## load genome description
data(hgA)
## partition genome into overlapping windows
windows <- partitionRegions(hgA)
## load genotype data from VCF file
vcfFile <- system.file("examples/example1.vcf.gz", package="podkat")
Z <- readGenotypeMatrix(vcfFile)
## read phenotype data from CSV file (continuous trait + covariates)
phenoFile <- system.file("examples/example1lin.csv", package="podkat")
pheno <-read.table(phenoFile, header=TRUE, sep=",")
## train null model with all covariates in data frame 'pheno'
nm.lin <- nullModel(y ~ ., pheno)
## perform association test for multiple regions
res <- assocTest(Z, nm.lin, windows)
res.adj <- p.adjust(res, method="BH")
## show filtered results
res.f <- filterResult(res.adj)
print(res.f)
res.f <- filterResult(res.adj, filterBy="p.value.adj")
print(res.f)
## compute contributions
contrib <- weights(res.f, Z, nm.lin)
contrib
## extract most indicative variants
filterResult(contrib[[1]])
filterResult(contrib)
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