartiles(test) } \arguments{ \item{test}{data that needs to be divided into quartiles} } \value{ output Dataframe with quartiles (categories and by number, 4 = highest quartile) } \description{ Function to make quartiles from a column within a dataframe --> taken from fashaR } \examples{ test2=makequartiles(test$resid.mtDNA) }
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testplot.R
datFig2 %>% filter(., scenario == "Fig2a") %>% arrange(desc(r2)) %>% ggtern(aes(x = env, z = spa, y = codist)) + scale_T_continuous(limits=c(0,1.0), breaks=seq(0,1,by=0.1), labels=seq(0,1,by=0.1)) + scale_L_continuous(limits=c(0.0,1), breaks=seq(0,1,by=0.1), labels=seq(0,1,by=0.1)) + scale_R_continuous(limits=c(0.0,1.0), breaks=seq(0,1,by=0.1), labels=seq(0,1,by=0.1)) + theme_showarrows() + labs(xarrow = "Environment", yarrow = "Codistribution", zarrow = "Spatial") + geom_point(aes(size = r2, shape = iteration, color = nicheOpt), alpha = 0.5) + scale_color_viridis_c() + #theme_minimal() + guides(size = guide_legend(order = 1, title = expression(paste(R^{2}))), shape = guide_legend(order = 2, title = NULL, override.aes = list(size = 4)), col = guide_colourbar(title = "Niche optima", order = 3)) + theme(legend.position = "bottom", legend.box = "vertical", axis.title = element_text(colour = "white"), panel.grid = element_line(colour = "darkgrey"), panel.border = element_rect(colour = "darkgrey"), panel.background = element_rect(fill = "white"))
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wind22zhu/rDNAse
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getGenbank.R
#' Get DNA/RNA Sequences from Genbank by GI ID #' #' Get DNA/RNA Sequences from Genbank by GI ID #' #' This function get DNA/RNA sequences from Genbank by GI ID(s). #' #' @param id A character vector, as the GI ID(s). #' #' @return A list, each component contains one of the DNA/RNA sequences. #' #' @keywords Genbank #' #' @aliases getGenbank #' #' @author Min-feng Zhu <\email{wind2zhu@@163.com}> #' #' @seealso See \code{\link{readFASTA}} for reading FASTA format files. #' #' @export getGenbank #' #' @examples #' \donttest{ #' # Network latency may slow down this example #' # Only test this when your connection is fast enough #' require(RCurl) #' #' ids = c(2, 11) #' getGenbank(ids)} getGenbank = function (id) { id = as.character(id) n = length(id) dna = vector('list', n) for (i in 1:n) { url = paste('http://www.ncbi.nlm.nih.gov/sviewer/viewer.cgi?tool=portal&sendto=on&log$=seqview&db=nuccore&dopt=fasta&sort=&val=', id[i], '&from=begin&to=end&maxplex=1', sep = '') genb = RCurl::getURL(url) sequences = strsplit(genb[[1]], split = "\n")[[1]] start = 2 end = length(sequences) dna[[i]]= paste(sequences[start:end], collapse = "") } gi_name = lapply(1:n, function(i) paste('gi', id[i], sep = "_")) names(dna) = gi_name return(dna) }
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permKS.R
`permKS` <- function (x, ...){ UseMethod("permKS") } `permKS.formula` <- function(formula, data, subset, na.action, ...){ ## mostly copied from wilcox.test.formula if (missing(formula) || (length(formula) != 3) || (length(attr(terms(formula[-2]), "term.labels")) != 1)) stop("'formula' missing or incorrect") m <- match.call(expand.dots = FALSE) if (is.matrix(eval(m$data, parent.frame()))) m$data <- as.data.frame(data) m[[1]] <- as.name("model.frame") m$... <- NULL mf <- eval(m, parent.frame()) DNAME <- paste(names(mf), collapse = " by ") groupname<-names(mf)[2] names(mf) <- NULL response <- attr(attr(mf, "terms"), "response") g <- factor(mf[[-response]]) resp <- mf[[response]] out <- do.call("permKS", c(list(x=resp,g=g), list(...))) out$data.name <- DNAME out } `permKS.default` <- function(x, g, exact = NULL, method=NULL, methodRule=methodRuleKS1, control=permControl(),...){ cm<-control$cm nmc<-control$nmc seed<-control$seed digits<-control$digits p.conf.level<-control$p.conf.level setSEED<-control$setSEED if (!is.numeric(x) | (!is.character(g) & !is.factor(g))) stop("x must be numeric and g must be character or factor vectors") if (is.null(method)) method<-methodRule(x,g,exact) method.OK<-(method=="pclt" | method=="exact.mc") if (!method.OK) stop("method not one of: 'pclt', 'exact.mc'") mout<-switch(method, pclt=ksample.pclt(x,g), exact.mc=ksample.exact.mc(x,g,nmc,seed,digits,p.conf.level,setSEED)) p.values<-mout$p.values PVAL<-p.values["p.twosided"] if (method=="pclt") METHOD<-"K-Sample Asymptotic Permutation Test" else if (method=="exact.mc") METHOD<-"K-Sample Exact Permutation Test Estimated by Monte Carlo" xname<-deparse(substitute(x)) gname<-deparse(substitute(g)) if (length(xname)>1) xname<-c("x") if (length(gname)>1) gname<-c("g") DNAME <- paste(xname, "and", gname) chisq<-mout$chisq.value if (!is.null(chisq)) names(chisq)<-"Chi Square" df<-mout$df if (!is.null(df)) names(df)<-"df" if (method!="exact.mc") nmc<-NULL OUT <- list(statistic = chisq, parameter=df, estimate=NULL, p.value = as.numeric(PVAL), method = METHOD, data.name = DNAME, p.conf.int=mout$p.conf.int, nmc=nmc) if (method=="exact.mc"){ class(OUT) <- "mchtest" } else class(OUT) <- "htest" return(OUT) }
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CuriousPICTians/lifematters
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#!/usr/bin/env Rscript #Usage : # 1) From Command line : $ cd /var/www/html/lifematters; Rscript kmeans.R '<email_id>' # 2) From PHP : exec("Rscript kmeans.R <email_id>", $out); library(rJava) library(RMongo) i <- commandArgs(TRUE) #i <- '1018@hotmail.com' rootkea <- mongoDbConnect('organ') donors <- dbGetQuery(rootkea, 'donorinfo', '{"approved": "1"}', skip = 0, limit = 10000) receivers <- dbGetQuery(rootkea, 'receiverinfo', '{"approved": "1"}', skip = 0, limit = 20000) donor_ds <- donors[, c("email", "organ", "blood")] receiver_ds <- receivers[, c("email", "organ", "blood")] donor_clusters <- kmeans(donor_ds[, c("organ", "blood")], 8) receiver_clusters <- kmeans(receiver_ds[, c("organ", "blood")], 8) j <- 1 ans <- 0 for (email in donor_ds$email) { if (email == i) { ans <- j break; } j <- j + 1 } cd_cluster <- donor_clusters$cluster[ans] organ_diff <- receiver_clusters$centers[,"organ"] - donor_clusters$centers[cd_cluster,"organ"] blood_diff <- receiver_clusters$centers[,"blood"] - donor_clusters$centers[cd_cluster,"blood"] ans_cluster_l <- which.min(abs(organ_diff) + abs(blood_diff)) temp <- receiver_ds[receiver_clusters$cluster == ans_cluster_l, ] final <- temp[(temp$organ == donor_ds[ans, ]$organ) & (temp$blood == donor_ds[ans,]$blood),] #print(final) print(final$email) #for (email in final$email) #{ # query <- gsub(' ', '', paste('{"email":"', email, '"}')) # print(query) # dbInsertDocument(rootkea, "result", query) #} #k <- 1 #rows <- nrow(final) #while (k <= rows) #{ # docs <- gsub('[]\\[]', "", toJSON(final[k,], dataframe = c("rows"))) #print(docs) # dbInsertDocument(rootkea, "result", doc = docs) # k <- k + 1 #}
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args <- commandArgs(T) print( args ) #args <- c( 'EPI/', 'TOPUP/', '2', '2' ) #setwd('/media/alessiofracasso/storage2/SpinozaTest/HighRes/AF_HighRes_04112016/topUpDataset2') # get actual dir mainDir <- getwd() # get EPIs setwd( args[1] ) epiFiles <- dir( pattern=sprintf('*.nii') ) # get TOPUPs setwd( mainDir ) setwd( args[2] ) topFiles <- dir( pattern=sprintf('*.nii') ) # get selected EPI selectedEpi <- as.numeric(args[3]) if (is.numeric(selectedEpi)==FALSE) { # selected epi is not numeric! msg <- sprintf( 'the third argument MUST be a number (which EPI do you want to realign all the data to??)' ) warning( msg ) stopifnot(flagDir) } # get selected TOP UP selectedTop <- as.numeric(args[4]) if (is.numeric(selectedTop)==FALSE) { # selected TOP is not numeric! msg <- sprintf( 'the third argument MUST be a number (which TOP UP do you want to realign all the data to??)' ) warning( msg ) stopifnot(flagDir) } # get EPI n of TRs setwd( mainDir ) instr <- sprintf('3dinfo %s%s > infoEPI.1D',args[1],epiFiles[selectedEpi]) system( instr ) trString <- scan( file='infoEPI.1D', what=c('character'), skip=17, nlines=1 ) nTRs <- as.numeric( trString[6] ) system('rm infoEPI.1D') # get TOPUP n of TRs setwd( mainDir ) instr <- sprintf('3dinfo %s%s > infoTOPUP.1D',args[2],topFiles[selectedTop]) system( instr ) trString <- scan( file='infoTOPUP.1D', what=c('character'), skip=17, nlines=1 ) nTRsTOPUP <- as.numeric( trString[6] ) system('rm infoTOPUP.1D') # motionCorrect EPIs print('##################') print('##################') print('motionCorrect EPIs') print('##################') print('##################') setwd( args[1] ) for ( nEpi in 1:length(epiFiles) ) { filename <- strsplit(epiFiles[nEpi],'.nii')[[1]][1] prefixName <- sprintf('pb.%s.volreg+orig', filename) motion1DfileAff <- sprintf('pb.%s.volreg', filename) motion1DfileLin <- sprintf('pb.%s.lin.volreg', filename) instr <- sprintf('3dvolreg -verbose -zpad 1 -base %s[%1.0f] -1Dfile %s -1Dmatrix_save %s -prefix %s -Fourier %s ', epiFiles[selectedEpi], nTRs-1, motion1DfileLin, motion1DfileAff, prefixName, epiFiles[nEpi] ) print( instr ) system( instr ) } setwd( mainDir ) targetDir <- 'motionCorrectEpi' flagDir <- dir.create( file.path(mainDir, targetDir) ) if (flagDir==FALSE) { # directory already exists! msg <- sprintf( 'Remove the directory %s_folder to proceed', targetDir ) warning( msg ) stopifnot(flagDir) } setwd( args[1] ) filesToMove <- dir(pattern='*volreg*') setwd( mainDir ) for ( nFiles in 1:length(filesToMove) ) { instr <- sprintf('mv %s%s %s/%s', args[1], filesToMove[nFiles], targetDir, filesToMove[nFiles] ) system( instr ) } # EPI for Top Up print('####################') print('####################') print('copy EPI for top up') print('####################') print('####################') setwd( args[1] ) instr <- sprintf( '3dTcat -prefix ../epiForTopUp.nii %s[%1.0f]', epiFiles[selectedEpi], nTRs-1 ) system( instr ) setwd( mainDir ) # TOP UP for Top Up print('##################################') print('##################################') print('copy top up volume EPIs for top up') print('##################################') print('##################################') setwd( args[2] ) instr <- sprintf( '3dTcat -prefix ../topUp.nii %s[%1.0f]', topFiles[selectedTop], 0 ) system( instr ) setwd( mainDir ) # Compute non-linear transformation print('#########################') print('#########################') print('compute top up transform') print('#########################') print('#########################') setwd( mainDir ) print('estimate non-linear transformation, it might take a while...') instr <- sprintf('3dQwarp -source epiForTopUp.nii -base topUp.nii -prefix warpTop -verb -iwarp -pblur 0.05 0.05 -blur -1 -1 -noweight -minpatch 9 -plusminus' ) print( instr ) system( instr ) # Apply non-linear transformation, create target dir print('#######################') print('#######################') print('apply top up transform') print('#######################') print('#######################') targetDir <- 'motionCorrect_topUp_Epi' flagDir <- dir.create( file.path(mainDir, targetDir) ) if (flagDir==FALSE) { # directory already exists! msg <- sprintf( 'Remove the directory %s_folder to proceed', targetDir ) warning( msg ) stopifnot(flagDir) } # apply non-linear transformation to the files and save them in target dir setwd('motionCorrectEpi') motionCorrAffine <- dir(pattern='*aff12.1D') setwd( mainDir ) for ( nEpi in 1:length(epiFiles) ) { namePrefix <- strsplit( epiFiles[nEpi], '.nii' )[[1]][1] filenameBlip <- sprintf( 'pb.%s.volreg+orig', namePrefix ) instr <- sprintf('3dNwarpApply -master %s%s -source %s%s -nwarp motionCorrectEpi/%s warpTop_PLUS_WARP+orig -interp wsinc5 -prefix %s/%s', args[1], epiFiles[nEpi], args[1], epiFiles[nEpi], motionCorrAffine[nEpi], targetDir, filenameBlip) print( instr ) system( instr ) } # storage directory print('###################') print('###################') print('clean up transform') print('###################') print('###################') targetDir <- 'topUpDir' flagDir <- dir.create( file.path(mainDir, targetDir) ) if (flagDir==FALSE) { # directory already exists! msg <- sprintf( 'Remove the directory %s_folder to proceed', targetDir ) warning( msg ) stopifnot(flagDir) } system('mv warpTop* topUpDir/') system('mv epiForTopUp.nii topUpDir/') system('mv topUp.nii topUpDir/')
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/predictions_on_na.R
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edples/Predictions-of-8-levels
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predictions_on_na.R
