{
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  "Title": "Tools for Genome Wide Association Studies",
  "Description": "Classes for storing very large GWAS data sets and\nannotation, and functions for GWAS data cleaning and analysis.",
  "Authors@R": "c(\nperson(\"Stephanie M.\", \"Gogarten\", role = \"aut\"),\nperson(\"Cathy\", \"Laurie\", role = \"aut\"),\nperson(\"Tushar\", \"Bhangale\", role = \"aut\"),\nperson(\"Matthew P.\", \"Conomos\", role = \"aut\"),\nperson(\"Cecelia\", \"Laurie\", role = \"aut\"),\nperson(\"Michael\", \"Lawrence\", role = \"aut\"),\nperson(\"Caitlin\", \"McHugh\", role = \"aut\"),\nperson(\"Ian\", \"Painter\", role = \"aut\"),\nperson(\"Xiuwen\", \"Zheng\", role = \"aut\"),\nperson(\"Jess\", \"Shen\", role = \"aut\"),\nperson(\"Rohit\", \"Swarnkar\", role = \"aut\"),\nperson(\"Adrienne\", \"Stilp\", role = \"aut\"),\nperson(\"Sarah\", \"Nelson\", role = \"aut\"),\nperson(\"David\", \"Levine\", role = \"aut\"),\nperson(\"Sonali\", \"Kumari\", role = \"ctb\",\ncomment = \"Converted vignettes from Sweave to RMarkdown / HTML.\"),\nperson(\"Stephanie M.\", \"Gogarten\",\nemail = \"sdmorris@uw.edu\", role = \"cre\"))",
  "License": "Artistic-2.0",
  "URL": "https://github.com/smgogarten/GWASTools",
  "LazyData": "yes",
  "biocViews": "SNP, GeneticVariability, QualityControl, Microarray",
  "Collate": "utils.R AllGenerics.R AllClasses.R genotypeToCharacter.R\nMethods-ScanAnnotationDataFrame.R\nMethods-SnpAnnotationDataFrame.R Methods-ScanAnnotationSQLite.R\nMethods-SnpAnnotationSQLite.R Methods-GdsReader.R\nMethods-GdsGenotypeReader.R Methods-GdsIntensityReader.R\nMethods-NcdfReader.R Methods-NcdfGenotypeReader.R\nMethods-NcdfIntensityReader.R Methods-MatrixGenotypeReader.R\nMethods-GenotypeData.R Methods-IntensityData.R\nMethods-Iterator.R createDataUtils.R createDataFile.R\ncreateAffyIntensityFile.R checkGenotypeFile.R\ncheckIntensityFile.R setMissingGenotypes.R imputedDosageFile.R\ncheckImputedDosageFile.R gdsSubset.R gdsSubsetCheck.R\nplinkUtils.R snpStats.R vcfWrite.R asVCF.R convertNcdfGds.R\nBAFfromClusterMeans.R BAFfromGenotypes.R genoClusterPlot.R\ngenoClusterPlotByBatch.R chromIntensityPlot.R\npseudoautoIntensityPlot.R intensityOutliersPlot.R\nsdByScanChromWindow.R medianSdOverAutosomes.R\nmeanSdByChromWindow.R findBAFvariance.R anomSegmentBAF.R\nanomFilterBAF.R anomDetectBAF.R LOHfind.R LOHselectAnoms.R\nanomDetectLOH.R anomSegStats.R anomStatsPlot.R\nanomIdentifyLowQuality.R alleleFrequency.R apartSnpSelection.R\nhetByScanChrom.R hetBySnpSex.R missingGenotypeByScanChrom.R\nmissingGenotypeBySnpSex.R meanIntensityByScanChrom.R\nqualityScoreByScan.R qualityScoreBySnp.R batchChisqTest.R\nbatchFisherTest.R duplicateDiscordanceAcrossDatasets.R\ndupDosageCorAcrossDatasets.R duplicateDiscordance.R\nduplicateDiscordanceProbability.R assocRegression.R\nassocCoxPH.R exactHWE.R mendelErr.R qqPlot.R manhattanPlot.R\nsnpCorrelationPlot.R ibdAreasDraw.R ibdAssignRelatedness.R\nibdPlot.R findRelationsMeanVar.R pedigreeCheck.R\npedigreeDeleteDuplicates.R pedigreePairwiseRelatedness.R\npedigreeMaxUnrelated.R simulateGenotypeMatrix.R\nsimulateIntensityMatrix.R",
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  "Repository": "https://bioc-release.r-universe.dev",
  "Date/Publication": "2026-04-28 12:35:56 UTC",
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  "RemoteRef": "RELEASE_3_23",
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  "NeedsCompilation": "no",
  "Packaged": {
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  "Author": "Stephanie M. Gogarten [aut],\nCathy Laurie [aut],\nTushar Bhangale [aut],\nMatthew P. Conomos [aut],\nCecelia Laurie [aut],\nMichael Lawrence [aut],\nCaitlin McHugh [aut],\nIan Painter [aut],\nXiuwen Zheng [aut],\nJess Shen [aut],\nRohit Swarnkar [aut],\nAdrienne Stilp [aut],\nSarah Nelson [aut],\nDavid Levine [aut],\nSonali Kumari [ctb] (Converted vignettes from Sweave to RMarkdown /\nHTML.),\nStephanie M. Gogarten [cre]",
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    "allequal",
    "anomDetectBAF",
    "anomDetectLOH",
