run_sampleContamination: Main function to run sample contamination analysis

Description Usage Arguments Value References

View source: R/run_sampleContamination.R

Description

This function detects sample contamination base on variant allele frequency (VAF) and variant coverage

Usage

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run_sampleContamination(data_path, output_path, config_file="config.txt",
rmSNPcv_cutoff=0,manualsetPara=FALSE,manual_localPcomm=10,manual_center=50,filterCOV=0)

Arguments

data_path

character, mutation VAF and coverage file directory

output_path

character, output directory

config_file

character, configuration file

rmSNPcv_cutoff

numeric, TRUE: filter SNPs with low covariance of coefficient (COV) (default: FALSE)

manualsetPara

logical, TRUE: manual setting base on distribution of pairwise samples commonality (default: FALSE)

manual_localPcomm

numeric, manual setting of localPcomm for low or high contamination (default: 10)

manual_center

numeric, manual setting of center cutoff for same subject determination (default: 50)

filterCOV

numeric, filter mutation below this cutoff

Value

list, containing pcomm, center cutoff, target cutoff, source cutoff, region cutoff and number of sample

References

TBA


lpwgit/sampleContamination documentation built on May 21, 2019, 7:51 a.m.