setwd("C:/comply") m_data <- read.csv("M.csv") profile_data <- read.csv("ProfileMetadata.csv") library(tidyverse) class(m_data) class(profile_data) str(m_data) str(profile_data) glimpse(m_data) glimpse(profile_data) head(m_data) colSums(is.na(m_data)) #no NA's, the n.a.'s are characters colSums(is.na(profile_data)) # the same as above head(profile_data) summary(m_data) summary(profile_data) # The problem is clasification type , the target variable m_data$M having 8 levels. library(stringr) sum(str_count(profile_data$Number.of.Years.of.Births.in.profile , "n.a.")) #count the number of n.a.'s sum(str_count(profile_data$Difference.in.Years.between.Max.Min.Year.of.Birth , "n.a.")) # as the last 2 columns of the profile_data have 84025 of "n.a." from 96737 observations, they are no longer relevant to the case. profile_data <- profile_data[, 1:9] #slice the data, dropping the above 2 columns glimpse(profile_data) identical(m_data$Profile_id, profile_data$Profile_id)#check if the"Profile_id" columns of the both data sets are identical, # meaning that the order is the same in both datasets. profile_data$m_var <-m_data$M #addin the M column to the relevant dataset, which the model will train and predict on. na_profile_data <-subset(profile_data, m_var == "n.a.") # choose only the n.a. rows,this will be dataset that the model will make predictions on. glimpse(na_profile_data) profile_data<- subset(profile_data, !m_var == "n.a.")# choose only the rows without n.a.,this will be the training dataset glimpse(profile_data) profile_data$has_year_of_birth<- as.factor(profile_data$has_year_of_birth)#convert the relevant columns of the datasets to factors profile_data$has_country <- as.factor(profile_data$has_country) profile_data$is_sanction <- as.factor(profile_data$is_sanction) profile_data$is_pep <- as.factor(profile_data$is_pep) profile_data$is_adverse_media <- as.factor(profile_data$is_adverse_media) profile_data$Number.of.Source.Docs.for.Profile <- as.factor(profile_data$Number.of.Source.Docs.for.Profile) na_profile_data$has_year_of_birth<- as.factor(na_profile_data$has_year_of_birth) na_profile_data$has_country <- as.factor(na_profile_data$has_country) na_profile_data$is_sanction <- as.factor(na_profile_data$is_sanction) na_profile_data$is_pep <- as.factor(na_profile_data$is_pep) na_profile_data$is_adverse_media <- as.factor(na_profile_data$is_adverse_media) na_profile_data$Number.of.Source.Docs.for.Profile <- as.factor(na_profile_data$Number.of.Source.Docs.for.Profile) profile_data$m_var <- as.numeric(profile_data$m_var) library(vtreat) library(dplyr) library(magrittr) # I consider the below variables significant as predictors. vars_test <- c("has_year_of_birth", " has_country ", "is_sanction ", "is_pep", "is_adverse_media", "Number.of.Source.Docs.for.Profile") treatplan <- designTreatmentsZ(profile_data,vars_test)#design a treatment plan for the variables which handles the missing values, to be used in XGBoost (scoreFrame <- treatplan %>% use_series(scoreFrame) %>% select(varName, origName, code)) (newvars <- scoreFrame %>% filter(code %in% c("clean", "lev")) %>% use_series(varName)) trainingframe.treat <- prepare(treatplan, profile_data, varRestriction = newvars) # this makes the data compatible to XgBoost testframe.treat <-prepare(treatplan, na_profile_data, varRestriction = newvars) library(xgboost) set.seed(123) # for reproducibility model <- xgb.cv(data = as.matrix(trainingframe.treat), #perform cross-validation to find the optimal number of trees label = profile_data$m_var, nrounds = 100, num_class = 8, nfold = 5, objective = "multi:softmax",# multiclass target eta = 0.3, max_depth = 6, early_stopping_rounds = 10, verbose = 0 # silent ) (evlog <- model$evaluation_log) evlog %>% summarize(ntrees.train = which.min(train_merror_mean), # find the index of min(train_merror_mean) ntrees.test = which.min(test_merror_mean)) # find the index of min(test_merror_mean) #from the above lines, optimal ntrees= 1 ntrees <- 1 m_var_xgb <- xgboost(data = as.matrix(trainingframe.treat), # training data as matrix label = profile_data$m_var, # column of outcomes nrounds = ntrees,# number of trees to build num_class = 8, objective = "multi:softmax", # objective eta = 0.3, depth = 6, verbose = 0 # silent ) na_profile_data$predicted <- predict(m_var_xgb, as.matrix(testframe.treat)) #predict on the test set and add the predictions column # to the na_profile_data set head(na_profile_data) #check the structure of the data set summary(na_profile_data$predicted) unique(na_profile_data$predicted) # to see which distinct values were predicted unique(profile_data$m_var) library(funModeling) df_status(na_profile_data)
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cielavenir/codeiq_solutions
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tyama_codeiq711_next.R
#!/usr/bin/Rscript next_permutation<-function(env,name,n=NA){ a=get(name,env) if(is.na(n))n<-length(a) if(n<0||length(a)<n)return(FALSE) i<-0 a<-c(a[1:n],rev(a[-n:0])) for(i in rev(1:(length(a)-1)))if(a[i]<a[i+1])break # r doesn't go beyond the range if(a[i]>=a[i+1]){ assign(name,rev(a),env) return(FALSE) } k<-i for(i in rev((k+1):length(a)))if(a[k]<a[i])break l<-i z<-a[k];a[k]<-a[l];a[l]<-z assign(name,a<-c(a[1:k],rev(a[-k:0])),env) return(TRUE) } env<-new.env() N<-6 e0<-1:(N*2) f0<-1:(N*2) i<-0 r<-0 for(i in 1:N){ e0[i]=f0[i]=0 e0[N+i]=f0[N+i]=1 } assign("e0",e0,env) assign("f0",f0,env) repeat{ e0=get("e0",env) repeat{ f0=get("f0",env) flg<-0 zero1<-0 zero2<-N one1<-0 one2<-N for(i in 1:(N*2)){ if(e0[i]==0)zero1=zero1+1 if(e0[i]==1)one1=one1+1 if(f0[N*2+1-i]==0)zero2=zero2-1 if(f0[N*2+1-i]==1)one2=one2-1 if(zero1==zero2)flg=flg+1 if(one1==one2)flg=flg+1 } if(flg>=2)r=r+1 if(!next_permutation(env,"f0"))break } if(!next_permutation(env,"e0"))break } cat(r) cat("\n")
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getStartingData.Rd
% Generated by roxygen2: do not edit by hand % Please edit documentation in R/getStartingData.R \name{getStartingData} \alias{getStartingData} \title{Retrieves user or budget names} \usage{ getStartingData(i, param.token.code, param.token.env) } \arguments{ \item{i}{name of endpoint} \item{param.token}{Your YNAB API personal access token} } \description{ Gets the following YNAB data for a YNAB subscriber: "user", "budgets" } \examples{ endpoint <- "budgets" mytoken <- "1234567890ABCDE" df_budgets <- getStartingData(i = endpoint, param.token = mytoken) } \keyword{getStartingData}
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secs-lab/hackathon-2020
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merge_ele_data.R
library(reshape2) setwd(dirname(rstudioapi::getSourceEditorContext()$path)) #read in caluclated elephant poaching and population datasets load("data/raw/SH_AnnualModelPreds.Rdata") ele_sums <- readRDS("data/raw/ele_sums.Rdata") #read in raw populaion survery data, select relevant columns #and filter to relevant years pop.dat <- read.csv("data/raw/Copy of all_popn_estimates_mikesites_140401.csv", header = TRUE) pop.dat <- pop.dat[-154,] # remove duplicate survey in same year pop.dat <- pop.dat[pop.dat$year > 2001, c("sitecode", "year", "area", "est", "var", "dens")] #read in poaching survey data, select relevant columns #and filter to relevant years pike.stats <- read.csv("data/raw/Copy of 170810_PikeStatsUpTo2016.csv", header = TRUE) pike.stats <- pike.stats[pike.stats$year > 2001, c("siteid", "year", "totcarc", "illegal")] names(pike.stats)[1] <- "sitecode" #'convert arrays to data frames ele.dat <- as.data.frame.table(site_quants.pike.full) ele.sums <- as.data.frame.table(ele_sums) #expand quantile values to individual columns ele.dat.wide <- dcast(ele.dat, Var2 + Var3 ~ Var1, value.var="Freq") ele.sums.wide <- dcast(ele.sums, Var2 + Var3 ~ Var1, value.var="Freq") #rename columns names(ele.dat.wide) <- c("sitecode", "year", "poach_q5", "poach_q50", "poach_q95") names(ele.sums.wide) <- c("sitecode", "year", "pop_q5", "pop_q50", "pop_q95") #create list of datafraes to be merged df.list <- list(ele.dat.wide, ele.sums.wide, pop.dat, pike.stats) #merge all dataframes in the list in turn, keeping only records with matches #in the poaching rate dataset ele.all <- Reduce(function(x, y) merge(x, y, by = c("sitecode", "year"), all.x = TRUE, all.y = FALSE), df.list, accumulate = FALSE) #export combined dataframe as a csv write.table(ele.all, "data/processed/ele_data.csv", sep=",", row.names = FALSE)
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cachematrix.R
## source file contains two functions to handle the mechanims ## to calculate the inverse of a matrix in a very efficient way by caching ## the result if does not change ## object for working whit a cacheable inverse of a matrix makeCacheMatrix <- function(x = matrix()) { i <- NULL # inverse set <- function(y) { # set data and clear cache x <<- y i <<- NULL } get <- function() x # get data setinv <- function(inv) i <<- inv # set inverse getinv <- function() i # get inverse list(set = set, get = get, setinv = setinv, getinv = getinv) } ## Write a short comment describing this function cacheSolve <- function(x, ...) { ## Return a matrix that is the inverse of 'x' i <- x$getinv() if(!is.null(i)) { message("getting cached data") return(i) } data <- x$get() i <- solve(data) x$setinv(i) i }
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cran/WindCurves
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plot.fitcurve.Rd
% Generated by roxygen2: do not edit by hand % Please edit documentation in R/fitcurve_plot.R \name{plot.fitcurve} \alias{plot.fitcurve} \title{A function to plot the curves fitted with fitcurve() function} \usage{ \method{plot}{fitcurve}(x, ...) } \arguments{ \item{x}{is object returned by fitcurve() function} \item{\dots}{Additional graphical parameters given to plot function.} } \value{ Plot the curves fitted with fitcurve() function } \description{ A function to plot the curves fitted with fitcurve() function } \examples{ s <- pcurves$Speed p <- pcurves$`Nordex N90` da <- data.frame(s,p) x <- fitcurve(da) plot(x) }
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derrickwilliams/phymoo
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bedr.sort.region.Rd.R
library(bedr) ### Name: bedr.sort.region ### Title: sort a region file ### Aliases: bedr.sort.region ### Keywords: sort ### ** Examples if (check.binary("bedtools")) { index <- get.example.regions(); a <- index[[1]]; b <- bedr.sort.region(a); }
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StephenElston/DataScience410
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SQLandR.R
##-------------------------------------------- ## ## Using SQL from R ## ## Class: PCE Data Science Methods Class ## ##-------------------------------------------- getwd() #setwd('C:/Users/Steve/Dropbox/UW/DataSci350/Lecture 2') ##-----Getting/Storing Data----- # txt files ?read.table # csv files. Is wraper on read.table ?read.csv # Note the option stringsAsFactors = FALSE # web/html ?readLines ## Example: get a data frame read.auto <- function(path = '.'){ require(stringr) ## Function to read the csv file filePath <- file.path(path, 'Automobile price data _Raw_.csv') auto.price <- read.csv(filePath, header = TRUE, stringsAsFactors = FALSE) ## Coerce some character columns to numeric numcols <- c('price', 'bore', 'stroke', 'horsepower', 'peak.rpm') auto.price[, numcols] <- lapply(auto.price[, numcols], as.numeric) auto.price } ## Read the csv file ## Note that SQL databases don't like '.' characters in column names Auto.Price = read.auto(path = 'C:/Users/Steve/GIT/DataScience350/Lecture1') ## Read the csv file nams <- names(Auto.Price) names(Auto.Price) <- gsub('\\.', '_', nams) ## replace '.' with '_' ##-----SQLite Access----- ## Set up the connection to the database library(RSQLite) # Name of the db db.name = 'auto_db' # Create the connection db_conn = dbConnect(dbDriver("SQLite"), db_name) # Write dataframe to a table dbWriteTable(db_conn,"Auto_Price", Auto.Price, overwrite = TRUE) # Simple query database query = 'SELECT * FROM Auto_Price LIMIT 5;' test = dbSendQuery(db_conn, query) fetch(test) ## Query to find turbo cars. Note the excape required ## arround the '. query = 'SELECT * FROM Auto_Price WHERE aspiration = \'turbo\';' turbo.q = dbSendQuery(db_conn, query) turbo = fetch(high.milage.q) ## Query to find high milage cars query = 'SELECT * FROM Auto_Price WHERE city_mpg > 24;' high.milage.q = dbSendQuery(db_conn, query) high.milage = fetch(high.milage.q) ## make a plot of the high milage subset require(ggplot2) ggplot(high.milage, aes(city_mpg, price)) + geom_point(aes(size = 2, color = factor(fuel_type))) + ggtitle('Price vs. city mpg for high milage autos') # Disconnect, because we have clean R code. dbDisconnect(db_conn) ## Example: Use an existing database ## Create the database from the con = dbConnect(dbDriver("SQLite"), dbname = 'nyc_flights/nycflights13.sqlite') alltables = dbListTables(con) alltables ## Look at a few tables query = 'SELECT * FROM flights LIMIT 5;' test = dbSendQuery(con, query) fetch(test) query = 'SELECT * FROM airports LIMIT 5;' test = dbSendQuery(con, query) fetch(test) ##----Try/Catch Pattern ---- # # The tryCatch is used to create robust, produciton quality, R code # It should be used a lot more. This pattern shows how to use it: # # result = tryCatch({ # your code # }, # error=function(error_condition){ # message('Your error message here') # message(error_condition) # }, # warning=function(warning_condition){ # message('Your warning message here') # message(warning_condition) # }, # finally={ # Always execute these commands to cleanup. # } # ) # execute.query <- function(query, db = 'nyc_flights/nycflights13.sqlite'){ stopifnot(is.character(query)) if(!file.exists(db)) stop('ERROR, database not found') tryCatch({ con = dbConnect(dbDriver("SQLite"), dbname = 'nyc_flights/nycflights13.sqlite') message('Opened database connection') dbGetQuery(con, query) }, error = function(error_condition){ message('ERROR: The query has failed') message(error_condition) }, warning = function(warning_condition){ message('WARRNING: warrning conditon for query') message(error_condition) }, finally = { dbDisconnect(con) message('\nDatabase connection closed') } ) } ## Test the function query = 'SELECT * FROM flights LIMIT 5;' execute.query(query) ## A query that fails query = 'SELECT * FROM no_table LIMIT 5;' execute.query(query)
