Description Usage Arguments Value Examples
Subset Maf object
| 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 | subMaf(
  maf,
  mafObj = FALSE,
  patient.id = NULL,
  geneList = NULL,
  chrSilent = NULL,
  mutType = "All",
  use.indel = TRUE,
  min.vaf = 0,
  max.vaf = 1,
  min.average.vaf = 0,
  min.ccf = 0,
  min.ref.depth = 0,
  min.alt.depth = 0,
  min.total.depth = 0,
  clonalStatus = NULL,
  use.adjVAF = FALSE,
  use.tumorSampleLabel = FALSE
)
 | 
| maf | Maf or MafList object generated by  | 
| mafObj | return Maf class. (Default: FALSE). | 
| patient.id | Select the specific patients. Default NULL, all patients are included. | 
| geneList | A list of genes to restrict the analysis. Default NULL. | 
| chrSilent | Chromosomes excluded in the analysis. e.g, 1, 2, X, Y. Default NULL. | 
| mutType | Select Proper variant classification you need. Default "All". Option: "nonSyn". | 
| use.indel | Logical value. Whether to use INDELs besides somatic SNVs. (Default: TRUE). | 
| min.vaf | The minimum VAF for filtering variants. Default 0. | 
| max.vaf | The maximum VAF for filtering variants. Default 1. | 
| min.average.vaf | The minimum tumor average VAF for filtering variants. Default 0. | 
| min.ccf | The minimum CCF for filtering variants. Default NULL. | 
| min.ref.depth | The minimum reference allele depth for filtering variants. Default 0. | 
| min.alt.depth | The minimum alteratation allele depth for filtering variants. Default 0. | 
| min.total.depth | The minimum total allele depth for filtering variants. Default 0. | 
| clonalStatus | Subset by clonal status. Default NULL. Option: "Clonal","Subclonal". | 
| use.adjVAF | Use adjusted VAF in analysis when adjusted VAF or CCF is available. Default FALSE. | 
| use.tumorSampleLabel | Logical (Default: FALSE). Rename the 'Tumor_Sample_Barcode' by 'Tumor_Sample_Label'. | 
Maf object or Maf data.
| 1 2 3 4 5 | maf.File <- system.file("extdata/", "CRC_HZ.maf", package = "MesKit")
clin.File <- system.file("extdata/", "CRC_HZ.clin.txt", package = "MesKit")
ccf.File <- system.file("extdata/", "CRC_HZ.ccf.tsv", package = "MesKit")
maf <- readMaf(mafFile=maf.File, clinicalFile = clin.File, ccfFile=ccf.File, refBuild="hg19")
maf_data <- subMaf(maf)
 | 
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