API for ChristofferFlensburg/superFreq
Calls and tracks CNAs, SNVs and clones over multiple cancer exomes.

Global functions
CNVregionsPerBP Source code
D3colour Source code
D3colours Source code
DEposterior Source code
GLFC Source code
GR Source code
QCsnp Source code
QCsnps Source code
SNP2GRanges Source code
VAconsequenceToSeverityRank Man page Source code
VAseverityToConsequence Man page Source code
XRank Source code
addAnnotationToOutput Source code
addBindingStrength Man page Source code
addCCGDannotation Source code
addCNAs Source code
addCOSMICannotation Source code
addCOSMICmouseHomologs Source code
addCall Source code
addChromosomeLines Source code
addClinvarAnnotation Source code
addMostSevereHit Source code
addNullAnnotation Source code
addPointMutations Source code
addStream Source code
addStreamSegment Source code
addSubclone Source code
addTheoreticalCNVerrors Source code
addVAnullAnnotation Source code
adjustBG Source code
allCalls Source code
alternativeFrequency Source code
analyse Man page Source code
annotateQ Man page Source code
annotateSomaticQs Man page Source code
annotationColumns Source code
annotationToChr Source code
annotationToX Source code
annotationToX1X2 Source code
bamToPileup Man page Source code
bamToVariants Source code
baseScore Source code
baseStrength Source code
batchToAnalysisDirectory Source code
bestGuess Source code
blurN Source code
boostCRwidth Source code
boostCRwidthRNA Source code
bringAnnotation Source code
callCNVs Source code
callCancerNormalCNVs Source code
callCloneTofM Source code
callConsistencies Source code
callConsistency Source code
callConsistencyNumeric Source code
callPrior Source code
callToColHeatmap Source code
callToColMaypole Source code
callTofM Source code
calledFromSingleSNP Source code
callsToColMaypole Source code
captureRegionToAnnotation Source code
captureRegionsToBQoffset Source code
captureRegionsToBed Source code
captureRegionsToGenome Source code
captureRegionsToNormalPath Source code
checkForMissedLOH Source code
checkRelatedness Source code
checkRelatednessCrossBatch Source code
checkSystem Source code
chrLengths Man page Source code
chrToX Man page Source code
cleanVariantRownames Source code
cleanVariants Source code
cloneStoryRMS Source code
cloneToCol Source code
clonesInTree Source code
clusterToConsistencies Source code
cnvsToStories Source code
cohortAnalyseBatch Man page Source code
cohortAnalyseBatchContrast Man page Source code
cohortGeneScore Source code
colmeans Source code
colorGradient Source code
colsums Source code
combineStories Source code
compareGroups Man page Source code
convertVariantsToVCF Source code
correctForGeneSize Source code
correctedFrequency Source code
createDirectories Source code
createOfflineTxDbs Source code
defaultSuperParameters Man page Source code
defaultSuperRuntimeSettings Man page Source code
defaultSuperSettings Man page Source code
deleteDebugFiles Source code
dibaseScore Source code
dibaseStrength Source code
doPlotBayes Source code
downloadCaptureRegions Source code
downloadFile Source code
downloadSuperFreqAnnotation Source code
downloadSuperFreqCOSMIC Source code
downloadSuperFreqDbSNP Source code
downloadSuperFreqSignatures Source code
downloadTemplate Man page Source code
dumpInput Man page Source code
enforceTransitive Source code
ensureDirectoryExists Source code
excludeClonesFromTree Source code
expandFlags Source code
explainSuperCaptureRegions Source code
explainSuperDbSNPdirectory Source code
explainSuperMetaData Source code
explainSuperNormalDirectory Source code
explainSuperReference Source code
extractClonalities Source code
extractqBAF Source code
fillInMissingVariants Source code
findBamWithBai Source code
findChildren Source code
findCloneTree Source code
findCorrespondingNormal Source code
findFinishedCohortIndividuals Source code
findGLFC Source code
findGLFCandPV Source code
findGoI Source code
findLocalCNV Source code
findMirror Source code
findReferenceBams Source code
findSNPclonalities Source code
findSNPstories Source code
findShift Source code
findShiftManually Source code
