Predict feature vectors from enhanced PCs.
enhanceFeatures( sce.enhanced, sce.ref, feature_names = NULL, model = c("xgboost", "dirichlet", "lm"), use.dimred = "PCA", assay.type = "logcounts", altExp.type = NULL, feature.matrix = NULL, nrounds = 0, train.n = round(ncol(sce.ref) * 2/3) )
sce.enhanced | SingleCellExperiment object with enhanced PCs. |
---|---|
sce.ref | SingleCellExperiment object with original PCs and expression. |
feature_names | List of genes/features to predict expression/values for. |
model | Model used to predict enhanced values. |
use.dimred | Name of dimension reduction to use. |
assay.type | Expression matrix in |
altExp.type | Expression matrix in |
feature.matrix | Expression/feature matrix to predict, if not directly
attached to |
nrounds | Nonnegative integer to set the |
train.n | Number of spots to use in the training dataset for tuning nrounds. By default, 2/3 the total number of spots are used. |
If assay.type
or altExp.type
are specified, the
enhanced features are stored in the corresponding slot of
sce.enhanced
and the modified SingleCellExperiment object is
returned.
If feature.matrix
is specified, or if a subset of features are
requested, the enhanced features are returned directly as a matrix.
Enhanced features are computed by fitting a predictive model to a
low-dimensional representation of the original expression vectors. By
default, a linear model is fit for each gene using the top 15 principal
components from each spot, i.e. lm(gene ~ PCs)
, and the fitted model
is used to predict the enhanced expression for each gene from the subspots'
principal components.
Diagnostic measures, such as RMSE for xgboost
or R.squared for linear
regression, are added to the `rowData` of the enhanced experiment if the
features are an assay of the original experiment. Otherwise they are stored
as an attribute of the returned matrix/altExp.
Note that feature matrices will be returned and are expected to be input as \(p \times n\) matrices of \(p\)-dimensional feature vectors over the \(n\) spots.
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