View source: R/r-functions.selection.R
find.outliers | R Documentation |
Find hypo- and hyper-mutated samples
find.outliers(input.file.name, output.folder, output.prefix)
input.file.name: |
A VCF-formatted file to read SnpEff annotated somatic variants. This input file shall contain these fields: Tumor_Sample_Barcode, Chromosome, Start_Position, dbSNP_RS, Reference_Allele, Tumor_Seq_Allele2, FILTER, One_Consequence, Hugo_Symbol, Gene, Feature, ENSP, HGVSc, HGVSp_Short, Amino_acids, Codons, ENSP, RefSeq, Entrez_Gene_Id. |
output.folder: |
the folder to write the output files |
output.prefix: |
prefix used to name the output file as prefix.outlier.txt . |
find.outliers(input.file.name='./examples/TCGA.ACC.mutect.somatic.maf.gz', output.folder='./examples/', output.prefix='TCGA.ACC');
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