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06 - Predicting with unlabel dataset.R
# Doing prediction with the unlabel dataset require(randomForest) #Load Data unlabel data_unlabel <- read.csv(file.path(data_dir, "UnlabeledWiDS2021.csv")) View(data_unlabel) sum(is.na(data_unlabel)) # Predicting values ?predict predictions_unlabel <- predict(modelo, newdata = data_unlabel, type = 'prob', na.action=na.fail) # Result View(predictions_unlabel) #performance ?performance ?prediction
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pollutantmean.R
pollutantmean <- function(directory, pollutant, id=1:332) { data <- NULL for(idn in id) { datap <- read.csv(paste0(directory,"/",formatC(idn,width=3,flag="0"),".csv")) data <- rbind(data, datap) } mean(data[,pollutant], na.rm=TRUE) }
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impact_CNA_pipeline.R
library(data.table) library(dplyr) library(tidyr) master.ref <- fread('/ifs/work/bergerm1/zhengy1/RET_all/Sample_mapping/master_ref_080719.csv') cna.dir <- paste0('/ifs/work/bergerm1/zhengy1/RET_all/Analysis_files/cna_',format(Sys.time(),'%m%d%y')) # cna.dir <- paste0('/ifs/work/bergerm1/zhengy1/RET_all/Analysis_files/cna_',format(Sys.time(),'%m%d%y'),'_no_ret') dir.create(cna.dir) # manifests for tumor and normals ----------------------------------------- dir.create(paste0(cna.dir,'/manifests/')) write.table(master.ref[!Tumor_Sample_Barcode.plasma %in% c('DA-ret-041-pl-T02_IGO_05500_FF_27','C-YP5R0K-L001-d','DA-ret-004-pl-T01_IGO_05500_FF_18', 'C-02WK6K-L001-d','C-02WK6K-L002-d',' DA-ret-028-pl-T01_IGO_05500_FF_24', 'DA-ret-028-pl-T02_IGO_05500_FF_25','C-2UW6JP-L002-d','C-2UW6JP-L003-d'), .(BAM_path.plasma = gsub('-duplex','',gsub('duplex_bams','unfiltered_bams',BAM_path.plasma)), Sex = ifelse(Sex == 'M','Male','Female'))], paste0(cna.dir,'/manifests/tumor_manifest.txt'),sep = '\t',quote = F,row.names = F,col.names = F) # low depth buffy coat (not good because pool A vs B ratio is diff -------- # write.table(master.ref[!is.na(BAM_path.normal), # .(BAM_path.normal = gsub('-duplex','',gsub('duplex_bams','unfiltered_bams',BAM_path.normal)), # Sex = ifelse(Sex == 'M','Male','Female'))], # paste0(cna.dir,'/manifests/normal_manifest.txt'),sep = '\t',quote = F,row.names = F,col.names = F) # # # high depth normal (not perfect because no spike in ret probes) ---------- # write.table(data.frame(bam_paths = list.files('/ifs/work/bergerm1/brannona/ACCESS_M1.8/ACCESSv1-VAL-20190004/unfiltered',pattern = 'DONOR[0-9]+-T.*.bam',full.names = T),Sex = 'Male'), # paste0(cna.dir,'/manifests/normal_manifest.txt'),sep = '\t',quote = F,row.names = F,col.names = F) # # curated low/no tumor content plasma bams -------------------------------- write.table(master.ref[Tumor_Sample_Barcode.plasma %in% c('DA-ret-041-pl-T02_IGO_05500_FF_27','C-YP5R0K-L001-d','DA-ret-004-pl-T01_IGO_05500_FF_18', 'C-02WK6K-L001-d','C-02WK6K-L002-d',' DA-ret-028-pl-T01_IGO_05500_FF_24', 'DA-ret-028-pl-T02_IGO_05500_FF_25','C-2UW6JP-L002-d','C-2UW6JP-L003-d'), .(BAM_path.plasma = gsub('-duplex','',gsub('duplex_bams','unfiltered_bams',BAM_path.plasma)), Sex = ifelse(Sex == 'M','Male','Female'))], paste0(cna.dir,'/manifests/normal_manifest.txt'),sep = '\t',quote = F,row.names = F,col.names = F) # running pipeline -------------------------------------------------------- system(paste0( 'bsub -sla Berger -q sol -cwd ',cna.dir,' -J ','cna_',format(Sys.time(),'%m%d%y'),' -o %J.o -e %J.e', ' -We 24:00 -R "rusage[mem=8]" -M 8 -n 1 ', ' /home/ptashkir/.conda/envs/py27/bin/python /home/ptashkir/CNV_ACCESS/cBX_pipeline/scripts/cfdna_scna.py', ' -t ',cna.dir,'/manifests/tumor_manifest.txt', ' -n ',cna.dir,'/manifests/normal_manifest.txt', ' -tr 25 -b /ifs/work/bergerm1/zhengy1/RET_all/Original_files/MSK-ACCESS-v1_0.sorted.RET.bed', ' -g /ifs/depot/resources/dmp/data/pubdata/hg-fasta/VERSIONS/hg19/Homo_sapiens_assembly19.fasta', ' -r /opt/common/CentOS_6/R/R-3.2.0/bin/R -q sol -o ',cna.dir, ' -bsub /common/lsf/9.1/linux2.6-glibc2.3-x86_64/bin/bsub -id EDD_ret', ' -l /home/ptashkir/CNV_ACCESS/cBX_pipeline/scripts/loessnormalize_nomapq_cfdna.R', ' -cn /home/ptashkir/CNV_ACCESS/cBX_pipeline/scripts/copynumber_tm.batchdiff_cfdna.R', ' -ta /ifs/work/bergerm1/zhengy1/RET_all/Original_files/MSK-ACCESS-v1_0.sorted.RET.merged.txt' )) # bed.file <- fread('/ifs/work/bergerm1/zhengy1/RET/Original_file/MSK-ACCESS-v1_0-probe-A.sorted.RET.bed') # write.table(bed.file[,!c('V4'),with = F], # '/ifs/work/bergerm1/zhengy1/RET_all/Original_files/MSK-ACCESS-v1_0-probe-A.sorted.RET.bed', # sep = '\t',quote = F,row.names = F,col.names = F) # system('bedtools nuc -fi /ifs/depot/resources/dmp/data/pubdata/hg-fasta/VERSIONS/hg19/Homo_sapiens_assembly19.fasta -bed /ifs/work/bergerm1/zhengy1/RET_all/Original_files/MSK-ACCESS-v1_0-probe-A.sorted.RET.bed > /ifs/work/bergerm1/zhengy1/RET_all/Original_files/MSK-ACCESS-v1_0-probe-A.sorted.RET.txt') # # using non ret bed file -------------------------------------------------- # # system(paste0( # 'bsub -sla Berger -q sol -cwd ',cna.dir,' -J ','cna_',format(Sys.time(),'%m%d%y'),'_no_ret -o %J.o -e %J.e', # ' -We 24:00 -R "rusage[mem=8]" -M 8 -n 1 ', # ' /home/ptashkir/.conda/envs/py27/bin/python /home/ptashkir/CNV_ACCESS/cBX_pipeline/scripts/cfdna_scna.py', # ' -t ',cna.dir,'/manifests/tumor_manifest.txt', # ' -n ',cna.dir,'/manifests/normal_manifest.txt', # ' -tr 25 -b /ifs/work/bergerm1/zhengy1/RET_all/Original_files/MSK-ACCESS-v1_0.sorted.woRET.bed', # ' -g /ifs/depot/resources/dmp/data/pubdata/hg-fasta/VERSIONS/hg19/Homo_sapiens_assembly19.fasta', # ' -r /opt/common/CentOS_6/R/R-3.2.0/bin/R -q sol -o ',cna.dir, # ' -bsub /common/lsf/9.1/linux2.6-glibc2.3-x86_64/bin/bsub -id EDD_ret', # ' -l /home/ptashkir/CNV_ACCESS/cBX_pipeline/scripts/loessnormalize_nomapq_cfdna.R', # ' -cn /home/ptashkir/CNV_ACCESS/cBX_pipeline/scripts/copynumber_tm.batchdiff_cfdna.R', # ' -ta /ifs/work/bergerm1/zhengy1/RET_all/Original_files/MSK-ACCESS-v1_0.sorted.woRET.merged.txt' # )) #
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#' @importFrom stringr str_glue #' @noRd .onAttach <- function(libname, pkgname) { packageStartupMessage( cli::rule(right = "Legal", line = 2, col = crayon::magenta), "\n", stringr::str_glue( " SomaDataIO\u2122 Copyright \u00A9 2021 SomaLogic, Inc. Permission is hereby granted, free of charge, to any person obtaining a copy of the SomaDataIO software and associated documentation files (the \"Software\"), to deal in the Software without restriction, including without limitation the rights to use, copy, modify, merge, publish, distribute, sublicense, and/or sell copies of the Software, and to permit persons to whom the Software is furnished to do so, subject to the following conditions outlined below. Further, SomaDataIO and SomaLogic are trademarks owned by SomaLogic, Inc. No license is hereby granted to these trademarks other than for purposes of identifying the origin or source of the Software. The above copyright notice and this permission notice shall be included in all copies or substantial portions of the Software. THE SOFTWARE IS PROVIDED \"AS IS\", WITHOUT WARRANTY OF ANY KIND, EXPRESS OR IMPLIED, INCLUDING BUT NOT LIMITED TO THE WARRANTIES OF MERCHANTABILITY, FITNESS FOR A PARTICULAR PURPOSE AND NONINFRINGEMENT. IN NO EVENT SHALL THE AUTHORS OR COPYRIGHT HOLDER(S) BE LIABLE FOR ANY CLAIM, DAMAGES, WHETHER DIRECT OR INDIRECT, OR OTHER LIABILITY, WHETHER IN AN ACTION OF CONTRACT, TORT OR OTHERWISE, ARISING FROM, OUT OF OR IN CONNECTION WITH THE SOFTWARE OR THE USE OR OTHER DEALINGS IN THE SOFTWARE. " ), "\n", cli::rule(line = 2, col = crayon::magenta) ) }
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temp_risks.R
#' temp_risks #' #' Compute the number of days per each location over the span of the data set where there is risk of heat stroke, comfortable weather, and freezing at 3 PM. #' @param data data frame with columns Date, Location, Temp3pm #' @author Gage Clawson #' @example temp_risks(data) #' @return Returns a table containing, #' \describe{ #' \item{Location}{Location in Australia} #' \item{heat_stroke_n}{Number of days for a particular location where there has been a risk of heat stroke} #' \item{comfort_n}{Number of days for a particular location where the weather has been comfortable} #' \item{freezing_n}{Number of days for a particular location where there has been a risk of freezing} #' } temp_risks = function(data){ clim_df <- data %>% dplyr::mutate(year = lubridate::year(Date), month = lubridate::month(Date), day = lubridate::day(Date)) %>% mutate(risk = case_when( Temp3pm >40 ~ "heat stroke", Temp3pm < 40 & Temp3pm >= 0 ~ "comfortable", Temp3pm < 0 ~ "freezing" ) ) risk_df <- clim_df %>% group_by(Location) %>% summarise(heat_stroke_n = sum(risk == "heat stroke", na.rm = TRUE), comfortable_n = sum(risk == "comfortable", na.rm = TRUE), freezing_n = sum(risk == "freezing", na.rm = TRUE)) %>% ungroup() return(list(table = risk_df) ) }
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# What: LCS in R # Changes GPL(C) moshahmed@gmail.com # See c:/doc3/algo/malgo/dynamic/lcs/lcs.htm # See lcs3.R 2016-10-15 lcs4p <- function(B, X, i, j) { # cat("lcs4p",i,j,"\n") if ( i==0 || j==0 ) return() if (B[i+1, j+1] == '/') { lcs4p(B, X, i-1, j-1) print (X[i]) } else if (B[i+1, j+1] == '^') { lcs4p(B, X, i-1, j) } else { # '<' lcs4p(B, X, i, j-1) } } lcs4 <- function(Xm, Yn) { X <- unlist(strsplit(Xm,split="")) Y <- unlist(strsplit(Yn,split="")) m <- nchar(Xm) n <- nchar(Yn) if (m<1 || n < 1) return(0) L <- matrix(0, nrow=m+2, ncol=n+2) B <- L for (i in 1:m+1) { for (j in 1:n+1) { if (i == 1 || j == 1) { L[i,j] = 0 } else if (X[i-1] == Y[j-1]) { L[i, j] = L[i-1, j-1] + 1 B[i, j] = '/' } else if (L[i-1,j] >= L[i,j-1]) { L[i, j] = L[i-1, j] B[i, j] = '^' } else { L[i, j] = L[i,j-1] B[i, j] = '<' } } } lcs4p(B, X, m, n) return(list("L"=L,"B"=B)) } Xm <- "ABABAD" Yn <- "ACAADD" ans <- lcs4(Xm,Yn)
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Hospital.R
