removedInstFhet | R Documentation |
Remove subjects with great autosomal heterozygosity deviation.
removedInstFhet(plink, Fhet, inputPrefix, outputPrefix)
plink |
an executable program in either the current working directory or somewhere in the command path. |
Fhet |
the cutoff of the autosomal heterozygosity deviation. |
inputPrefix |
the prefix of the input PLINK binary files. |
outputPrefix |
the prefix of the output PLINK binary files. |
If the cutoff of the autosomal heterozygosity deviation is set to be greater than 0.2, i.e. |Fhet| >= 0.2, then this analysis will automatically skip haploid markers (male X and Y chromosome markers).
The output PLINK binary files after removing subjects with great autosomal heterozygosity deviation.
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, " .")) Fhet <- 0.2 inputPrefix <- "genoUpdatedData" outputPrefix <- "2_06_removedInstFhet" ## Not run: Requires an executable program PLINK, e.g. ## plink <- "/home/tools/plink" ## removedInstFhet(plink, Fhet, inputPrefix, outputPrefix)
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