Spaces:
Sleeping
Sleeping
File size: 12,419 Bytes
ef677f1 1c47445 b32645b 1c47445 dbe81c1 37a1b01 dbe81c1 1c47445 37a1b01 1c47445 37a1b01 1c47445 37a1b01 1c47445 c4a8601 b32645b 1c47445 b32645b 1c47445 dbe81c1 1c47445 dbe81c1 1c47445 dbe81c1 1c47445 b32645b 1c47445 b32645b 1c47445 b32645b 1c47445 b32645b 1c47445 b32645b 1c47445 37a1b01 dbe81c1 1c47445 b32645b 1c47445 ef677f1 1c47445 |
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 100 101 102 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 119 120 121 122 123 124 125 126 127 128 129 130 131 132 133 134 135 136 137 138 139 140 141 142 143 144 145 146 147 148 149 150 151 152 153 154 155 156 157 158 159 160 161 162 163 164 165 166 167 168 169 170 171 172 173 174 175 176 177 178 179 180 181 182 183 184 185 186 187 188 189 190 191 192 193 194 195 196 197 198 199 200 201 202 203 204 205 206 207 208 209 210 211 212 213 214 215 216 217 218 219 220 221 222 223 224 225 226 227 228 229 230 231 232 233 234 235 236 237 238 239 240 241 242 243 244 245 246 247 248 249 250 251 252 253 254 255 256 257 258 259 260 261 262 263 264 265 266 267 268 269 270 271 272 273 274 275 276 277 |
import gradio as gr
from main import run_fc_analysis
import os
import numpy as np
from sklearn.metrics import mean_squared_error, r2_score
import json
import pickle
from rcf_prediction import train_predictor_from_latents
def calculate_fc_accuracy(original_fc, reconstructed_fc):
"""
Calculate accuracy metrics between original and reconstructed FC matrices
"""
# Mean Squared Error (lower is better)
mse = mean_squared_error(original_fc, reconstructed_fc)
# Root Mean Squared Error (lower is better)
rmse = np.sqrt(mse)
# R² Score (higher is better, 1 is perfect)
r2 = r2_score(original_fc, reconstructed_fc)
# Correlation between matrices (higher is better)
corr = np.corrcoef(original_fc.flatten(), reconstructed_fc.flatten())[0, 1]
# Custom similarity score based on normalized dot product (higher is better)
norm_dot = np.dot(original_fc.flatten(), reconstructed_fc.flatten()) / (
np.linalg.norm(original_fc.flatten()) * np.linalg.norm(reconstructed_fc.flatten()))
return {
"MSE": float(mse),
"RMSE": float(rmse),
"R²": float(r2),
"Correlation": float(corr),
"Cosine Similarity": float(norm_dot)
}
def save_latents(latents, demographics, subjects=None, file_path='latents.pkl'):
"""
Save latent representations and associated demographics to file
"""
os.makedirs('results', exist_ok=True)
# Create a dictionary with latents and demographics
data = {
'latents': latents,
'demographics': demographics
}
if subjects is not None:
data['subjects'] = subjects
# Save as pickle for easy loading in Python
with open(os.path.join('results', file_path), 'wb') as f:
pickle.dump(data, f)
# Also save as JSON for more universal access
json_data = {
'latents': latents.tolist() if isinstance(latents, np.ndarray) else latents,
'demographics': {k: v.tolist() if isinstance(v, np.ndarray) else v
for k, v in demographics.items()}
}
if subjects is not None:
json_data['subjects'] = subjects
with open(os.path.join('results', file_path.replace('.pkl', '.json')), 'w') as f:
json.dump(json_data, f)
return os.path.join('results', file_path)
def gradio_fc_analysis(data_source, latent_dim, nepochs, bsize, use_hf_dataset):
"""Run the full VAE analysis pipeline with accuracy metrics"""
# Run the original analysis
fig, results = run_fc_analysis(
data_dir=data_source,
demographic_file=None, # We're now getting demographics directly from the dataset
latent_dim=latent_dim,
nepochs=nepochs,
bsize=bsize,
save_model=True,
use_hf_dataset=use_hf_dataset,
return_data=True # New parameter to return data, will need to update main.py
)
if results:
vae = results.get('vae')
X = results.get('X')
latents = results.get('latents')
demographics = results.get('demographics')
reconstructed_fc = results.get('reconstructed_fc')
generated_fc = results.get('generated_fc')
outcome_measures = results.get('outcome_measures', None)
# Calculate accuracy metrics
accuracy_metrics = {}
if X is not None and reconstructed_fc is not None:
for i in range(min(5, len(X))): # Calculate for up to 5 samples
metrics = calculate_fc_accuracy(X[i], reconstructed_fc[i])
accuracy_metrics[f"Subject_{i+1}"] = metrics
# Average metrics across subjects
avg_metrics = {}
for metric in ["MSE", "RMSE", "R²", "Correlation", "Cosine Similarity"]:
avg_metrics[metric] = np.mean([subject_metrics[metric]
for subject_metrics in accuracy_metrics.values()])
accuracy_metrics["Average"] = avg_metrics
# Save latent representations if available
if latents is not None and demographics is not None:
latents_path = save_latents(latents, demographics, file_path=f'latents_dim{latent_dim}.pkl')
print(f"Saved latents to {latents_path}")
# Train a predictor model if we have outcome measures
predictor_results = None
if outcome_measures is not None and 'wab_aq' in outcome_measures:
try:
print("Training WAB-AQ prediction model from latent representations...")
