API for drramki-chop/edm
Scalable workflow to identify copy Number variants from exome sequencing data

Global functions
AddAnnotations,ExomeDepth-method Man page
AnnotateExtra Man page
AnnotateExtra,ExomeDepth-method Man page
AnnotateExtra-methods Man page
CallCNVs Man page
CallCNVs,ExomeDepth-method Man page
Conrad.hg19.common.CNVs Man page
ExomeCount Man page
ExomeDepth Man page
ExomeDepth-class Man page
ExomeDepth-package Man page
TestCNV Man page
TestCNV,ExomeDepth-method Man page
call.variants Source code
check.exons.def Source code
check.yaml Source code
count.everted.reads Man page
countBam.everted Man page
countBamInGRanges.exomeDepth Man page
exons.hg19 Man page
exons.hg19.X Man page
gather.mosdepth.coverage Source code
gather.variant.calls Source code
genes.hg19 Man page
get.bam.counts.mosdepth Source code
get.power.betabinom Man page
getBamCounts Man page
initialize,ExomeDepth-method Man page
initialize-methods Man page
plot,ANY-method Man page
plot,ExomeDepth,ANY-method Man page
plot,ExomeDepth-method Man page
plot-methods Man page
plot.ExomeDepth Man page
plot.sample.max.correlation Source code
qbetabinom Man page
qbetabinom.ab Man page
select.exons Source code
select.reference.panel Source code
select.reference.set Man page
show,ExomeDepth-method Man page
show-methods Man page
somatic.CNV.call Man page
variant.annotations Source code
viterbi.hmm Man page
wrapper.script Source code
drramki-chop/edm documentation built on June 6, 2020, 8:48 a.m.