liana.pl.feature_by_group#
- liana.pl.feature_by_group(adata=None, groupby=None, spatial_key='spatial', labels=None, feature=None, figure_size=(10, 6), normalize=True, percentile_scaling=None, show_counts=True)#
Plot inflow scores for single feature across spatial coordinates.
- Parameters:
- adata
AnnData|None(default:None) Annotated data object.
- groupby
str|None(default:None) Key to be used for grouping.
- spatial_key
str(default:'spatial') Key in
adata.obsmthat contains the spatial coordinates.- labels
list[str] |None(default:None) List of labels to compare, from groupby.
- feature
str|None(default:None) From adata.var_names.
- figure_size
tuple[float,float] (default:(10, 6)) Figure x,y size
- normalize
bool(default:True) Normalize expression values between 0 and 1 for each cell type.
- percentile_scaling
tuple[int,int] |None(default:None) Tuple specifying percentiles for scaling.
- show_counts
bool(default:True) Show counts of expression cells (expression > 0).
- adata
- Return type:
- Returns:
A tuple of the matplotlib
Figureand its mainAxes.
Examples
adatais typically the output ofliana.mt.inflow, whosevar_namesare'source^ligand^receptor'triplets. Each label inlabelsgets its own colormap and colorbar, so the groups can be compared in place:>>> import liana as li >>> adata = li.ds.generate_toy_spatial() >>> lrdata = li.mt.inflow(adata, groupby="bulk_labels", resource_name="consensus") >>> fig, ax = li.pl.feature_by_group( ... lrdata, groupby="bulk_labels", labels=["Dendritic", "CD14+ Monocyte"], feature=lrdata.var_names[0] ... )