scanpy.pl.MatrixPlot
- class scanpy.pl.MatrixPlot(adata, var_names, groupby, use_raw=None, log=False, num_categories=7, categories_order=None, title=None, figsize=None, gene_symbols=None, var_group_positions=None, var_group_labels=None, var_group_rotation=None, layer=None, standard_scale=None, ax=None, values_df=None, vmin=None, vmax=None, vcenter=None, norm=None, **kwds)
Allows the visualization of values using a color map.
- Parameters:
- adata :
AnnData
Annotated data matrix.
- var_names :
Union
[str
,Sequence
[str
],Mapping
[str
,Union
[str
,Sequence
[str
]]]] var_names
should be a valid subset ofadata.var_names
. Ifvar_names
is a mapping, then the key is used as label to group the values (seevar_group_labels
). The mapping values should be sequences of validadata.var_names
. In this case either coloring or ‘brackets’ are used for the grouping of var names depending on the plot. Whenvar_names
is a mapping, then thevar_group_labels
andvar_group_positions
are set.- groupby :
Union
[str
,Sequence
[str
]] The key of the observation grouping to consider.
- use_raw :
Optional
[bool
] (default:None
) Use
raw
attribute ofadata
if present.- log :
bool
(default:False
) Plot on logarithmic axis.
- num_categories :
int
(default:7
) Only used if groupby observation is not categorical. This value determines the number of groups into which the groupby observation should be subdivided.
- categories_order :
Optional
[Sequence
[str
]] (default:None
) Order in which to show the categories. Note: add_dendrogram or add_totals can change the categories order.
- figsize :
Optional
[Tuple
[float
,float
]] (default:None
) Figure size when
multi_panel=True
. Otherwise thercParam['figure.figsize]
value is used. Format is (width, height)- dendrogram
If True or a valid dendrogram key, a dendrogram based on the hierarchical clustering between the
groupby
categories is added. The dendrogram information is computed usingscanpy.tl.dendrogram()
. Iftl.dendrogram
has not been called previously the function is called with default parameters.- gene_symbols :
Optional
[str
] (default:None
) Column name in
.var
DataFrame that stores gene symbols. By defaultvar_names
refer to the index column of the.var
DataFrame. Setting this option allows alternative names to be used.- var_group_positions :
Optional
[Sequence
[Tuple
[int
,int
]]] (default:None
) Use this parameter to highlight groups of
var_names
. This will draw a ‘bracket’ or a color block between the given start and end positions. If the parametervar_group_labels
is set, the corresponding labels are added on top/left. E.g.var_group_positions=[(4,10)]
will add a bracket between the fourthvar_name
and the tenthvar_name
. By giving more positions, more brackets/color blocks are drawn.- var_group_labels :
Optional
[Sequence
[str
]] (default:None
) Labels for each of the
var_group_positions
that want to be highlighted.- var_group_rotation :
Optional
[float
] (default:None
) Label rotation degrees. By default, labels larger than 4 characters are rotated 90 degrees.
- layer :
Optional
[str
] (default:None
) Name of the AnnData object layer that wants to be plotted. By default adata.raw.X is plotted. If
use_raw=False
is set, thenadata.X
is plotted. Iflayer
is set to a valid layer name, then the layer is plotted.layer
takes precedence overuse_raw
.- title :
Optional
[str
] (default:None
) Title for the figure.
- expression_cutoff
Expression cutoff that is used for binarizing the gene expression and determining the fraction of cells expressing given genes. A gene is expressed only if the expression value is greater than this threshold.
- mean_only_expressed
If True, gene expression is averaged only over the cells expressing the given genes.
- standard_scale :
Optional
[Literal
['var'
,'group'
]] (default:None
) Whether or not to standardize that dimension between 0 and 1, meaning for each variable or group, subtract the minimum and divide each by its maximum.
- values_df :
Optional
[DataFrame
] (default:None
) Optionally, a dataframe with the values to plot can be given. The index should be the grouby categories and the columns the genes names.
- kwds
Are passed to
matplotlib.pyplot.scatter()
.
- adata :
See also
matrixplot()
Simpler way to call MatrixPlot but with less options.
rank_genes_groups_matrixplot()
to plot marker genes identified using the
rank_genes_groups()
function.
Examples
Simple visualization of the average expression of a few genes grouped by the category ‘bulk_labels’.
import scanpy as sc adata = sc.datasets.pbmc68k_reduced() markers = ['C1QA', 'PSAP', 'CD79A', 'CD79B', 'CST3', 'LYZ'] sc.pl.MatrixPlot(adata, markers, groupby='bulk_labels').show()
Same visualization but passing var_names as dict, which adds a grouping of the genes on top of the image:
markers = {'T-cell': 'CD3D', 'B-cell': 'CD79A', 'myeloid': 'CST3'} sc.pl.MatrixPlot(adata, markers, groupby='bulk_labels').show()
Attributes
Methods
add_dendrogram
([show, dendrogram_key, size])Show dendrogram based on the hierarchical clustering between the
groupby
categories.add_totals
([show, sort, size, color])Show barplot for the number of cells in in
groupby
category.get_axes
()getdoc
()legend
([show, title, width])Configure legend parameters
Renders the image but does not call
matplotlib.pyplot.show()
.savefig
(filename[, bbox_inches])Save the current figure
show
([return_axes])Show the figure
style
([cmap, edge_color, edge_lw])Modifies plot visual parameters.
swap_axes
([swap_axes])Plots a transposed image.