rsemstar.Rd
This function executes the docker container rsemstar1, where RSEM is used to calculate gene/isoforms counts using as mapper STAR, Dubin et al. Bioinformatics. 2013 Jan 1;29(1):15-21
a character string. Two options: "sudo"
or "docker"
, depending to which group the user belongs
a character string indicating where gzip fastq files are located
a character string indicating the scratch folder where docker container will be mounted
a character string indicating the folder where the indexed reference genome for STAR is located. IMPORTANT the present function only suport genomic indexes made using ensembl genom and the corresponding gtf
a character string indicating the type of reads to be trimmed. Two options: "se"
or "pe"
respectively for single end and pair end sequencing
a character string indicating the type ofsequencing protocol used for the analysis. Three options: "none"
, "forward"
, "reverse"
respectively for non strand selection, forward for Illumina strandness protocols, reverse for ACCESS Illumina protocol
a number indicating the number of cores to be used from the application
a boolean TRUE FALSE to decide if bam files are saved
three files: dedup_reads.bam, which is sorted and duplicates marked bam file, dedup_reads.bai, which is the index of the dedup_reads.bam, and dedup_reads.stats, which provides mapping statistics
if (FALSE) {
#downloading fastq files
system("wget http://130.192.119.59/public/test_R1.fastq.gz")
system("wget http://130.192.119.59/public/test_R2.fastq.gz")
library(docker4seq)
#running rsemstar nostrand pe
rsemstar(group="docker",fastq.folder=getwd(), scratch.folder="/data/scratch/",
genome.folder="/data/genomes/hg38star/", seq.type="pe", strandness="none",
threads=8, save.bam = FALSE)
}