SCRIPsimu | R Documentation |
Simulate count data for single cell RNA-sequencing using SCIRP method
SCRIPsimu( data, params, method = "single", base_allcellmeans_SC = NULL, pre.bcv.df = NULL, libsize = NULL, bcv.shrink = 1, Dropout_rate = NULL, mode = "GP-trendedBCV", de.prob = NULL, de.downProb = NULL, de.facLoc = NULL, de.facScale = NULL, path.skew = NULL, batch.facLoc = NULL, batch.facScale = NULL, path.nSteps = NULL, ... )
data |
data matrix required to fit the mean-BCV trend for simulation |
params |
SplatParams object containing parameters for the simulation |
method |
"single", "groups" or "paths" |
base_allcellmeans_SC |
base mean vector provided to help setting DE analysis |
pre.bcv.df |
BCV.df enables us to change the variation of BCV values |
libsize |
library size can be provided directly |
bcv.shrink |
factor to control the BCV levels |
Dropout_rate |
factor to control the dropout rate directly |
mode |
"GP-commonBCV", "BP-commonBCV", "BP", "BGP-commonBCV" and "BGP-trendedBCV" |
de.prob |
the proportion of DE genes |
de.downProb |
the proportion of down-regulated DE genes |
de.facLoc |
DE location factor |
de.facScale |
DE scale factor |
path.skew |
Controls how likely cells are from the start or end point of the path |
batch.facLoc |
DE location factor in batch |
batch.facScale |
DE scale factor in batch |
path.nSteps |
number of steps between the start point and end point for each path |
... |
Other parameters |
SingleCellExperiment file
data(params_acinar) data(acinar.data) sim_trend = SCRIPsimu(data=acinar.data, params=params_acinar, mode="GP-trendedBCV")
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