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    "anomIdentifyLowQuality",
    "anomSegmentBAF",
    "anomSegStats",
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    "assocCoxPH",
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    "autosomeCode",
    "BAFfromClusterMeans",
    "BAFfromGenotypes",
    "batchChisqTest",
    "batchFisherTest",
    "checkGenotypeFile",
    "checkImputedDosageFile",
    "checkIntensityFile",
    "checkNcdfGds",
    "chromIntensityPlot",
    "close",
    "convertGdsNcdf",
    "convertNcdfGds",
    "createAffyIntensityFile",
    "createDataFile",
    "currentFilter",
    "dupDosageCorAcrossDatasets",
    "duplicateDiscordance",
    "duplicateDiscordanceAcrossDatasets",
    "duplicateDiscordanceProbability",
    "exactHWE",
    "findBAFvariance",
    "GdsGenotypeReader",
    "GdsIntensityReader",
    "GdsReader",
    "gdsSubset",
    "gdsSubsetCheck",
    "genoClusterPlot",
    "genoClusterPlotByBatch",
    "genoDataAsVCF",
    "GenotypeBlockIterator",
    "GenotypeData",
    "GenotypeIterator",
    "genotypeToCharacter",
    "getAlleleA",
    "getAlleleB",
    "getAnnotation",
    "getAttribute",
    "getBAlleleFreq",
    "getChromosome",
    "getDimension",
    "getDimensionNames",
    "getGenotype",
    "getGenotypeSelection",
    "getLogRRatio",
    "getMetadata",
    "getNodeDescription",
    "getobj",
    "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",
    "hetByScanChrom",
    "hetBySnpSex",
    "ibdAreasDraw",
    "ibdAssignRelatedness",
    "ibdAssignRelatednessKing",
    "ibdPlot",
    "imputedDosageFile",
    "IntensityData",
    "intensityOutliersPlot",
    "iterateFilter",
    "kingIBS0FSCI",
    "lastFilter",
    "lastFilter<-",
    "manhattanPlot",
    "MatrixGenotypeReader",
    "MchromCode",
    "meanIntensityByScanChrom",
    "meanSdByChromWindow",
    "medianSdOverAutosomes",
    "mendelErr",
    "mendelList",
    "mendelListAsDataFrame",
    "minorAlleleDetectionAccuracy",
    "missingGenotypeByScanChrom",
    "missingGenotypeBySnpSex",
    "NcdfGenotypeReader",
    "NcdfIntensityReader",
    "NcdfReader",
    "nscan",
    "nsnp",
    "open",
    "pasteSorted",
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    "pedigreeDeleteDuplicates",
    "pedigreeMaxUnrelated",
    "pedigreePairwiseRelatedness",
    "plinkCheck",
    "plinkWrite",
    "pseudoautoIntensityPlot",
    "qqPlot",
    "qualityScoreByScan",
    "qualityScoreBySnp",
    "readWriteFirst",
    "resetIterator",
    "saveas",
    "ScanAnnotationDataFrame",
    "ScanAnnotationSQLite",
    "sdByScanChromWindow",
    "setMissingGenotypes",
    "show",
    "simulateGenotypeMatrix",
    "simulateIntensityMatrix",
    "SnpAnnotationDataFrame",
    "SnpAnnotationSQLite",
    "snpCorrelationPlot",
    "snpFilter",
    "vcfCheck",
    "vcfWrite",
    "writeAnnotation",
    "writeMetadata",
    "XchromCode",
    "XYchromCode",
    "YchromCode"
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      "title": "Regions of SNP-PC correlation to filter for Principal Component Analysis",
      "object": "pcaSnpFilters.hg19",
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      "name": "pseudoautosomal.hg18",
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      "object": "pseudoautosomal.hg18",
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        "end.base"
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      "tojson": true
    },
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      "name": "pseudoautosomal.hg38",
      "title": "Pseudoautosomal region base positions",
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        "region",
        "start.base",
        "end.base"
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      "name": "relationsMeanVar",
      "title": "Mean and Variance information for full-sibs, half-sibs, first-cousins",
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        "list"
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    {
      "page": "GWASTools-package",
      "title": "Tools for Genome Wide Association Studies",
