rsemanno | R Documentation |
This function executes the docker container annotate.1, where Bioconductor is used to annotated gene.results output of RSEM using ENSEMBL annotation
rsemanno(
group = c("sudo", "docker"),
rsem.folder = getwd(),
scratch.folder = "/data/scratch",
org = c("hg19", "hg38", "mm10", "mm9"),
truncating.expected.counts = FALSE,
protein.anno = FALSE
)
group |
a character string. Two options: |
rsem.folder |
a character string indicating where gene.results and isoforms.results are located |
scratch.folder |
a character string indicating the scratch folder where docker container will be mounted |
org |
a character string indicating the genome assembly used for mapping and counting with |
truncating.expected.counts |
a boolean logical variable indicating if the expected counts calculated by RSEM need to be converted in integer to be compliant with differnetial expression Bioconductor packages as DESeq2. Default is FALSE |
protein.anno |
a boolean logical variable indicating if instead of gene SYMBOL SWISSPROT symbol are used. This option is useful for integrating transcriptomics data with proteomics data |
one file: annotated_genes.results, which is the annotated version of gene.results.
## Not run:
#downloading fastq files
system("wget http://130.192.119.59/public/genes.results.gz")
gzip -d genes.results.gz
#running rsemanno
rsemanno(group="docker",rsem.folder=getwd(), scratch.folder="/data/scratch",
org="hg38", truncating.expected.counts=FALSE,
protein.anno=FALSE)
## End(Not run)
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