mutSelection | R Documentation |
Select candidate variants for cancer research.
mutSelection(
maf,
dbVAF = 0.01,
ExAC = TRUE,
Genomesprojects1000 = TRUE,
ESP6500 = TRUE,
gnomAD = TRUE,
dbSNP = FALSE,
keepCOSMIC = TRUE,
keepType = "exonic",
bedFile = NULL,
bedHeader = FALSE,
bedFilter = TRUE,
progressbar = TRUE,
verbose = TRUE
)
maf |
An MAF data frame, generated by |
dbVAF |
Threshold of VAF of certain population for variants in database. Default: 0.01 |
ExAC |
Whether to filter variants listed in ExAC with VAF higher than cutoff(set in VAF parameter). Default: TRUE. |
Genomesprojects1000 |
Whether to filter variants listed in Genomesprojects1000 with VAF higher than cutoff(set in VAF parameter). Default: TRUE. |
ESP6500 |
Whether to filter variants listed in ESP6500 with VAF higher than cutoff(set in VAF parameter). Default: TRUE. |
gnomAD |
Whether to filter variants listed in gnomAD with VAF higher than cutoff(set in VAF parameter). Default: TRUE. |
dbSNP |
Whether to filter variants listed in dbSNP. Default: FALSE. |
keepCOSMIC |
Whether to keep variants in COSMIC even they have are present in germline database. Default: TRUE. |
keepType |
A group of variant classifications will be kept, including 'exonic', 'nonsynonymous' and 'all'. Default: 'exonic'. |
bedFile |
A file in bed format that contains region information. Default: NULL |
bedHeader |
Whether the input bed file has a header or not. Default: FALSE. |
bedFilter |
Whether to filter the information in bed file or not, which only leaves segments in Chr1-Ch22, ChrX and ChrY. Default: TRUE |
progressbar |
Whether to show progress bar when running this function Default: TRUE |
verbose |
Whether to generate message/notification during the filtration process. Default: TRUE. |
An MAF data frame with variants after selection.
maf <- vcfToMAF(system.file("extdata",
"WES_EA_T_1_mutect2.vep.vcf", package="CaMutQC"))
mafF <- mutSelection(maf)
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