runTSCANDEG | R Documentation |
Wrapper for identifying genes with significant changes with respect to one of the TSCAN pseudotime paths
runTSCANDEG(inSCE, pathIndex, useAssay = "logcounts", discardCluster = NULL)
inSCE |
Input SingleCellExperiment object. |
pathIndex |
Path index for which the pseudotime values should be used.
This corresponds to the terminal node of specific path from the root
node to the terminal node. Run |
useAssay |
Character. The name of the assay to use for testing the
expression change. Should be log-normalized. Default |
discardCluster |
Cluster(s) which are not of use or masks other
interesting effects can be discarded. Default |
The input inSCE
with results updated in metadata
.
Nida Pervaiz
data("mouseBrainSubsetSCE", package = "singleCellTK")
mouseBrainSubsetSCE <- runTSCAN(inSCE = mouseBrainSubsetSCE,
useReducedDim = "PCA_logcounts")
terminalNodes <- listTSCANTerminalNodes(mouseBrainSubsetSCE)
mouseBrainSubsetSCE <- runTSCANDEG(inSCE = mouseBrainSubsetSCE,
pathIndex = terminalNodes[1])
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