Plot smoothed trends for selected genes across pseudotime approximated from embeddings or grouped by clusters.
Usage
VisGeneTrend(
object,
features,
by = "pseudotime",
reduction = "umap",
dims = 1:2,
smooth.method = "loess",
palette = "C",
point_size = 2,
point_alpha = 0.3,
smooth_alpha = 0.3,
smooth_linewidth = 1.5
)Arguments
- object
A
Seuratobject; UMAP/PCA is computed when absent.- features
Character vector of gene names; required.
- by
Either
'pseudotime'or a metadata column to group by. Default:'pseudotime'.- reduction
Reduction used for pseudotime when
by='pseudotime'('umap'or'pca'). Default:'umap'.- dims
Dimensions used for pseudotime ranking. Default:
1:2.- smooth.method
Smoothing method:
'loess'or'gam'. Default:'loess'.- palette
Viridis palette option for color/fill. Default:
"C".- point_size
Point size. Default:
2.- point_alpha
Point alpha. Default:
0.3.- smooth_alpha
Smooth alpha. Default:
0.3.- smooth_linewidth
Smooth line width. Default:
1.5.
Examples
obj <- SeuratVisProExample(
n_cells = 300,
n_genes = 1000,
n_clusters = 10,
seed = 123,
genes_mt = "^MT-",
neighbor_dims = 10,
cluster_res = 0.5,
umap_dims = 10,
spatial = FALSE)
#> Modularity Optimizer version 1.3.0 by Ludo Waltman and Nees Jan van Eck
#>
#> Number of nodes: 300
#> Number of edges: 4508
#>
#> Running Louvain algorithm...
#> Maximum modularity in 10 random starts: 0.9485
#> Number of communities: 10
#> Elapsed time: 0 seconds
p <- VisGeneTrend(
obj,
features = c("G10", "G20", "G30"),
by = "pseudotime",
reduction = "umap",
dims = 1:2,
smooth.method = "loess",
palette = "C",
point_size = 2,
point_alpha = 0.3,
smooth_alpha = 0.3,
smooth_linewidth = 1.5)
p
#> `geom_smooth()` using formula = 'y ~ x'