#R Programming #Assignment for Week 4 #Author: Yige #Date: Nov.6, 2018 rm(list=ls()) setwd("~/Desktop/Data Science @Coursera/Assignments/2_3") #1 plot the 30-day mortality rates for heart attack outcome <- read.csv("outcome-of-care-measures.csv",colClasses = "character") names(outcome) ncol(outcome) nrow(outcome) deathrates <- as.numeric(outcome[,11]) hist(deathrates) #2 function to find best hosipital in a state best <- function(state,outcome){ setwd("~/Desktop/Data Science @Coursera/Assignments/2_3") dat <- read.csv("outcome-of-care-measures.csv",colClasses = "character") dat <- dat[,c(1:10,11,17,23)] #dat[,c(11,12,13)] <- as.numeric(dat[,c(11,12,13)]) #colnames(dat)[c(11,12,13)] <- c("heart attack","heart failure","pneumonia") #subset hospital info & 30 day death rate of "heart attack","heart failure","pneumonia" if(!state %in% dat$State){ stop("invalid state") } else if(!outcome %in% c("heart attack","heart failure","pneumonia")){ stop("invalid outcome") } switch(outcome,'heart attack'={col =11},'heart failure'={col=12}, 'pneumonia'={col=13}) dat[, col] = as.numeric(dat[, col]) hop_state <- dat[dat$State == state,c(2,col)] hop_state <- na.omit(hop_state) hop_state <- hop_state[order(hop_state[,2],hop_state[,1]),] hop_state[1,1] #hop_state[which.min(hop_state[,2]), 1] } #TEST best("TX", "heart attack") best("TX", "heart failure") best("MD", "heart attack") best("MD", "pneumonia") best("BB", "heart attack") best("NY", "hear attack") #3 Ranking hospital by outcome in a state rankhospital <- function(state, outcome, num = "best"){ setwd("~/Desktop/Data Science @Coursera/Assignments/2_3") dat <- read.csv("outcome-of-care-measures.csv",colClasses = "character") dat <- dat[,c(1:10,11,17,23)] if(!state %in% dat$State){ stop("invalid state") } else if(!outcome %in% c("heart attack","heart failure","pneumonia")){ stop("invalid outcome") } switch(outcome,'heart attack'={col =11},'heart failure'={col=12}, 'pneumonia'={col=13}) dat[, col] = as.numeric(dat[, col]) dat_state <- dat[dat$State == state,c(2,col)] dat_state <- na.omit(dat_state) nhospital <- nrow(dat_state) switch(num,'best'={num=1},'worst'={num=nhospital}) if(num > nhospital){ return(NA) } dat_state <- dat_state[order(dat_state[,2],dat_state[,1]),] dat_state[num,1] } #TEST rankhospital("TX", "heart failure", 4) rankhospital("MD", "heart attack", "worst") rankhospital("MN", "heart attack", 5000) #4 Ranking hospital in all states rankall <- function(outcome,num){ setwd("~/Desktop/Data Science @Coursera/Assignments/2_3") dat <- read.csv("outcome-of-care-measures.csv",colClasses = "character") switch(outcome,'heart attack'={col =11},'heart failure'={col=17}, 'pneumonia'={col=23},stop("invalid outcome")) dat[, col] = as.numeric(dat[, col]) dat <- dat[,c(2,7,col)] #name,state,death rate dat <- na.omit(dat) states=unique(dat$State) rankstate <- function(state){ dat_state <- dat[dat$State == state,] nhospital <- nrow(dat_state) switch(num,'best'={num=1},'worst'={num=nhospital}) if(num > nhospital){ return(NA) } dat_order <- order(dat_state[,3], dat_state[,1]) #order by death rate/name name <- dat_state[dat_order,][num,1] c(name,state) } result = do.call(rbind, lapply(states, rankstate)) result = result[order(result[, 2]), ] rownames(result) = result[, 2] colnames(result) = c("hospital", "state") data.frame(result) } #TEST head(rankall("heart attack", 20), 10) tail(rankall("pneumonia", "worst"), 3) tail(rankall("heart failure"), 10)
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test-tri-graticule.R
test_that("tri_graticule works", { mesh <- tri_graticule() %>% expect_s3_class( "mesh3d") expect_s3_class(tri_graticule(xlim = c(10, 20)), "mesh3d") expect_s3_class(tri_graticule(ylim = c(-80, -70)), "mesh3d") expect_s3_class(tri_graticule(xlim = c(100, 150), ylim = c(-80, -70)), "mesh3d") expect_s3_class(tri_graticule(hull = TRUE), "mesh3d") expect_s3_class(tri_graticule(xlim = c(10, 20),hull = TRUE), "mesh3d") expect_s3_class(tri_graticule(ylim = c(-80, -70),hull = TRUE), "mesh3d") expect_s3_class(tri_graticule(xlim = c(100, 150), ylim = c(-80, -70),hull = TRUE), "mesh3d") expect_s3_class(tri_graticule(hull = TRUE, sub = 1), "mesh3d") expect_s3_class(tri_graticule(ylim = c(-80, -70), sub = 2, hull = TRUE), "mesh3d") mesh2 <- tri_graticule(n = 15) %>% expect_s3_class( "mesh3d") expect_true(ncol(mesh$vb) < ncol(mesh2$vb)) expect_s3_class(tri_graticule(n = 20, ylim = c(-80, -70), sub = 2, hull = TRUE), "mesh3d") }) test_that("quad_graticule works", { mesh <- quad_graticule() %>% expect_s3_class( "mesh3d") expect_s3_class(quad_graticule(xlim = c(10, 20)), "mesh3d") expect_s3_class(quad_graticule(ylim = c(-80, -70)), "mesh3d") expect_s3_class(quad_graticule(xlim = c(100, 150), ylim = c(-80, -70)), "mesh3d") expect_warning(expect_s3_class(quad_graticule(hull = TRUE), "mesh3d")) expect_warning(expect_s3_class(quad_graticule(xlim = c(10, 20),hull = TRUE), "mesh3d")) expect_warning(expect_s3_class(quad_graticule(ylim = c(-80, -70),hull = TRUE), "mesh3d")) expect_warning(expect_s3_class(quad_graticule(xlim = c(100, 150), ylim = c(-80, -70),hull = TRUE), "mesh3d")) expect_warning(expect_s3_class(quad_graticule(hull = TRUE, sub = 1), "mesh3d")) expect_warning(expect_s3_class(quad_graticule(ylim = c(-80, -70), sub = 2, hull = TRUE), "mesh3d")) mesh2 <- quad_graticule(n = 15) %>% expect_s3_class( "mesh3d") expect_true(ncol(mesh$vb) < ncol(mesh2$vb)) expect_warning(expect_s3_class(quad_graticule(n = 20, ylim = c(-80, -70), sub = 2, hull = TRUE), "mesh3d")) }) test_that("hull_graticule works", { mesh <- hull_graticule() %>% expect_s3_class( "mesh3d") expect_warning(hull_graticule(xlim = c(10, 20))) expect_warning(hull_graticule(ylim = c(-80, -70))) expect_warning(hull_graticule(xlim = c(100, 150), ylim = c(-80, -70))) expect_warning(hull_graticule(hull = TRUE)) expect_warning(hull_graticule(xlim = c(10, 20),hull = TRUE)) expect_warning(hull_graticule(ylim = c(-80, -70),hull = TRUE)) expect_warning(hull_graticule(xlim = c(100, 150), ylim = c(-80, -70),hull = TRUE)) expect_warning(expect_s3_class(hull_graticule(hull = TRUE, sub = 1), "mesh3d")) expect_warning(expect_s3_class(hull_graticule(ylim = c(-80, -70), sub = 2, hull = TRUE), "mesh3d")) mesh2 <- hull_graticule(n_coords = 15) %>% expect_s3_class( "mesh3d") expect_true(ncol(mesh$vb) > ncol(mesh2$vb)) expect_warning(expect_s3_class(hull_graticule(n_coords = 20, ylim = c(-80, -70), sub = 2, hull = TRUE), "mesh3d")) expect_warning(hull_graticule(n_coords = 10, coords = geosphere::randomCoordinates(100))) })
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#' @importFrom htmltools a #' @importFrom htmltools css #' @importFrom htmltools div #' @importFrom htmltools img #' @importFrom htmltools tags #' @importFrom htmltools tagList #' @importFrom rlang list2 #' @keywords internal "_PACKAGE"
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Temporal_ordering_of_TF_programs.R
library(Seurat) library(Signac) library(monocle3) library(SeuratWrappers) library(ggplot2) library(patchwork) library(reshape2) library(cicero) library(gplots) library(dplyr) library(plyr) blank_theme <- theme_minimal()+ theme( panel.border = element_blank(), panel.grid=element_blank(), axis.ticks = element_blank(), plot.title=element_text(size=14, face="bold"), panel.background = element_rect(fill = "white", colour = "grey50") ) ################ temporal order of transcriptional programs, Figure 3 ###use alpha cell lineage as an example load("/oasis/tscc/scratch/hazhu/share/upload/diff_atac_chromvar.rds") diff_ds_sub<-subset(diff_ds,subset=anno%in%c("diff_ENP1","diff_ENPalpha","diff_alpha")) col_dna<-c("diff_ENP1"="thistle1", "diff_ENPalpha"="mediumorchid2","diff_alpha"="purple2") dna_all_cds <- as.cell_data_set(diff_ds_sub) dna_all_cds <- cluster_cells(cds = dna_all_cds, reduction_method = "UMAP") dna_all_cds <- learn_graph(dna_all_cds, use_partition = F,close_loop = F, learn_graph_control=list(ncenter=500,minimal_branch_len=10)) dna_all_cds <- order_cells(dna_all_cds, reduction_method = "UMAP") ######manually select alpha cell lineage cds_subset<-choose_graph_segments(dna_all_cds) cds_subset<-dna_all_cds[,colnames(cds_subset)] p2<-plot_cells(dna_all_cds, color_cells_by = "anno", label_groups_by_cluster=FALSE, trajectory_graph_color = "grey0", trajectory_graph_segment_size = 1.5, group_label_size = 5, label_cell_groups = FALSE, label_leaves=FALSE, label_branch_points=FALSE, label_roots = FALSE)+ scale_color_manual(values =col_dna )+NoLegend() alpha.pseudotime.mtx<-cds_subset@assays@data$counts alpha.pseudotime.mtx<-alpha.pseudotime.mtx[rownames(alpha.pseudotime.mtx)%in%rownames(ccre.umap)[ccre.umap$module%in%c("ENP1","ENP_alpha","SC_alpha")],] alpha.pseudotime.mtx<-as.data.frame(t(alpha.pseudotime.mtx)) alpha.pseudotime.mtx<-cbind(alpha.pseudotime.mtx,"pseudotime"=pseudotime(cds_subset)) alpha.pseudotime.mtx<-alpha.pseudotime.mtx[order(alpha.pseudotime.mtx$pseudotime),] #####cCRE pseudotime alpha.ccre.pseudotime<-matrix(0,0,2) for (i in colnames(alpha.pseudotime.mtx[,-5961])) { temp.pseudotime<-alpha.pseudotime.mtx$pseudotime[alpha.pseudotime.mtx[,i]==1] pseodotime.sumit<-density(temp.pseudotime)$x[which.max(density(temp.pseudotime)$y)] temp<-c(i,pseodotime.sumit) alpha.ccre.pseudotime<-rbind(alpha.ccre.pseudotime,temp) } rownames(alpha.ccre.pseudotime)<-colnames(alpha.pseudotime.mtx[,-5961]) alpha.pseudotime.umap<-ccre.umap[rownames(alpha.ccre.pseudotime),] alpha.pseudotime.umap$pseudotime<-as.numeric(alpha.ccre.pseudotime[,2]) ############Plot cCRE pseudotime on cCRE UMAP, fupplementary figure 3j ccre.umap<-read.csv("/oasis/tscc/scratch/hazhu/share/upload/sc.islet.diff.ccre.umap.csv",row.names = 1) p.umap.pseudotime<-ggplot(ccre.umap,aes(x=UMAP1,y=UMAP2))+geom_point(size=0.01,colour = "grey80")+ geom_point(data = alpha.pseudotime.umap,aes(x=UMAP1,y=UMAP2,color=pseudotime),size=0.01)+ scale_colour_viridis_c(option = "inferno")+ blank_theme ############construct RNA pseudotime diff_rna<-readRDS("/oasis/tscc/scratch/hazhu/share/upload/diff_rna.rds") rna_all_cds <- as.cell_data_set(diff_rna) rna_all_cds <- cluster_cells(cds = rna_all_cds, reduction_method = "UMAP") rna_subset<-rna_all_cds[,colnames(cds_subset)] rm(rna_all_cds) rm(diff_rna) #######look for alpha genes and alpha TFs alpha.peaks<-colnames(alpha.pseudotime.mtx[,1:(ncol(alpha.pseudotime.mtx)-1)]) alpha.genes<-sig_target_gene_predicton[sig_target_gene_predicton$peak_id%in%alpha.peaks,"gene"] ############include master TFs found in Figure 2d master.tfs<-read.csv("/oasis/tscc/scratch/hazhu/share/upload/sc.islet.diff.module.specific.tf.sig.csv",row.names = 1) alpha.master.TFs<-master.tfs[master.tfs$module%in%c("ENP1","ENP_alpha","SC_alpha"),"TF"] alpha.genes<-unique(c(alpha.genes,alpha.master.TFs)) alpha.rna.pseudotime.mtx<-rna_subset@assays@data$logcounts alpha.rna.pseudotime.mtx<-alpha.rna.pseudotime.mtx[rownames(alpha.rna.pseudotime.mtx)%in%alpha.genes,] alpha.rna.pseudotime.mtx<-as.data.frame(t(alpha.rna.pseudotime.mtx)) alpha.rna.pseudotime.mtx<-cbind(alpha.rna.pseudotime.mtx,"pseudotime"=pseudotime(cds_subset)) alpha.rna.pseudotime.mtx<-alpha.rna.pseudotime.mtx[order(alpha.rna.pseudotime.mtx$pseudotime),] alpha.rna.pseudotime<-matrix(0,0,2) for (i in colnames(alpha.rna.pseudotime.mtx[,1:(ncol(alpha.rna.pseudotime.mtx)-1)])) { temp.fit<-smooth.spline(alpha.rna.pseudotime.mtx$pseudotime,alpha.rna.pseudotime.mtx[,colnames(alpha.rna.pseudotime.mtx)==i]) temp.pseudotime<-temp.fit$x[which.max(temp.fit$y)] temp<-c(i,temp.pseudotime) alpha.rna.pseudotime<-rbind(alpha.rna.pseudotime,temp) } rownames(alpha.rna.pseudotime)<-colnames(alpha.rna.pseudotime.mtx[,1:(ncol(alpha.rna.pseudotime.mtx)-1)]) colnames(alpha.rna.pseudotime)<-c("names","pseudotime") alpha.rna.pseudotime<-as.data.frame(alpha.rna.pseudotime) alpha.rna.pseudotime$pseudotime<-as.numeric(alpha.rna.pseudotime$pseudotime) alpha.rna.pseudotime$module<-NA alpha.rna.pseudotime$origin<-rep("RNA",nrow(alpha.rna.pseudotime)) colnames(alpha.ccre.pseudotime)<-c("names","pseudotime") alpha.ccre.pseudotime<-as.data.frame(alpha.ccre.pseudotime) alpha.ccre.pseudotime$pseudotime<-as.numeric(alpha.ccre.pseudotime$pseudotime) alpha.ccre.pseudotime$module<-alpha.pseudotime.umap$module alpha.ccre.pseudotime$origin<-rep("cCRE",nrow(alpha.ccre.pseudotime)) alpha.all.pseudotime<-rbind(alpha.rna.pseudotime,alpha.ccre.pseudotime) alpha.all.pseudotime$axis<-rep(1,nrow(alpha.all.pseudotime)) alpha.all.pseudotime<-alpha.all.pseudotime[order(alpha.all.pseudotime$pseudotime),] alpha.all.pseudotime$rank<-c(1:nrow(alpha.all.pseudotime)) #######plot TF, TF target cCREs and TF target genes TF.gene<-"ZNF414" TF.bs<-C_TF[C_TF$gene==TF.gene & C_TF$stat>0.5,] TF.bs<-TF.bs[TF.bs$peak_ID%in%rownames(alpha.all.pseudotime),] alpha.all.pseudotime$scc<-rep(0,nrow(alpha.all.pseudotime)) for (i in TF.bs$peak_ID) { alpha.all.pseudotime$scc[rownames(alpha.all.pseudotime)==i]<-TF.bs[TF.bs$peak_ID==i,"stat"] } pseudotime.TF.bs<-alpha.all.pseudotime[!alpha.all.pseudotime$scc==0,] tf.exp<-alpha.all.pseudotime[TF.gene,] ccre.target<-sig_target_gene_predicton[sig_target_gene_predicton$peak_id%in%rownames(pseudotime.TF.bs),"gene"] ccre.target<-unique(ccre.target) ccre.target.pseudotime<-alpha.all.pseudotime[ccre.target,] p.pseudotime.2<-ggplot(alpha.all.pseudotime,aes(x=pseudotime,y=origin))+geom_point(size=0.5,colour="grey85")+ geom_point(data = ccre.target.pseudotime,aes(x=pseudotime,y=origin),size=0.5,colour="tan3")+ geom_point(data =tf.exp, aes(x=pseudotime,y=origin),size=2, colour="forestgreen")+ geom_point(data=pseudotime.TF.bs,aes(x=pseudotime,y=origin,color=scc),size=0.5)+ scale_color_gradientn(colours = c("grey90","Tomato1","red4"))+ blank_theme
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% Generated by roxygen2: do not edit by hand % Please edit documentation in R/torro.R \docType{data} \name{shifts} \alias{shifts} \title{Shifts} \format{tibble} \usage{ data(shifts) } \description{ Tibble with the following columns } \details{ \itemize{ \item shift_name name of the shift \item shift_T_start starting time of the shift \item win_expanding logical, TRUE for expanding/growing window, FALSE for moving \item win_start_lenght length of the first window \item n_shifts number of window shifts } See also toy version, \code{shifts_toy}. } \keyword{datasets}
