Process and analyze tissue images from spatial transcriptomics data using Squidpy. Extract image features, segment cells/nuclei, and compute morphological features from H&E or IF images. Use when processing tissue images for spatial transcriptomics.
Scanned 2/12/2026
Install via CLI
openskills install mdbabumiamssm/LLMs-Universal-Life-Science-and-Clinical-Skills----
name: bio-spatial-transcriptomics-image-analysis
description: Process and analyze tissue images from spatial transcriptomics data using Squidpy. Extract image features, segment cells/nuclei, and compute morphological features from H&E or IF images. Use when processing tissue images for spatial transcriptomics.
tool_type: python
primary_tool: squidpy
---
# Image Analysis for Spatial Transcriptomics
Extract features and segment tissue images in spatial transcriptomics data.
## Required Imports
```python
import squidpy as sq
import scanpy as sc
import numpy as np
import matplotlib.pyplot as plt
from skimage import io, filters, segmentation
```
## Access Tissue Images
```python
# Get image from Visium data
library_id = list(adata.uns['spatial'].keys())[0]
img_dict = adata.uns['spatial'][library_id]['images']
# High and low resolution images
hires = img_dict['hires']
lowres = img_dict['lowres']
print(f'Hires shape: {hires.shape}')
print(f'Lowres shape: {lowres.shape}')
# Get scale factors
scalef = adata.uns['spatial'][library_id]['scalefactors']
spot_diameter = scalef['spot_diameter_fullres']
hires_scale = scalef['tissue_hires_scalef']
```
## Create ImageContainer
```python
# Squidpy's ImageContainer for organized image handling
img = sq.im.ImageContainer(adata.uns['spatial'][library_id]['images']['hires'])
print(img)
# Or load from file
img = sq.im.ImageContainer('tissue_image.tif')
# Access the image array
arr = img['image'].values
```
## Extract Image Features per Spot
```python
# Calculate image features for each spot
sq.im.calculate_image_features(
adata,
img,
features=['summary', 'histogram', 'texture'],
key_added='img_features',
spot_scale=1.0, # Fraction of spot diameter
n_jobs=4,
)
# Features stored in adata.obsm['img_features']
print(f"Image features shape: {adata.obsm['img_features'].shape}")
```
## Available Image Features
```python
# Summary statistics
sq.im.calculate_image_features(adata, img, features='summary')
# Mean, std, etc. per channel
# Histogram features
sq.im.calculate_image_features(adata, img, features='histogram', features_kwargs={'histogram': {'bins': 16}})
# Intensity distribution
# Texture features (GLCM)
sq.im.calculate_image_features(adata, img, features='texture')
# Contrast, homogeneity, correlation, ASM
# Custom features
sq.im.calculate_image_features(
adata, img,
features=['summary', 'texture'],
features_kwargs={
'summary': {'quantiles': [0.1, 0.5, 0.9]},
'texture': {'distances': [1, 2], 'angles': [0, np.pi/4, np.pi/2]},
}
)
```
## Segment Cells/Nuclei
```python
# Segment using watershed
sq.im.segment(
img,
layer='image',
method='watershed',
channel=0, # Use first channel
thresh=0.5,
)
# Access segmentation mask
seg_mask = img['segmented_watershed'].values
```
## Segment with Cellpose
```python
# Cellpose provides better cell segmentation
from cellpose import models
# Load model
model = models.Cellpose(model_type='nuclei')
# Get image array
image = img['image'].values[:, :, 0] # Single channel
# Segment
masks, flows, styles, diams = model.eval(image, diameter=30, channels=[0, 0])
# Add to ImageContainer
img.add_img(masks, layer='cellpose_masks')
```
## Extract Spot Image Crops
```python
# Get image crop around each spot
def get_spot_crop(adata, img_arr, spot_idx, crop_size=100):
coords = adata.obsm['spatial'][spot_idx]
scalef = adata.uns['spatial'][library_id]['scalefactors']['tissue_hires_scalef']
x, y = int(coords[0] * scalef), int(coords[1] * scalef)
half = crop_size // 2
crop = img_arr[max(0, y-half):y+half, max(0, x-half):x+half]
return crop
# Get crop for spot 0
crop = get_spot_crop(adata, hires, 0)
plt.imshow(crop)
```
## Color Deconvolution (H&E)
```python
from skimage.color import rgb2hed, hed2rgb
# Separate H&E stains
hed = rgb2hed(hires)
hematoxylin = hed[:, :, 0]
eosin = hed[:, :, 1]
dab = hed[:, :, 2]
# Visualize
fig, axes = plt.subplots(1, 3, figsize=(15, 5))
axes[0].imshow(hematoxylin, cmap='gray')
axes[0].set_title('Hematoxylin')
axes[1].imshow(eosin, cmap='gray')
axes[1].set_title('Eosin')
axes[2].imshow(hires)
axes[2].set_title('Original')
plt.tight_layout()
```
## Compute Morphological Features
```python
from skimage.measure import regionprops_table
# Get properties from segmentation
props = regionprops_table(
seg_mask,
intensity_image=hires[:, :, 0],
properties=['label', 'area', 'eccentricity', 'solidity', 'mean_intensity']
)
import pandas as pd
morph_df = pd.DataFrame(props)
print(morph_df.describe())
```
## Use Image Features for Clustering
```python
# Combine expression and image features
import numpy as np
# Get expression PCA
expr_pca = adata.obsm['X_pca'][:, :20]
# Get image features
img_features = adata.obsm['img_features']
# Scale and combine
from sklearn.preprocessing import StandardScaler
expr_scaled = StandardScaler().fit_transform(expr_pca)
img_scaled = StandardScaler().fit_transform(img_features)
# Weight combination
alpha = 0.3 # Image weight
combined = np.hstack([
(1 - alpha) * expr_scaled,
alpha * img_scaled
])
adata.obsm['X_combined'] = combined
# Cluster on combined features
sc.pp.neighbors(adata, use_rep='X_combined')
sc.tl.leiden(adata, key_added='combined_leiden')
```
## Smooth Expression with Image
```python
# Use image similarity to smooth expression
from scipy.spatial.distance import cdist
# Compute image similarity matrix
img_features = adata.obsm['img_features']
img_sim = 1 / (1 + cdist(img_features, img_features, metric='euclidean'))
# Normalize
img_sim = img_sim / img_sim.sum(axis=1, keepdims=True)
# Smooth expression
X_smoothed = img_sim @ adata.X
adata.layers['img_smoothed'] = X_smoothed
```
## Related Skills
- spatial-data-io - Load spatial data with images
- spatial-visualization - Visualize images with expression
- spatial-domains - Use image features for domain detection
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