| removedSnpFemaleChrXmiss | R Documentation | 
Remove SNPs on the chromosome X with a pre-defined cutoff for missingness in females.
removedSnpFemaleChrXmiss( plink, femaleChrXmissCutoff, inputPrefix, outputPrefix )
plink | 
 an executable program in either the current working directory or somewhere in the command path.  | 
femaleChrXmissCutoff | 
 the cutoff of the missingness in female chromosome X SNPs.  | 
inputPrefix | 
 the prefix of the input PLINK binary files.  | 
outputPrefix | 
 the prefix of the output PLINK binary files.  | 
The output PLINK binary files.
Junfang Chen
 
## In the current working directory
bedFile <- system.file("extdata", "genoUpdatedData.bed", package="Gimpute")
bimFile <- system.file("extdata", "genoUpdatedData.bim", package="Gimpute") 
famFile <- system.file("extdata", "genoUpdatedData.fam", package="Gimpute")
system(paste0("scp ", bedFile, bimFile, famFile, " ."))  
femaleChrXmissCutoff <- 0.05
inputPrefix <- "genoUpdatedData"  
outputPrefix <- "2_10_removedSnpFemaleChrXmiss" 
## Not run: Requires an executable program PLINK, e.g.
## plink <- "/home/tools/plink"
## removedSnpFemaleChrXmiss(plink, femaleChrXmissCutoff, 
##                          inputPrefix, outputPrefix)
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