cellrefiner.preprocessing.spatial_mapping
- cellrefiner.preprocessing.spatial_mapping(ad_st, ad_sc, db, scale=None, cluster_key_sc=None, spatial_key='spatial', pca_key='X_pca', uns_key='rank_genes_groups', n_rank_gene=100, n_cell=5, device='cuda:0', enable_cupy=True, enable_lr_force=False, return_mapping=False, seed=0)[source]
Perform mapping of single-cell data to spatial transcriptomics data and spatial refinement.
- Parameters:
ad_st (AnnData) –
Spatial transcriptomics AnnData object.
Must contain spatial coordinates in .obsm[spatial_key].
ad_sc (AnnData) – Single-cell RNA-seq AnnData object.
db (DataFrame) – Ligand-receptor interaction database.
scale (float) – Spatial scale parameter that determines the interaction distance, representing the size of spatial transcriptomics spot.
cluster_key_sc (str, Optional) – Key in ad_sc.obs that contains cell type annotations, used for scanpy.tl.rank_genes_groups(ad_sc, groupby=cluster_key_sc)
spatial_key (str, default 'spatial') – Key in ad_st.obsm that contains spatial coordinates
pca_key (str, default 'X_pca') –
Key in ad_sc.obsm that contains PCA embeddings.
If not in ad_sc.obsm, scanpy.pp.pca() will be computed.
uns_key (str, default 'rank_genes_groups') –
Key in ad_sc.uns containing ranked genes results from scanpy.tl.rank_genes_groups()
If not present, scanpy.tl.rank_genes_groups(ad_sc, groupby=cluster_key_sc) will be computed.
n_rank_gene (int or None, default 100) –
Number of top-ranked genes for each cell type that will be used in spatial mapping.
If None, all genes will be used.
n_cell (int, default 5) – Number of cells to map to each spatial location.
device (str, default 'cuda:0') – Device used by pytorch.
enable_lr_force (bool, default False) – Whether to enable ligand-receptor force.
enable_cupy (bool, default True) – Whether to enable CuPy. If CuPy is not available, will automatically fall back to CPU.
seed (int, default 0) – random seed
- Returns:
AnnData object containing mapped cells with refined spatial coordinates.
.obsm[‘spatial’]: Refined spatial coordinates. If .obsm[‘spatial’] is present in ad_sc, then stored as .obsm[‘spatial_refined’].
Same gene expression data as input single-cell RNA-seq data
- Return type:
AnnData
Examples
>>> adata_cr = spatial_mapping(adata_st,adata_sc,db_lr,scale=125,cluster_key_sc = 'cell_type')