View source: R/PrepareBam_EP.R
| PrepareBam_EP | R Documentation | 
Prepares the information contained in .bam files to be analyzed by EventPointer
PrepareBam_EP(
  Samples,
  SamplePath,
  Ref_Transc = "Ensembl",
  fileTransc = NULL,
  cores = 1,
  Alpha = 2
)
| Samples | Name of the .bam files to be analyzed (Sample1.bam,Sample2.bam,...,etc). | 
| SamplePath | Path where the bam files are stored. | 
| Ref_Transc | Reference transcriptome used to name the genes found in bam files. Options are: Ensembl, UCSC or GTF. | 
| fileTransc | Path to the GTF reference transcriptome ff Ref_Transc is GTF. | 
| cores | Number of cores used for parallel processing. | 
| Alpha | Internal SGSeq parameter to include or exclude regions | 
SGFeaturesCounts object. It contains a GRanges object with the corresponding elements to build the different splicing graphs found and the counts related to each of the elements.
## Not run: 
 # Obtain the samples and directory for .bam files
   BamInfo<-si
   Samples<-BamInfo[,2]
   PathToSamples <- system.file('extdata/bams', package = 'SGSeq')
   PathToGTF<-paste(system.file('extdata',package='EventPointer'),'/FBXO31.gtf',sep='')
  # Run PrepareBam function
   SG_RNASeq<-PrepareBam_EP(Samples=Samples,
                            SamplePath=PathToSamples,
                            Ref_Transc='GTF',
                            fileTransc=PathToGTF,
                            cores=1)
## End(Not run)
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