removedSnpMissDiff | R Documentation |
Remove SNPs with difference in SNP missingness between cases and controls. To test for differential call rates between cases and controls for each SNP
removedSnpMissDiff( plink, inputPrefix, snpMissDifCutOff, outputPrefix, groupLabel )
plink |
an executable program in either the current working directory or somewhere in the command path. |
inputPrefix |
the prefix of the input PLINK binary files. |
snpMissDifCutOff |
the cutoff of the difference in missingness between cases and controls. |
outputPrefix |
the prefix of the output PLINK binary files. |
groupLabel |
a string value indicating the outcome label: "control",
or, "case" or "caseControl" for both existing groups. For more details, see
|
Only if both case-control groups exist in the input genotype data, differential SNPs are removed.
The output PLINK binary files.
Junfang Chen
getGroupLabel
.
## 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, " .")) inputPrefix <- "genoUpdatedData" snpMissDifCutOff <- 0.02 outputPrefix <- "2_09_removedSnpMissDiff" groupLabel <- "control" ## Not run: Requires an executable program PLINK, e.g. ## plink <- "/home/tools/plink" ## removedSnpMissDiff(plink, inputPrefix, snpMissDifCutOff, ## outputPrefix, groupLabel)
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