@sjcrh/proteinpaint-server 2.14.4 → 2.16.0

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package/shared/common.js CHANGED
@@ -472,7 +472,8 @@ export const tkt = {
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  mds2: 'mds2', // mds 2nd gen
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  mds3: 'mds3', // 3rd gen
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  bedgraphdot: 'bedgraphdot',
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- bam: 'bam'
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+ bam: 'bam',
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+ ld: 'ld'
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  }
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  export function validtkt(what) {
@@ -0,0 +1,129 @@
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+ # Usage:
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+ # time Rscript fastclust.R in.json
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+
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+ # Image is in Rplots.pdf
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+
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+ # Checking if all R packages are installed or not, if not installing each one of them
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+
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+ ggplot2_path <- system.file(package='ggplot2')
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+ if (nchar(ggplot2_path) == 0) {
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+ install.packages("ggplot2", repos='https://cran.case.edu/')
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+ }
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+
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+ jsonlite_path <- system.file(package='jsonlite')
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+ if (nchar(jsonlite_path) == 0) {
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+ install.packages("jsonlite", repos='https://cran.case.edu/')
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+ }
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+
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+ dendextend_path <- system.file(package='dendextend')
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+ if (nchar(dendextend_path) == 0) {
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+ install.packages("dendextend", repos='https://cran.case.edu/')
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+ }
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+
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+ reshape_path <- system.file(package='reshape')
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+ if (nchar(reshape_path) == 0) {
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+ install.packages("reshape", repos='https://cran.case.edu/')
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+ }
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+
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+ #flashClust_path <- system.file(package='flashClust')
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+ #if (nchar(flashClust_path) == 0) {
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+ # install.packages("flashClust", repos='https://cran.case.edu/')
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+ #}
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+
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+ suppressPackageStartupMessages(library(dendextend))
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+ library(jsonlite)
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+ #library(flashClust)
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+ library(dendextend)
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+ library(reshape)
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+ library(ggplot2)
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+
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+ # Distance matrix
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+ args <- commandArgs(trailingOnly = T)
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+ if (length(args) != 1) stop("Usage: Rscript test.R in.json > results")
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+ infile <- args[1]
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+ input <- fromJSON(infile)
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+
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+ # For columns (i.e samples)
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+ RowDist <- dist(input$matrix, method = "euclidean") # Transposing the matrix
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+
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+ # Hierarchical clustering
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+ print (input$cluster_method)
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+ RowDend <- hclust(RowDist, method = tolower(input$cluster_method))
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+ #RowDend <- flashClust(RowDist, method = tolower(input$cluster_method))
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+ #print (RowDend$order)
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+ #print ("Merge")
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+ #print (RowDend$merge)
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+ #print ("Height")
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+ #print (RowDend$height)
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+ #print ("Labels")
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+ #print (RowDend$labels)
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+ #print ("Calls")
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+ #print (RowDend$call)
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+ #print ("Attributes")
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+ #attributes(RowDend)
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+ #print ("methods")
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+ #methods(class=class(RowDend))
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+ RowDendro <- as.dendrogram(RowDend)
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+ #print ("Attributes as.dendrogram")
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+ #attributes(RowDendro)
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+ plot(RowDendro)
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+
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+ node_coordinates <- get_nodes_xy(
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+ RowDendro,
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+ type = "rectangle"
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+ )
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+ print (node_coordinates)
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+
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+ # For columns (i.e samples)
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+ ColumnDist <- dist(t(input$matrix), method = "euclidean") # Transposing the matrix
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+
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+ # Hierarchical clustering
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+
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+ ColumnDend <- hclust(ColumnDist, method = tolower(input$cluster_method))
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+ #ColumnDend <- flashClust(ColumnDist,method = tolower(input$cluster_method))
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+ ColumnDendro <- as.dendrogram(ColumnDend)
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+ plot (ColumnDendro)
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+
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+ # Sorting the matrix
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+
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+ SortedMatrix <- input$matrix[RowDend$order, ColumnDend$order]
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+ SortedRowNames <- input$row_names[RowDend$order]
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+ SortedColumnNames <- input$col_names[ColumnDend$order]
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+
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+ m <- matrix(SortedMatrix,length(SortedRowNames),length(SortedColumnNames))
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+ colnames(m) <- SortedColumnNames
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+ rownames(m) <- SortedRowNames
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+
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+ df <- melt(m)
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+ colnames(df) <- c("Genes", "Samples", "value")
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+
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+ ggplot(df, aes(x = Genes, y = Samples, fill = value)) +
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+ geom_tile() + scale_fill_gradient(low="blue", high="red")
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+
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+ #ggsave("heatmap.png")
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+
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+
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+ ##print (SortedMatrix)
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+ #df <- as.data.frame(SortedMatrix)
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+ #rownames(df) <- SortedRowNames
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+ #colnames(df) <- SortedColumnNames
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+ #print ("DataFrame")
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+ #print (df)
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+ ##plt <- ggplot(as.data.frame(SortedMatrix), aes(SortedColumnNames,SortedRowNames)) + geom_tile() + theme_minimal()
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+ #plt <- ggplot(df,aes(x=colname,y=rownames(df))) + geom_tile() + theme_minimal()
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+ #
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+ ## setting gradient color as red and white
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+ #plt <- plt + scale_fill_gradient(low="blue", high="red")
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+ #
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+ ## setting the title and subtitles using
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+ ## title and subtitle
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+ #plt <- plt + labs(title = "Heatmap")
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+ #plt <- plt + labs(subtitle = "A simple heatmap using geom_tile()")
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+ #
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+ ## setting x and y labels using labs
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+ #plt <- plt + labs(x ="Samples", y ="Genes")
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+ #
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+ ## plotting the Heatmap
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+ #plt
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+ #png("heatmap.png")
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+ #dev.off()
package/utils/lowess.R ADDED
@@ -0,0 +1,9 @@
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+ library(jsonlite)
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+
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+ # read in data
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+ args <- commandArgs(trailingOnly = T)
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+ if (length(args) != 1) stop("input coordinates needed")
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+ infile <- args[1]
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+ data <- fromJSON(infile)
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+ result = lowess(data$X, data$Y)
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+ toJSON(result)
@@ -1 +0,0 @@
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- //!!! DO NOT USE FOR geneVariant filterCTE constructor