Identify spatial domains and tissue regions in spatial transcriptomics data using Squidpy and Scanpy. Cluster spots considering both expression and spatial context to define anatomical regions. Use when identifying tissue domains or spatial regions.
Install with Codex or Claude Copy this prompt, paste it into Codex, Claude, or another assistant, and let it review the skill page and install it for you.
A direct command skips the review prompt. Inspect the source before running it.
Identify spatial domains and tissue regions in spatial transcriptomics data using Squidpy and Scanpy. Cluster spots considering both expression and spatial context to define anatomical regions. Use when identifying tissue domains or spatial regions.
tool_type
python
primary_tool
squidpy
Spatial Domain Detection
Identify spatial domains and tissue regions by combining expression and spatial information.
Required Imports
import squidpy as sq
import scanpy as sc
import numpy as np
import matplotlib.pyplot as plt
Standard Clustering (Expression Only)
# Standard Leiden clustering (ignores spatial context)
sc.pp.neighbors(adata, n_neighbors=15, n_pcs=30)
sc.tl.leiden(adata, resolution=0.5, key_added='leiden')
# Visualize on tissue
sq.pl.spatial_scatter(adata, color='leiden', size=)
1.3
Spatial-Aware Clustering with Squidpy
# Build spatial neighbors
sq.gr.spatial_neighbors(adata, coord_type='generic', n_neighs=6)
# Run Leiden on spatial graph
sc.tl.leiden(adata, resolution=0.5, key_added='spatial_leiden', neighbors_key='spatial_neighbors')
sq.pl.spatial_scatter(adata, color='spatial_leiden', size=1.3)
# Compare different clustering approachesfrom sklearn.metrics import adjusted_rand_score
methods = ['leiden', 'spatial_leiden', 'combined_leiden']
for i, m1 inenumerate(methods):
for m2 in methods[i+1:]:
ari = adjusted_rand_score(adata.obs[m1], adata.obs[m2])
print(f'{m1} vs {m2}: ARI = {ari:.3f}')
Domain Markers
# Find marker genes for each domain
sc.tl.rank_genes_groups(adata, groupby='spatial_leiden', method='wilcoxon')
# Get top markers
markers = sc.get.rank_genes_groups_df(adata, group=None)
print(markers.groupby('group').head(5))
# Plot top markers on tissue
top_markers = markers.groupby('group').head(1)['names'].tolist()
sq.pl.spatial_scatter(adata, color=top_markers[:6], ncols=3)