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scripts/train_baselines.py β Baseline comparison models for the paper.
Baselines:
1. MFCC+MLP β 40 MFCCs (mean+std = 80 features) β 2-layer MLP
2. MFCC+LR β same features β Logistic Regression (linear baseline)
3. Random β majority class predictor
Runs on: COPD binary and Pneumonia binary datasets.
Uses same train/val/test splits as OPERA models for fair comparison.
Pneumonia uses 5-fold CV (same as OPERA evaluation).
Output: outputs/results_baselines.json
outputs/baseline_comparison.png
"""
import os
import sys
import json
import warnings
import numpy as np
import pandas as pd
import librosa
from tqdm import tqdm
from sklearn.linear_model import LogisticRegression
from sklearn.neural_network import MLPClassifier
from sklearn.preprocessing import StandardScaler
from sklearn.model_selection import StratifiedKFold
from sklearn.metrics import (
f1_score, recall_score, precision_score,
roc_auc_score, accuracy_score, classification_report
)
import matplotlib
matplotlib.use('Agg')
import matplotlib.pyplot as plt
warnings.filterwarnings('ignore')
sys.path.insert(0, os.path.dirname(os.path.dirname(__file__)))
os.makedirs('outputs', exist_ok=True)
SAMPLE_RATE = 16000
DURATION = 8 # seconds β same as OPERA
N_MFCC = 40
RANDOM_STATE = 42
# ββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββ
# Feature extraction
# ββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββ
def extract_mfcc(file_path: str) -> np.ndarray | None:
"""
Extract 40 MFCCs β mean + std = 80-dim feature vector.
Returns None on failure.
"""
try:
y, sr = librosa.load(file_path, sr=SAMPLE_RATE, duration=DURATION, mono=True)
if len(y) < SAMPLE_RATE: # skip files shorter than 1 second
return None
mfcc = librosa.feature.mfcc(y=y, sr=sr, n_mfcc=N_MFCC)
return np.concatenate([mfcc.mean(axis=1), mfcc.std(axis=1)])
except Exception:
return None
def extract_features_from_df(df: pd.DataFrame, desc: str) -> tuple[np.ndarray, np.ndarray]:
"""Extract MFCC features for all rows. Returns (X, y) dropping failed files."""
X, y = [], []
failed = 0
for _, row in tqdm(df.iterrows(), total=len(df), desc=desc):
feat = extract_mfcc(str(row['file_path']))
if feat is not None:
X.append(feat)
y.append(int(row['label']))
else:
failed += 1
if failed:
print(f" Skipped {failed} files (too short or unreadable)")
return np.array(X), np.array(y)
# ββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββ
# Model evaluation helpers
# ββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββ
def eval_binary(y_true, y_pred, y_prob, model_name, disease):
metrics = {
'model': model_name,
'disease': disease,
'accuracy': float(accuracy_score(y_true, y_pred)),
'f1_macro': float(f1_score(y_true, y_pred, average='macro', zero_division=0)),
'recall': float(recall_score(y_true, y_pred, pos_label=1, zero_division=0)),
'precision': float(precision_score(y_true, y_pred, pos_label=1, zero_division=0)),
'auroc': float(roc_auc_score(y_true, y_prob)) if len(np.unique(y_true)) > 1 else 0.0,
}
print(f" {model_name:20s} | Acc:{metrics['accuracy']:.3f} | "
f"F1:{metrics['f1_macro']:.3f} | Recall:{metrics['recall']:.3f} | AUROC:{metrics['auroc']:.3f}")
return metrics
def run_baselines_single_split(train_df, test_df, disease):
"""Run baselines on a fixed train/test split (COPD)."""
print(f"\n Extracting MFCC features...")
