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Update app.py
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app.py
CHANGED
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@@ -314,7 +314,7 @@ def update_viability_realtime(blue_threshold, stored_masks, stored_image_np):
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# Create the Gradio interface
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with gr.Blocks(title="Cell Viability Counter with Trypan Blue Analysis", theme=gr.themes.Soft()) as demo:
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gr.Markdown("# Cell Viability Counter with Trypan Blue Analysis")
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gr.Markdown("Upload a trypan blue stained microscopy image and analyze cell viability. Dead cells appear blue, alive cells are unstained.")
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# Define State components to store masks and image data across function calls
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masks_state = gr.State(value=None)
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@@ -466,7 +466,7 @@ with gr.Blocks(title="Cell Viability Counter with Trypan Blue Analysis", theme=g
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2. **Analysis Results**:
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- **Cell Count**: Total number of detected cells
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- **Confluency**: Percentage of image area covered by cells (useful for assessing cell density)
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3. **Real-time Viability Assessment (Trypan Blue)**:
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- After segmentation, the viability section will become visible.
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# Create the Gradio interface
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with gr.Blocks(title="Cell Viability Counter with Trypan Blue Analysis", theme=gr.themes.Soft()) as demo:
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gr.Markdown("# Cell Viability Counter with Trypan Blue Analysis")
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gr.Markdown("Upload a trypan blue stained microscopy image and analyze cell viability. Dead cells appear blue, alive cells are unstained. For accurate cell confluency, crop the image to display only desired area.")
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# Define State components to store masks and image data across function calls
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masks_state = gr.State(value=None)
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2. **Analysis Results**:
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- **Cell Count**: Total number of detected cells
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- **Confluency**: Percentage of image area covered by cells (useful for assessing cell density). Note that cell confluency is calculated per the entire area of the image input.
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3. **Real-time Viability Assessment (Trypan Blue)**:
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- After segmentation, the viability section will become visible.
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