      "topics": [
        "GWASTools-package",
        "GWASTools"
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    },
    {
      "page": "alleleFrequency",
      "title": "Allelic frequency",
      "topics": [
        "alleleFrequency"
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    },
    {
      "page": "allequal",
      "title": "Test if two objects have the same elements",
      "topics": [
        "allequal"
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    {
      "page": "anomDetectBAF",
      "title": "BAF Method for Chromosome Anomaly Detection",
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        "anomDetectBAF",
        "anomFilterBAF",
        "anomSegmentBAF"
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    {
      "page": "anomDetectLOH",
      "title": "LOH Method for Chromosome Anomaly Detection",
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      "title": "Identify low quality samples",
      "topics": [
        "anomIdentifyLowQuality"
      ]
    },
    {
      "page": "anomSegStats",
      "title": "Calculate LRR and BAF statistics for anomalous segments",
      "topics": [
        "anomSegStats",
        "anomStatsPlot"
      ]
    },
    {
      "page": "apartSnpSelection",
      "title": "Random selection of SNPs",
      "topics": [
        "apartSnpSelection"
      ]
    },
    {
      "page": "snpStats",
      "title": "Utilities for snpStats",
      "topics": [
        "asSnpMatrix"
      ]
    },
    {
      "page": "assocCoxPH",
      "title": "Cox proportional hazards",
      "topics": [
        "assocCoxPH"
      ]
    },
    {
      "page": "assocRegression",
      "title": "Association testing with regression",
      "topics": [
        "assocRegression"
      ]
    },
    {
      "page": "BAFfromClusterMeans",
      "title": "B Allele Frequency & Log R Ratio Calculation",
      "topics": [
        "BAFfromClusterMeans"
      ]
    },
    {
      "page": "BAFfromGenotypes",
      "title": "B Allele Frequency & Log R Ratio Calculation",
      "topics": [
        "BAFfromGenotypes"
      ]
    },
    {
      "page": "batchTest",
      "title": "Batch Effects of Genotyping",
      "topics": [
        "batchChisqTest",
        "batchFisherTest"
      ]
    },
    {
      "page": "centromeres",
      "title": "Centromere base positions",
      "topics": [
        "centromeres",
        "centromeres.hg18",
        "centromeres.hg19",
        "centromeres.hg38"
      ]
    },
    {
      "page": "chromIntensityPlot",
      "title": "Plot B Allele Frequency and/or Log R Ratio, R or Theta values for samples by probe position on a chromosome",
      "topics": [
        "chromIntensityPlot"
      ]
    },
    {
      "page": "convertNcdfGds",
      "title": "Convert between NetCDF and GDS format",
      "topics": [
        "checkNcdfGds",
        "convertGdsNcdf",
        "convertNcdfGds"
      ]
    },
    {
      "page": "createDataFile",
      "title": "Write genotypic calls and/or associated metrics to a GDS or netCDF file.",
      "topics": [
        "checkGenotypeFile",
        "checkIntensityFile",
        "createAffyIntensityFile",
        "createDataFile"
      ]
    },
    {
      "page": "duplicateDiscordance",
      "title": "Duplicate discordance",
      "topics": [
        "duplicateDiscordance"
      ]
    },
    {
      "page": "duplicateDiscordanceAcrossDatasets",
      "title": "Functions to check discordance and allelic dosage correlation across datasets",
      "topics": [
        "dupDosageCorAcrossDatasets",
        "duplicateDiscordanceAcrossDatasets",
        "minorAlleleDetectionAccuracy"
      ]
    },
    {
      "page": "duplicateDiscordanceProbability",
      "title": "Probability of duplicate discordance",
      "topics": [
        "duplicateDiscordanceProbability"
      ]
    },
    {
      "page": "exactHWE",
      "title": "Hardy-Weinberg Equilibrium testing",
      "topics": [
        "exactHWE"
      ]
    },
    {
      "page": "findBAFvariance",