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BiocManager::install('org.Mm.eg.db') BiocManager::install('org.Hs.eg.db') install.packages ("xml2") BiocManager::install("biomaRt") install.packages("sqldf") library (org.Mm.eg.db) library (org.Hs.eg.db) library(biomaRt) library (WGCNA) library(sqldf) load (file = "2-gtex-InfoWithModule.RData") annot = read.csv ("GeneAnotation.csv",sep=",") annot probes = names (datExpr) probes probes2annot = match (probes,annot$GeneName) probes2annot ensembl.genes = annot$id [probes2annot] # ensembl.genes <- readLines ('ensemble_id.csv') ensembl.genes ensembl.genes <- gsub('.{0,2}$', '', ensembl.genes) ensembl.genes <- gsub("[^0-9A-Za-z///' ]","#" , ensembl.genes ,ignore.case = TRUE) ensembl.genes <- gsub("#","", ensembl.genes ,ignore.case = TRUE) values <- as.vector (ensembl.genes) values # values [is.na(values)] <- "ENSG00000270040" # values # mart <- useDataset("hsapiens_gene_ensembl", useMart("ensembl")) mart = useMart("ensembl", dataset = "hsapiens_gene_ensembl", host="uswest.ensembl.org") entrezgene = getBM(attributes=c('ensembl_gene_id', 'entrezgene'), filters = 'ensembl_gene_id', values = values, mart = mart) names(entrezgene)[2]<-"genenum" entrezgene entrezgene<- entrezgene[!duplicated(entrezgene[1]), ] entrezgene value_dataframe = data.frame (values) value_dataframe names(value_dataframe)[1]<-"ensembl_gene_id" value_dataframe # write.csv (entrezgene,"entrezgene.xls") # write.csv (value_dataframe,"value_dataframe.xls") combined_df <- sqldf("Select f.*, most.genenum from value_dataframe f left JOIN (select distinct ensembl_gene_id,genenum from entrezgene) as most on f.ensembl_gene_id = most.ensembl_gene_id ") combined_df # allLLIDs = as.data.frame.matrix(entrezgene) allLLIDs <- as.vector (combined_df[[2]]) allLLIDs GOenr = GOenrichmentAnalysis (moduleColors,allLLIDs,organism="human",nBestP = 10) tab = GOenr$bestPTerms [[4]]$enrichment write.table (tab,"0-GOenrichementtable.csv",sep=",",quote= TRUE,row.names=FALSE)
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plotExons-old.R
source("~/Desktop/research/notes/R_code/getExons.R") source("~/Desktop/research/notes/R_code/getExonsIntrons.R") source("~/Desktop/research/notes/R_code/parseExonTable.R") plotExons <- function (egid,sp) { exons <- getExons(egid,sp) if (!is.null(exons)) { sap <- apply(exons[seq(1,nrow(exons),by=2),], 1, function (x) { lines(c(x[1],x[2]),c(.01,.01),type="l",lwd=5) } ) sap <- apply(exons[seq(2,nrow(exons),by=2),], 1, function (x) { lines(c(x[1],x[2]),c(-0.01,-.01),type="l",lwd=5) } ) } else { cat("No exon or sts information available. Bummer.\n") } } plot.Exons <- function (exons) { if (!is.null(exons)) { sap <- apply(exons[seq(1,nrow(exons),by=2),], 1, function (x) { lines(c(x[1],x[2]),c(.01,.01),type="l",lwd=5) } ) sap <- apply(exons[seq(2,nrow(exons),by=2),], 1, function (x) { lines(c(x[1],x[2]),c(-0.01,-.01),type="l",lwd=5) } ) } else { cat("No exon or sts information available. Bummer.\n") } } plotExonsIntrons <- function (egid,sp) { exons <- getExonTable(egid,sp) if (!is.null(exons)) { for (e in 1:nrow(exons)) { lines(exons[e,],c(0,0),type="l",lwd=5) } } else { cat("No exon or sts information available. Bummer.\n") } }
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UScpiqs.Rd
% Generated by roxygen2: do not edit by hand % Please edit documentation in R/midasr-package.R \docType{data} \name{UScpiqs} \alias{UScpiqs} \title{US quartely seasonaly adjusted consumer price index} \format{A \code{\link{data.frame}} object.} \source{ \href{http://www.bea.gov/national/xls/gdplev.xls}{FRED} } \description{ US quarterly CPI from 1960Q1 to 2017Q3s } \keyword{datasets}
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logisticRidge.Rd.R
library(ridge) ### Name: logisticRidge ### Title: Logistic ridge regression. ### Aliases: logisticRidge coef.ridgeLogistic plot.ridgeLogistic ### predict.ridgeLogistic print.ridgeLogistic summary.ridgeLogistic ### print.summary.ridgeLogistic ### ** Examples data(GenBin) mod <- logisticRidge(Phenotypes ~ ., data = as.data.frame(GenBin)) summary(mod)
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% Generated by roxygen2: do not edit by hand % Please edit documentation in R/dim_red.R \name{run_umap} \alias{run_umap} \title{Runs UMAP on an scRNA-seq PCA matrix.} \usage{ run_umap(mat, n_pcs = NULL) } \arguments{ \item{mat}{A cells x PCs matrix.} \item{n_pcs}{The number of PCs to include.} } \value{ A cells x 2 matrix holding the UMAP coordinates. } \description{ Runs the umap version of UMAP on a cells x PCs matrix from an scRNA-seq dataset. }
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% Generated by roxygen2: do not edit by hand % Please edit documentation in R/methods.R \name{setBibliography,easyreporting-method} \alias{setBibliography,easyreporting-method} \title{setBibliography} \usage{ \S4method{setBibliography}{easyreporting}(object, bibfile = NULL) } \arguments{ \item{object}{an easyreporting class object} \item{bibfile}{a string with the name of the bib file} } \value{ none } \description{ add a bibfile name to the object that will be reflected into the report as a bibliography section } \examples{ \dontrun{ # TBD } } \keyword{internal}
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% Generated by roxygen2: do not edit by hand % Please edit documentation in R/GetLines.R \name{GetLines} \alias{GetLines} \title{Betting lines.} \usage{ GetLines(sport = "NBA", year, type = "Both") } \arguments{ \item{sport}{either "NBA", "NFL", or "WNBA"} \item{year}{season (e.g. 2008 for 2007-08 season)} \item{type}{either "Regular Season" or "Playoffs" or "Both"} } \value{ data frame with schedule and line for each game in that season } \description{ Betting lines. } \examples{ GetLines("NBA", 2014, "playoffs") } \keyword{betting} \keyword{line,} \keyword{odds,} \keyword{schedule,}
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comext_data.r
library(tidyverse) #------ # CANADIAN EXPORTS (FOB) canexport <- read.csv(file = "csv/canexport.csv", header = TRUE, colClasses = c(rep("character",3),"numeric",rep("character",2),"numeric"), sep = ";") canexport <- as.tibble(canexport) canexport$DECLARANT <- "CAN" # rename FLOW canexport <- canexport %>% select(-FLOW) canexport$FLOW <- "EXPORTS" # calculate average over three calendar years canexport_avg <- canexport %>% group_by(DECLARANT, PARTNER, PRODUCT, FLOW, INDICATORS) %>% summarize(avg=mean(INDICATOR_VALUE, na.rm=FALSE)) # rename header for better merging with import data colnames(canexport_avg) <- c("reporter","partner","hs6","flow","indicator","avg") # ----- # CANADIAN IMPORTS (CIF) canimport <- read.csv(file = "csv/canimport.csv", header = TRUE, colClasses = c(rep("character",3),"numeric",rep("character",2),"numeric"), sep = ";") canimport <- as.tibble(canimport) canimport$DECLARANT <- "CAN" # rename FLOW canimport <- canimport %>% select(-FLOW) canimport$FLOW <- "IMPORTS" # rename to ROW and to EU_28 canimport[canimport$PARTNER=="otherthanEUAgg",]$PARTNER <- "ROW" canimport[canimport$PARTNER=="myEU",]$PARTNER <- "EU_28" # calculate average over three calendar years canimport_avg <- canimport %>% group_by(DECLARANT, PARTNER, PRODUCT, FLOW, INDICATORS) %>% summarize(avg=mean(INDICATOR_VALUE, na.rm=FALSE)) # rename header for better merging with export data colnames(canimport_avg) <- c("reporter","partner","hs6","flow","indicator","avg") # ------ # EU-ROW trade data (both CIB and FOB) eurow <- read.csv(file = "csv/eu_row.csv", header = TRUE, colClasses = c(rep("character",3),"numeric",rep("character",3),"numeric"), sep = ";") eurow <- as.tibble(eurow) eurow <- eurow %>% select(-Statistical.Procedure) # rename indicators eurow <- eurow %>% mutate_if(is.character, str_replace_all, pattern = "CUM_QUANTITY_TON", replacement = "QUANTITY") eurow <- eurow %>% mutate_if(is.character, str_replace_all, pattern = "CUM_VALUE_1000ECU", replacement = "VALUE_1000EURO") # separate import and export flows (note that the declarant is always the EU) euimp <- eurow %>% filter(Flow == 1) euexp <- eurow %>% filter(Flow == 2) # rename FLOW euimp <- euimp %>% select(-Flow) euimp$Flow <- "IMPORTS" euexp <- euexp %>% select(-Flow) euexp$Flow <- "EXPORTS" # rename ROW and EU euimp$Partner.Country <- "ROW" euexp$Partner.Country <- "ROW" euimp$DECLARANT <- "EU_28" euexp$DECLARANT <- "EU_28" # calculate average euimp_avg <- euimp %>% group_by(DECLARANT, Partner.Country, PRODUCT_NC, Flow, INDICATORS) %>% summarize(avg=mean(INDICATOR_VALUE, na.rm=FALSE)) euexp_avg <- euexp %>% group_by(DECLARANT, Partner.Country, PRODUCT_NC, Flow, INDICATORS) %>% summarize(avg=mean(INDICATOR_VALUE, na.rm=FALSE)) # rename for easier merge colnames(euimp_avg) <- c("reporter", "partner", "hs6", "flow", "indicator", "avg") colnames(euexp_avg) <- c("reporter", "partner", "hs6", "flow", "indicator", "avg") #----- # EU imports and exports to CAN euflows <- read.csv(file = "csv/eu_cif_fob.csv", header = TRUE, colClasses = c(rep("character",3),"numeric",rep("character",3),"numeric"), sep = ";") euflows <- as.tibble(euflows) euflows <- euflows %>% select(-Statistical.Procedure) # rename indicators euflows <- euflows %>% mutate_if(is.character, str_replace_all, pattern = "CUM_QUANTITY_TON", replacement = "QUANTITY") euflows <- euflows %>% mutate_if(is.character, str_replace_all, pattern = "CUM_VALUE_1000ECU", replacement = "VALUE_1000EURO") # separate import and export flows # Note that the declarant is always the EU # and the partner is CANADA euflows <- euflows %>% filter(Partner.Country == "0404") euflows$Partner.Country <- "CAN" euflows$DECLARANT <- "EU_28" euflows[euflows$Flow == "1",]$Flow <- "IMPORTS" euflows[euflows$Flow == "2",]$Flow <- "EXPORTS" euflows_avg <- euflows %>% group_by(DECLARANT, Partner.Country, PRODUCT_NC, Flow, INDICATORS) %>% summarize(avg=mean(INDICATOR_VALUE, na.rm=FALSE)) colnames(euflows_avg) <- c("reporter", "partner", "hs6", "flow", "indicator", "avg") #---- # do the merge and save to disk trade_data <- canexport_avg %>% full_join(canimport_avg) %>% full_join(euimp_avg) %>% full_join(euexp_avg) %>% full_join(euflows_avg) save(trade_data, file = "data/trade_data.RData")
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#' Install conda #' #' @details #' Download the [Miniconda](https://docs.conda.io/en/latest/miniconda.html) #' installer, and use it to install Miniconda. #' All function and descriptions from [reticulate package](https://github.com/rstudio/reticulate/blob/master/R/miniconda.R) #' #' @examples #' \dontrun{ #' install_conda() #' } #' @export install_conda <- function() { message("Please install reticulate(>= 1.14) package and use install_miniconda() function.") } #' install `java` #' #' @description #' install `corretto` which is one of openjdk(java) distro. #' Case of `MacOS`, remove all java and reinstall `corretto` version 11. #' #' @examples #' \dontrun{ #' install_java() #' install_jdk() #' } #' @export install_java <- function() { os <- get_os() dest <- crt_dest_loc() java_download(os, dest) loc <- crt_path(os) crt_unc(os, dest, exdir = loc) set_java_home(os) post_process( "install.packages('rJava', type = 'binary');library(rJava);.jinit();rstudioapi::restartSession()" ) } #' @rdname install_java #' @export install_jdk <- install_java install_nodejs <- function() { return(T) } install_go <- function() { return(T) } install_rust <- function() { return(T) }
