View source: R/DownsampleMatrix.R
downSampleCells | R Documentation |
Estimate numbers of detected genes, significantly differentially expressed genes, and median significant effect size
downSampleCells(
originalData,
useAssay = "counts",
minCountDetec = 10,
minCellsDetec = 3,
minCellnum = 10,
maxCellnum = 1000,
realLabels,
depthResolution = 10,
iterations = 10,
totalReads = 1e+06
)
originalData |
The SingleCellExperiment object storing all assay data from the shiny app. |
useAssay |
Character. The name of the assay to be used for subsampling. |
minCountDetec |
Numeric. The minimum number of reads found for a gene to be considered detected. |
minCellsDetec |
Numeric. The minimum number of cells a gene must have at least 1 read in for it to be considered detected. |
minCellnum |
Numeric. The minimum number of virtual cells to include in the smallest simulated dataset. |
maxCellnum |
Numeric. The maximum number of virtual cells to include in the largest simulated dataset |
realLabels |
Character. The name of the condition of interest. Must match a name from sample data. If only two factors present in the corresponding colData, will default to t-test. If multiple factors, will default to ANOVA. |
depthResolution |
Numeric. How many different read depth should the script simulate? Will simulate a number of experimental designs ranging from 10 reads to maxReadDepth, with logarithmic spacing. |
iterations |
Numeric. How many times should each experimental design be simulated? |
totalReads |
Numeric. How many aligned reads to put in each simulated dataset. |
A 3-dimensional array, with dimensions = c(iterations, depthResolution, 3). [,,1] contains the number of detected genes in each simulated dataset, [,,2] contains the number of significantly differentially expressed genes in each simulation, and [,,3] contains the mediansignificant effect size in each simulation. If no genes are significantly differentially expressed, the median effect size defaults to infinity.
data("mouseBrainSubsetSCE")
subset <- mouseBrainSubsetSCE[seq(100),]
res <- downSampleCells(subset,
realLabels = "level1class",
iterations=2)
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