API for rCNV
Detect Copy Number Variants from SNPs Data

Global functions
ADnorm	Man page
ADtable	Man page
TMM	Source code
TMMex	Source code
ad.correct	Man page Source code
allele.freq	Man page Source code
allele.info	Man page Source code
alleleINF	Man page
apply_pb	Source code
chisq_test	Source code
cnv	Man page Source code
cnv_0	Source code
colorize	Source code
combn_pb	Source code
cpm.normal	Man page Source code
depthVsSample	Man page Source code
dp.cov	Source code
dp.covZ	Source code
dup.plot	Man page Source code
dup.validate	Man page Source code
dupGet	Man page Source code
dupGet_0	Source code
ex.prop	Source code
exportVCF	Man page Source code
get.eHpvals	Source code
get.miss	Man page Source code
get.pvals	Source code
gg	Source code
gt.format	Man page Source code
gt2	Source code
h.zygosity	Man page Source code
het.sity1	Source code
het.sity2	Source code
hetTgen	Man page Source code
index_to_mean	Source code
lapply_pb	Source code
maf	Man page Source code
makeTransparent	Source code
non_bi_rm	Source code
norm.fact	Man page Source code
plot_svd	Source code
power.bias	Man page Source code
quantile_normalisation	Source code
readVCF	Man page Source code
relatedness	Man page Source code
sapply_pb	Source code
sig.hets	Man page Source code
sim	Source code
sim.als	Man page Source code
vcf.stat	Man page Source code
vst	Man page Source code
vstPermutation	Man page Source code
wind	Source code