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data(Sonar, package = "mlbench", envir = environment()) data(BreastCancer, package = "mlbench", envir = environment()) binaryclass.df = Sonar binaryclass.formula = Class~. binaryclass.target = "Class" binaryclass.train.inds = c(1:50, 100:150) binaryclass.test.inds = setdiff(seq_len(nrow(binaryclass.df)), binaryclass.train.inds) binaryclass.train = binaryclass.df[binaryclass.train.inds, ] binaryclass.test = binaryclass.df[binaryclass.test.inds, ] binaryclass.class.col = 61 binaryclass.class.levs = levels(binaryclass.df[, binaryclass.class.col]) binaryclass.task = makeClassifTask("binary", data = binaryclass.df, target = binaryclass.target) multiclass.df = iris multiclass.formula = Species~. multiclass.target = "Species" multiclass.train.inds = c(1:30, 51:80, 101:130) multiclass.test.inds = setdiff(1:150, multiclass.train.inds) multiclass.train = multiclass.df[multiclass.train.inds, ] multiclass.test = multiclass.df[multiclass.test.inds, ] multiclass.class.col = 5 multiclass.task = makeClassifTask("multiclass", data = multiclass.df, target = multiclass.target) multiclass.small.df = iris[c(1:3, 51:53, 101:103), ] multiclass.small.formula = Species~. multiclass.small.target = "Species" multiclass.small.train.inds = c(1:2, 4:5, 7:8) multiclass.small.test.inds = setdiff(1:9, multiclass.small.train.inds) multiclass.small.train = multiclass.small.df[multiclass.small.train.inds, ] multiclass.small.test = multiclass.small.df[multiclass.small.test.inds, ] multiclass.small.class.col = 5 multiclass.small.task = makeClassifTask("multiclass", data = multiclass.small.df, target = multiclass.small.target) multilabel.df = iris multilabel.df[, "y1"] = rep(c(TRUE, FALSE), 75L) multilabel.df[, "y2"] = rep(c(FALSE, TRUE), 75L) multilabel.target = c("y1", "y2") multilabel.train.inds = c(1:30, 51:80, 101:130) multilabel.test.inds = setdiff(1:150, multilabel.train.inds) multilabel.train = multilabel.df[multilabel.train.inds, ] multilabel.test = multilabel.df[multilabel.test.inds, ] multilabel.task = makeMultilabelTask("multilabel", data = multilabel.df, target = multilabel.target) multilabel.formula.cbind = as.formula(paste("cbind(", paste(multilabel.target, collapse = ",", sep = " "), ") ~ .", sep = "")) multilabel.formula = as.formula(paste(paste(multilabel.target, collapse = "+"), "~.")) multilabel.small.inds = c(1, 52, 53, 123) noclass.df = iris[, -5] noclass.train.inds = c(1:30, 51:80, 101:130) noclass.test.inds = setdiff(1:150, noclass.train.inds) noclass.train = noclass.df[noclass.train.inds, ] noclass.test = noclass.df[noclass.test.inds, ] noclass.task = makeClusterTask("noclass", data = noclass.df) data(BostonHousing, package = "mlbench", envir = environment()) regr.df = BostonHousing regr.formula = medv ~ . regr.target = "medv" regr.train.inds = seq(1, 506, 7) regr.test.inds = setdiff(seq_len(nrow(regr.df)), regr.train.inds) regr.train = regr.df[regr.train.inds, ] regr.test = regr.df[regr.test.inds, ] regr.class.col = 14 regr.task = makeRegrTask("regrtask", data = regr.df, target = regr.target) regr.small.df = BostonHousing[150:160, ] regr.small.formula = medv ~ . regr.small.target = "medv" regr.small.train.inds = 1:7 regr.small.test.inds = setdiff(seq_len(nrow(regr.small.df)), regr.small.train.inds) regr.small.train = regr.small.df[regr.small.train.inds, ] regr.small.test = regr.small.df[regr.small.test.inds, ] regr.small.class.col = 14 regr.small.task = makeRegrTask("regrtask", data = regr.small.df, target = regr.small.target) regr.num.df = regr.df[, sapply(regr.df, is.numeric)] regr.num.formula = regr.formula regr.num.target = regr.target regr.num.train.inds = regr.train.inds regr.num.test.inds = regr.test.inds regr.num.train = regr.num.df[regr.num.train.inds, ] regr.num.test = regr.num.df[regr.num.test.inds, ] regr.num.class.col = 13 regr.num.task = makeRegrTask("regrnumtask", data = regr.num.df, target = regr.num.target) getSurvData = function(n = 100, p = 10) { set.seed(1) beta = c(rep(1, 10), rep(0, p - 10)) x = matrix(rnorm(n * p), n, p) colnames(x) = sprintf("x%01i", 1:p) real.time = - (log(runif(n))) / (10 * exp(drop(x %*% beta))) cens.time = rexp(n, rate = 1 / 10) status = ifelse(real.time <= cens.time, TRUE, FALSE) obs.time = ifelse(real.time <= cens.time, real.time, cens.time) + 1 return(cbind(data.frame(time = obs.time, status = status), x)) } surv.df = getSurvData() surv.formula = survival::Surv(time, status) ~ . surv.target = c("time", "status") surv.train.inds = seq(1, floor(2 / 3 * nrow(surv.df))) surv.test.inds = setdiff(seq_len(nrow(surv.df)), surv.train.inds) surv.train = surv.df[surv.train.inds, ] surv.test = surv.df[surv.test.inds, ] surv.task = makeSurvTask("survtask", data = surv.df, target = surv.target) rm(getSurvData) costsens.feat = iris costsens.costs = matrix(runif(150L * 3L, min = 0, max = 1), 150L, 3L) costsens.task = makeCostSensTask("costsens", data = costsens.feat, costs = costsens.costs) ns.svg = c(svg = "http://www.w3.org/2000/svg") black.circle.xpath = "/svg:svg//svg:circle[contains(@style, 'fill: #000000')]" grey.rect.xpath = "/svg:svg//svg:rect[contains(@style, 'fill: #EBEBEB;')]" red.circle.xpath = "/svg:svg//svg:circle[contains(@style, 'fill: #F8766D')]" blue.circle.xpath = "/svg:svg//svg:circle[contains(@style, 'fill: #619CFF')]" green.circle.xpath = "/svg:svg//svg:circle[contains(@style, 'fill: #00BA38')]" black.line.xpath = "/svg:svg//svg:polyline[not(contains(@style, 'stroke:'))]" black.line.xpath2 = "/svg:svg//svg:polyline[contains(@style, 'stroke: #000000')]" blue.line.xpath = "/svg:svg//svg:polyline[contains(@style, 'stroke: #00BFC4;')]" mediumblue.line.xpath = "/svg:svg//svg:polyline[contains(@style, 'stroke: #3366FF;')]" red.line.xpath = "/svg:svg//svg:polyline[contains(@style, 'stroke: #F8766D;')]" red.rug.line.xpath = "/svg:svg//svg:line[contains(@style, 'stroke: #FF0000;')]" black.bar.xpath = "/svg:svg//svg:rect[contains(@style, 'fill: #595959;')]"
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require(sqldf) # set your working directory to the folder where you have the raw data file stored # If you don't have the file,get it from here https://d396qusza40orc.cloudfront.net/exdata%2Fdata%2Fhousehold_power_consumption.zip #read the file file <- c("household_power_consumption.txt") a2 <- read.csv.sql(file, header = T, sep=";", sql = "select * from file where (Date == '1/2/2007' OR Date == '2/2/2007')" ) #combining the Date and Time variables to create one datetime variable of class character a2$datetime <- paste(a2$Date,a2$Time,sep = " ") #convert the character class datetime variable into a2$datetime <- as.POSIXct(strptime(a2$datetime,"%d/%m/%Y %H:%M:%S")) #head(a2) #Open the file device using png() png("plot2.png",width = 480,height = 480,units = "px",bg = "transparent",pointsize = 12) #windows() --use this to test, send to your screen #plot the graph using base plotting system and function plot() plot(a2$datetime,a2$Global_active_power,type = "l",ylab = "Global Active Power (kilowatts)",xlab = "") # close the device connection. dev.off()
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vcf2eqtl <- function(vcf, expr, pops=NULL, minHet=3, minHetDP=10, mc.cores=1, alpha=0.05, calculateFst=T, outliers=T, testDE=F, all3=F, hweFilter=T, hweAlpha=0.05, covariates=NULL, propExplained=T, withinPop=T, format='bcftools', transcripts=NULL){ if(is.null(pops)){ calculateFst=F testDE=F propExplained=F withinPop=F } #extract SNP genotype and SNP depth data from vcf globalFst=NULL cat('reading vcf...\n') currvcf<-suppressWarnings(readVcf(vcf,genome='curr')) genoInfo<-geno(currvcf) genos<-make012(genoInfo$GT) cat(paste('vcf contains',nrow(genos),'variants\n')) if(format=='freebayes'){ AOs<-apply(genoInfo$AO,2,as.numeric) ROs<-apply(genoInfo$RO,2,as.numeric) } else if (format=='bcftools'){ ad<-apply(geno(currvcf)$AD,c(1,2),function(l) l[[1]]) ROs<-ad[1,,] AOs<-ad[2,,] } else{ stop('format must be either bcftools or freebayes') } BOs<-AOs+ROs AOs[genos!=1]<-NA BOs[genos!=1]<-NA AOs[BOs<minHetDP]<-NA BOs[BOs<minHetDP]<-NA rownames(AOs)<-rownames(genos) rownames(BOs)<-rownames(genos) cat('getting reference and alternate observations...\n') alleleObs<-vector('list',nrow(genos)) names(alleleObs)<-rownames(genos) for(i in 1:nrow(AOs)){ if(i%%10000==0) cat(paste(i,'\n')) alleleObs[[i]]<-na.omit(data.frame(row.names=colnames(genos),x=AOs[i,],size=BOs[i,])) } cat('organizing SNP info...\n') CHROM=as.vector(seqnames(rowRanges(currvcf))) POS=as.numeric(as.character(start(ranges(rowRanges(currvcf))))) REF=as.character(mcols(rowRanges(currvcf))[,'REF']) ALT=as.character(unlist(mcols(rowRanges(currvcf))[,'ALT'])) AF=as.numeric(unlist(info(currvcf)$AC))/as.numeric(unlist(info(currvcf)$AN)) snpInfo<-data.frame(CHROM=CHROM,POS=POS,REF=REF,ALT=ALT,AF=AF,stringsAsFactors=F) rownames(snpInfo)<-rownames(genos) cat('organizing expression data...\n') #organize and normalize expression data if(is.null(transcripts)) transcripts=CHROM expr<-expr[rownames(expr)%in%transcripts,] designMatrix<-NULL dmatComponents<-NULL if(withinPop) dmatComponents ='pops' if(!is.null(covariates)) dmatComponents =c('covariates', dmatComponents) if(!is.null(dmatComponents)){ form<-as.formula(paste('~',paste(dmatComponents,collapse='+'))) designMatrix<-model.matrix(form) } voomExpr<-voom(expr,design=designMatrix) rownames(voomExpr$weights)<-rownames(expr) currexpr<-as.matrix(voomExpr$E[transcripts,]) currweights<-as.matrix(voomExpr$weights[transcripts,]) rownames(currexpr)<-rownames(genos) rownames(currweights)<-rownames(genos) #if desired, filter genotypes if(all3){ cat('filtering for sites with all three genotypes...\n') num_gts<-apply(genos,1,function(v) length(table(v))) genos<-genos[num_gts==3,] } if(hweFilter){ cat('filtering out sites out of HWE in at least one population...\n') hwepops=pops hwe=rep(1,nrow(genos)) if(is.null(pops)) hwepops=rep(1,ncol(genos)) for(pop in unique(hwepops)){ hwe<-pmin(hwe,apply(genos[,which(pops==pop)],1,function(v) HWExact(table(factor(v,levels=c(0,1,2))),verbose=F)$pval)) } genos<-genos[hwe>hweAlpha,] } cat('filtering out sites without minimum number of informative heterozygotes\n') alleleObs<-alleleObs[rownames(genos)] imbalanceInfo<-unlist(lapply(alleleObs,function(df) nrow(df)>minHet)) alleleObs<-alleleObs[imbalanceInfo] genos<-genos[names(alleleObs),] if(nrow(genos)==0){ stop('No sites left after filtering, check to make sure you have a freebayes VCF of biallelic SNPs with allele observations in it') } #subset other data sets after filtering genos currexpr<-currexpr[rownames(genos),] snpInfo<-snpInfo[rownames(genos),] cat(paste(nrow(genos),'sites left after filtering, testing for eQTL status...\n')) #single-threaded test if(mc.cores==1){ cat('imbalance test...\n') imb.out<-do.call(rbind,lapply(alleleObs,bbLRT)) } else{ #multithreaded test cat('mulithreaded imbalance test...\n') imb.out<-do.call(rbind,mclapply(alleleObs,bbLRT,mc.cores=mc.cores)) } #single-threaded test if(mc.cores==1){ cat('association test...\n') assoc.out<-t(sapply(rownames(genos),associationTest, currexpr=currexpr,currweights=currweights,genos=genos,withinPop=withinPop)) } else{ #multithreaded test cat('mulithreaded association test...\n') assoc.out<-do.call(rbind,mclapply(rownames(genos),associationTest, currexpr=currexpr,currweights=currweights,genos=genos, withinPop=withinPop,mc.cores=mc.cores)) } #collect results and calculate p values using Fisher's method res<-cbind(imb.out,assoc.out) colnames(res)<-c('AImu','AIp','AIlog2fc','ASSOCz','ASSOCp','ASSOClog2fc') rownames(res)<-rownames(genos) res<-as.data.frame(res) #compare alternate homozygotes for fc combineP<-function(v){ if(NA%in%v) return(NA) return(sumlog(v)$p) } res$ASSOClog2fc<-2*res$ASSOClog2fc res$p<-apply(cbind(res$AIp,res$ASSOCp),1,combineP) res$padj<-p.adjust(res$p,method='BH') res$AIpadj<-p.adjust(res$AIp,method='BH') res$ASSOCpadj<-p.adjust(res$ASSOCp,method='BH') res$eQTL<-res$padj<alpha res<-cbind(snpInfo,res) #calculate Fst and call outliers using OutFLANK if(calculateFst){ cat('calculating Fst...\n') genosOutFLANK=genos genosOutFLANK[is.na(genosOutFLANK)]<-9 wc.out<-MakeDiploidFSTMat(t(genosOutFLANK),rownames(genos),pops) res$Fst=wc.out$FST res$FstNum<-wc.out$T1 res$FstDen<-wc.out$T2 res$He<-wc.out$He globalFst=sum(res$FstNum)/sum(res$FstDen) if(outliers){ fl.out<-OutFLANK(wc.out,NumberOfSamples=ncol(genos),qthreshold=alpha)$results res$FstOutlier=fl.out$OutlierFlag res$FstOutlierP=fl.out$pvaluesRightTail } } #test for differential expression using DESeq2 DEres =NULL if(testDE){ cat('testing for differential expression with DESeq2...\n') currdat<-data.frame(pops=pops) cds<-DESeqDataSetFromMatrix(expr,currdat,~pops) cds<-DESeq(cds,test='LRT',reduced=~1) DEres <-results(cds) res$DE<-DEres[res$CHROM,'padj']<alpha res$DEp<-DEres[res$CHROM,'pvalue'] res$DEpadj<-DEres[res$CHROM,'padj'] } #calculate reduction in population differentiation after accounting for eQTL if(propExplained){ cat('calculating proportion of population differences explained by eQTLs...\n') if(mc.cores==1){ propE<-sapply(rownames(genos)[which(res$eQTL)],propExplain,currexpr=currexpr,genos=genos,pops=pops) } else{ cat('\tmulithreading...\n') propE<-unlist(mclapply(rownames(genos)[which(res$eQTL)],propExplain, currexpr=currexpr,genos=genos,pops=pops,mc.cores=mc.cores)) } res$popDiffExplained<-NA res$popDiffExplained[which(res$eQTL)]=propE } return(list(res=res,snpContigExpr=currexpr,genos=genos,alleleObs=alleleObs,globalFst=globalFst,pops=pops,DEres= DEres)) }
