workbench 0.8.201__py3-none-any.whl → 0.8.204__py3-none-any.whl

workbench/model_scripts/chemprop/generated_model_script.py

@@ -25,6 +25,7 @@
 # - argparse, file loading, S3 writes
 # =============================
 
+import glob
 import os
 import argparse
 import json
@@ -39,11 +40,13 @@ from sklearn.model_selection import train_test_split, KFold, StratifiedKFold
 from sklearn.preprocessing import LabelEncoder
 from sklearn.metrics import (
     mean_absolute_error,
+    median_absolute_error,
     r2_score,
     root_mean_squared_error,
     precision_recall_fscore_support,
     confusion_matrix,
 )
+from scipy.stats import spearmanr
 import joblib
 
 # ChemProp imports
@@ -51,12 +54,12 @@ from chemprop import data, models, nn
 
 # Template Parameters
 TEMPLATE_PARAMS = {
-    "model_type": "classifier",
-    "target": "solubility_class",
-    "feature_list": ['smiles'],
-    "model_metrics_s3_path": "s3://sandbox-sageworks-artifacts/models/aqsol-chemprop-class/training",
-    "train_all_data": False,
-    "hyperparameters": {'max_epochs': 400, 'hidden_dim': 300, 'depth': 3, 'n_folds': 5},
+    "model_type": "uq_regressor",
+    "targets": ['udm_asy_res_efflux_ratio'],  # List of target columns (single or multi-task)
+    "feature_list": ['smiles', 'smr_vsa4', 'tpsa', 'nhohcount', 'mollogp', 'peoe_vsa1', 'smr_vsa3', 'nitrogen_span', 'numhdonors', 'minpartialcharge', 'vsa_estate3', 'vsa_estate6', 'tertiary_amine_count', 'hba_hbd_ratio', 'peoe_vsa8', 'estate_vsa4', 'xc_4dv', 'vsa_estate2', 'molmr', 'xp_2dv', 'mi', 'molecular_axis_length', 'vsa_estate4', 'xp_6dv', 'qed', 'estate_vsa8', 'chi1v', 'asphericity', 'axp_1d', 'bcut2d_logphi', 'kappa3', 'axp_7d', 'num_s_centers', 'amphiphilic_moment', 'molecular_asymmetry', 'charge_centroid_distance', 'estate_vsa3', 'vsa_estate8', 'aromatic_interaction_score', 'molecular_volume_3d', 'axp_7dv', 'peoe_vsa3', 'smr_vsa6', 'bcut2d_mrhi', 'radius_of_gyration', 'xpc_4dv', 'minabsestateindex', 'axp_0dv', 'chi4n', 'balabanj', 'bcut2d_mwlow'],
+    "id_column": "udm_mol_bat_id",
+    "model_metrics_s3_path": "s3://ideaya-sageworks-bucket/models/caco2-er-chemprop-reg-hybrid/training",
+    "hyperparameters": {'n_folds': 5, 'hidden_dim': 700, 'depth': 6, 'dropout': 0.15, 'ffn_hidden_dim': 2000, 'ffn_num_layers': 2},
 }
 
 
@@ -108,14 +111,14 @@ def expand_proba_column(df: pd.DataFrame, class_labels: list[str]) -> pd.DataFra
 
 def create_molecule_datapoints(
     smiles_list: list[str],
-    targets: list[float] | None = None,
+    targets: list[float] | np.ndarray | None = None,
     extra_descriptors: np.ndarray | None = None,
 ) -> tuple[list[data.MoleculeDatapoint], list[int]]:
     """Create ChemProp MoleculeDatapoints from SMILES strings.
 
     Args:
         smiles_list: List of SMILES strings
-        targets: Optional list of target values (for training)
+        targets: Optional target values as 2D array (n_samples, n_targets). NaN allowed for missing targets.
         extra_descriptors: Optional array of extra features (n_samples, n_features)
 
     Returns:
@@ -127,6 +130,12 @@ def create_molecule_datapoints(
     valid_indices = []
     invalid_count = 0
 
