Description Usage Format Details Source Examples
A toy dataset containing a single-cell RNA-seq (scRNA-seq) read counts matrix, ERCC spike-ins counts and spike-in concentration.
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CountData. A matrix of raw read counts of scRNA-seq data which has 500 genes (rows) and 200 cells (columns).
SpikeCounts. A matrix of read counts for spik-in transcripts to estimate the capture efficiencies of the cells.
SpikeConc. A vector of the molecular concentration for spike-in transcripts.
group. A vector specifying the two groups and can be generated by: group <- c(rep(1,100), rep(2,100))
.
CellCluster. A vector specifying the cell cluster memberships of the cells in CountData
and for example can be generated by: CellCluster <- c(rep(1,20), rep(2,30), rep(3, 40), rep(4, 50), rep(5, 60))
.
CountData. A matrix of raw read counts of scRNA-seq data which has 200 genes (rows) and 200 cells (columns).
SpikeCounts. A matrix of read counts for spik-in transcripts to estimate the capture efficiencies of the cells.
SpikeConc. A vector of the molecular concentration for spike-in transcripts.
group. A vector specifying the two groups and can be generated by: group <- c(rep(1,100), rep(2,100))
CellCluster. A vector specifying the cell cluster memberships of the cells in CountData
and for example can be generated by: CellCluster <- c(rep(1,20), rep(2,30), rep(3, 40), rep(4, 50), rep(5, 60))
.
Petropoulos S, et al. Cell, 2016, 165(4): 1012-1026.
1 2 3 4 5 6 7 8 9 10 11 12 13 | # Load test data for DEsingle
data(TestData)
CountData = TestData$CountData
SpikeCounts = TestData$SpikeCounts
SpikConc = TestData$SpikeConc
# Specifying the two groups to be compared
# The sample number in group 1 and group 2 is 100 and 100 cells respectively
group <- c(rep(1,100), rep(2,100))
# Specifying the cluster-memberships of the cells.
CellCluster <- c(rep(1,20), rep(2,30), rep(3, 40), rep(4, 50), rep(5, 60))
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