      "title": "Find chromosomal areas with high BAlleleFreq (or LogRRatio) standard deviation",
      "topics": [
        "findBAFvariance",
        "meanSdByChromWindow",
        "medianSdOverAutosomes",
        "sdByScanChromWindow"
      ]
    },
    {
      "page": "GdsGenotypeReader-class",
      "title": "Class GdsGenotypeReader",
      "topics": [
        "autosomeCode,GdsGenotypeReader-method",
        "GdsGenotypeReader",
        "GdsGenotypeReader-class",
        "getAlleleA,GdsGenotypeReader-method",
        "getAlleleB,GdsGenotypeReader-method",
        "getChromosome,GdsGenotypeReader-method",
        "getGenotype,GdsGenotypeReader-method",
        "getGenotypeSelection,GdsGenotypeReader-method",
        "getPosition,GdsGenotypeReader-method",
        "getScanID,GdsGenotypeReader-method",
        "getSnpID,GdsGenotypeReader-method",
        "getVariable,GdsGenotypeReader-method",
        "MchromCode,GdsGenotypeReader-method",
        "nscan,GdsGenotypeReader-method",
        "nsnp,GdsGenotypeReader-method",
        "XchromCode,GdsGenotypeReader-method",
        "XYchromCode,GdsGenotypeReader-method",
        "YchromCode,GdsGenotypeReader-method"
      ]
    },
    {
      "page": "GdsIntensityReader-class",
      "title": "Class GdsIntensityReader",
      "topics": [
        "autosomeCode,GdsIntensityReader-method",
        "GdsIntensityReader",
        "GdsIntensityReader-class",
        "getBAlleleFreq,GdsIntensityReader-method",
        "getChromosome,GdsIntensityReader-method",
        "getLogRRatio,GdsIntensityReader-method",
        "getPosition,GdsIntensityReader-method",
        "getQuality,GdsIntensityReader-method",
        "getScanID,GdsIntensityReader-method",
        "getSnpID,GdsIntensityReader-method",
        "getVariable,GdsIntensityReader-method",
        "getX,GdsIntensityReader-method",
        "getY,GdsIntensityReader-method",
        "hasBAlleleFreq,GdsIntensityReader-method",
        "hasLogRRatio,GdsIntensityReader-method",
        "hasQuality,GdsIntensityReader-method",
        "hasX,GdsIntensityReader-method",
        "hasY,GdsIntensityReader-method",
        "MchromCode,GdsIntensityReader-method",
        "nscan,GdsIntensityReader-method",
        "nsnp,GdsIntensityReader-method",
        "XchromCode,GdsIntensityReader-method",
        "XYchromCode,GdsIntensityReader-method",
        "YchromCode,GdsIntensityReader-method"
      ]
    },
    {
      "page": "GdsReader-class",
      "title": "Class GdsReader",
      "topics": [
        "close,GdsReader-method",
        "GdsReader",
        "GdsReader-class",
        "getAttribute,GdsReader-method",
        "getDimension,GdsReader-method",
        "getNodeDescription,GdsReader-method",
        "getVariable,GdsReader-method",
        "getVariableNames,GdsReader-method",
        "hasVariable,GdsReader-method",
        "open,GdsReader-method",
        "show,GdsReader-method"
      ]
    },
    {
      "page": "gdsSubset",
      "title": "Write a subset of data in a GDS file to a new GDS file",
      "topics": [
        "gdsSubset",
        "gdsSubsetCheck"
      ]
    },
    {
      "page": "genoClusterPlot",
      "title": "SNP cluster plots",
      "topics": [
        "genoClusterPlot",
        "genoClusterPlotByBatch"
      ]
    },
    {
      "page": "GenotypeData-class",
      "title": "Class GenotypeData",
      "topics": [
        "autosomeCode,GenotypeData-method",
        "close,GenotypeData-method",
        "GenotypeData",
        "GenotypeData-class",
        "getAlleleA,GenotypeData-method",
        "getAlleleB,GenotypeData-method",
        "getChromosome,GenotypeData-method",
        "getGenotype,GenotypeData-method",
        "getGenotypeSelection,GenotypeData-method",
        "getPosition,GenotypeData-method",
        "getScanAnnotation,GenotypeData-method",
        "getScanID,GenotypeData-method",
        "getScanVariable,GenotypeData-method",
        "getScanVariableNames,GenotypeData-method",
        "getSex,GenotypeData-method",
        "getSnpAnnotation,GenotypeData-method",
        "getSnpID,GenotypeData-method",
