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NAMESPACE
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NAMESPACE
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useDynLib("GENESIS")
import(grDevices)
import(graphics)
import(methods)
import(stats)
importFrom(utils, read.table)
import(Biobase)
import(gdsfmt)
import(Matrix)
import(data.table)
#import(foreach)
importFrom(BiocParallel,
bpiterate,
bpparam,
bpnworkers)
importFrom(GWASTools,
GdsGenotypeReader,
GenotypeData,
GenotypeBlockIterator)
importClassesFrom(GWASTools,
GdsGenotypeReader,
GenotypeData,
GenotypeIterator,
GenotypeBlockIterator,
ScanAnnotationDataFrame)
importMethodsFrom(GWASTools,
close,
getAlleleA,
getAlleleB,
getChromosome,
getGenotypeSelection,
getPosition,
getScanAnnotation,
getScanID,
getSnpID,
getSnpVariable,
getVariable,
getSex,
hasSex,
snpFilter,
XchromCode,
YchromCode)
import(SeqArray)
import(SeqVarTools)
importFrom(SNPRelate,
snpgdsPCA,
snpgdsPCASNPLoading,
snpgdsPCASampLoading)
importFrom(BiocGenerics, start, end)
importFrom(GenomicRanges, GRanges)
importFrom(IRanges, IRanges, findOverlaps)
importFrom(S4Vectors, mcols, queryHits, subjectHits)
exportMethods(assocTestSingle,
assocTestAggregate,
effectAllele,
fitNullModel,
fitNullModelFastScore,
kingToMatrix,
makeSparseMatrix,
pcair,
pcrelate,
pcrelateToMatrix)
export(admixMap,
calcISAFBeta,
calcScore,
computeVSIF,
computeVSIFNullModel,
correctKin,
correctK0,
correctK2,
isNullModelFastScore,
isNullModelSmall,
jointScoreTest,
kin2gds,
mat2gds,
nullModelFastScore,
nullModelInvNorm,
nullModelSmall,
pcairPartition,
pcrelateSampBlock,
samplesGdsOrder,
varCompCI)
S3method(plot, pcair)
S3method(summary, pcair)
S3method(print, pcair)
S3method(print, summary.pcair)