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"""logreg_cdr_compare — compare LogReg AUCs across GT / base-UNet / fine-tuned-UNet CDR sources.
Lets us answer: how much of the apparent +0.11 AUC from the LogReg(clinical+CDR-GT)
result is from the GT source quality vs the CDR features themselves? Tritower
uses per-fold-fine-tuned UNet — this script reproduces that pipeline as a 5-fold
LogReg baseline so the numbers are directly comparable to v4 cd_solo_geom and
tritower runs.
5-fold StratifiedGroupKFold (patient-grouped), LogReg with StandardScaler.
Run:
python -m v4.scripts.analysis.logreg_cdr_compare
"""
from __future__ import annotations
import sys, time
from pathlib import Path
import numpy as np
from sklearn.linear_model import LogisticRegression
from sklearn.preprocessing import StandardScaler
from sklearn.pipeline import make_pipeline
from sklearn.model_selection import StratifiedGroupKFold
from sklearn.metrics import roc_auc_score
REPO_ROOT = Path(__file__).resolve().parents[3]
sys.path.insert(0, str(REPO_ROOT))
from v4.classes.profiles.v4papila import build_data
from v4.classes.profiles.fundus_images import (
build_geometry_loader,
_PapilaUNetMaskPipeline,
compute_geometry_features,
)
CONTOUR_DIR = REPO_ROOT / "Papila/ExpertsSegmentations/Contours"
UNET_WEIGHTS = REPO_ROOT / "models/v2/refuge/segmentation/per_image/best.pt"
def main():
data = build_data({
"image_dir": "Papila/FundusImages",
"clinical_dir": "Papila/ClinicalData",
"iop_corr_method": "ratio",
"iop_drop_raw": True,
"exclude_cols": ["Axial_Length"],
})
df = data.df[data.df[data.label_col].isin([0, 1])].reset_index(drop=True)
samples = data.collect_samples(df)
y = df[data.label_col].astype(int).values
groups = df["Patient ID"].astype(int).values
view = data.matrix
X_clin = np.array([view.vectorize_entity(int(r["Patient ID"]), str(r["eyeID"]))
for _, r in df.iterrows()])
print(f"n eyes={len(df)} n patients={len(set(groups))} "
f"label balance={np.bincount(y).tolist()}")
# ─── GT CDR ───────────────────────────────────────────────────────────────
print("\n[1/3] GT CDR (rasterise expert contours; split-independent)")
gt = build_geometry_loader("gt", contour_dir=str(CONTOUR_DIR))
gt.precompute(samples)
gt_vecs = gt.all_vectors()
X_cdr_gt = np.array([gt_vecs[(int(r["Patient ID"]), str(r["eyeID"]))]
for _, r in df.iterrows()])
# ─── Base UNet CDR (no fine-tune; same masks every fold) ──────────────────
print("\n[2/3] base UNet CDR (REFUGE weights, no fine-tune)")
t0 = time.time()
unet_base = build_geometry_loader("unet",
weights_path=str(UNET_WEIGHTS),
contour_dir=str(CONTOUR_DIR),
finetune_epochs=0,
)
unet_base.precompute(samples)
base_vecs = unet_base.all_vectors()
X_cdr_unet_base = np.array([base_vecs[(int(r["Patient ID"]), str(r["eyeID"]))]
for _, r in df.iterrows()])
print(f" base inference done in {time.time()-t0:.1f}s")
# ─── Build the 5 folds (used for both per-fold UNet ft AND for LogReg CV) ─
sgkf = StratifiedGroupKFold(n_splits=5, shuffle=True, random_state=42)
splits = list(sgkf.split(np.arange(len(df)), y, groups))
# ─── Per-fold fine-tuned UNet CDR ─────────────────────────────────────────
print("\n[3/3] per-fold-fine-tuned UNet CDR (matches tritower / cd_solo_geom)")
X_cdr_unet_ft = np.zeros((len(df), 5), dtype=np.float32)
pipe = _PapilaUNetMaskPipeline(
str(UNET_WEIGHTS),
contour_dir=str(CONTOUR_DIR),
finetune_epochs=10,
finetune_lr=1e-5,
finetune_batch_size=4,
)
for fold, (tr, te) in enumerate(splits):
t1 = time.time()
train_samples = [samples[i] for i in tr]
test_samples = [samples[i] for i in te]
pipe.reset_weights()
pipe.finetune(train_samples)
masks = pipe.predict(test_samples)
for j, (pid, eye, _) in zip(te, test_samples):
disc, cup = masks[(pid, eye)]
X_cdr_unet_ft[j] = compute_geometry_features(disc, cup)
print(f" fold {fold+1}/5 done ({time.time()-t1:.0f}s)")
# ─── LogReg CV ────────────────────────────────────────────────────────────
def cv(X, label):
aucs = []
for tr, te in splits:
clf = make_pipeline(StandardScaler(),
LogisticRegression(max_iter=2000, C=1.0))
clf.fit(X[tr], y[tr])
aucs.append(roc_auc_score(y[te], clf.predict_proba(X[te])[:, 1]))
print(f" {label:32s}: {np.mean(aucs):.4f} ± {np.std(aucs):.4f}")
print("\n=== StratifiedGroupKFold LogReg AUCs ===")
cv(X_clin, "clinical only")
cv(X_cdr_gt, "CDR-GT only")
cv(X_cdr_unet_base, "CDR-UNet (base) only")
cv(X_cdr_unet_ft, "CDR-UNet (per-fold ft) only")
print()
cv(np.concatenate([X_clin, X_cdr_gt], axis=1), "clinical + CDR-GT")
cv(np.concatenate([X_clin, X_cdr_unet_base], axis=1), "clinical + CDR-UNet (base)")
cv(np.concatenate([X_clin, X_cdr_unet_ft], axis=1), "clinical + CDR-UNet (ft)")
if __name__ == "__main__":
main()