load.data | R Documentation |
This function loads a series of data tables or VCFs into a dataset object which is in essense a list of tables, one for each type of information
load.data(list_of_data_files, cellularity, Chromosome, position, WT.count,
mut.count, subclonal.CN, no.chrs.bearing.mut, mutation.copy.number,
subclonal.fraction, phase = NULL, is.male = T, is.vcf = F,
ref.genome.version = "hg19", supported_chroms = c(1:22))
list_of_data_files |
A list of data file names to be read in |
cellularity |
A vector containing the cellularity estimates for each sample |
Chromosome |
String that contains the name of the column with chromosome denomination for each mutation |
position |
String that contains the name of the column with position denomination for each mutation |
WT.count |
String the colname of the column in the data files that contains the number of wild type reads |
mut.count |
String, the colname of the column in the data files that contains the number of mutant reads |
subclonal.CN |
String, the name of the total copynumber column |
no.chrs.bearing.mut |
String, the column that contains the number of chromosomes not bearing any mutations |
mutation.copy.number |
String, colname with mutation copy number estimates |
subclonal.fraction |
String, colname of the column that contains the subclonal fraction (or CCF) estimate for each mutation |
phase |
String, colname of the copy number to mutation phasing info column |
is.male |
Optional boolean that represents the sex, set to TRUE if male, FALSE if female. This information is used to decide whether to include X chromosome mutations |
is.vcf |
Optional boolean parameter whether the files to be read in are in VCF format |
ref.genome.version |
Optional string that represents the reference genome, required when reading in VCF files |
A list of tables, one for each type of information
sd11
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