All functions
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addGenome()
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Add your own Genome |
availableGenomes()
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List of available genomes |
bt771
|
scRNA-seq data from a patient with Glioblastoma |
clip()
|
Squish matrix values into range |
cnaCor()
|
Cell - Tumour CNA Correlations |
cnaHotspotGenes()
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Find the Genes with the highest CNA signal |
cnaPlot()
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Plot a Heatmap of CNA Values |
cnaScatterPlot()
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Visualise Malignant and Non-Malignant Subsets |
cnaSignal()
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Calculate the Means of Absolute CNA Values |
colCenter()
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Center a matrix column-wise |
currentGenome()
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List the current genome name |
expandToClones()
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FUNCTION_TITLE |
fetchModes()
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FUNCTION_TITLE |
filterGenes()
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Filter Genes by their Genome Features |
findClones()
|
Find Clones |
findMalignant()
|
Find Malignant Subset of Cells |
fitBimodal() fitModal()
|
Fit a Bimodal Gaussian Distribution |
genesOn()
|
Retrieve Genes by their Genome Features |
infercna()
|
Infer Copy-Number Alterations From Single-Cell RNA-Seq Data |
mgh125
|
scRNA-seq data from a patient with Glioblastoma |
modality()
|
Test Distribution For Modality |
orderGenes()
|
Order Genes by their Genomic Positions |
refCells
|
Normal Cell IDs in a cohort of 28 Glioblastoma samples. |
refCorrect()
|
Convert Relative CNA Values To Absolute |
retrieveGenome()
|
Retrieve genome data |
rowCenter()
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Center a matrix row-wise |
runMean()
|
Rolling Means |
splitGenes()
|
Split Genes By Chromosome (Arm) |
useData()
|
Load Example Data |
useGenome()
|
Select a Genome for infercna to use |