@sjcrh/proteinpaint-server 2.24.1 → 2.26.0
This diff represents the content of publicly available package versions that have been released to one of the supported registries. The information contained in this diff is provided for informational purposes only and reflects changes between package versions as they appear in their respective public registries.
- package/dataset/clinvar.hg19.js +3 -3
- package/dataset/clinvar.hg38.js +20 -3
- package/genome/cgc.js +7 -0
- package/genome/hg19.js +2 -0
- package/genome/hg38.js +9 -2
- package/package.json +19 -5
- package/routes/genelookup.ts +58 -0
- package/routes/healthcheck.ts +72 -0
- package/server.js +1 -1
- package/utils/cuminc.R +9 -7
- package/utils/fastclust.R +8 -6
package/utils/cuminc.R
CHANGED
|
@@ -13,13 +13,15 @@
|
|
|
13
13
|
|
|
14
14
|
# Input JSON:
|
|
15
15
|
# {
|
|
16
|
-
#
|
|
17
|
-
#
|
|
18
|
-
#
|
|
19
|
-
#
|
|
20
|
-
#
|
|
21
|
-
#
|
|
22
|
-
#
|
|
16
|
+
# data:
|
|
17
|
+
# chartId: [
|
|
18
|
+
# {
|
|
19
|
+
# time: time to event
|
|
20
|
+
# event: event code (0 = censored, 1 = event, 2 = competing risk event)
|
|
21
|
+
# series: series ID
|
|
22
|
+
# }
|
|
23
|
+
# ],
|
|
24
|
+
# startTime: custom start time of cuminc curve
|
|
23
25
|
# }
|
|
24
26
|
#
|
|
25
27
|
# Output JSON:
|
package/utils/fastclust.R
CHANGED
|
@@ -42,9 +42,9 @@ args <- commandArgs(trailingOnly = T)
|
|
|
42
42
|
if (length(args) != 1) stop("Usage: Rscript test.R in.json > results")
|
|
43
43
|
infile <- args[1]
|
|
44
44
|
input <- fromJSON(infile)
|
|
45
|
-
|
|
45
|
+
normalized_matrix <- t(scale(t(input$matrix))) # Applying z-score normalization
|
|
46
46
|
# For columns (i.e samples)
|
|
47
|
-
RowDist <- dist(
|
|
47
|
+
RowDist <- dist(normalized_matrix, method = "euclidean") # Transposing the matrix
|
|
48
48
|
|
|
49
49
|
# Hierarchical clustering
|
|
50
50
|
print (input$cluster_method)
|
|
@@ -76,7 +76,7 @@ print ("RowCoordinates")
|
|
|
76
76
|
print (row_node_coordinates)
|
|
77
77
|
|
|
78
78
|
# For columns (i.e samples)
|
|
79
|
-
ColumnDist <- dist(t(
|
|
79
|
+
ColumnDist <- dist(t(normalized_matrix), method = "euclidean") # Transposing the matrix
|
|
80
80
|
|
|
81
81
|
# Hierarchical clustering
|
|
82
82
|
|
|
@@ -95,7 +95,7 @@ print (col_node_coordinates)
|
|
|
95
95
|
print ("Done")
|
|
96
96
|
# Sorting the matrix
|
|
97
97
|
|
|
98
|
-
SortedMatrix <-
|
|
98
|
+
SortedMatrix <- normalized_matrix[RowDend$order, ColumnDend$order]
|
|
99
99
|
SortedRowNames <- input$row_names[RowDend$order]
|
|
100
100
|
SortedColumnNames <- input$col_names[ColumnDend$order]
|
|
101
101
|
|
|
@@ -104,9 +104,11 @@ colnames(m) <- SortedColumnNames
|
|
|
104
104
|
rownames(m) <- SortedRowNames
|
|
105
105
|
cat("rownames",RowDend$order,"\n",sep="\t")
|
|
106
106
|
cat("colnames",ColumnDend$order,"\n",sep="\t")
|
|
107
|
+
cat ("OutputMatrix",normalized_matrix,"\n",sep="\t") # This outputs the 2D array in 1D column-wise. This is later converted to 2D array in nodejs.
|
|
108
|
+
|
|
107
109
|
|
|
108
|
-
df <- melt(m)
|
|
109
|
-
colnames(df) <- c("Genes", "Samples", "value")
|
|
110
|
+
#df <- melt(m)
|
|
111
|
+
#colnames(df) <- c("Genes", "Samples", "value")
|
|
110
112
|
|
|
111
113
|
#ggplot(df, aes(x = Genes, y = Samples, fill = value)) + geom_tile() + scale_fill_gradient(low="blue", high="red") + theme(axis.text.x = element_text(angle = 90, vjust = 0.5, hjust=1))
|
|
112
114
|
|