API for CNVrd2
CNVrd2: a read depth-based method to detect and genotype complex common copy number variants from next generation sequencing data.

Global functions
.Random.seed Man page
CNVrd2-class Man page
CNVrd2-package Man page
allGroups Man page
bamFiles Man page
calculateLDSNPandCNV Man page Source code
ccl3l1data Man page
clusteringCNVs-class Man page
copynumberGroups Man page
countReadInWindow Man page
countReadInWindow,CNVrd2-method Man page
countReadInWindow-methods Man page
emnormalCNV Man page
emnormalCNV,clusteringCNVs-method Man page
emnormalCNV-methods Man page
fcgr3bMXL Man page
groupBayesianCNVs Man page Source code
groupCNVs Man page
groupCNVs,clusteringCNVs-method Man page
groupCNVs-methods Man page
identifyPolymorphicRegion Man page
identifyPolymorphicRegion,CNVrd2-method Man page
identifyPolymorphicRegion-methods Man page
numericOrNULL-class Man page
objectCNVrd2 Man page
objectCluster Man page
plotCNVrd2 Man page
plotCNVrd2,CNVrd2-method Man page
plotCNVrd2-methods Man page
plotPolymorphicRegion Man page
plotPolymorphicRegion,CNVrd2-method Man page
plotPolymorphicRegion-methods Man page
readCountMatrix Man page
resultSegment Man page
searchGroupCNVs Man page
searchGroupCNVs,clusteringCNVs-method Man page
searchGroupCNVs-methods Man page
segmentSamples Man page
segmentSamples,CNVrd2-method Man page
segmentSamples-methods Man page
segmentSamplesUsingPopInformation Man page
segmentSamplesUsingPopInformation,CNVrd2-method Man page
segmentSamplesUsingPopInformation-methods Man page
vectorORfactor-class Man page
CNVrd2 documentation built on Nov. 17, 2017, noon