fitNoDE | R Documentation |
Fit the DECENT model assuming no differentially-expressed (DE) genes
fitNoDE(data.obs, spikes, spike.conc, use.spikes, CE.range, tau.init, tau.global, tau.est, normalize, GQ.approx, maxit, parallel)
data.obs |
Observed count matrix for endogeneous genes, rows represent genes, columns represent cells. |
spike.conc |
A vector of theoretical count for each spike-in in one cell (Only needed if spikes = |
use.spikes |
If |
CE.range |
A two-element vector of the lower limit and upper limit for the estimated range of
capture efficiencies (ONLY needed if spikes = |
tau.init |
initial estimates (intcp,slope) that link Beta-Binomial dispersion parameter to the mean expression. |
tau.global |
whether to use the same tau parameters across cell. Default TRUE |
tau.est |
Methods to estimate tau parameters. The default 'endo' corresponds to using endogeneous genes. Other options are 'none' which means tau.init is not further estimated and 'spikes' corresponds to using spike-ins. |
normalize |
Method for estimating size factors, either 'ML' (maximum likelihood, Ye et al., 2017) or 'TMM' (Robinson et al., 2010). |
GQ.approx |
If |
maxit |
maximum number of iterations for EM algorithm. |
parallel |
If |
spike |
Observed count matrix for spike-ins, rows represent spike-ins, columns represent cells. Only needed if spikes = |
A list containing estimates of DE model
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