View source: R/postImputation.R
postImpQC | R Documentation |
Perform quality control and data management after imputation.
postImpQC( plink, inputPrefix, out1, out2, out3, out4, outputInfoFile, infoScore = 0.6, outputMonoSNPfile, prefixAlign2ref, missCutoff = 20, outRemovedSNPfile, outRetainSNPfile, referencePanel )
plink |
an executable program in either the current working directory or somewhere in the command path. |
inputPrefix |
the prefix of the final imputed PLINK files. |
out1 |
the prefix of well imputed PLINK files with the index. |
out2 |
the prefix of well imputed PLINK files after removing any SNPs with the same positions (if any), the index is also appended. |
out3 |
the prefix of well imputed PLINK files with the index after adding previously identified monomorphic SNPs if any. |
out4 |
the prefix of final well imputed PLINK files with the index. |
outputInfoFile |
the output file of impute2 info scores consisting of two columns: all imputed SNPs and their info scores. |
infoScore |
the cutoff of filtering imputation quality score for each variant. The default value is 0.6. |
outputMonoSNPfile |
the output pure text file that stores the removed monomorphic SNPs, one per line, if any. |
prefixAlign2ref |
the prefix of the output PLINK binary files after removing SNPs whose alleles are not in the imputation reference, taking their genomic positions into account. |
missCutoff |
the cutoff of the least number of instances for a SNP that is not missing. The default is 20. |
outRemovedSNPfile |
the output file of SNPs with pre-defined missing values that are removed. |
outRetainSNPfile |
the output file of SNPs that are retained. |
referencePanel |
a string indicating the type of imputation reference panels is used: c("1000Gphase1v3_macGT1", "1000Gphase3"). |
All imputed genotype data in PLINK format, well imputed data and its variants, as well as a set of pure text files containing removed or retained SNPs.
Junfang Chen
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