| salmon | R Documentation | 
This function calls
salmon
using system2(). To run in parallel, register a parallel backend, e.g.,
using doParallel::registerDoParallel().
salmon(
  filepaths,
  samples,
  indexDir,
  outputDir = "salmon_output",
  cmd = "salmon",
  args = c("-l A -q --seqBias --gcBias --no-version-check -p",
    foreach::getDoParWorkers()),
  compress = TRUE
)
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 ";".  | 
samples | 
 Corresponding sample names for fastq files.  | 
indexDir | 
 Directory that contains salmon index.  | 
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.  | 
compress | 
 Logical indicating whether to gzip the quantification file (quant.sf) from salmon. Does not affect downstream analysis.  | 
A vector of exit codes, invisibly.
seeker(), getSalmonMetadata()
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