View source: R/snvPreprocessing.R
snvPreprocessing | R Documentation |
This function executes the docker container snvPreprocessing. IMPORTANT: the working folder require the presence of GenomeAnalysisTK.tar.bz2 files
snvPreprocessing(
group = c("sudo", "docker"),
bam.folder = getwd(),
scratch.folder = "/data/scratch",
genome.folder,
threads = 8,
gatk.file
)
group |
a character string. Two options: |
bam.folder |
a character string indicating where bam file generated by bwa is located |
scratch.folder |
a character string indicating the scratch folder where docker container will be mounted |
genome.folder |
a character string indicating the folder where the index reference genome for bwa is located |
threads |
a number indicating the number of cores to be used by the application |
gatk.file |
a character string for GenomeAnalysisTK-X.Y.tar.bz2, this file should be located in the bam.folder |
bam and bai after indel relignment and quality recalibration.
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")
#required for bwa 61Gb At the present time this is required to run mutect1
system("wget http://130.192.119.59/public/hg19_exome.tar.gz")
#this genome index is prepared to be used for indel realignment and quality recalibration
#running snvPreprocessing
snvPreprocessing(group="docker",bam.folder=getwd(),
scratch.folder="/data/scratch",
genome.folder="/data/scratch/hg19_exome",
threads=24, gatk.file="GenomeAnalysisTK-3.7.tar.bz2")
## End(Not run)
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