Description Usage Arguments Details Value Examples
This is a modification of the M3Drop method. Instead of fitting a Michaelis-Menten model to the log expression-dropout relation, we fit a linear model. Namely, the linear model is build on the log(expression) versus log(dropout) distribution. After fitting a linear model important features are selected as the top N residuals of the linear model.
1 2 3 4 5 6 7 | selectFeatures(object, n_features = 500, suppress_plot = TRUE)
selectFeatures.SingleCellExperiment(object, n_features, suppress_plot)
## S4 method for signature 'SingleCellExperiment'
selectFeatures(object, n_features = 500,
suppress_plot = TRUE)
|
object |
an object of |
n_features |
number of the features to be selected |
suppress_plot |
boolean parameter, which defines whether to plot log(expression) versus log(dropout) distribution for all genes. Selected features are highlighted with the red colour. |
Please note that feature_symbol
column of rowData(object)
must be
present in the input object and should not contain any duplicated feature names.
This column defines feature names used during projection. Feature symbols
in the reference dataset must correpond to the feature symbols
in the projection dataset, otherwise the mapping will not work!
an object of SingleCellExperiment
class with a new column in
rowData(object)
slot which is called scmap_features
. It can be accessed
by using as.data.frame(rowData(object))$scmap_features
.
1 2 3 4 5 6 7 8 9 10 11 | library(SingleCellExperiment)
sce <- SingleCellExperiment(assays = list(normcounts = as.matrix(yan)), colData = ann)
# this is needed to calculate dropout rate for feature selection
# important: normcounts have the same zeros as raw counts (fpkm)
counts(sce) <- normcounts(sce)
logcounts(sce) <- log2(normcounts(sce) + 1)
# use gene names as feature symbols
rowData(sce)$feature_symbol <- rownames(sce)
# remove features with duplicated names
sce <- sce[!duplicated(rownames(sce)), ]
sce <- selectFeatures(sce)
|
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