Simulate single-cell RNA-seq count data using the method described in Lun, Bach and Marioni "Pooling across cells to normalize single-cell RNA sequencing data with many zero counts".
lunSimulate(params = newLunParams(), verbose = TRUE, ...)
params | LunParams object containing Lun simulation parameters. |
---|---|
verbose | logical. Whether to print progress messages. |
... | any additional parameter settings to override what is provided in
|
SingleCellExperiment object containing the simulated counts and intermediate values.
The Lun simulation generates gene mean expression levels from a gamma
distribution with shape = mean.shape
and rate = mean.rate
.
Counts are then simulated from a negative binomial distribution with
mu = means
and size = 1 / bcv.common
. In addition each cell is
given a size factor (2 ^ rnorm(nCells, mean = 0, sd = 0.5)
) and
differential expression can be simulated with fixed fold changes.
See LunParams
for details of the parameters.
Lun ATL, Bach K, Marioni JC. Pooling across cells to normalize single-cell RNA sequencing data with many zero counts. Genome Biology (2016).
Paper: dx.doi.org/10.1186/s13059-016-0947-7
Code: https://github.com/MarioniLab/Deconvolution2016
sim <- lunSimulate()#>#>#>#>#>#>