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All functions

AncestryCheck()
AncestryCheck: Evaluation of the samples' ancestry label.
ClumpLD()
ClumpLD: Clumping SNPs using linkage disequilibrium between SNPs
ComputeGeneticPC()
ComputeGeneticPC: Computing principal components from genetic relationship matrix
ComputeLD()
ComputeLD: Compute Linkage Disequilibrium (LD) for SNP Data
ComputePRS()
ComputePRS: Computing polygenic risk score (PRS)
DiffZeroOne()
DiffZeroOne: Assessing the Z-score for deviation from one and zero.
DummyCovar()
DummyCovar: Recode a categorical variable to a set of binary dummy variables.
EstimateHerit()
EstimateHerit: Computing SNP heritability i.e., the proportion of phenotypic variance explained by SNPs.
Example_covarfile
Example of covariate dataframe
Example_h2data
Example dataset for h2 estimation between male and female for eight different traits
Example_phenofile
Example dataset for phenotype file
Example_pthresoldfile
Example dataset with p-value threshold
Example_rgdata
Example dataset for running DiffZerOne function
Ffile
Example dataset for FemaleWAS
FilterAllele()
FilterAllele: Filtering out the multi-allelic variants
FilterPlinkSample()
FilterPlinkSample: Making PLINK files with desired samples.
FilterRegion()
FilterRegion: Filter chromosomal regions.
FilterSNP()
FilterSNP: Filter out SNPs.
GXWASmiami()
Miami plot
GXwas()
GXwas: Running genome-wide association study (GWAS) and X-chromosome-wide association study (XWAS) models.
GXwasR_data()
GXwasR Data
GeneticCorrBT()
GeneticCorrBT: Computing genetic correlation between two traits.
GetMFPlink()
GetMFPlink: Getting male and female PLINK binary files.
LDPrune()
LDPrune: Performs LD pruning on SNP data using PLINK
MAFdiffSexControl()
MAFdiffSexControl: Test for significantly different minor allele frequency (MAF) between sexes in control samples
MergeRegion()
MergeRegion: Merging two sets of PLINK binary files.
MetaGWAS()
MetaGWAS: Combining summary-level results from two or more GWA studies into a single estimate.
Mfile
Example dataset for MaleWAS
PlinkSummary()
PlinkSummary: Summary of PLINK format genotype dataset
PvalComb()
PvalComb
QCsample()
QCsample: Quality control for samples in the PLINK binary files.
QCsnp()
QCsnp: Quality control (QC) for SNPs.
Regression_Ex
Example dataset for regression
SexCheck()
SexCheck: Compare sex assignments in the input PLINK files with those imputed from X chromosome inbreeding coefficients
SexDiff()
SexDiff: Sex difference in effect size for each SNP using t-test.
SexDiffZscore()
SexDiffZscore: Z-score-based sex difference test.
SexRegress()
SexRegress: Performing linear regression analysis with quantitative response variable.
Summary_Stat_Ex1
Example dataset for GWAS summary statistics
Summary_Stat_Ex2
Example dataset for GWAS summary statistics
SumstatGenCorr()
SumstatGenCorr: Genetic Correlation Calculation from GWAS Summary Statistics
TestXGene()
TestXGene: Performing gene-based association test using GWAS/XWAS summary statistics.
XWAS_Summary_Example
Example dataset for XWAS summary statistics
Xhwe()
Xhwe: Filter X-chromosome variants for HWE in females.
example_data_study_sample_ancestry
Example of ancestry dataframe of samples
executePlinkMAF()
executePlinkMAF: Execute PLINK to Calculate Minor Allele Frequencies (MAF)
highLD_hg19
Example dataset for high LD regions in hg19 built
plinkVCF()
plinkVCF: Converting VCF files to PLINK binary files and vice-versa.
validate_reference_data()
Validate Path to Reference Data Set