gtexJunctionReadsFormat <- function() {
list(
tablename = "Junction quantification",
filename = "GTEx_Analysis_v6_RNA-seq_Flux1.6_junction_reads.txt",
description = "Read counts of splicing junctions",
dataType = "Junction quantification",
# Transpose data before parsing? If so, a row in the transposed dataset
# would be a column in the original
skip = 1, # Rows to skip when parsing file (include header)
transpose = FALSE,
# Format checker information
rowCheck = TRUE, # Check a row (TRUE) or a column (FALSE)
checkIndex = 1, # Index of row/column to check the format
# File string to check
check = c("TargetID", "Gene_Symbol", "Chr", "Coord"),
# Parsing information
delim = "\t", # Delimiter used to separate fields
colNames = 1, # Row to use for column names
rowNames = 1, # Column to use for row names
ignoreCols = seq(4), # Columns to ignore
ignoreRows = 1, # Rows to ignore
commentChar = NULL, # Ignore lines starting with this string
# Remove duplicated rows
unique = TRUE,
# Identity of rows and columns
rows = "splice junctions",
columns = "samples",
# Default columns to show (NULL to show all)
show = NULL,
process = function(data) {
# Clean gtf filenames of columns
colnames(data) <- gsub("\\.gtf$", "", colnames(data))
# Transform junction positions for easier parsing
cols <- str_split_fixed(rownames(data), "_", 3)
rownames(data) <- sprintf("chr%s:%s:%s",
cols[ , 1], cols[ , 2], cols[ , 3])
return(data)
}
)
}
attr(gtexJunctionReadsFormat, "loader") <- "formats"
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