        "getSnpVariable,GenotypeData-method",
        "getSnpVariableNames,GenotypeData-method",
        "getVariable,GenotypeData-method",
        "hasScanAnnotation,GenotypeData-method",
        "hasScanVariable,GenotypeData-method",
        "hasSex,GenotypeData-method",
        "hasSnpAnnotation,GenotypeData-method",
        "hasSnpVariable,GenotypeData-method",
        "hasVariable,GenotypeData-method",
        "MchromCode,GenotypeData-method",
        "nscan,GenotypeData-method",
        "nsnp,GenotypeData-method",
        "open,GenotypeData-method",
        "show,GenotypeData-method",
        "XchromCode,GenotypeData-method",
        "XYchromCode,GenotypeData-method",
        "YchromCode,GenotypeData-method"
      ]
    },
    {
      "page": "GenotypeIterator-class",
      "title": "Class GenotypeIterator",
      "topics": [
        "currentFilter",
        "currentFilter,GenotypeIterator-method",
        "GenotypeBlockIterator",
        "GenotypeBlockIterator-class",
        "GenotypeIterator",
        "GenotypeIterator-class",
        "getAlleleA,GenotypeIterator-method",
        "getAlleleB,GenotypeIterator-method",
        "getChromosome,GenotypeIterator-method",
        "getGenotypeSelection,GenotypeIterator-method",
        "getPosition,GenotypeIterator-method",
        "getSnpID,GenotypeIterator-method",
        "getSnpVariable,GenotypeIterator-method",
        "iterateFilter",
        "iterateFilter,GenotypeIterator-method",
        "lastFilter",
        "lastFilter,GenotypeIterator-method",
        "lastFilter<-",
        "lastFilter<-,GenotypeIterator,numeric-method",
        "resetIterator",
        "resetIterator,GenotypeIterator-method",
        "snpFilter",
        "snpFilter,GenotypeIterator-method"
      ]
    },
    {
      "page": "genotypeToCharacter",
      "title": "Convert number of A alleles to character genotypes",
      "topics": [
        "genotypeToCharacter"
      ]
    },
    {
      "page": "getobj",
      "title": "Get an R object stored in an Rdata file",
      "topics": [
        "getobj"
      ]
    },
    {
      "page": "getVariable",
      "title": "Accessors for variables in GenotypeData and IntensityData classes and their component classes",
      "topics": [
        "autosomeCode",
        "getAlleleA",
        "getAlleleB",
        "getAnnotation",
        "getAttribute",
        "getBAlleleFreq",
        "getChromosome",
        "getDimension",
        "getGenotype",
        "getGenotypeSelection",
        "getLogRRatio",
        "getMetadata",
        "getNodeDescription",
        "getPosition",
        "getQuality",
        "getQuery",
        "getScanAnnotation",
        "getScanID",
        "getScanVariable",
        "getScanVariableNames",
        "getSex",
        "getSnpAnnotation",
        "getSnpID",
        "getSnpVariable",
        "getSnpVariableNames",
        "getVariable",
        "getVariableNames",
        "getX",
        "getY",
        "hasBAlleleFreq",
        "hasLogRRatio",
        "hasQuality",
        "hasScanAnnotation",
        "hasScanVariable",
        "hasSex",
        "hasSnpAnnotation",
        "hasSnpVariable",
        "hasVariable",
        "hasX",
        "hasY",
        "MchromCode",
        "nscan",
        "nsnp",
        "writeAnnotation",
        "writeMetadata",
        "XchromCode",
        "XYchromCode",
        "YchromCode"
      ]
    },
    {
      "page": "defunct",
      "title": "Defunct Functions in Package 'GWASTools'",
      "topics": [
        "assocTestCPH",
        "assocTestFisherExact",
        "assocTestRegression",
        "convertVcfGds",
        "gdsCheckImputedDosage",
        "gdsImputedDosage",
        "gdsSetMissingGenotypes",
        "gwasExactHW",
        "GWASTools-defunct",
        "ncdfAddData",
        "ncdfAddIntensity",
        "ncdfCheckGenotype",
        "ncdfCheckIntensity",
        "ncdfCreate",
        "ncdfImputedDosage",
        "ncdfSetMissingGenotypes",
        "ncdfSubset",
        "ncdfSubsetCheck",
        "plinkToNcdf"
      ]
    },
    {
      "page": "hetByScanChrom",