findSubclones Source code
fisherTest Source code
fixFalseSNPcall Source code
flagFromNormals Source code
forceMerge Source code
forceRedoEverything Man page Source code
forceRedoNothing Man page Source code
fragmentLength Source code
freqToDirectionProb Source code
frequencyError Source code
generateBody Source code
generateCnaTab Source code
generateHead Source code
generateHtml Source code
generateNullFit Source code
generateOverviewTab Source code
generateRiverTab Source code
generateScatterTab Source code
generateScript Source code
generateTabs Source code
genomeToAssembly Source code
genomeToMPgenome Source code
get104profile Man page Source code
get96signature Source code
getAllIndividualVariants Source code
getAllVEPdata Source code
getBestSigma Source code
getCNV Source code
getCNVrates Source code
getCNVstories Source code
getCohortCNAmatrix Source code
getCohortMutationMatrix Man page Source code
getCohortSNVmatrix Source code
getCorrectedCR Source code
getCosmicCensusDensity Source code
getCosmicCounts Man page Source code
getDeviation Source code
getDodgyness Source code
getFit Source code
getFlatPrior Source code
getHetRatio Source code
getIndelSignature Source code
getIndividualSmallVariants Source code
getIndividualVariants Source code
getMaxCov Source code
getMeanCNV Source code
getMoreVEPinfo Man page Source code
getNormalVariant Source code
getNormalVariants Source code
getPosterior Source code
getPriorNullDeviation Source code
getPriors Source code
getProjectVariants Source code
getProjects Source code
getQuality Source code
getRownamesFor96signatures Source code
getSNVrates Source code
getSettings Man page Source code
getStories Man page Source code
getSubgroups Source code
getSystematicVariance Source code
getTheoreticalError Source code
getVariant Source code
getVariantsByIndividual Man page Source code
getWBreaks Source code
heatmapStories Source code
hg38ChrLengths Source code
humanAllChrLengths Source code
humanChrLengths Source code
identifyTooLowHetRatio Source code
importCOSMICsignatures Source code
importCaptureRegions Man page Source code
importEnsemblData Source code
importMutagenSignatures Source code
importQualityScores Source code
importReferenceGenome Source code
importSampleMetaData Man page Source code
importTCGAsignatures Source code
inGene Source code
inProject Source code
inSubgroup Source code
interpolate Source code
interpolates Source code
isAB Source code
isCNV Source code
isSaneMetaData Source code
libNorm Source code
linkBams Source code
loadAndPlotProfiles Source code
loadAnyCaptureRegions Source code
loadClusterList Source code
loadCohortMethods Source code
loadData Man page Source code
loadQsList Source code
loessNorm Source code
loessNormAll Source code
loessNormAllToReference Source code
loessNormToReference Source code
makeCNAbatchHeatmap Source code
makeCNAheatmap Source code
makeCNVplots Source code
makeCSVofAllPointMutations Source code
makeCaptureFromFeatureCountRegions Source code
makeCloneScatterPlots Source code
makeFitPlots Man page Source code
makeFitPlots2 Source code
makeHeatmap Man page Source code
makeMetaData Source code
makeMetaDataFromBatch Source code
makeRiverPlots Source code
makeSNPprogressionPlots Source code
makeScatterPlots Source code
makeSummaryPlot Source code
makeTreeConsistent Source code
makepHeatmap Man page Source code
markSomatics Source code
matchFlagVariants Source code
matchInternalQs Source code
matchQs Source code
matchToExac Source code
matchTodbSNPs Source code
matchVariants Source code
mcri Man page Source code
meanDistribution Source code
mergeBatches Man page Source code
mergeChromosomes Source code
mergeDoubleLoss Source code
mergeRegions Source code
mergeStories Source code
mergeStrs Source code
mergeToOneRegion Source code
mergeVariantList Source code
metaToSamplePairs Source code
metaToTimeSeries Source code
mirrorDown Source code
moreVEPnames Man page Source code
mouseChrLengths Source code
multiBlur Source code
nameCaptureRegions Source code
newBamToVariants Source code
newFlagFromNormals Source code
newVariants Source code
