checkAlign2ref | Check the alignment with the imputation reference panel |
chrWiseSplit | Split genome-wide genotyping data into chromosome-wide PLINK... |
chunk4eachChr | Chunk each chromosome into multiple segments |
computeInfoByQctool | Calculate the info score by QCTOOL |
dot-convertImpute2ByGtool | Convert IMPUTE2 format files into PLINK format |
dot-filterImputeData | Filter genetic variants |
dot-filterImputeData2 | Filter genetic variants |
dot-getInfoScoreImpute2 | Extract info score |
dot-imputedByImpute2 | Impute genotypes using IMPUTE2 |
dot-imputedByImpute4 | Impute genotypes using IMPUTE4 |
dot-mergePlinkData | Merge chunk-wise PLINK files |
dot-prepareLegend2bim | Prepare a bim-like reference file |
dot-prePhasingByShapeit | Prephasing genotypes using SHAPEIT |
dot-snpSharedPos | Find shared genomic position between two files. |
extractByGenipe | Extract imputed markers using Genipe |
genoQC | Quality control for genotype data |
getGroupLabel | Get the outcome label of the genotype data |
imputedByGenipe | Impute genotypes using Genipe |
mergeByGenipe | Merge imputed files using Genipe |
phaseImpute | Phasing and imputation |
plotPCA4plink | Population outlier detection |
postImpQC | Post imputation quality control |
prepareAnnoFile4affy | prepare Affymetrix chip annotation file |
reductExpand | Post imputation data extraction and expansion |
removedDoubleProbes | Remove duplicated SNPs |
removedExclProbe | Remove improper SNPs |
removedInstFhet | Remove subjects with abnormal autosomal heterozygosity... |
removedInstMiss | Remove subjects with missing values |
removedMaleHetX | Remove male subjects with haploid heterozygous SNPs |
removedMendelErr | Check Mendel errors for family-based data |
removedMonoSnp | Exclude monomorphic SNPs |
removedParentIdsMiss | Reset paternal and maternal codes |
removedSnpFemaleChrXhweControl | Hardy Weinberg Equilibrium test for chromosome X SNPs in... |
removedSnpFemaleChrXmiss | remove chromosome X SNPs in females |
removedSnpHetX | Remove heterozygous SNPs in male chromosome X |
removedSnpHWEauto | Hardy Weinberg Equilibrium test for autosomal SNPs |
removedSnpMiss | Remove SNPs with missing values |
removedSnpMissDiff | Remove SNPs with difference in SNP missingness between cases... |
removedSnpMissPostImp | Remove SNPs after post imputation |
removedUnmapProbes | Remove SNPs not in the chip annotation file |
removedWrongAnceInst | Remove samples with incorrect ancestry |
removedYMtSnp | Remove SNPs on the chromosome Y and mitochondrial DNA |
removeNoGroupId | Remove samples without group information |
removeOutlierByPCs | Remove population outliers |
removeSampID | Remove samples in PLINK files |
renamePlinkBFile | Rename PLINK binary files |
setHeteroHaploMissing | Set haploid heterozygous SNPs as missing |
splitXchr | Split chromosome X into pseudoautosomal region and... |
updatedSnpInfo | Update the SNP information |
updateGenoInfo | Update genotype information |
updateGroupIdAndSex | Update group and geneder information |
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