      "title": "Heterozygosity rates by scan and chromosome",
      "topics": [
        "hetByScanChrom"
      ]
    },
    {
      "page": "hetBySnpSex",
      "title": "Heterozygosity by SNP and sex",
      "topics": [
        "hetBySnpSex"
      ]
    },
    {
      "page": "HLA",
      "title": "HLA region base positions",
      "topics": [
        "HLA",
        "HLA.hg18",
        "HLA.hg19",
        "HLA.hg38"
      ]
    },
    {
      "page": "ibdPlot",
      "title": "Plot theoretical and observed identity by descent values and assign relationships",
      "topics": [
        "ibdAreasDraw",
        "ibdAssignRelatedness",
        "ibdAssignRelatednessKing",
        "ibdPlot",
        "kingIBS0FSCI"
      ]
    },
    {
      "page": "imputedDosageFile",
      "title": "Create and check a GDS or NetCDF file with imputed dosages",
      "topics": [
        "checkImputedDosageFile",
        "imputedDosageFile"
      ]
    },
    {
      "page": "IntensityData-class",
      "title": "Class IntensityData",
      "topics": [
        "autosomeCode,IntensityData-method",
        "close,IntensityData-method",
        "getBAlleleFreq,IntensityData-method",
        "getChromosome,IntensityData-method",
        "getLogRRatio,IntensityData-method",
        "getPosition,IntensityData-method",
        "getQuality,IntensityData-method",
        "getScanID,IntensityData-method",
        "getScanVariable,IntensityData-method",
        "getScanVariableNames,IntensityData-method",
        "getSex,IntensityData-method",
        "getSnpID,IntensityData-method",
        "getSnpVariable,IntensityData-method",
        "getSnpVariableNames,IntensityData-method",
        "getVariable,IntensityData-method",
        "getX,IntensityData-method",
        "getY,IntensityData-method",
        "hasBAlleleFreq,IntensityData-method",
        "hasLogRRatio,IntensityData-method",
        "hasQuality,IntensityData-method",
        "hasScanAnnotation,IntensityData-method",
        "hasScanVariable,IntensityData-method",
        "hasSex,IntensityData-method",
        "hasSnpAnnotation,IntensityData-method",
        "hasSnpVariable,IntensityData-method",
        "hasVariable,IntensityData-method",
        "hasX,IntensityData-method",
        "hasY,IntensityData-method",
        "IntensityData",
        "IntensityData-class",
        "MchromCode,IntensityData-method",
        "nscan,IntensityData-method",
        "nsnp,IntensityData-method",
        "open,IntensityData-method",
        "show,IntensityData-method",
        "XchromCode,IntensityData-method",
        "XYchromCode,IntensityData-method",
        "YchromCode,IntensityData-method"
      ]
    },
    {
      "page": "intensityOutliersPlot",
      "title": "Plot mean intensity and highlight outliers",
      "topics": [
        "intensityOutliersPlot"
      ]
    },
    {
      "page": "manhattanPlot",
      "title": "Manhattan plot for genome wide association tests",
      "topics": [
        "manhattanPlot"
      ]
    },
    {
      "page": "MatrixGenotypeReader-class",
      "title": "Class MatrixGenotypeReader",
      "topics": [
        "autosomeCode,MatrixGenotypeReader-method",
        "getChromosome,MatrixGenotypeReader-method",
        "getGenotype,MatrixGenotypeReader-method",
        "getGenotypeSelection,MatrixGenotypeReader-method",
        "getPosition,MatrixGenotypeReader-method",
        "getScanID,MatrixGenotypeReader-method",
        "getSnpID,MatrixGenotypeReader-method",
        "MatrixGenotypeReader",
        "MatrixGenotypeReader-class",
        "MchromCode,MatrixGenotypeReader-method",
        "nscan,MatrixGenotypeReader-method",
        "nsnp,MatrixGenotypeReader-method",
        "show,MatrixGenotypeReader-method",
        "XchromCode,MatrixGenotypeReader-method",
        "XYchromCode,MatrixGenotypeReader-method",
        "YchromCode,MatrixGenotypeReader-method"
      ]
    },
    {
      "page": "meanIntensityByScanChrom",
      "title": "Calculate Means and Standard Deviations of Intensities",
      "topics": [
        "meanIntensityByScanChrom"
      ]
    },
    {
