suppressPackageStartupMessages(library(optparse))
suppressPackageStartupMessages(library(rcrispr))
###############################################################################
#* -- -- *#
#* -- OPTIONS -- *#
#* -- -- *#
###############################################################################
option_list = c(
count_path_options(),
library_annotation_options(),
crisprcleanr_output_options(),
crisprcleanr_correction_options(),
shared_output_options(),
count_format_options(),
count_column_index_options(),
library_annotation_format_options(),
library_annotation_column_index_options(),
library_annotation_genomic_column_index_options()
)
opt_parser <- OptionParser(option_list = option_list)
opt <- tryCatch({
parse_args(opt_parser)
}, error = function(e) {
# Stop if there is an error
stop(paste("Cannot parse arguments (error):", e, sep = "\n"))
}, warning = function(w) {
# Stop if there is a warning
stop(paste("Cannot parse arguments (warning):", w, sep = "\n"))
})
###############################################################################
#* -- -- *#
#* -- OPTION VALIDATION -- *#
#* -- -- *#
###############################################################################
# Check whether required fields are provided
for (n in c('counts', 'library', 'lfc_matrix')) {
check_option(n, opt[[n]])
}
if (is.null(opt$count_matrix_outfile))
opt$count_matrix_outfile <- 'count_matrix.CRISPRcleanR_input.tsv'
if (is.null(opt$lfc_matrix_outfile))
opt$lfc_matrix_outfile <- 'fold_change_matrix.sgrna.CRISPRcleanR_input.tsv'
if (is.null(opt$library_outfile))
opt$library_outfile <- 'library.CRISPRcleanR_input.tsv'
###############################################################################
#* -- -- *#
#* -- MAIN SCRIPT -- *#
#* -- -- *#
###############################################################################
# Read in library
message("Reading library annotation...")
library_annotations_object <-
read_library_annotation_file(
filepath = opt$library,
id_column = opt$library_id_column_index,
gene_column = opt$library_gene_column_index,
chr_column = opt$library_chr_column_index,
chr_start_column = opt$library_start_column_index,
chr_end_column = opt$library_end_column_index,
file_separator = opt$library_delim,
file_header = ifelse(opt$no_library_header,FALSE,TRUE),
check.names = FALSE
)
# Read in sample count matrix
message("Reading count matrix...")
sample_count_matrix <- read_count_matrix_file(
filepath = opt$counts,
id_column = opt$count_id_column_index,
gene_column = opt$count_gene_column_index,
count_column = opt$count_count_column_index,
file_separator = opt$counts_delim,
file_header = ifelse(opt$no_counts_header,FALSE,TRUE),
processed = TRUE,
check.names = FALSE
)
# Read in fold change matrix
message("Reading fold change matrix...")
fold_change_matrix <- read_count_matrix_file(
filepath = opt$lfc_matrix,
id_column = opt$lfc_id_column_index,
gene_column = opt$lfc_gene_column_index,
count_column = opt$lfc_lfc_column_index,
file_separator = opt$lfc_delim,
file_header = ifelse(opt$no_lfc_header,FALSE,TRUE),
processed = TRUE,
check.names = FALSE
)
# Compare sgRNA IDs and gene names between count matrix and library
message("Comparing count matrix to library...")
mat_lib_match <- compare_count_matrix_to_library(
count_matrix = sample_count_matrix,
id_column = 1,
gene_column = 2,
library_annotation_object = library_annotations_object)
# Compare sgRNA IDs and gene names between fold change matrix and library
message("Comparing fold change matrix to library...")
mat_lib_match <- compare_count_matrix_to_library(
count_matrix = fold_change_matrix,
id_column = 1,
gene_column = 2,
library_annotation_object = library_annotations_object)
# Get CRISPRcleanR-formatted library
message("Preparing CRISPRcleanR-formatted library...")
processed_library <- get_library_annotations(library_annotations_object, processed = T, crisprcleanr = T)
# Get CRISPRcleanR-formatted count matrix
message("Preparing CRISPRcleanR-formatted count matrix...")
processed_count_matrix <- sample_count_matrix
colnames(processed_count_matrix)[1:2] <- c('sgRNA', 'gene')
# Get CRISPRcleanR-formatted count matrix
message("Preparing CRISPRcleanR-formatted fold change matrix...")
processed_fold_change_matrix <- fold_change_matrix
colnames(processed_fold_change_matrix)[1:2] <- c('sgRNA', 'gene')
# Write processed count matrix to file
message("Writing count matrix to file...")
outfile <- write_dataframe_to_file(data = processed_count_matrix,
outfile = opt$count_matrix_outfile,
outdir = opt$outdir,
prefix = opt$prefix,
suffix = opt$suffix,
row.names = FALSE,
quote = FALSE,
sep = "\t")
message(paste("Count matrix written to:", outfile))
# Write processed fold change matrix to file
message("Writing fold change matrix to file...")
outfile <- write_dataframe_to_file(data = processed_fold_change_matrix,
outfile = opt$lfc_matrix_outfile,
outdir = opt$outdir,
prefix = opt$prefix,
suffix = opt$suffix,
row.names = FALSE,
quote = FALSE,
sep = "\t")
message(paste("Fold change matrix written to:", outfile))
# Write processed library to file
message("Writing processed library to file...")
outfile <- write_dataframe_to_file(data = processed_library,
outfile = opt$library_outfile,
outdir = opt$outdir,
prefix = opt$prefix,
suffix = opt$suffix,
row.names = FALSE,
quote = FALSE,
sep = "\t")
message(paste("Fold change matrix written to:", outfile))
# Write Rdata to file
if (!is.null(opt$rdata)) {
message("Writing R data to file...")
rdata_outfile <- write_rdata_to_file(prefix = opt$prefix,
suffix = opt$suffix,
outfile = opt$rdata,
outdir = opt$outdir,
data = list(sample_count_matrix,
fold_change_matrix,
library_annotations_object,
processed_count_matrix,
processed_fold_change_matrix,
processed_library))
message(paste("R data written to:", rdata_outfile))
}
# Script exited without error
message("DONE")
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