View source: R/oncosnpIllumina.R
oncosnp | R Documentation |
This function executes a ubuntu docker that produces as output oncosnp and request as input a tabl delimited file with Name Chromosome Position Log R Ratio B Allele Freq, where Name is the snp id from Illumina arrays, Chromosome is the chr, POsition is the SNP location in the chr Log R Ratio B Allele Freq are genrated from genomestudio
oncosnp(
group = c("sudo", "docker"),
data.folder,
scratch.folder,
sample.name = NULL,
blood.name = NULL
)
group |
a character string. Two options: sudo or docker, depending to which group the user belongs |
data.folder |
a character string indicating the folder where input data are located and where output will be written |
scratch.folder |
a character string indicating the scratch folder for temporary operations |
sample.name |
a character string indicating snp data file name |
blood.name |
a character string indicating snp data file name for blood snp |
cnv1.cnvs, cnv2,cnvs and other oncosnp elements, see oncosnp help page for further information
Raffaele Calogero, raffaele.calogero [at] unito [dot] it, University of Torino
## Not run:
system("wget http://130.192.119.59/public/testcnv.zip")
#running fastqc
oncosnp(group="docker", data.folder=getwd(), scratch.folder="/data/scratch", sample.name="sampleXX.txt", blood.name=NULL)
## End(Not run)
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