+    # Convert targets to 2D array if provided
+    if targets is not None:
+        targets = np.atleast_2d(np.array(targets))
+        if targets.shape[0] == 1 and len(smiles_list) > 1:
+            targets = targets.T  # Shape was (1, n_samples), transpose to (n_samples, 1)
+
     for i, smi in enumerate(smiles_list):
         # Validate SMILES with RDKit first
         mol = Chem.MolFromSmiles(smi)
@@ -134,8 +143,9 @@ def create_molecule_datapoints(
             invalid_count += 1
             continue
 
-        # Build datapoint with optional target and extra descriptors
-        y = [targets[i]] if targets is not None else None
+        # Build datapoint with optional target(s) and extra descriptors
+        # For multi-task, y is a list of values (can include NaN for missing targets)
+        y = targets[i].tolist() if targets is not None else None
         x_d = extra_descriptors[i] if extra_descriptors is not None else None
 
         dp = data.MoleculeDatapoint.from_smi(smi, y=y, x_d=x_d)
@@ -152,9 +162,11 @@ def build_mpnn_model(
     hyperparameters: dict,
     task: str = "regression",
     num_classes: int | None = None,
+    n_targets: int = 1,
     n_extra_descriptors: int = 0,
     x_d_transform: nn.ScaleTransform | None = None,
     output_transform: nn.UnscaleTransform | None = None,
+    task_weights: np.ndarray | None = None,
 ) -> models.MPNN:
     """Build an MPNN model with the specified hyperparameters.
 
@@ -162,19 +174,21 @@ def build_mpnn_model(
         hyperparameters: Dictionary of model hyperparameters
         task: Either "regression" or "classification"
         num_classes: Number of classes for classification tasks
+        n_targets: Number of target columns (for multi-task regression)
         n_extra_descriptors: Number of extra descriptor features (for hybrid mode)
         x_d_transform: Optional transform for extra descriptors (scaling)
         output_transform: Optional transform for regression output (unscaling targets)
+        task_weights: Optional array of weights for each task (multi-task learning)
 
     Returns:
         Configured MPNN model
     """
     # Model hyperparameters with defaults
-    hidden_dim = hyperparameters.get("hidden_dim", 300)
-    depth = hyperparameters.get("depth", 3)
-    dropout = hyperparameters.get("dropout", 0.0)
-    ffn_hidden_dim = hyperparameters.get("ffn_hidden_dim", 300)
-    ffn_num_layers = hyperparameters.get("ffn_num_layers", 1)
+    hidden_dim = hyperparameters.get("hidden_dim", 700)
+    depth = hyperparameters.get("depth", 6)
+    dropout = hyperparameters.get("dropout", 0.15)
+    ffn_hidden_dim = hyperparameters.get("ffn_hidden_dim", 2000)
+    ffn_num_layers = hyperparameters.get("ffn_num_layers", 2)
 
     # Message passing component
     mp = nn.BondMessagePassing(d_h=hidden_dim, depth=depth, dropout=dropout)
@@ -197,12 +211,20 @@ def build_mpnn_model(
         )
     else:
         # Regression with optional output transform to unscale predictions
+        # n_tasks controls the number of output heads for multi-task learning
+        # task_weights goes here (in RegressionFFN) to weight loss per task
+        weights_tensor = None
+        if task_weights is not None:
+            weights_tensor = torch.tensor(task_weights, dtype=torch.float32)
+
         ffn = nn.RegressionFFN(
             input_dim=ffn_input_dim,
             hidden_dim=ffn_hidden_dim,
             n_layers=ffn_num_layers,
             dropout=dropout,
+            n_tasks=n_targets,
             output_transform=output_transform,
+            task_weights=weights_tensor,
         )
 
     # Create the MPNN model
@@ -227,31 +249,26 @@ def model_fn(model_dir: str) -> dict:
     Returns:
         Dictionary with ensemble models and metadata
     """
-    # Load ensemble metadata
+    # Load ensemble metadata (required)
     ensemble_metadata_path = os.path.join(model_dir, "ensemble_metadata.joblib")
-    if os.path.exists(ensemble_metadata_path):
-        ensemble_metadata = joblib.load(ensemble_metadata_path)
-        n_ensemble = ensemble_metadata["n_ensemble"]
-    else:
-        # Backwards compatibility: single model without ensemble metadata
-        n_ensemble = 1
+    ensemble_metadata = joblib.load(ensemble_metadata_path)
+    n_ensemble = ensemble_metadata["n_ensemble"]
+    target_columns = ensemble_metadata["target_columns"]
 
