View source: R/dada2_upto_qualPlots.R
dada2.upto.qualPlots | R Documentation |
This function runs the first part of the pipeline, up through making quality plots, allowing the user to manually choose the truncation lengths based on those results.
dada2.upto.qualPlots( fastq.path, file.split.pattern = "--", maxCores = 4, random.seed = 42, user.output.path = NULL, force = FALSE, ask = TRUE )
fastq.path |
Path to raw FASTQ files. |
file.split.pattern |
A character string containg the pattern you want to use to separate the sample name and R1/R2 in the symlink names. Default is '–'. |
maxCores |
The maximum number of cores to utilize in steps that are parallelizabe. Default is 4. |
random.seed |
A integer utilized by 'set.seed' to make pipeline reproducible |
force |
Logical. By default the pipeline will skip steps if their corresponding output objects already exist. Set to TRUE to force the pipeline to run through all steps. Default is FALSE. |
ask |
Logical. Whether to prompt user to verify files in 'fastq.path'. FALSE skips this verification. Default TRUE. |
user.out.path |
Path to a directory if you want to use a specific output directory instead of the one programmatically generated by the pipeline. Primarily used if you are re-running a pipeline and want to save to previously generated output path. Default is NULL (which will autogenerate the output path). |
dada2
, plotQualityProfile
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