S4 Tools for Reading and Organizing Genetic Data


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Documentation for package ‘SNPkit’ version 0.1.0

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as_snpmatrix Convert a genotype matrix or data.frame to snpStats::SnpMatrix
cbind_SnpMatrix Safe cbind for SnpMatrix preserving dimnames
check.call.rate Check SNP call rate
check.ibs Check Identity-By-State (IBS) for a genotype pair
check.identical.samples Check identical samples based on distance
check.identical.samples.by.block Check identical samples by block
check.mendelian.inconsistencies Check Mendelian inconsistencies
check.mendelian.inconsistencies.pair Check Mendelian inconsistencies for a pair
check.sample.call.rate Check Sample Call Rate
check.sample.heterozygosity Check sample heterozygosity
check.snp.chromo Check SNP by chromosome
check.snp.hwe Check SNP Hardy-Weinberg equilibrium deviation
check.snp.hwe.chi2 Check SNPs for Hardy-Weinberg equilibrium deviation using chi-square p-values
check.snp.maf Check SNP minor allele frequency
check.snp.mgf Check SNP missing genotype frequencies
check.snp.monomorf Check SNP monomorphic status
check.snp.no.position Check SNP no position
check.snp.same.position Check SNPs mapped to the same position
combineSNPData Combine multiple SNPDataLong objects
doPCA Do genome relationship matrix PCA
exploratory.plots Exploratory plots for SNP and sample summary
FImputeExport-class FImputeExport Class
FImputeRunner Build FImputeRunner object
FImputeRunner-class FImputeRunner Class
genoToDF Convert geno slot from SNPDataLong to a data.frame
get.correl.fc Get correlation (fc method)
get.gender Get gender based on heterozygosity
get.hwe.chi2 Get HWE chi-square p-values
getGeno Flexible and efficient genotype file reading with autodetection using fread
getGeno-method Flexible and efficient genotype file reading with autodetection using fread
ibs.pair IBS pair statistics
importAllGenos Import and combine multiple genotype configurations
importAllGenos-method Import and combine multiple genotype configurations
importFImputeResults Import imputed FImpute results from disk
import_geno_list Import multiple genotype datasets from a list of configurations
pairs2sets Convert pairs to sets
plotPCAgroups Plot PCA groups from anticlustering result
print.summary.SNPDataLong Print method for SNPDataLong summary
qcSamples Quality control on samples
qcSamples-method Quality control on samples
qcSNPs Quality Control for SNPDataLong with optional criteria
qcSNPs-method Quality Control for SNPDataLong with optional criteria
qc_header Formatted header message
rbindSnpFlexible Faster row-bind for SnpMatrix objects with differing columns
rbind_SnpMatrix Safe rbind for SnpMatrix preserving dimnames
read.fimpute Read imputed genotypes from FImpute output and return SNPDataLong object
runAnticlusteringPCA Run PCA and anticlustering on SNPDataLong
runFImpute Run FImpute from a FImputeRunner object
runFImpute-method Run FImpute from a FImputeRunner object
run_admixture Run ADMIXTURE analysis
saveFImpute Save genotype and map files in FImpute format
saveFImpute-method Save genotype and map files in FImpute format
saveFImputeRaw Export genotypes and map using basic arguments
savePlink Save SNPDataLong object to PLINK format
SNPFileConfig-class SNPFileConfig Class
SNPImportList-class SNPImportList Class
Subset Subset an SNPDataLong object
Subset-method Subset an SNPDataLong object
summary-method Summary for SNPDataLong objects