noneg Source code
normaliseCoverage Source code
normaliseCoverageToHets Source code
outputData Source code
outputMeanCNV Source code
outputNewVariants Source code
outputSomaticVariants Source code
pBinom Source code
pToSigma Source code
pTwoBinom Source code
pairScore Source code
parseMutagenSignatures Source code
pasteLines Source code
performPreliminaryVariantCallingOnMissingVCFs Source code
plot104profilesByClone Source code
plot104profilesBySample Source code
plotBayesPDFs Source code
plotCNAbatchHeatmap Source code
plotCNAheatmap Source code
plotCNAheatmapOverGoI Man page Source code
plotCNAheatmapWithGoI Man page Source code
plotCR Man page Source code
plotClones Source code
plotCohortMutationHeatmap Man page Source code
plotColourScatter Man page Source code
plotFrequencyDiagnostics Source code
plotHR Source code
plotMA Man page Source code
plotMAFLFC Source code
plotMeanCNV Source code
plotMeanCNVtoFile Source code
plotMultipageMutationMatrix Source code
plotMutationMatrix Source code
plotPost Source code
plotProfiles Source code
plotRiver Man page Source code
plotShiftedMAFLFC Source code
plotShrunk Source code
plotSimilarSignatures Source code
plotStories Man page Source code
plotSubgroupCNVtoFile Source code
plotSubgroupMutationMatrix Source code
plotSummary Source code
plotVolcano Source code
plotXRank Source code
postAnalyseVEP Man page Source code
postProcess Source code
postRank Source code
postWidth Source code
posteriors Source code
preprocessCCGD Source code
preprocessClinvar Source code
printHTML Man page Source code
projectMeanCNV Source code
propagateForceRedo Source code
qToGR Source code
qToGRanges Man page Source code
qToVCF Source code
qsToGRL Source code
qualityProgression Source code
qualityScatter Man page Source code
randomCol Source code
randomCols Source code
randomLtys Source code
rangesToBindingScore Source code
readsToPileup Source code
redoHetCalculations Source code
refBias Source code
refBiasMirror Source code
refUnbias Source code
regionalGCcorrect Source code
removeChrFromDump Source code
renameCloneTree Source code
renameClones Source code
renameGoIs Source code
reorderStories Source code
requireFileExists Man page Source code
resetMargins Source code
reverseCall Source code
rowmeans Source code
rowsums Source code
runDE Man page Source code
runSummaryPostAnalysis Man page Source code
runVEP Man page Source code
sameCNV Source code
sameCallAsNeighbour Source code
sameClone Source code
sampleToIndividual Source code
sampleToRdir Source code
samplesToRdirs Source code
saveMetaData Source code
scalarNorm Source code
scoreConsistencies Source code
selectGermlineHets Source code
selectGermlineHetsFromCancer Source code
selectedProtectedHets Source code
setVariantLoss Source code
setupCohortPlot Source code
severityToType Man page Source code
shareSNPs Source code
shareVariants Source code
shortenCalls Source code
solveCigars Source code
splitEvents Source code
splitMeanCNV Source code
splitMetaData Source code
splitRegions Source code
spreadPositions Source code
spreadPositions2D Source code
storiesToCloneStories Source code
storyToLabel Source code
stoufferTest Source code
subsetFit Source code
superCohort Man page Source code
superFreq Man page Source code
superInputFiles Man page Source code
superOutputDirectories Man page Source code
superVersion Man page Source code
third Source code
topXRank Source code
trimVariantsByIndividual Source code
twoBinom Source code
typeToSeverity Man page Source code
unifyCaptureRegions Source code
updateCNVplots Source code
updateDeletions Source code
updateInsertions Source code
updateMultisamplePlots Source code
updateScatterPlots Source code
updateStory Source code
vafScatter Man page Source code
variantLoss Source code
vcfToPositions Source code
vecNorm Source code
whichDistribution Source code
whichUnitarityViolating Source code
writeToVCF Man page Source code
xToChr Man page Source code
xToGene Man page Source code
xToGeneFromDB Source code
xToPos Man page Source code
ChristofferFlensburg/superFreq documentation built on Nov. 15, 2023, 6:15 a.m.