View source: R/SiftCellBoost.R
SiftCellBoost | R Documentation |
This function runs SiftCell-Boost, it generates a file of barcode of infered cell-containing droplets
SiftCellBoost(
workingdir,
threshold = 100,
expectedN = 1000,
dataName = "Sample",
mitoGenes = TRUE,
otherFlagGenes = NULL,
N.PCs = 100,
geneUMIthreshold = 50,
seed = 0,
quantileReg = FALSE,
labels = FALSE
)
workingdir |
working director with DGE and shuffleDGE two folders. Within DGE or shuffleDGE foler, |
threshold |
UMI threshold; By default threshold = 100 |
expectedN |
number of expected cell-containing droplets in the dataset. |
dataName |
name of the dataset. For example:PBMC |
mitoGenes |
Default true |
otherFlagGenes |
f0lag genes that characterize unwanted celltypes. For example:PPBP, a marker |
N.PCs |
PCs |
geneUMIthreshold |
genes less than the threshold is discarded |
seed |
seed for randomization |
quantileReg |
default if use top 1000 HVG |
labels |
external labels |
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