xenome | R Documentation |
This function executes the docker container bwa1 where BWA is installed BWA is a read alignment package that efficiently align short sequencing reads against a large reference sequence This aligner provides optimal results with DNA-seq data
xenome(
group = c("sudo", "docker"),
fastq.folder = getwd(),
scratch.folder = "/data/scratch",
xenome.folder,
seq.type = "pe",
threads = 1
)
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 |
xenome.folder |
a character string indicating the folder where the indexed reference genomes generated by xenome are locates |
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 |
ambiguous, both, neither, hs and mm fastq.gz files. xeno_hs_R1.fastq.gz and xeno_hs_R2.fastq.gz are fastq file free of mouse reads and are used for further analysis.
Raffaele Calogero
## Not run:
#downloading examples 1 million reads of mcf7 exome mixed with 1 million of mouse derived by human exome capturing
system("wget http://130.192.119.59/public/hs1m_mm1m_R1.fastq.gz")
system("wget http://130.192.119.59/public/hs1m_mm1m_R2.fastq.gz")
#running xenome
xenome(group="docker",fastq.folder=getwd(), scratch.folder="/data/scratch",
xenome.folder="/data/scratch/hg19.mm10", seq.type="pe",
threads=24)
## End(Not run)
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