| ciri2 | R Documentation | 
This function executes the docker container ciri2 where CIRI v2.0.6 is installed and it provides the list of circRNAs predicted from a RNA-Seq experiment. For CIRI 2 tool detail refer to: "Gao, Y., Zhang, J., & Zhao, F. (2017). Circular RNA identification based on multiple seed matching. Brief Bioinform. 2018 Sep 28;19(5):803-810."
ciri2(
  group = c("sudo", "docker"),
  scratch.folder,
  sam.file,
  genome.file,
  annotation.file = NA,
  max.span = 2e+05,
  stringency.value = c("high", "low", "zero"),
  quality.threshold = 10,
  threads = 1
)
| group | a character string. Two options:  | 
| scratch.folder | a character string indicating the scratch folder where docker container will be mounted | 
| sam.file | a character string indicating the path to the RNA-Seq alignment SAM file from BWA | 
| genome.file | a character string indicating the path to the Fasta file of the reference genomic sequence (it should be the same reference indexed for the BWA alignment) | 
| annotation.file | a character string indicating the path to the GTF/GFF file reporting the reference gene annotations | 
| max.span | an integer reporting the maximum spanning distance of a circRNA (default = 200000 bp) | 
| stringency.value | the selected stringency level of the analysis. Three possible options are available: "high" (high stringency, default), in which CIRI2 only provides circRNAs supported by more than 2 distinct Paired Chiastic Clipping (PCC) signals; "low" (low stringency), CIRI2 only provides circRNAs supported by more than 2 junction reads; "zero", CIRI2 provides all circRNAs regardless junction read counts or PCC signals | 
| quality.threshold | integer indicating the threshold for mapping quality of each segment of junction reads (default=10) | 
| threads | integer indicating the number of threads used for the analysis (default=1) | 
The list of CIRI 2 predicted circRNAs
Nicola Licheri and Giulio Ferrero
## Not run: 
    #retrieve the example data
    system("wget https://sourceforge.net/projects/ciri/files/CIRI2/CIRI_v2.0.6.zip") #retrieve the example data
    system("unzip CIRI_v2.0.6.zip")
    #running ciri2 function
    ciri2(group="docker", scratch.folder="/data/scratch", sam.file=paste(getwd(),"/CIRI_v2.0.6/data/sample.sam", sep=""), genome.file=paste(getwd(),"/CIRI_v2.0.6/data/chr1.fa", sep=""), annotation.file="", max.span=200000, stringency.value="high", quality.threshold=10, threads=1)
## End(Not run)
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