wab_scores = np.array(outcome_measures['wab_aq'])
# Filter out any NaN values
valid_indices = ~np.isnan(wab_scores)
if np.sum(valid_indices) > 5: # Only train with sufficient data
filtered_latents = latents[valid_indices]
filtered_wab = wab_scores[valid_indices]
# Extract demographic features for the model
filtered_demographics = {}
for key, values in demographics.items():
if isinstance(values, (list, np.ndarray)) and len(values) >= len(valid_indices):
filtered_demographics[key] = np.array(values)[valid_indices]
# Train the prediction model with cross-validation
predictor_results = train_predictor_from_latents(
filtered_latents,
filtered_wab,
filtered_demographics,
cv=5, # 5-fold cross-validation
n_estimators=100, # Number of trees in Random Forest
prediction_type="regression"
)
print("WAB-AQ prediction model training complete!")
except Exception as e:
print(f"Error training prediction model: {str(e)}")
# Prepare status message with accuracy metrics
if accuracy_metrics:
avg = accuracy_metrics["Average"]
status = (f"Analysis complete! Model trained with {latent_dim} dimensions.\n\n"
f"Reconstruction Accuracy Metrics (Average):\n"
f"• MSE: {avg['MSE']:.6f}\n"
f"• RMSE: {avg['RMSE']:.6f}\n"
f"• R²: {avg['R²']:.6f}\n"
f"• Correlation: {avg['Correlation']:.6f}\n"
f"• Cosine Similarity: {avg['Cosine Similarity']:.6f}\n\n")
# Add prediction model results if available
if predictor_results is not None:
cv_results = predictor_results.get('cv_results', {})
mean_metrics = cv_results.get('mean_metrics', {})
if mean_metrics and 'r2' in mean_metrics:
prediction_r2 = mean_metrics.get('r2', 0)
prediction_rmse = mean_metrics.get('rmse', 0)
status += (f"WAB-AQ Prediction Model Performance:\n"
f"• R²: {prediction_r2:.4f}\n"
f"• RMSE: {prediction_rmse:.4f}\n\n")
status += f"Latent representations saved to results/latents_dim{latent_dim}.pkl"
else:
status = "Analysis complete! VAE model has been trained and demographic relationships analyzed."
else:
status = "Analysis complete, but no results were returned for accuracy calculation."
return fig, status
def create_interface():
with gr.Blocks(title="Aphasia fMRI to FC Analysis using VAE") as iface:
gr.Markdown("""
# Aphasia fMRI to FC Analysis using VAE
This demo uses a Variational Autoencoder (VAE) to analyze functional connectivity patterns in the brain and their relationship to demographic variables.
## Dataset Information
By default, this uses the SreekarB/OSFData dataset from HuggingFace with the following variables:
- ID: Subject identifier
- wab_aq: Aphasia severity score
- age: Age of the subject
- mpo: Months post onset
- education: Years of education
- gender: Subject gender
- handedness: Subject handedness (ignored in the analysis)
""")
with gr.Row():
with gr.Column(scale=1):
# Configuration parameters
data_source = gr.Textbox(
label="Data Source (HF Dataset ID or Local Directory)",
value="SreekarB/OSFData"
)
latent_dim = gr.Slider(
minimum=8, maximum=64, step=8,
label="Latent Dimensions", value=32
)
nepochs = gr.Slider(
minimum=100, maximum=5000, step=100,
label="Number of Epochs", value=200 # Reduced for faster demos
)
bsize = gr.Slider(
minimum=8, maximum=64, step=8,
label="Batch Size", value=16
)
use_hf_dataset = gr.Checkbox(
label="Use HuggingFace Dataset", value=True
)
# Training button
train_button = gr.Button("Start Training", variant="primary")
status_text = gr.Textbox(label="Status", value="Ready to start training")
with gr.Column(scale=2):
# Output plot
output_plot = gr.Plot(label="Analysis Results")
accuracy_box = gr.Markdown("### Accuracy Metrics\nRun analysis to see reconstruction accuracy metrics here")
# Link the training button to the analysis function
train_button.click(
fn=gradio_fc_analysis,
inputs=[data_source, latent_dim, nepochs, bsize, use_hf_dataset],
outputs=[output_plot, status_text]
)
# Custom function to update the accuracy box
def update_accuracy_display(status_text):
if "Accuracy Metrics" in status_text:
# Extract the accuracy metrics section
parts = status_text.split("Reconstruction Accuracy Metrics (Average):")
if len(parts) > 1:
metrics_text = parts[1].split("\n\n")[0]
return f"### Reconstruction Accuracy Metrics\n{metrics_text}"
return "### Accuracy Metrics\nNo metrics available yet. Run analysis to generate metrics."
# Update accuracy box when status changes
status_text.change(
fn=update_accuracy_display,
inputs=[status_text],
outputs=[accuracy_box]
)
# Add examples
gr.Examples(
examples=[
["SreekarB/OSFData", 32, 200, 16, True], # Fewer epochs for faster demo
],
inputs=[data_source, latent_dim, nepochs, bsize, use_hf_dataset],
)
# Add explanation of the workflow
gr.Markdown("""
## How this works
1. **Data Loading**: The system downloads NIfTI files (P01_rs.nii format) from the SreekarB/OSFData dataset
2. **Preprocessing**: The fMRI data is processed using the Power 264 atlas and converted to functional connectivity (FC) matrices
3. **VAE Training**: A conditional VAE model learns the latent representation of brain connectivity
4. **Predictive Modeling**: The system trains a Random Forest regressor on latent features to predict WAB-AQ scores (aphasia severity)
5. **Analysis**: The system analyzes relationships between latent brain connectivity patterns and demographic variables
6. **Visualization**: Results are displayed showing original FC, reconstructed FC, generated FC, and demographic correlations
Note: This app works with the SreekarB/OSFData dataset that contains NIfTI files and demographic information.
""")
return iface
if __name__ == "__main__":
iface = create_interface()
iface.launch(share=True)
|