Description Usage Arguments Details Value References Examples
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".
1 | lunSimulate(params = newLunParams(), sparsify = TRUE, verbose = TRUE, ...)
|
params |
LunParams object containing Lun simulation parameters. |
sparsify |
logical. Whether to automatically convert assays to sparse matrices if there will be a size reduction. |
verbose |
logical. Whether to print progress messages. |
... |
any additional parameter settings to override what is provided in
|
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.
SingleCellExperiment object containing the simulated counts and intermediate values.
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
1 | sim <- lunSimulate()
|
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