importFrom(grDevices, adjustcolor) importFrom(graphics, abline, plot, text) importFrom(stats, as.formula, binom.test, binomial, coef, complete.cases, glm, lm, median, model.matrix, na.omit, pchisq, qchisq, setNames, vcov) import(methods) import(gdsfmt) import(SeqArray) importFrom(BiocGenerics, end) importFrom(S4Vectors, elementMetadata, mcols, "mcols<-", queryHits, subjectHits) importFrom(IRanges, IRanges, findOverlaps, mergeByOverlaps, subsetByOverlaps) importFrom(GenomicRanges, GRanges, GRangesList, seqnames) import(Biobase) import(logistf) import(data.table) importFrom(GWASExactHW, HWExact) importFrom(Matrix, Matrix) exportClasses(SeqVarData, SeqVarIterator, SeqVarBlockIterator, SeqVarRangeIterator, SeqVarWindowIterator, SeqVarListIterator) exportMethods(show, sampleData, "sampleData<-", variantData, "variantData<-", validateSex, granges, variantFilter, lastFilter, "lastFilter<-", variantBlock, variantRanges, iterateFilter, resetIterator, currentRanges, currentVariants, applyMethod, refChar, altChar, nAlleles, isVariant, isSNV, getGenotype, getGenotypeAlleles, refDosage, altDosage, alleleDosage, expandedAltDosage, expandedVariantIndex, variantInfo, getVariableLengthData, imputedDosage, titv, alleleFrequency, alleleCount, minorAlleleCount, missingGenotypeRate, heterozygosity, hethom, homozygosity, meanBySample, countSingletons, pca, hwe, inbreedCoeff, mendelErr, duplicateDiscordance, alternateAlleleDetection, refFrac, refFracOverHets, refFracPlot, regression, chromWithPAR) export(SeqVarData, SeqVarIterator, SeqVarBlockIterator, SeqVarRangeIterator, SeqVarWindowIterator, SeqVarListIterator, setVariantID)