samcell 1.1.0

Generalized label-free biological cell segmentation with Segment Anything

SAMCell: Generalized Label-Free Biological Cell Segmentation

SAMCell is a state-of-the-art deep learning model for automated cell segmentation in microscopy images. Built on Meta's Segment Anything Model (SAM), SAMCell provides superior performance for label-free cell segmentation across diverse cell types and imaging conditions.

🌟 Key Features

• State-of-the-art Performance: Outperforms existing methods like Cellpose, Stardist, and CALT-US
• Zero-shot Generalization: Works on new cell types and microscopes without retraining
• Distance Map Regression: Novel approach using Euclidean distance maps for robust segmentation
• Comprehensive Metrics: Calculate 30+ morphological and intensity-based cell metrics
• Easy Integration: Simple Python API with minimal setup
• Multiple Interfaces: Command-line tool, Python API, GUI, and Napari plugin

📊 Performance

SAMCell demonstrates superior performance in both test-set and zero-shot cross-dataset evaluation:

Method	PBL-HEK (OP_CSB)	PBL-N2a (OP_CSB)
SAMCell-Generalist	0.598	0.824
Cellpose	0.320	0.764
Stardist	0.189	0.724

Results on zero-shot cross-dataset evaluation

🚀 Quick Start

Installation

# Install from PyPI (recommended)
pip install samcell

# Or install from source
git clone https://github.com/saahilsanganeriya/SAMCell.git
cd SAMCell
pip install -e .

Download Pre-trained Weights

Download the pre-trained SAMCell model weights:

# SAMCell-Generalist (recommended)
wget https://github.com/saahilsanganeriya/SAMCell/releases/download/v1/samcell-generalist.pt

# Or SAMCell-Cyto
wget https://github.com/saahilsanganeriya/SAMCell/releases/download/v1/samcell-cyto.pt

Basic Usage

import cv2
import samcell

# Load your microscopy image
image = cv2.imread('your_image.png', cv2.IMREAD_GRAYSCALE)

# Initialize SAMCell
model = samcell.FinetunedSAM('facebook/sam-vit-base')
model.load_weights('samcell-generalist.pt')

# Create pipeline
pipeline = samcell.SAMCellPipeline(model, device='cuda')

# Segment cells
labels = pipeline.run(image)

# Calculate metrics
metrics_df = pipeline.calculate_metrics(labels, image)
print(f"Found {len(metrics_df)} cells")

# Export results
pipeline.export_metrics(labels, 'cell_metrics.csv', image)

Command Line Interface

# Basic segmentation
samcell segment image.png --model samcell-generalist.pt --output results/

# With comprehensive metrics
samcell segment image.png --model samcell-generalist.pt --output results/ --export-metrics

# Custom thresholds
samcell segment image.png --model samcell-generalist.pt --peak-threshold 0.5 --fill-threshold 0.1

📋 Requirements

• Python ≥ 3.8
• PyTorch ≥ 1.9.0
• transformers ≥ 4.26.0
• OpenCV ≥ 4.5.0
• scikit-image ≥ 0.19.0
• pandas ≥ 1.3.0

For GPU acceleration:

• CUDA-compatible GPU
• CUDA Toolkit ≥ 11.0

🔧 Advanced Usage

Custom Thresholds

SAMCell uses two key thresholds for post-processing:

# Default values (optimized across datasets)
pipeline = samcell.SAMCellPipeline(model, device='cuda')
labels = pipeline.run(image, cells_max=0.47, cell_fill=0.09)

Batch Processing

# Process multiple images
images = [cv2.imread(f'image_{i}.png', 0) for i in range(10)]

results = []
for image in images:
    labels = pipeline.run(image)
    metrics = pipeline.calculate_metrics(labels, image)
    results.append(metrics)

# Combine all metrics
import pandas as pd
all_metrics = pd.concat(results, ignore_index=True)

Comprehensive Metrics

SAMCell calculates 30+ morphological and intensity metrics:

# Basic metrics (fast)
basic_metrics = samcell.calculate_basic_metrics(labels, image)

# Include neighbor analysis
neighbor_metrics = samcell.calculate_neighbor_metrics(labels)

# Full analysis including texture (slower)
full_metrics = samcell.calculate_all_metrics(
    labels, image, include_texture=True
)

