skewer | R Documentation |
This function executes the docker container skewer1 to remove sequencing adapters from RNAseq reads
skewer(
group = c("sudo", "docker"),
fastq.folder = getwd(),
scratch.folder = "/data/scratch",
adapter5,
adapter3,
seq.type = c("se", "pe"),
threads = 1,
min.length = 18
)
group |
a character string. Two options: |
fastq.folder |
a character string indicating where gzip fastq files are located |
scratch.folder |
a character string indicating the scratch folder where docker container will be mounted |
adapter5 |
a character string indicating the fwd adapter |
adapter3 |
a character string indicating the rev adapter |
seq.type |
a character string indicating the type of reads to be trimmed. Two options: |
threads |
a number indicating the number of cores to be used from the application |
min.length |
a number indicating minimal length required to return a trimmed read |
One or two gzip fastq files ending with trimmed-pair1.fastq.gz and trimmed-pair1.fastq.gz, a log file of the trimming with the extensione trimmed.log, run.info file descring the analysis steps done by the docker. The latter file is useful to understand where the docker stop in case of unexpected end
Raffaele Calogero
## Not run:
system("wget http://130.192.119.59/public/test_R1.fastq.gz")
system("wget http://130.192.119.59/public/test_R2.fastq.gz")
skewer(group="docker",fastq.folder=getwd(), scratch.folder="/data/scratch",
adapter5="AGATCGGAAGAGCACACGTCTGAACTCCAGTCA",
adapter3="AGATCGGAAGAGCGTCGTGTAGGGAAAGAGTGT",
seq.type="pe", threads=10, min.length=40)
## End(Not run)
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