X_train, y_train = extract_features_from_df(train_df, f" Train ({disease})")
X_test, y_test = extract_features_from_df(test_df, f" Test ({disease})")
scaler = StandardScaler()
X_train = scaler.fit_transform(X_train)
X_test = scaler.transform(X_test)
results = []
# 1. Logistic Regression (linear probe)
lr = LogisticRegression(max_iter=1000, class_weight='balanced', random_state=RANDOM_STATE, C=1.0)
lr.fit(X_train, y_train)
y_pred = lr.predict(X_test)
y_prob = lr.predict_proba(X_test)[:, 1]
results.append(eval_binary(y_test, y_pred, y_prob, 'MFCC + LR', disease))
# 2. MLP
mlp = MLPClassifier(
hidden_layer_sizes=(256, 64), activation='relu',
max_iter=300, early_stopping=True, validation_fraction=0.1,
random_state=RANDOM_STATE, learning_rate_init=1e-3
)
mlp.fit(X_train, y_train)
y_pred = mlp.predict(X_test)
y_prob = mlp.predict_proba(X_test)[:, 1]
results.append(eval_binary(y_test, y_pred, y_prob, 'MFCC + MLP', disease))
# 3. Majority class baseline
majority = int(np.bincount(y_train).argmax())
y_pred = np.full_like(y_test, majority)
y_prob = np.zeros_like(y_test, dtype=float)
results.append(eval_binary(y_test, y_pred, y_prob, 'Majority Class', disease))
return results
def run_baselines_cv(df, disease, n_folds=5):
"""Run baselines with stratified CV (Pneumonia)."""
print(f"\n Extracting MFCC features (full dataset)...")
X_all, y_all = extract_features_from_df(df, f" {disease}")
skf = StratifiedKFold(n_splits=n_folds, shuffle=True, random_state=RANDOM_STATE)
model_names = ['MFCC + LR', 'MFCC + MLP']
oof_probs = {m: np.zeros(len(X_all)) for m in model_names}
oof_preds = {m: np.zeros(len(X_all), dtype=int) for m in model_names}
for fold, (ti, vi) in enumerate(skf.split(X_all, y_all)):
X_tr, X_vl = X_all[ti], X_all[vi]
y_tr = y_all[ti]
scaler = StandardScaler()
X_tr = scaler.fit_transform(X_tr)
X_vl = scaler.transform(X_vl)
lr = LogisticRegression(max_iter=1000, class_weight='balanced', random_state=RANDOM_STATE)
lr.fit(X_tr, y_tr)
oof_probs['MFCC + LR'][vi] = lr.predict_proba(X_vl)[:, 1]
oof_preds['MFCC + LR'][vi] = lr.predict(X_vl)
mlp = MLPClassifier(hidden_layer_sizes=(256, 64), activation='relu',
max_iter=300, early_stopping=True, validation_fraction=0.1,
random_state=RANDOM_STATE, learning_rate_init=1e-3)
mlp.fit(X_tr, y_tr)
oof_probs['MFCC + MLP'][vi] = mlp.predict_proba(X_vl)[:, 1]
oof_preds['MFCC + MLP'][vi] = mlp.predict(X_vl)
print(f" Fold {fold+1}/{n_folds} done")
results = []
for m in model_names:
results.append(eval_binary(y_all, oof_preds[m], oof_probs[m], m, disease))
majority = int(np.bincount(y_all).argmax())
y_pred = np.full_like(y_all, majority)
y_prob = np.zeros_like(y_all, dtype=float)
results.append(eval_binary(y_all, y_pred, y_prob, 'Majority Class', disease))
return results
# ββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββ
# COPD
# ββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββ
print("\n" + "="*60)
print("COPD BASELINES (train/test split)")
print("="*60)
copd_train = pd.read_csv('data/copd_train_split.csv')
copd_val = pd.read_csv('data/copd_val_split.csv')
copd_test = pd.read_csv('data/copd_test_split.csv')
# Combine train+val to match OPERA training set size
copd_trainval = pd.concat([copd_train, copd_val], ignore_index=True)
print(f" Train+Val: {len(copd_trainval)} | Test: {len(copd_test)}")
