Agent skill

spatial-domains

Stars 2,009
Forks 275

Install this agent skill to your Project

npx add-skill https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills/tree/main/skills/spatial-transcriptomics-analysis/bioSkills/spatial-domains

SKILL.md


name: bio-spatial-transcriptomics-spatial-domains description: 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 measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools:

  • read_file
  • run_shell_command

Spatial Domain Detection

Identify spatial domains and tissue regions by combining expression and spatial information.

Required Imports

python
import squidpy as sq
import scanpy as sc
import numpy as np
import matplotlib.pyplot as plt

Standard Clustering (Expression Only)

python
# 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

python
# 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)

Combined Expression + Spatial Graph

python
from scipy.sparse import csr_matrix
from sklearn.preprocessing import normalize

# Build both graphs
sq.gr.spatial_neighbors(adata, coord_type='generic', n_neighs=6)
sc.pp.neighbors(adata, n_neighbors=15, n_pcs=30)

# Combine graphs (weighted average)
spatial_weight = 0.3
spatial_conn = adata.obsp['spatial_connectivities']
expr_conn = adata.obsp['connectivities']

# Normalize
spatial_norm = normalize(spatial_conn, norm='l1', axis=1)
expr_norm = normalize(expr_conn, norm='l1', axis=1)

# Combine
combined = spatial_weight * spatial_norm + (1 - spatial_weight) * expr_norm
adata.obsp['combined_connectivities'] = csr_matrix(combined)

# Cluster on combined graph
sc.tl.leiden(adata, resolution=0.5, key_added='combined_leiden', adjacency=adata.obsp['combined_connectivities'])

BayesSpace (R Integration)

python
# BayesSpace provides spatial smoothing for domain detection
# Run in R, then import results

# R code (run separately):
# library(BayesSpace)
# sce <- readRDS("sce.rds")
# sce <- spatialPreprocess(sce, platform="Visium")
# sce <- spatialCluster(sce, q=7, nrep=10000)
# saveRDS(sce, "sce_bayesspace.rds")

# Import BayesSpace results
import rpy2.robjects as ro
from rpy2.robjects import pandas2ri
pandas2ri.activate()

ro.r('sce <- readRDS("sce_bayesspace.rds")')
spatial_clusters = ro.r('colData(sce)$spatial.cluster')
adata.obs['bayesspace'] = list(spatial_clusters)

STAGATE for Spatial Domains

python
# STAGATE uses graph attention for spatial domain detection
import STAGATE

# Build graph
STAGATE.Cal_Spatial_Net(adata, rad_cutoff=150)
STAGATE.Stats_Spatial_Net(adata)

# Train STAGATE
adata = STAGATE.train_STAGATE(adata, alpha=0)

# Cluster on STAGATE embeddings
sc.pp.neighbors(adata, use_rep='STAGATE')
sc.tl.leiden(adata, resolution=0.5, key_added='stagate_leiden')

Evaluate Domain Quality

python
# Check if domains are spatially coherent
from sklearn.metrics import silhouette_score

coords = adata.obsm['spatial']
labels = adata.obs['spatial_leiden'].values

# Spatial silhouette score
spatial_silhouette = silhouette_score(coords, labels)
print(f'Spatial silhouette score: {spatial_silhouette:.3f}')

# Expression silhouette score
expr_silhouette = silhouette_score(adata.obsm['X_pca'], labels)
print(f'Expression silhouette score: {expr_silhouette:.3f}')

Refine Domain Boundaries

python
# Smooth domain assignments using spatial neighbors
from scipy import sparse

def smooth_domains(adata, cluster_key, n_iter=1):
    conn = adata.obsp['spatial_connectivities']
    labels = adata.obs[cluster_key].values
    categories = adata.obs[cluster_key].cat.categories

    for _ in range(n_iter):
        new_labels = []
        for i in range(adata.n_obs):
            neighbors = conn[i].nonzero()[1]
            if len(neighbors) > 0:
                neighbor_labels = labels[neighbors]
                # Majority vote
                unique, counts = np.unique(neighbor_labels, return_counts=True)
                new_labels.append(unique[counts.argmax()])
            else:
                new_labels.append(labels[i])
        labels = np.array(new_labels)

    adata.obs[f'{cluster_key}_smoothed'] = pd.Categorical(labels, categories=categories)

smooth_domains(adata, 'leiden', n_iter=2)
sq.pl.spatial_scatter(adata, color=['leiden', 'leiden_smoothed'], ncols=2)

Compare Domain Methods

python
# Compare different clustering approaches
from sklearn.metrics import adjusted_rand_score

methods = ['leiden', 'spatial_leiden', 'combined_leiden']
for i, m1 in enumerate(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

python
# 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)

Annotate Domains

python
# Manual annotation based on markers
domain_annotations = {
    '0': 'White matter',
    '1': 'Cortex layer 1',
    '2': 'Cortex layer 2/3',
    '3': 'Cortex layer 4',
    '4': 'Cortex layer 5',
    '5': 'Cortex layer 6',
}

adata.obs['domain'] = adata.obs['spatial_leiden'].map(domain_annotations)
sq.pl.spatial_scatter(adata, color='domain', size=1.3)

Related Skills

  • spatial-neighbors - Build spatial graphs (prerequisite)
  • spatial-statistics - Compute spatial statistics per domain
  • single-cell/clustering - Standard clustering methods

Expand your agent's capabilities with these related and highly-rated skills.

FreedomIntelligence/OpenClaw-Medical-Skills

vcf-annotator

Annotate VCF variants with VEP, ClinVar, gnomAD frequencies, and ancestry-aware context. Generates prioritised variant reports.

2,009 275
Explore
FreedomIntelligence/OpenClaw-Medical-Skills

chemist-analyst

Analyzes events through chemistry lens using molecular structure, reaction mechanisms, thermodynamics, kinetics, and analytical techniques (spectroscopy, chromatography, mass spectrometry). Provides insights on chemical processes, material properties, reaction pathways, synthesis, and analytical methods. Use when: Chemical reactions, material analysis, synthesis planning, process optimization, environmental chemistry. Evaluates: Molecular structure, reaction mechanisms, yield, selectivity, safety, environmental impact.

2,009 275
Explore
FreedomIntelligence/OpenClaw-Medical-Skills

bio-alignment-io

Read, write, and convert multiple sequence alignment files using Biopython Bio.AlignIO. Supports Clustal, PHYLIP, Stockholm, FASTA, Nexus, and other alignment formats for phylogenetics and conservation analysis. Use when reading, writing, or converting alignment file formats.

2,009 275
Explore
FreedomIntelligence/OpenClaw-Medical-Skills

sleep-analyzer

分析睡眠数据、识别睡眠模式、评估睡眠质量,并提供个性化睡眠改善建议。支持与其他健康数据的关联分析。

2,009 275
Explore
FreedomIntelligence/OpenClaw-Medical-Skills

metabolomics-workbench-database

Access NIH Metabolomics Workbench via REST API (4,200+ studies). Query metabolites, RefMet nomenclature, MS/NMR data, m/z searches, study metadata, for metabolomics and biomarker discovery.

2,009 275
Explore
FreedomIntelligence/OpenClaw-Medical-Skills

bio-hi-c-analysis-matrix-operations

Balance, normalize, and transform Hi-C contact matrices using cooler and cooltools. Apply iterative correction (ICE), compute expected values, and generate observed/expected matrices. Use when normalizing or transforming Hi-C matrices.

2,009 275
Explore

Didn't find tool you were looking for?

Be as detailed as possible for better results