import(graphics) import(stats) import(utils) import(methods) import(Biobase) import(DBI) import(RSQLite) import(gdsfmt) #import(ncdf4) # moved to Suggests importFrom(GWASExactHW, HWExact) importFrom(DNAcopy, getbdry, CNA, smooth.CNA, segment) importFrom(survival, Surv, coxph) # used in assocCoxPH importFrom(sandwich, vcovHC, vcovHC.default) # used in assocRegression importFrom(lmtest, lrtest, lrtest.default) # used in assocRegression importFrom(logistf, logistf) # used in assocRegression importFrom(quantsmooth, paintCytobands, lengthChromosome) # used to plot ideograms importFrom(data.table, fread, fwrite, rbindlist) exportClasses( SnpAnnotationDataFrame, SnpAnnotationSQLite, ScanAnnotationDataFrame, ScanAnnotationSQLite, NcdfReader, NcdfGenotypeReader, NcdfIntensityReader, GdsReader, GdsGenotypeReader, GdsIntensityReader, MatrixGenotypeReader, GenotypeData, IntensityData, GenotypeIterator, GenotypeBlockIterator ) export( ## Class constructor functions SnpAnnotationDataFrame, SnpAnnotationSQLite, ScanAnnotationDataFrame, ScanAnnotationSQLite, NcdfReader, NcdfGenotypeReader, NcdfIntensityReader, GdsReader, GdsGenotypeReader, GdsIntensityReader, MatrixGenotypeReader, GenotypeData, IntensityData, GenotypeIterator, GenotypeBlockIterator, ## Ordinary functions (i.e. not generic): alleleFrequency, anomSegmentBAF, anomFilterBAF, anomDetectBAF, anomDetectLOH, anomIdentifyLowQuality, anomSegStats, anomStatsPlot, apartSnpSelection, asSnpMatrix, assocCoxPH, assocRegression, BAFfromClusterMeans, BAFfromGenotypes, batchChisqTest, batchFisherTest, checkGenotypeFile, checkImputedDosageFile, checkIntensityFile, checkNcdfGds, chromIntensityPlot, convertGdsNcdf, convertNcdfGds, createDataFile, createAffyIntensityFile, dupDosageCorAcrossDatasets, duplicateDiscordance, duplicateDiscordanceAcrossDatasets, duplicateDiscordanceProbability, exactHWE, findBAFvariance, gdsSubset, gdsSubsetCheck, genoClusterPlot, genoClusterPlotByBatch, genotypeToCharacter, hetByScanChrom, hetBySnpSex, ibdAreasDraw, ibdAssignRelatedness, ibdAssignRelatednessKing, ibdPlot, imputedDosageFile, intensityOutliersPlot, kingIBS0FSCI, manhattanPlot, meanIntensityByScanChrom, meanSdByChromWindow, medianSdOverAutosomes, mendelErr, mendelList, mendelListAsDataFrame, minorAlleleDetectionAccuracy, missingGenotypeByScanChrom, missingGenotypeBySnpSex, pedigreeCheck, pedigreeDeleteDuplicates, pedigreeMaxUnrelated, pedigreePairwiseRelatedness, pasteSorted, plinkCheck, plinkWrite, pseudoautoIntensityPlot, qqPlot, qualityScoreByScan, qualityScoreBySnp, sdByScanChromWindow, setMissingGenotypes, simulateGenotypeMatrix, simulateIntensityMatrix, snpCorrelationPlot, vcfCheck, vcfWrite, genoDataAsVCF, allequal, getobj, saveas, readWriteFirst ) exportMethods( ## Methods associated with the generic functions defined in ## this package: getAlleleA, getAlleleB, getAnnotation, getAttribute, getBAlleleFreq, getChromosome, getDimension, getDimensionNames, getGenotype, getGenotypeSelection, getLogRRatio, getMetadata, getNodeDescription, getPosition, getQuality, getQuery, getScanAnnotation, getScanID, getScanVariable, getScanVariableNames, getSex, getSnpAnnotation, getSnpID, getSnpVariable, getSnpVariableNames, getVariable, getVariableNames, getX, getY, hasBAlleleFreq, hasCoordVariable, hasLogRRatio, hasQuality, hasScanAnnotation, hasScanVariable, hasSex, hasSnpAnnotation, hasSnpVariable, hasVariable, hasX, hasY, nsnp, nscan, writeAnnotation, writeMetadata, autosomeCode, XchromCode, YchromCode, XYchromCode, MchromCode, snpFilter, lastFilter, "lastFilter<-", iterateFilter, currentFilter, resetIterator, ## Methods associated with generic functions defined somewhere else: open, close, show )