| rsemstar | R Documentation | 
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
rsemstar(
  group = c("sudo", "docker"),
  fastq.folder = getwd(),
  scratch.folder = "/data/scratch",
  genome.folder,
  seq.type = c("se", "pe"),
  strandness = c("none", "forward", "reverse"),
  threads = 1,
  save.bam = TRUE
)
| 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 | 
| genome.folder | 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 | 
| seq.type | a character string indicating the type of reads to be trimmed. Two options:  | 
| strandness | a character string indicating the type ofsequencing protocol used for the analysis. Three options:  | 
| threads | a number indicating the number of cores to be used from the application | 
| save.bam | 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
Raffaele Calogero
## Not run: 
    #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)
## End(Not run)
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