      "page": "mendelErr",
      "title": "Mendelian Error Checking",
      "topics": [
        "mendelErr"
      ]
    },
    {
      "page": "mendelList",
      "title": "Mendelian Error Checking",
      "topics": [
        "mendelList",
        "mendelListAsDataFrame"
      ]
    },
    {
      "page": "missingGenotypeByScanChrom",
      "title": "Missing Counts per Scan per Chromosome",
      "topics": [
        "missingGenotypeByScanChrom"
      ]
    },
    {
      "page": "missingGenotypeBySnpSex",
      "title": "Missing Counts per SNP by Sex",
      "topics": [
        "missingGenotypeBySnpSex"
      ]
    },
    {
      "page": "NcdfGenotypeReader-class",
      "title": "Class NcdfGenotypeReader",
      "topics": [
        "autosomeCode,NcdfGenotypeReader-method",
        "getChromosome,NcdfGenotypeReader-method",
        "getGenotype,NcdfGenotypeReader-method",
        "getPosition,NcdfGenotypeReader-method",
        "getScanID,NcdfGenotypeReader-method",
        "getSnpID,NcdfGenotypeReader-method",
        "getVariable,NcdfGenotypeReader-method",
        "MchromCode,NcdfGenotypeReader-method",
        "NcdfGenotypeReader",
        "NcdfGenotypeReader-class",
        "nscan,NcdfGenotypeReader-method",
        "nsnp,NcdfGenotypeReader-method",
        "XchromCode,NcdfGenotypeReader-method",
        "XYchromCode,NcdfGenotypeReader-method",
        "YchromCode,NcdfGenotypeReader-method"
      ]
    },
    {
      "page": "NcdfIntensityReader-class",
      "title": "Class NcdfIntensityReader",
      "topics": [
        "autosomeCode,NcdfIntensityReader-method",
        "getBAlleleFreq,NcdfIntensityReader-method",
        "getChromosome,NcdfIntensityReader-method",
        "getLogRRatio,NcdfIntensityReader-method",
        "getPosition,NcdfIntensityReader-method",
        "getQuality,NcdfIntensityReader-method",
        "getScanID,NcdfIntensityReader-method",
        "getSnpID,NcdfIntensityReader-method",
        "getVariable,NcdfIntensityReader-method",
        "getX,NcdfIntensityReader-method",
        "getY,NcdfIntensityReader-method",
        "hasBAlleleFreq,NcdfIntensityReader-method",
        "hasLogRRatio,NcdfIntensityReader-method",
        "hasQuality,NcdfIntensityReader-method",
        "hasX,NcdfIntensityReader-method",
        "hasY,NcdfIntensityReader-method",
        "MchromCode,NcdfIntensityReader-method",
        "NcdfIntensityReader",
        "NcdfIntensityReader-class",
        "nscan,NcdfIntensityReader-method",
        "nsnp,NcdfIntensityReader-method",
        "XchromCode,NcdfIntensityReader-method",
        "XYchromCode,NcdfIntensityReader-method",
        "YchromCode,NcdfIntensityReader-method"
      ]
    },
    {
      "page": "NcdfReader-class",
      "title": "Class NcdfReader",
      "topics": [
        "close,NcdfReader-method",
        "getAttribute,NcdfReader-method",
        "getDimension,NcdfReader-method",
        "getDimensionNames",
        "getDimensionNames,NcdfReader-method",
        "getVariable,NcdfReader-method",
        "getVariableNames,NcdfReader-method",
        "hasCoordVariable",
        "hasCoordVariable,NcdfReader-method",
        "hasVariable,NcdfReader-method",
        "NcdfReader",
        "NcdfReader-class",
        "open,NcdfReader-method",
        "show,NcdfReader-method"
      ]
    },
    {
      "page": "pasteSorted",
      "title": "Paste two vectors sorted pairwise",
      "topics": [
        "pasteSorted"
      ]
    },
    {
      "page": "pcaSnpFilters",
      "title": "Regions of SNP-PC correlation to filter for Principal Component Analysis",
      "topics": [
        "pcaSnpFilters",
        "pcaSnpFilters.hg18",
        "pcaSnpFilters.hg19",
        "pcaSnpFilters.hg38"
      ]
    },
    {
      "page": "pedigreeCheck",
      "title": "Testing for internal consistency of pedigrees",
      "topics": [
        "pedigreeCheck"
      ]
    },
    {
      "page": "pedigreeDeleteDuplicates",
      "title": "Remove duplicates from a pedigree",
      "topics": [
        "pedigreeDeleteDuplicates"
      ]
    },
    {
      "page": "pedigreeMaxUnrelated",
