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milk10k_effb2_dermoscopic_metadata/__pycache__/data.cpython-314.pyc
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Binary file (27.8 kB). View file
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milk10k_effb2_dermoscopic_metadata/data.py
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@@ -113,6 +113,10 @@ def synthetic_mask(df: pd.DataFrame) -> np.ndarray:
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return mask
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def create_or_load_split(
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df: pd.DataFrame, manifest: Path, val_size: float, seed: int,
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synthetic_train_only: bool = False, fold_index: int = 0, k_folds: int = 1,
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@@ -138,12 +142,18 @@ def create_or_load_split(
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raise ValueError(f"Split manifest has overlapping train/validation IDs: {manifest}")
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unknown = (train_ids | val_ids) - all_ids
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missing = all_ids - (train_ids | val_ids)
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-
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raise ValueError(f"Split manifest does not match dataset (unknown={len(unknown)}, missing={len(missing)}).")
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else:
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synthetic = synthetic_mask(df)
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base = df.loc[~synthetic].copy() if synthetic_train_only else df.copy()
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extra_train_ids = set(df.loc[synthetic, "lesion_id"].astype(str)) if synthetic_train_only else set()
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folds = []
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if k_folds == 1:
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train_rows, val_rows = train_test_split(base, test_size=val_size, stratify=base["label"], random_state=seed)
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@@ -155,9 +165,23 @@ def create_or_load_split(
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splitter = StratifiedKFold(k_folds, shuffle=True, random_state=seed)
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pairs = [(base.iloc[tr], base.iloc[va]) for tr, va in splitter.split(base, base["label"])]
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for train_rows, val_rows in pairs:
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folds.append({
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"train_lesion_ids": sorted(set(train_rows["lesion_id"].astype(str)) | extra_train_ids),
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"val_lesion_ids": sorted(set(val_rows["lesion_id"].astype(str))),
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})
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train_ids = set(folds[fold_index]["train_lesion_ids"]); val_ids = set(folds[fold_index]["val_lesion_ids"])
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manifest.parent.mkdir(parents=True, exist_ok=True)
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@@ -180,6 +204,14 @@ def append_augmented_rows(base_df: pd.DataFrame, train_df: pd.DataFrame, args) -
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if args.augmented_data_dir is None: return train_df
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augmented = load_dermoscopic_dataframe(args.augmented_data_dir)
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augmented = augmented[~augmented["lesion_id"].astype(str).isin(set(base_df["lesion_id"].astype(str)))].copy()
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if args.augmented_classes:
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allowed = {name.upper() for name in args.augmented_classes}
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unknown = allowed - {name.upper() for name in base_df["label"].unique()}
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return mask
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def source_lesion_id(value: Any) -> str:
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return str(value).split("__sdpair_", 1)[0]
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def create_or_load_split(
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df: pd.DataFrame, manifest: Path, val_size: float, seed: int,
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synthetic_train_only: bool = False, fold_index: int = 0, k_folds: int = 1,
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raise ValueError(f"Split manifest has overlapping train/validation IDs: {manifest}")
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unknown = (train_ids | val_ids) - all_ids
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missing = all_ids - (train_ids | val_ids)
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allowed_missing = set()
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if synthetic_train_only:
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allowed_missing = {
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lesion_id for lesion_id in missing
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if "__sdpair_" in lesion_id and source_lesion_id(lesion_id) in val_ids
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}
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unexpected_missing = missing - allowed_missing
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if unknown or unexpected_missing:
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raise ValueError(f"Split manifest does not match dataset (unknown={len(unknown)}, missing={len(missing)}).")
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else:
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synthetic = synthetic_mask(df)
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base = df.loc[~synthetic].copy() if synthetic_train_only else df.copy()
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folds = []
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if k_folds == 1:
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train_rows, val_rows = train_test_split(base, test_size=val_size, stratify=base["label"], random_state=seed)
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splitter = StratifiedKFold(k_folds, shuffle=True, random_state=seed)
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pairs = [(base.iloc[tr], base.iloc[va]) for tr, va in splitter.split(base, base["label"])]
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for train_rows, val_rows in pairs:
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train_real_ids = set(train_rows["lesion_id"].astype(str))
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val_real_ids = set(val_rows["lesion_id"].astype(str))
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extra_train_ids = set()
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excluded_synthetic_ids = set()
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if synthetic_train_only:
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for lesion_id in df.loc[synthetic, "lesion_id"].astype(str):
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source_id = source_lesion_id(lesion_id)
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if source_id in train_real_ids:
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extra_train_ids.add(lesion_id)
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elif source_id in val_real_ids:
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excluded_synthetic_ids.add(lesion_id)
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else:
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raise ValueError(f"Synthetic lesion has unknown source ID: {lesion_id}")
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folds.append({
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"train_lesion_ids": sorted(set(train_rows["lesion_id"].astype(str)) | extra_train_ids),
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"val_lesion_ids": sorted(set(val_rows["lesion_id"].astype(str))),
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"excluded_synthetic_lesion_ids": sorted(excluded_synthetic_ids),
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})
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train_ids = set(folds[fold_index]["train_lesion_ids"]); val_ids = set(folds[fold_index]["val_lesion_ids"])
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manifest.parent.mkdir(parents=True, exist_ok=True)
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if args.augmented_data_dir is None: return train_df
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augmented = load_dermoscopic_dataframe(args.augmented_data_dir)
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augmented = augmented[~augmented["lesion_id"].astype(str).isin(set(base_df["lesion_id"].astype(str)))].copy()
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train_source_ids = set(train_df["lesion_id"].astype(str).map(source_lesion_id))
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base_source_ids = set(base_df["lesion_id"].astype(str).map(source_lesion_id))
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augmented["source_lesion_id"] = augmented["lesion_id"].astype(str).map(source_lesion_id)
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unknown = ~augmented["source_lesion_id"].isin(base_source_ids)
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if unknown.any():
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examples = augmented.loc[unknown, "lesion_id"].astype(str).head(5).tolist()
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raise ValueError(f"Augmented lesions have unknown source IDs. Examples: {examples}")
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augmented = augmented[augmented["source_lesion_id"].isin(train_source_ids)].copy()
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if args.augmented_classes:
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allowed = {name.upper() for name in args.augmented_classes}
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unknown = allowed - {name.upper() for name in base_df["label"].unique()}
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