View source: R/genotypeInfoUpdate.R
removedDoubleProbes | R Documentation |
Remove duplicated SNPs that have same rs-names or duplicated genomic position.
removedDoubleProbes( plink, inputPrefix, chipAnnoFile, chipType, outputSNPdupFile, outputPrefix )
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. |
chipAnnoFile |
an input chip annotation file. If the chip annotation file is not available for your study, it can be downloaded from http://www.well.ox.ac.uk/~wrayner/strand/. |
chipType |
a string name defines the type of the chip annotation file:
'SNPIDstudy', and 'rsIDstudy'. The detail is described in
|
outputSNPdupFile |
a pure text file that stores the duplicated SNP IDs, which are detected by the use of the chip annotation file. |
outputPrefix |
the prefix of the output PLINK binary files. |
Duplicated SNPs have two levels of meaning: 1.) SNPs have same rs-names but different versions of SNP ID in chip annotation file. e.g. SNP-A IDs for Affymetrix chip. 2.) SNPs with duplicated genomic position: the combination of base pair position and chromosomal location.
The output PLINK binary files after removing duplicated SNP IDs.
Junfang Chen
prepareAnnoFile4affy
## In the current working directory bedFile <- system.file("extdata", "controlData.bed", package="Gimpute") bimFile <- system.file("extdata", "controlData.bim", package="Gimpute") famFile <- system.file("extdata", "controlData.fam", package="Gimpute") chipAnnoFile <- system.file("extdata", "chipAnno.txt", package="Gimpute") system(paste0("scp ", bedFile, bimFile, famFile, " .")) inputPrefix <- "controlData" chipType <- "rsIDstudy" outputSNPdupFile <- "snpDup.txt" outputPrefix <- "removedDoubleProbes" ## Not run: Requires an executable program PLINK, e.g. ## plink <- "/home/tools/plink" ## removedDoubleProbes(plink, inputPrefix, chipAnnoFile, ## chipType, outputSNPdupFile, outputPrefix)
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