GeneRelevance-class | R Documentation |
The relevance map is cached insided of the DiffusionMap
.
gene_relevance(
coords,
exprs,
...,
k = 20L,
dims = 1:2,
distance = NULL,
smooth = TRUE,
remove_outliers = FALSE,
verbose = FALSE
)
## S4 method for signature 'DiffusionMap,missing'
gene_relevance(
coords,
exprs,
...,
k = 20L,
dims = 1:2,
distance = NULL,
smooth = TRUE,
remove_outliers = FALSE,
verbose = FALSE
)
## S4 method for signature 'matrix,dMatrixOrMatrix'
gene_relevance(
coords,
exprs,
...,
pcs = NULL,
knn_params = list(),
weights = 1,
k,
dims,
distance,
smooth,
remove_outliers,
verbose
)
coords |
A |
exprs |
An cells |
... |
Unused. All parameters to the right of the |
k |
Number of nearest neighbors to use |
dims |
Index into columns of |
distance |
Distance measure to use for the nearest neighbor search. |
smooth |
Smoothing parameters |
remove_outliers |
Remove cells that are only within one other cell's nearest neighbor, as they tend to get large norms. |
verbose |
If TRUE, log additional info to the console |
pcs |
A cell |
knn_params |
A |
weights |
Weights for the partial derivatives. A vector of the same length as |
A GeneRelevance
object:
coords
A cells \times
dims matrix
or sparseMatrix
of coordinates (e.g. diffusion components), reduced to the dimensions passed as dims
exprs
A cells \times
genes matrix of expressions
partials
Array of partial derivatives wrt to considered dimensions in reduced space
(genes \times
cells \times
dimensions)
partials_norm
Matrix with norm of aforementioned derivatives. (n\_genes \times
cells)
nn_index
Matrix of k nearest neighbor indices. (cells \times
k)
dims
Column index for plotted dimensions. Can character
, numeric
or logical
distance
Distance measure used in the nearest neighbor search. See find_knn
smooth_window
Smoothing window used (see smth.gaussian
)
smooth_alpha
Smoothing kernel width used (see smth.gaussian
)
Gene Relevance methods, Gene Relevance plotting: plot_differential_map
/plot_gene_relevance
data(guo_norm)
dm <- DiffusionMap(guo_norm)
gr <- gene_relevance(dm)
m <- t(Biobase::exprs(guo_norm))
gr_pca <- gene_relevance(prcomp(m)$x, m)
# now plot them!
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