fastq_to_fasta | R Documentation |
Wrapper function for fastq_to_fasta
fastx_qtoa( fileToc, fqa = "fastq_to_fasta", discard_N = T, rename = F, outFile = paste0(file_path_sans_ext(fileToc), ".fa"), writelog = T, qEncoding = 33, stderr = file.path(dirname(fileToc), paste0(basename(fileToc), "_qtoa_stderr.txt")), stdout = file.path(dirname(fileToc), paste0(basename(fileToc), "_qtoa_stdout.txt")), useClipRConda = ifelse(is.null(getOption("CLIPflexR.condaEnv")), FALSE, TRUE), additional_Args = NULL, verbose = FALSE )
fileToc |
path to file to process (fastq). |
fqa |
path to fastx_trimmer from FastX toolkit. |
discard_N |
discard reads with unknown nucleotides (N), TRUE (default) or FALSE. |
rename |
replace sequence names with number identifiers, TRUE or FALSE (default). |
outFile |
output file path. |
writelog |
write stderr/stdout logs, TRUE (default) or FALSE. |
qEncoding |
quality encoding, set to either 33 (Sanger Phred+33 encoding/Illumina fastq; default) or NULL (Phred+64 fastq). |
stderr |
path to stderr file. |
stdout |
path to stdout file. |
useClipRConda |
use conda environment installed by Herper, TRUE (default) or FALSE. |
additional_Args |
additional arguments to be passed to system call. |
verbose |
print messages to screen, TRUE or FALSE (default). |
path to trimmed file
Kathryn Rozen-Gagnon
testFQ <- system.file("extdata/Fox3_Std_small.fq.gz",package="CLIPflexR") FqFile_FF <- ctk_fastqFilter(testFQ,qsFilter = "mean:0-29:20",verbose=TRUE) FqFile <- decompress(FqFile_FF,overwrite=TRUE) FqFile_fa <- fastx_qtoa(FqFile)
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