print(f" Test positives: {copd_test['label'].sum()}")
copd_results = run_baselines_single_split(copd_trainval, copd_test, 'COPD')
# ββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββ
# Pneumonia
# ββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββ
print("\n" + "="*60)
print("PNEUMONIA BASELINES (5-fold CV β same as OPERA)")
print("="*60)
pneu_df = pd.read_csv('data/pneumonia_binary_labels_with_embeddings.csv').dropna(
subset=['embedding_path'])
print(f" Total: {len(pneu_df)} | Positives: {pneu_df['label'].sum()}")
pneu_results = run_baselines_cv(pneu_df, 'Pneumonia')
# ββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββ
# Save results
# ββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββ
all_results = {
'COPD': copd_results,
'Pneumonia': pneu_results,
}
with open('outputs/results_baselines.json', 'w') as f:
json.dump(all_results, f, indent=2)
print("\n Saved: outputs/results_baselines.json")
# ββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββ
# Comparison chart β baselines vs OPERA
# ββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββ
opera_results = {
'COPD': {'f1_macro': 0.947, 'recall': 0.959, 'auroc': 0.995},
'Pneumonia': {'f1_macro': 0.869, 'recall': 0.731, 'auroc': 0.984},
}
fig, axes = plt.subplots(1, 2, figsize=(14, 5))
metrics_to_plot = ['f1_macro', 'recall', 'auroc']
metric_labels = ['Macro F1', 'Recall', 'AUROC']
colors = ['#90CAF9', '#A5D6A7', '#FFCC80', '#EF9A9A']
for ax, (disease, baseline_list) in zip(axes, all_results.items()):
models = [r['model'] for r in baseline_list] + ['OPERA-MLP (ours)']
x = np.arange(len(models))
width = 0.25
opera_row = opera_results[disease]
all_rows = baseline_list + [{'f1_macro': opera_row['f1_macro'],
'recall': opera_row['recall'],
'auroc': opera_row['auroc']}]
for i, (metric, label, color) in enumerate(zip(metrics_to_plot, metric_labels, colors)):
vals = [r[metric] for r in all_rows]
bars = ax.bar(x + i * width, vals, width, label=label, color=color, alpha=0.85, edgecolor='white')
for bar, v in zip(bars, vals):
if v > 0.01:
ax.text(bar.get_x() + bar.get_width()/2, bar.get_height() + 0.005,
f'{v:.2f}', ha='center', va='bottom', fontsize=7.5, fontweight='bold')
ax.set_xticks(x + width)
ax.set_xticklabels(models, fontsize=9, rotation=10, ha='right')
ax.set_ylim(0, 1.18)
ax.set_ylabel('Score', fontsize=11)
ax.set_title(f'{disease} Detection β Baseline vs OPERA-MLP', fontsize=12, fontweight='bold')
ax.legend(fontsize=9, loc='upper left')
ax.grid(axis='y', linestyle='--', alpha=0.4)
ax.axvline(x=len(models) - 1.4, color='gray', linestyle='--', alpha=0.5)
plt.tight_layout()
fig.savefig('outputs/baseline_comparison.png', dpi=150, bbox_inches='tight')
plt.close(fig)
print(" Saved: outputs/baseline_comparison.png")
# Print final summary table
print("\n" + "="*70)
print("FULL COMPARISON TABLE")
print("="*70)
print(f"{'Model':<22} {'Disease':<12} {'F1':>6} {'Recall':>8} {'AUROC':>8}")
print("-"*70)
for disease, results in all_results.items():
for r in results:
print(f" {r['model']:<20} {disease:<12} {r['f1_macro']:>6.3f} {r['recall']:>8.3f} {r['auroc']:>8.3f}")
opera = opera_results[disease]
print(f" {'OPERA-MLP (ours)':<20} {disease:<12} {opera['f1_macro']:>6.3f} {opera['recall']:>8.3f} {opera['auroc']:>8.3f}")
print()
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