addPhenodata | Adds phenotype data from a file to a QDNAseqReadCounts or a... |
applyFilters | Adjusts the filtering on which bins are used |
binReadCounts | Calculate binned read counts from a set of BAM files |
callBins | Call aberrations from segmented copy number data |
compareToReference | Divide binned read counts with those of reference samples |
correctBins | Correct binned read counts for GC content and mappability |
createBins | Builds bin annotation data for a particular bin size |
estimateCorrection | Estimate correction to read counts for GC content and... |
exportBins | Exports to a file |
frequencyPlot | Plot copy number aberration frequencies |
getBinAnnotations | Gets bin annotation data for a particular bin size |
highlightFilters | Highlights data points in a plotted profile to evaluate... |
isobarPlot | Plot median read counts as a function of GC content and... |
LGG150 | LGG150 chromosomes 7-10 |
makeCgh | Constructs a 'cghRaw', 'cghSeg', or 'cghCall' object |
noisePlot | Plot noise as a function of sequence depth |
normalizeBins | Normalizes binned read counts |
normalizeSegmentedBins | Normalize segmented bins |
plot | Plot copy number profile |
poolRuns | Pools binned read counts across samples |
QDNAseqCopyNumbers | Container for QDNAseq read count data |
QDNAseq-defunct | Defunct functions in package 'QDNAseq' |
QDNAseq-package | Package QDNAseq |
QDNAseqReadCounts | Container for QDNAseq read count data |
QDNAseqSignals | A parent class for containers of QDNAseq data |
segmentBins | Segments normalized copy number data |
smoothOutlierBins | Smooth outlier bins after normalization |
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