      "title": "Find a maximal set of unrelated individuals in a subset of a pedigree.",
      "topics": [
        "pedigreeMaxUnrelated"
      ]
    },
    {
      "page": "pedigreePairwiseRelatedness",
      "title": "Assign relatedness from pedigree data",
      "topics": [
        "pedigreePairwiseRelatedness"
      ]
    },
    {
      "page": "plinkUtils",
      "title": "Utilities to create and check PLINK files",
      "topics": [
        "plinkCheck",
        "plinkWrite"
      ]
    },
    {
      "page": "pseudoautoIntensityPlot",
      "title": "Plot B Allele Frequency and Log R Ratio for the X and Y chromosomes, overlaying XY SNPs",
      "topics": [
        "pseudoautoIntensityPlot"
      ]
    },
    {
      "page": "pseudoautosomal",
      "title": "Pseudoautosomal region base positions",
      "topics": [
        "pseudoautosomal",
        "pseudoautosomal.hg18",
        "pseudoautosomal.hg19",
        "pseudoautosomal.hg38"
      ]
    },
    {
      "page": "qqPlot",
      "title": "QQ plot for genome wide assocation studies",
      "topics": [
        "qqPlot"
      ]
    },
    {
      "page": "qualityScoreByScan",
      "title": "Mean and median quality score for scans",
      "topics": [
        "qualityScoreByScan"
      ]
    },
    {
      "page": "qualityScoreBySnp",
      "title": "Mean and median quality score for SNPs",
      "topics": [
        "qualityScoreBySnp"
      ]
    },
    {
      "page": "readWriteFirst",
      "title": "Read and write the first n lines of a file",
      "topics": [
        "readWriteFirst"
      ]
    },
    {
      "page": "relationsMeanVar",
      "title": "Mean and Variance information for full-sibs, half-sibs, first-cousins",
      "topics": [
        "relationsMeanVar"
      ]
    },
    {
      "page": "saveas",
      "title": "Save an R object with a new name",
      "topics": [
        "saveas"
      ]
    },
    {
      "page": "ScanAnnotationDataFrame-class",
      "title": "Class ScanAnotationDataFrame",
      "topics": [
        "getAnnotation,ScanAnnotationDataFrame-method",
        "getMetadata,ScanAnnotationDataFrame-method",
        "getScanID,ScanAnnotationDataFrame-method",
        "getSex,ScanAnnotationDataFrame-method",
        "getVariable,ScanAnnotationDataFrame-method",
        "getVariableNames,ScanAnnotationDataFrame-method",
        "hasSex,ScanAnnotationDataFrame-method",
        "hasVariable,ScanAnnotationDataFrame-method",
        "ScanAnnotationDataFrame",
        "ScanAnnotationDataFrame-class"
      ]
    },
    {
      "page": "ScanAnnotationSQLite-class",
      "title": "Class ScanAnotationSQLite",
      "topics": [
        "close,ScanAnnotationSQLite-method",
        "getAnnotation,ScanAnnotationSQLite-method",
        "getMetadata,ScanAnnotationSQLite-method",
        "getQuery,ScanAnnotationSQLite-method",
        "getScanID,ScanAnnotationSQLite-method",
        "getSex,ScanAnnotationSQLite-method",
        "getVariable,ScanAnnotationSQLite-method",
        "getVariableNames,ScanAnnotationSQLite-method",
        "hasSex,ScanAnnotationSQLite-method",
        "hasVariable,ScanAnnotationSQLite-method",
        "nscan,ScanAnnotationSQLite-method",
        "open,ScanAnnotationSQLite-method",
        "ScanAnnotationSQLite",
        "ScanAnnotationSQLite-class",
        "show,ScanAnnotationSQLite-method",
        "writeAnnotation,ScanAnnotationSQLite-method",
        "writeMetadata,ScanAnnotationSQLite-method"
      ]
    },
    {
      "page": "setMissingGenotypes",
      "title": "Write a new netCDF or GDS file, setting certain SNPs to missing",
      "topics": [
        "setMissingGenotypes"
      ]
    },
    {
      "page": "simulateGenotypeMatrix",
      "title": "Simulate Genotype or Intensity Matrix & Load into GDS/NetCDF File",
      "topics": [
        "simulateGenotypeMatrix",
        "simulateIntensityMatrix"
      ]
    },
    {
      "page": "SnpAnnotationDataFrame-class",
      "title": "Class SnpAnotationDataFrame",
      "topics": [
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