Files in CNVrd2
CNVrd2: a read depth-based method to detect and genotype complex common copy number variants from next generation sequencing data.
NAMESPACE
DESCRIPTION
build/vignette.rds
data/fcgr3bMXL.RData
data/ccl3l1data.txt.gz
R/emnormalCNV.R
R/segmentSamplesUsingPopInformation.R
R/identifyPolymorphicRegion.R
R/segmentSamples.R
R/AllGenerics.R
R/calculateLDSNPandCNV.R
R/plotCNVrd2.R
R/groupBayesianCNVs.R
R/searchGroupCNVs.R
R/AllClasses.R
R/countReadInWindow.R
R/groupCNVs.R
R/plotPolymorphicRegion.R
vignettes/CNVrd2.Rnw
vignettes/refCNVrd2.bib
man/segmentSamples.Rd
man/searchGroupCNVs.Rd
man/groupCNVs-methods.Rd
man/countReadInWindow.Rd
man/segmentSamplesUsingPopInformation-methods.Rd
man/plotPolymorphicRegion-methods.Rd
man/plotCNVrd2-methods.Rd
man/plotCNVrd2.Rd
man/identifyPolymorphicRegion-methods.Rd
man/groupCNVs.Rd
man/vectorORfactor-class.Rd
man/fcgr3bMXL.Rd
man/identifyPolymorphicRegion.Rd
man/numericOrNULL-class.Rd
man/calculateLDSNPandCNV.Rd
man/clusteringCNVs-class.Rd
man/segmentSamplesUsingPopInformation.Rd
man/emnormalCNV-methods.Rd
man/plotPolymorphicRegion.Rd
man/CNVrd2-class.Rd
man/CNVrd2-package.Rd
man/groupBayesianCNVs.Rd
man/segmentSamples-methods.Rd
man/searchGroupCNVs-methods.Rd
man/emnormalCNV.Rd
man/ccl3l1data.Rd
man/countReadInWindow-methods.Rd
inst/doc/CNVrd2.R
inst/doc/CNVrd2.pdf
inst/doc/CNVrd2.Rnw
inst/extdata/chr17.34800000.34830000.vcf.gz
inst/extdata/chr17.34800000.34830000.vcf.gz.tbi
inst/extdata/chr1.161600000.161611000.vcf.gz
inst/extdata/chr17.34815000.34823000.vcf.gz
inst/extdata/ccl3l1data.txt
inst/extdata/chr1.161600000.161611000.vcf.gz.tbi
inst/extdata/chr17.34815000.34823000.vcf.gz.tbi