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# Define the functions Dsquared <-function(obs = NULL, pred = NULL, model = NULL, adjust = FALSE) { # version 1.3 (3 Jan 2015) model.provided <- ifelse(is.null(model), FALSE, TRUE) if (model.provided) { if (!("glm" %in% class(model))) stop ("'model' must be of class 'glm'.") if (!is.null(pred)) message("Argument 'pred' ignored in favour of 'model'.") if (!is.null(obs)) message("Argument 'obs' ignored in favour of 'model'.") obs <- model$y pred <- model$fitted.values } else { # if model not provided if (is.null(obs) | is.null(pred)) stop("You must provide either 'obs' and 'pred', or a 'model' object of class 'glm'") if (length(obs) != length(pred)) stop ("'obs' and 'pred' must be of the same length (and in the same order).") if (!(obs %in% c(0, 1)) | pred < 0 | pred > 1) stop ("Sorry, 'obs' and 'pred' options currently only implemented for binomial GLMs (binary response variable with values 0 or 1) with logit link.") logit <- log(pred / (1 - pred)) model <- glm(obs ~ logit, family = "binomial") } D2 <- (model$null.deviance - model$deviance) / model$null.deviance if (adjust) { if (!model.provided) return(message("Adjusted D-squared not calculated, as it requires a model object (with its number of parameters) rather than just 'obs' and 'pred' values.")) n <- length(model$fitted.values) #p <- length(model$coefficients) p <- attributes(logLik(model))$df D2 <- 1 - ((n - 1) / (n - p)) * (1 - D2) } # end if adj return (D2) } prediction_analysis<- function(fit,release.next){ # Predict based on next release data. prediction <- predict(fit, newdata=release.next, type="response") # Use ROCR library calculate the performance. pred <- prediction(prediction,release.next$becomes_vulnerable) perf <- performance(pred, "prec", "rec") # Select the relevant values precision <- unlist(slot(perf, "y.values")) recall <- unlist(slot(perf, "x.values")) f_score = 2 * ((precision * recall)/(precision + recall)) mean_precision= mean(precision, na.rm=TRUE) mean_recall = mean(recall, na.rm=TRUE) mean_f_score = mean(f_score, na.rm=TRUE) # Create ROC Curve, # plot(perf, colorize=T) # Calculate the Area under the curve auc <- performance(pred,"auc") auc <- unlist(slot(auc, "y.values")) return (as.data.frame(cbind(mean_precision,mean_recall,mean_f_score,auc))) } release_modeling <- function(release,release.next){ options(warn=-1) # Remove files where there were no bugs of any kind, or if it had no SLOC # i.e. The subset must have at least on bug of ANY kind, and SLOC > 0 release <- subset(release, (release$num_pre_features !=0 | release$num_pre_compatibility_bugs !=0 | release$num_pre_regression_bugs !=0 | release$num_pre_security_bugs !=0 | release$num_pre_tests_fails_bugs != 0 | release$num_pre_stability_crash_bugs != 0 | release$num_pre_build_bugs != 0 | release$becomes_vulnerable != FALSE) & release$sloc > 0) release.next <- subset(release.next, (release.next$num_pre_features !=0 | release.next$num_pre_compatibility_bugs !=0 | release.next$num_pre_regression_bugs !=0 | release.next$num_pre_security_bugs !=0 | release.next$num_pre_tests_fails_bugs != 0 | release.next$num_pre_stability_crash_bugs != 0 | release.next$num_pre_build_bugs != 0 | release.next$becomes_vulnerable != FALSE) & release.next$sloc > 0) # Normalize and center data, added one to the values to be able to calculate log to zero. log(1)=0 release = cbind(as.data.frame(log(release[,c(1:19)] + 1)), becomes_vulnerable = release$becomes_vulnerable, was_buggy = release$was_buggy, becomes_buggy = release$becomes_buggy, was_vulnerable = release$was_vulnerable) release.next = cbind(as.data.frame(log(release.next[,c(1:19)] + 1)), becomes_vulnerable = release.next$becomes_vulnerable, was_buggy = release.next$was_buggy, becomes_buggy = release.next$becomes_buggy, was_vulnerable = release.next$was_vulnerable) # Modeling (forward selection) # Individual Models fit_null <- glm(formula = becomes_vulnerable ~ 1, data = release, family = "binomial") fit_control <- glm(formula = becomes_vulnerable ~ sloc, data = release, family = "binomial") fit_bugs <- glm (formula= becomes_vulnerable ~ sloc + num_pre_bugs, data = release, family = "binomial") # Category Based Models fit_features <- glm (formula= becomes_vulnerable ~ sloc + num_pre_features, data = release, family = "binomial") fit_security <- glm (formula= becomes_vulnerable ~ sloc + num_pre_security_bugs, data = release, family = "binomial") fit_stability <- glm (formula= becomes_vulnerable ~ sloc + num_pre_stability_crash_bugs + num_pre_compatibility_bugs + num_pre_regression_bugs, data = release, family = "binomial") fit_build <- glm (formula= becomes_vulnerable ~ sloc + num_pre_build_bugs + num_pre_tests_fails_bugs, data = release, family = "binomial") #history models fit_vuln_to_vuln <- glm(formula = becomes_vulnerable ~ sloc + was_vulnerable, data = release, family = "binomial") fit_bug_to_vuln <- glm(formula = becomes_vulnerable ~ sloc + was_buggy, data = release, family = "binomial") fit_bug_to_bug <- glm(formula = becomes_buggy ~ sloc + was_buggy, data = release, family = "binomial") # Experience Based Models fit_security_experienced <- glm (formula= becomes_vulnerable ~ sloc + avg_security_experienced_participants, data = release, family = "binomial") fit_bug_security_experienced <- glm (formula= becomes_vulnerable ~ sloc + avg_bug_security_experienced_participants, data = release, family = "binomial") fit_stability_experienced <- glm (formula= becomes_vulnerable ~ sloc + avg_stability_experienced_participants, data = release, family = "binomial") fit_build_experienced <- glm (formula= becomes_vulnerable ~ sloc + avg_build_experienced_participants, data = release, family = "binomial") fit_test_fail_experienced <- glm (formula= becomes_vulnerable ~ sloc + avg_test_fail_experienced_participants, data = release, family = "binomial") fit_compatibility_experienced <- glm (formula= becomes_vulnerable ~ sloc + avg_compatibility_experienced_participants, data = release, family = "binomial") # Display Results: cat("\nRelease Summary\n") print(summary(release)) cat("\nSpearman's Correlation for bug metrics\n") print(cor(release[,c(5:11)],method="spearman")) cat("\nSpearman's Correlation for experience metrics\n") print(cor(release[,c(14:19)],method="spearman", use = "complete")) release_v <- release[ which(release$becomes_vulnerable == TRUE), ] release_n <- release[ which(release$becomes_vulnerable == FALSE), ] cat("\n% Vulnerable\n") print(cbind(Total = length(release[,1]), Neutral = length(release_n[,1]), Vulnerable = length(release_v[,1]), Percentage = (length(release_v[,1])/length(release_n[,1]))*100)) cat("\nWilcoxon:\n") print(wilcox.test(release_v$sloc, release_n$sloc, alternative="greater")) print(cbind(median_v = median(release_v$sloc, na.rm=TRUE),median_n = median(release_n$sloc, na.rm=TRUE))) print(cbind(mean_v = mean(release_v$sloc, na.rm=TRUE),mean_n = mean(release_n$sloc, na.rm=TRUE))) # For bug metrics cat("\nFor bug metrics:\n") print(wilcox.test(release_v$num_pre_bugs, release_n$num_pre_bugs, alternative="greater")) print(cbind(median_v = median(release_v$num_pre_bugs, na.rm=TRUE),median_n = median(release_n$num_pre_bugs, na.rm=TRUE))) print(cbind(mean_v = mean(release_v$num_pre_bugs, na.rm=TRUE),mean_n = mean(release_n$num_pre_bugs, na.rm=TRUE))) print(wilcox.test(release_v$num_pre_features, release_n$num_pre_features, alternative="greater")) print(cbind(median_v = median(release_v$num_pre_features, na.rm=TRUE),median_n = median(release_n$num_pre_features, na.rm=TRUE))) print(cbind(mean_v = mean(release_v$num_pre_features, na.rm=TRUE),mean_n = mean(release_n$num_pre_features, na.rm=TRUE))) print(wilcox.test(release_v$num_pre_compatibility_bugs, release_n$num_pre_compatibility_bugs, alternative="greater")) print(cbind(median_v = median(release_v$num_pre_compatibility_bugs, na.rm=TRUE),median_n = median(release_n$num_pre_compatibility_bugs, na.rm=TRUE))) print(cbind(mean_v = mean(release_v$num_pre_compatibility_bugs, na.rm=TRUE),mean_n = mean(release_n$num_pre_compatibility_bugs, na.rm=TRUE))) print(wilcox.test(release_v$num_pre_regression_bugs, release_n$num_pre_regression_bugs, alternative="greater")) print(cbind(median_v = median(release_v$num_pre_regression_bugs, na.rm=TRUE),median_n = median(release_n$num_pre_regression_bugs, na.rm=TRUE))) print(cbind(mean_v = mean(release_v$num_pre_regression_bugs, na.rm=TRUE),mean_n = mean(release_n$num_pre_regression_bugs, na.rm=TRUE))) print(wilcox.test(release_v$num_pre_security_bugs, release_n$num_pre_security_bugs, alternative="greater")) print(cbind(median_v = median(release_v$num_pre_security_bugs, na.rm=TRUE),median_n = median(release_n$num_pre_security_bugs, na.rm=TRUE))) print(cbind(mean_v = mean(release_v$num_pre_security_bugs, na.rm=TRUE),mean_n = mean(release_n$num_pre_security_bugs, na.rm=TRUE))) print(wilcox.test(release_v$num_pre_tests_fails_bugs, release_n$num_pre_tests_fails_bugs, alternative="greater")) print(cbind(median_v = median(release_v$num_pre_tests_fails_bugs, na.rm=TRUE),median_n = median(release_n$num_pre_tests_fails_bugs, na.rm=TRUE))) print(cbind(mean_v = mean(release_v$num_pre_tests_fails_bugs, na.rm=TRUE),mean_n = mean(release_n$num_pre_tests_fails_bugs, na.rm=TRUE))) print(wilcox.test(release_v$num_pre_stability_crash_bugs, release_n$num_pre_stability_crash_bugs, alternative="greater")) print(cbind(median_v = median(release_v$num_pre_stability_crash_bugs, na.rm=TRUE),median_n = median(release_n$num_pre_stability_crash_bugs, na.rm=TRUE))) print(cbind(mean_v = mean(release_v$num_pre_stability_crash_bugs, na.rm=TRUE),mean_n = mean(release_n$num_pre_stability_crash_bugs, na.rm=TRUE))) print(wilcox.test(release_v$num_pre_build_bugs, release_n$num_pre_build_bugs, alternative="greater")) print(cbind(median_v = median(release_v$num_pre_build_bugs, na.rm=TRUE),median_n = median(release_n$num_pre_build_bugs, na.rm=TRUE))) print(cbind(mean_v = mean(release_v$num_pre_build_bugs, na.rm=TRUE),mean_n = mean(release_n$num_pre_build_bugs, na.rm=TRUE))) # For experience metrics cat("\nFor experience metrics:\n") print(wilcox.test(release_v$avg_security_experienced_participants, release_n$avg_security_experienced_participants, alternative="greater")) print(cbind(median_v = median(release_v$avg_security_experienced_participants, na.rm=TRUE),median_n = median(release_n$avg_security_experienced_participants, na.rm=TRUE))) print(cbind(mean_v = mean(release_v$avg_security_experienced_participants, na.rm=TRUE),mean_n = mean(release_n$avg_security_experienced_participants, na.rm=TRUE))) print(wilcox.test(release_v$avg_bug_security_experienced_participants, release_n$avg_bug_security_experienced_participants, alternative="greater")) print(cbind(median_v = median(release_v$avg_bug_security_experienced_participants, na.rm=TRUE),median_n = median(release_n$avg_bug_security_experienced_participants, na.rm=TRUE))) print(cbind(mean_v = mean(release_v$avg_bug_security_experienced_participants, na.rm=TRUE),mean_n = mean(release_n$avg_bug_security_experienced_participants, na.rm=TRUE))) print(wilcox.test(release_v$avg_stability_experienced_participants, release_n$avg_stability_experienced_participants, alternative="greater")) print(cbind(median_v = median(release_v$avg_stability_experienced_participants, na.rm=TRUE),median_n = median(release_n$avg_stability_experienced_participants, na.rm=TRUE))) print(cbind(mean_v = mean(release_v$avg_stability_experienced_participants, na.rm=TRUE),mean_n = mean(release_n$avg_stability_experienced_participants, na.rm=TRUE))) print(wilcox.test(release_v$avg_build_experienced_participants, release_n$avg_build_experienced_participants, alternative="greater")) print(cbind(median_v = median(release_v$avg_build_experienced_participants, na.rm=TRUE),median_n = median(release_n$avg_build_experienced_participants, na.rm=TRUE))) print(cbind(mean_v = mean(release_v$avg_build_experienced_participants, na.rm=TRUE),mean_n = mean(release_n$avg_build_experienced_participants, na.rm=TRUE))) print(wilcox.test(release_v$avg_test_fail_experienced_participants, release_n$avg_test_fail_experienced_participants, alternative="greater")) print(cbind(median_v = median(release_v$avg_test_fail_experienced_participants, na.rm=TRUE),median_n = median(release_n$avg_test_fail_experienced_participants, na.rm=TRUE))) print(cbind(mean_v = mean(release_v$avg_test_fail_experienced_participants, na.rm=TRUE),mean_n = mean(release_n$avg_test_fail_experienced_participants, na.rm=TRUE))) print(wilcox.test(release_v$avg_compatibility_experienced_participants, release_n$avg_compatibility_experienced_participants, alternative="greater")) print(cbind(median_v = median(release_v$avg_compatibility_experienced_participants, na.rm=TRUE),median_n = median(release_n$avg_compatibility_experienced_participants, na.rm=TRUE))) print(cbind(mean_v = mean(release_v$avg_compatibility_experienced_participants, na.rm=TRUE),mean_n = mean(release_n$avg_compatibility_experienced_participants, na.rm=TRUE))) cat("\nCohensD for Bug metrics:\n") print(cbind( sloc = cohensD(release_v$sloc, release_n$sloc), bugs = cohensD(release_v$num_pre_bugs, release_n$num_pre_bugs), features = cohensD(release_v$num_pre_features, release_n$num_pre_features), compatibility_bugs = cohensD(release_v$num_pre_compatibility_bugs, release_n$num_pre_compatibility_bugs), regression_bugs = cohensD(release_v$num_pre_regression_bugs, release_n$num_pre_regression_bugs), security_bugs = cohensD(release_v$num_pre_security_bugs, release_n$num_pre_security_bugs), tests_fails_bugs = cohensD(release_v$num_pre_tests_fails_bugs, release_n$num_pre_tests_fails_bugs), stability_crash_bugs = cohensD(release_v$num_pre_stability_crash_bugs, release_n$num_pre_stability_crash_bugs), build_bugs = cohensD(release_v$num_pre_build_bugs, release_n$num_pre_build_bugs) )) cat("\nCohensD for Experience metrics:\n") print(cbind( avg_security_experienced_participants = cohensD(release_v$avg_security_experienced_participants, release_n$avg_security_experienced_participants), avg_bug_security_experienced_participants = cohensD(release_v$avg_bug_security_experienced_participants, release_n$avg_bug_security_experienced_participants), avg_stability_experienced_participants = cohensD(release_v$avg_stability_experienced_participants, release_n$avg_stability_experienced_participants), avg_build_experienced_participants = cohensD(release_v$avg_build_experienced_participants, release_n$avg_build_experienced_participants), avg_test_fail_experienced_participants = cohensD(release_v$avg_test_fail_experienced_participants, release_n$avg_test_fail_experienced_participants), avg_compatibility_experienced_participants = cohensD(release_v$avg_compatibility_experienced_participants, release_n$avg_compatibility_experienced_participants) )) cat("\n# Summary Control Models\n") cat("fit_null\n") print(summary(fit_null)) cat("fit_control\n") print(summary(fit_control)) cat("fit_bugs\n") print(summary(fit_bugs)) cat("\n") cat("# Summary\n") cat("fit_security\n") print(summary(fit_security)) cat("fit_features\n") print(summary(fit_features)) cat("fit_stability\n") print(summary(fit_stability)) cat("fit_build\n") print(summary(fit_build)) cat("\n") cat("# Summary History Models\n") cat("fit_vuln_to_vuln\n") print(summary(fit_vuln_to_vuln)) cat("fit_bug_to_vuln\n") print(summary(fit_bug_to_vuln)) cat("fit_bug_to_bug\n") print(summary(fit_bug_to_bug)) cat("\n") cat("# Summary Experience Models\n") cat("fit_security_experienced\n") print(summary(fit_security_experienced)) cat("fit_bug_security_experienced\n") print(summary(fit_bug_security_experienced)) cat("fit_stability_experienced\n") print(summary(fit_stability_experienced)) cat("fit_build_experienced\n") print(summary(fit_build_experienced)) cat("fit_test_fail_experienced\n") print(summary(fit_test_fail_experienced)) cat("fit_compatibility_experienced\n") print(summary(fit_compatibility_experienced)) cat("\n") cat("# D^2 Analysys\n") cat("Control\n") cat("fit_control\n") print(Dsquared(model = fit_control)) cat("For fit_bugs\n") print(Dsquared(model = fit_bugs)) cat("\n") cat("# Categories\n") cat("fit_security\n") print(Dsquared(model = fit_security)) cat("For fit_features\n") print(Dsquared(model = fit_features)) cat("For fit_stability\n") print(Dsquared(model = fit_stability)) cat("For fit_build\n") print(Dsquared(model = fit_build)) cat("\n") cat("# Summary History Models\n") cat("fit_vuln_to_vuln\n") print(Dsquared(model = fit_vuln_to_vuln)) cat("fit_bug_to_vuln\n") print(Dsquared(model = fit_bug_to_vuln)) cat("fit_bug_to_bug\n") print(Dsquared(model = fit_bug_to_bug)) cat("\n") cat("# Summary Experience Models\n") cat("fit_security_experienced\n") print(Dsquared(model = fit_security_experienced)) cat("fit_bug_security_experienced\n") print(Dsquared(model = fit_bug_security_experienced)) cat("fit_stability_experienced\n") print(Dsquared(model = fit_stability_experienced)) cat("fit_build_experienced\n") print(Dsquared(model = fit_build_experienced)) cat("fit_test_fail_experienced\n") print(Dsquared(model = fit_test_fail_experienced)) cat("fit_compatibility_experienced\n") print(Dsquared(model = fit_compatibility_experienced)) cat("\n") cat("# Prediction Analysis\n") cat("Control\n") cat("For fit_control\n") print(prediction_analysis(fit_control,release.next)) cat("For fit_bugs\n") print(prediction_analysis(fit_bugs,release.next)) cat("\n") cat("# Categories\n") cat("For fit_security\n") print(prediction_analysis(fit_security,release.next)) cat("For fit_features\n") print(prediction_analysis(fit_features,release.next)) cat("For fit_stability\n") print(prediction_analysis(fit_stability,release.next)) cat("For fit_build\n") print(prediction_analysis(fit_build,release.next)) cat("\n") cat("# Summary History Models\n") cat("fit_vuln_to_vuln\n") print(prediction_analysis(fit_vuln_to_vuln,release.next)) cat("fit_bug_to_vuln\n") print(prediction_analysis(fit_bug_to_vuln,release.next)) cat("fit_bug_to_bug\n") print(prediction_analysis(fit_bug_to_bug,release.next)) cat("\n") cat("# Summary Experience Models\n") cat("fit_security_experienced\n") print(prediction_analysis(fit_security_experienced,release.next)) cat("fit_bug_security_experienced\n") print(prediction_analysis(fit_bug_security_experienced,release.next)) cat("fit_stability_experienced\n") print(prediction_analysis(fit_stability_experienced,release.next)) cat("fit_build_experienced\n") print(prediction_analysis(fit_build_experienced,release.next)) cat("fit_test_fail_experienced\n") print(prediction_analysis(fit_test_fail_experienced,release.next)) cat("fit_compatibility_experienced\n") print(prediction_analysis(fit_compatibility_experienced,release.next)) options(warn=0) }
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/R/tagtools/man/block_rms.Rd
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FlukeAndFeather/TagTools
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block_rms.Rd
% Generated by roxygen2: do not edit by hand % Please edit documentation in R/block_rms.R \name{block_rms} \alias{block_rms} \title{Compute RMS of sample blocks} \usage{ block_rms(X, n, nov = NULL) } \arguments{ \item{X}{A vector or a matrix containing samples of a signal in each column.} \item{n}{The number of samples from X to use in each analysis block.} \item{nov}{The number of samples that the next block overlaps the previous block.} } \value{ A list with 2 elements: \itemize{ \item{\strong{Y: }} A vector or matrix containing the RMS value of each block. If X is a mxn matrix, Y is pxn where p is the number of complete n-length blocks with nov that can be made out of m samples, i.e., n+(p-1)*(n-nov) < m \item{\strong{t: }} The time at which each output in Y is reported, in units of samples of X. So if t[1] = 12, then the value Y[1] corresponds to the “time” 12 samples in X. The times at which Y values are reported are the centers of the averaging windows. } } \description{ This function is used to compute the RMS (root-mean-square) of successive blocks of samples. } \note{ Output sampling rate is the same as the input sampling rate so s and v have the same size as p. Frame: This function assumes a [north,east,up] navigation frame and a [forward,right,up] local frame. In these frames, a positive pitch angle is an anti-clockwise rotation around the y-axis. A descending animal will have a negative pitch angle. } \examples{ X <- matrix(c(1:20), byrow = TRUE, nrow = 4) block_rms(X, n = 2, nov = NULL) }
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/Unit 5 Text Analytics/Assignment5_Spam1.R
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Assignment5_Spam1.R
# Assignment 5 # Separating Spam from Ham (Part 1) emails = read.csv("emails.csv", stringsAsFactors = FALSE) str(emails) summary(emails) table(emails$spam) emails$text[1] emails$text[2] # How many characters are in the longest email in the dataset? max(nchar(emails$text)) # Which row contains the shortest email in the dataset? which.min(nchar(emails$text)) # Follow the standard steps to build and pre-process the corpus: corpus = VCorpus(VectorSource(emails$text)) corpus = tm_map(corpus, content_transformer(tolower)) corpus = tm_map(corpus, removePunctuation) corpus = tm_map(corpus, removeWords, stopwords("english")) corpus = tm_map(corpus, stemDocument) dtm = DocumentTermMatrix(corpus) summary(dtm) # To obtain a more reasonable number of terms, limit dtm to contain terms appearing in at least 5% of documents, and store this result as spdtm spdtm = removeSparseTerms(dtm, 0.95) summary(spdtm) # Build a data frame called emailsSparse from spdtm, and use the make.names function to make the variable names of emailsSparse valid. emailsSparse = as.data.frame(as.matrix(spdtm)) colnames(emailsSparse) = make.names(colnames(emailsSparse)) # What is the word stem that shows up most frequently across all the emails in the dataset? sort(colSums(emailsSparse)) emailsSparse$spam = emails$spam # How many word stems appear at least 5000 times in the ham emails in the dataset? sort(colSums(subset(emailsSparse, spam == 0))) # How many word stems appear at least 1000 times in the spam emails in the dataset? sort(colSums(subset(emailsSparse, spam == 1))) # Do not count the dependent variable "spam" emailsSparse$spam = as.factor(emailsSparse$spam) set.seed(123) split = sample.split(emailsSparse$spam, 0.7) train = subset(emailsSparse, split == TRUE) test = subset(emailsSparse, split == FALSE) # Using the training set, train the following three machine learning models. The models should predict the dependent variable "spam", using all other available variables as independent variables. # Please be patient, as these models may take a few minutes to train. # 1) A logistic regression model called spamLog. You may see a warning message here - we'll discuss this more later. spamLog = glm(spam ~ ., data=train, family="binomial") predTrainLog = predict(spamLog, type="response") # 2) A CART model called spamCART, using the default parameters to train the model (don't worry about adding minbucket or cp). # Remember to add the argument method="class" since this is a binary classification problem. spamCART = rpart(spam ~ ., data=train, method="class") predTrainCART = predict(spamCART)[,2] # 3) A random forest model called spamRF, using the default parameters to train the model (don't worry about specifying ntree or nodesize). # Directly before training the random forest model, set the random seed to 123 # (even though we've already done this earlier in the problem, it's important to set the seed right before training the model so we all obtain the same results. # Keep in mind though that on certain operating systems, your results might still be slightly different). set.seed(123) spamRF = randomForest(spam ~ ., data=train) predTrainRF = predict(spamRF, type="prob")[,2] table(predTrainLog < 0.00001) table(predTrainLog > 0.99999) table(predTrainLog >= 0.00001 & predTrainLog <= 0.99999) # How many variables are labeled as significant (at the p=0.05 level) in the logistic regression summary output? summary(spamLog) # How many of the word stems "enron", "hou", "vinc", and "kaminski" appear in the CART tree? prp(spamCART) # What is the training set accuracy of spamLog, using a threshold of 0.5 for predictions? table(train$spam, predTrainLog > 0.5) (3052 + 954) / nrow(train) # Training set AUC of spamLog trainLogROCR = prediction(predTrainLog, train$spam) as.numeric(performance(trainLogROCR, "auc")@y.values) # What is the training set accuracy of spamCART, using a threshold of 0.5 for predictions? table(train$spam, predTrainCART > 0.5) (2885 + 894) / nrow(train) # What is the training set AUC of spamCART? trainCART.ROCR = prediction(predTrainCART, train$spam) as.numeric(performance(trainCART.ROCR, "auc")@y.values) # Training set accuracy of spamRF, using a threshold of 0.5 for predictions table(train$spam, predTrainRF > 0.5) (3015 + 916) / nrow(train) # Training set AUC of spamRF trainRF.ROCR = prediction(predTrainRF, train$spam) as.numeric(performance(trainRF.ROCR, "auc")@y.values) # What is the testing set accuracy of spamLog, using a threshold of 0.5 for predictions? predTestLog = predict(spamLog, newdata=test, type="response") table(test$spam, predTestLog > 0.5) (1257 + 376) / nrow(test) # Testing set AUC of spamLog testLogROCR = prediction(predTestLog, test$spam) as.numeric(performance(testLogROCR, "auc")@y.values) # What is the testing set accuracy of spamCART, using a threshold of 0.5 for predictions? predTestCART = predict(spamCART, newdata=test)[,2] table(test$spam, predTestCART > 0.5) (1228 + 386) / nrow(test) # Testing set AUC of spamCART testCART.ROCR = prediction(predTestCART, test$spam) as.numeric(performance(testCART.ROCR, "auc")@y.values) # What is the testing set accuracy of spamRF, using a threshold of 0.5 for predictions? predTestRF = predict(spamRF, newdata=test, type="prob")[,2] table(test$spam, predTestRF > 0.5) (1291 + 387) / nrow(test) # Testing set AUC of spamRF testRF.ROCR = prediction(predTestRF, test$spam) as.numeric(performance(testRF.ROCR, "auc")@y.values) # In terms of testing set performance, # the random forest outperformed logistic regression and CART in both measures, obtaining an impressive AUC of 0.997 on the test set. # Both CART and random forest had very similar accuracies on the training and testing sets. # However, logistic regression obtained nearly perfect accuracy and AUC on the training set and had far-from-perfect performance on the testing set. # This is an indicator of overfitting.