View source: R/varcall2HowMany.R
varcall2HowMany | R Documentation |
From an excel with mutation detected in each varian caller, the function convert the data in a table with information about in how many variant callers appeared the mutation.
varcall2HowMany( filename, chr_pos = 1, position = 2, gen_name = 3, varian_caller = 4, VAF = NA, others = NULL, var_cal_4 = c("mutect38", "somaticsniper", "strelka", "varscan") )
filename |
The name of the excel file with the mutations with choromosome, position, gen name and variant caller |
chr_pos |
Position of the chromosome name in the data frame |
position |
Position of the mega position in the data frame |
gen_name |
Position of the Gene name in the data frame |
varian_caller |
Position of the Variant Caller in the data frame |
VAF |
Position of the VAF name in the data frame (if is not present, NA will be presented) |
others |
Position of the other variables in the data frame that will be merged |
var_cal_4 |
Names of the four variant caller to calculate the How many field |
data frame with How many variant callers per mutation
## Not run: varcall2HowMany (filename) ## End(Not run)
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