trimgalore: Run Trim Galore!

In seeker: Simplified Fetching and Processing of Microarray and RNA-Seq Data

Run Trim Galore!

Description

This function calls trim_galore using system2(), and is only designed to handle standard adapter/quality trimming. To run in parallel, register a parallel backend, e.g., using doParallel::registerDoParallel().

Usage

trimgalore(
  filepaths,
  outputDir = "trimgalore_output",
  cmd = "trim_galore",
  args = NULL,
  pigzCmd = "pigz"
)

Arguments

filepaths	Paths to fastq files. For single-end reads, each element should be a single filepath. For paired-end reads, each element should be two filepaths separated by ";".
outputDir	Directory in which to store output. Will be created if it doesn't exist.
cmd	Name or path of the command-line interface.
args	Additional arguments to pass to the command-line interface. Output files will always be compressed. Arguments "–gzip", "–cores", "-j", and "–basename" are not allowed. Arguments "-o" and "–paired" should not be specified here.
pigzCmd	String for pigz command, which will gzip the output files.

Value

A vector of exit codes, invisibly.

See Also

seeker()

seeker documentation built on Sept. 11, 2024, 7:54 p.m.