🖥️ GUI and Napari Plugin

Standalone GUI

# Install GUI dependencies
pip install samcell[gui]

# Launch GUI
python -m samcell.gui

Napari Plugin

# Install napari plugin
pip install samcell[napari]

# Launch napari and find SAMCell in the plugins menu
napari

📖 Documentation

API Reference

FinetunedSAM

model = samcell.FinetunedSAM(sam_model='facebook/sam-vit-base')
model.load_weights(weight_path, map_location='cuda')

SAMCellPipeline

pipeline = samcell.SAMCellPipeline(
    model,                    # FinetunedSAM instance
    device='cuda',           # 'cuda' or 'cpu'
    crop_size=256,          # Patch size for sliding window
)

# Run segmentation
labels = pipeline.run(
    image,                   # Input grayscale image
    cells_max=0.47,         # Cell peak threshold
    cell_fill=0.09,         # Cell fill threshold
    return_dist_map=False   # Return distance map
)

Metrics Functions

# Calculate all metrics
metrics_df = samcell.calculate_all_metrics(
    labels,                  # Segmentation labels
    original_image=None,     # Original image for intensity metrics
    include_texture=False,   # Include texture analysis
    neighbor_distance=10     # Distance for neighbor analysis
)

# Export to CSV
success = samcell.export_metrics_csv(
    labels,
    'output.csv',
    original_image=image,
    include_texture=False
)

Available Metrics

SAMCell calculates comprehensive morphological metrics:

Shape Metrics:

• Area, Perimeter, Convex Area
• Compactness, Circularity, Roundness
• Aspect Ratio, Eccentricity, Solidity
• Major/Minor Axis Lengths

Spatial Metrics:

• Centroid coordinates
• Bounding box dimensions
• Number of neighbors
• Nearest neighbor distances

Intensity Metrics (when original image provided):

• Mean, Standard deviation, Min/Max intensity
• Intensity range and distribution

Texture Metrics (optional):

• GLCM-based features
• Contrast, Homogeneity, Energy
• Correlation, Dissimilarity

🔬 Method Overview

SAMCell introduces several key innovations:

1. Distance Map Regression: Instead of direct segmentation, predicts Euclidean distance from each pixel to cell boundaries
2. Watershed Post-processing: Converts distance maps to discrete cell masks using watershed algorithm
3. Sliding Window Inference: Processes large images in overlapping 256×256 patches
4. No Prompting Required: Works automatically without user-provided prompts

📊 Datasets

SAMCell was trained on:

• LIVECell: 5,000+ phase-contrast images, 8 cell types, 1.7M annotated cells
• Cellpose Cytoplasm: ~600 diverse microscopy images from internet sources

Evaluated on novel datasets:

• PBL-HEK: Human Embryonic Kidney 293 cells
• PBL-N2a: Neuro-2a cells

🤝 Contributing

We welcome contributions! Please see our Contributing Guidelines for details.

📄 Citation

If you use SAMCell in your research, please cite our paper:

@article{vandeloo2025samcell,
    title={SAMCell: Generalized label-free biological cell segmentation with segment anything},
    author={VandeLoo, Alexandra Dunnum and Malta, Nathan J and Sanganeriya, Saahil and Aponte, Emilio and van Zyl, Caitlin and Xu, Danfei and Forest, Craig},
    journal={bioRxiv},
    year={2025},
    publisher={Cold Spring Harbor Laboratory},
    doi={10.1101/2025.02.06.636835},
    url={https://www.biorxiv.org/content/10.1101/2025.02.06.636835v1}
}

📞 Support

• Issues: GitHub Issues
• Discussions: GitHub Discussions
• Email: [e-mail]

📜 License

This project is licensed under the MIT License - see the LICENSE file for details.

🏛️ Institutions

This work was developed at:

• Georgia Institute of Technology
  • School of Biological Sciences
  • School of Computer Science
  • Department of Biomedical Engineering
  • School of Mechanical Engineering
  • School of Interactive Computing

🙏 Acknowledgments

• Meta AI for the original Segment Anything Model
• The open-source community for tools and datasets
• Georgia Tech for computational resources
• All contributors and users of SAMCell

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SAMCell Team - Making cell segmentation accessible to everyone! 🔬✨