     # Load all ensemble models
     ensemble_models = []
     for ens_idx in range(n_ensemble):
         model_path = os.path.join(model_dir, f"chemprop_model_{ens_idx}.pt")
-        if not os.path.exists(model_path):
-            # Backwards compatibility: try old single model path
-            model_path = os.path.join(model_dir, "chemprop_model.pt")
         model = models.MPNN.load_from_file(model_path)
         model.eval()
         ensemble_models.append(model)
 
-    print(f"Loaded {len(ensemble_models)} ensemble model(s)")
+    print(f"Loaded {len(ensemble_models)} ensemble model(s), n_targets={len(target_columns)}")
 
     return {
         "ensemble_models": ensemble_models,
         "n_ensemble": n_ensemble,
+        "target_columns": target_columns,
     }
 
 
@@ -297,9 +314,10 @@ def predict_fn(df: pd.DataFrame, model_dict: dict) -> pd.DataFrame:
     model_type = TEMPLATE_PARAMS["model_type"]
     model_dir = os.environ.get("SM_MODEL_DIR", "/opt/ml/model")
 
-    # Extract ensemble models
+    # Extract ensemble models and metadata
     ensemble_models = model_dict["ensemble_models"]
     n_ensemble = model_dict["n_ensemble"]
+    target_columns = model_dict["target_columns"]
 
     # Load label encoder if present (classification)
     label_encoder = None
@@ -337,13 +355,14 @@ def predict_fn(df: pd.DataFrame, model_dict: dict) -> pd.DataFrame:
     valid_mask = np.array(valid_mask)
     print(f"Valid SMILES: {sum(valid_mask)} / {len(smiles_list)}")
 
-    # Initialize prediction column (use object dtype for classifiers to avoid FutureWarning)
+    # Initialize prediction columns (use object dtype for classifiers to avoid FutureWarning)
     if model_type == "classifier":
         df["prediction"] = pd.Series([None] * len(df), dtype=object)
     else:
-        df["prediction"] = np.nan
-        if n_ensemble > 1:
-            df["prediction_std"] = np.nan
+        # Regression: create prediction column for each target
+        for tc in target_columns:
+            df[f"{tc}_pred"] = np.nan
+            df[f"{tc}_pred_std"] = np.nan
 
     if sum(valid_mask) == 0:
         print("Warning: No valid SMILES to predict on")
@@ -408,10 +427,15 @@ def predict_fn(df: pd.DataFrame, model_dict: dict) -> pd.DataFrame:
             ens_preds = ens_preds.squeeze(axis=1)
         all_ensemble_preds.append(ens_preds)
 
-    # Stack and compute mean/std
+    # Stack and compute mean/std (std is 0 for single model)
     ensemble_preds = np.stack(all_ensemble_preds, axis=0)
     preds = np.mean(ensemble_preds, axis=0)
-    preds_std = np.std(ensemble_preds, axis=0) if n_ensemble > 1 else None
+    preds_std = np.std(ensemble_preds, axis=0)  # Will be 0s for n_ensemble=1
+
+    # Ensure 2D: (n_samples, n_targets)
+    if preds.ndim == 1:
+        preds = preds.reshape(-1, 1)
+        preds_std = preds_std.reshape(-1, 1)
 
     print(f"Inference: Ensemble predictions shape: {preds.shape}")
 
@@ -440,12 +464,15 @@ def predict_fn(df: pd.DataFrame, model_dict: dict) -> pd.DataFrame:
             decoded_preds = label_encoder.inverse_transform(class_preds)
             df.loc[valid_mask, "prediction"] = decoded_preds
     else:
-        # Regression: direct predictions
-        df.loc[valid_mask, "prediction"] = preds.flatten()
+        # Regression: store predictions for each target
+        for t_idx, tc in enumerate(target_columns):
+            df.loc[valid_mask, f"{tc}_pred"] = preds[:, t_idx]
+            df.loc[valid_mask, f"{tc}_pred_std"] = preds_std[:, t_idx]
 
-        # Add prediction_std for ensemble models
-        if preds_std is not None:
-            df.loc[valid_mask, "prediction_std"] = preds_std.flatten()
+        # Add prediction/prediction_std aliases for first target
+        first_target = target_columns[0]
+        df["prediction"] = df[f"{first_target}_pred"]
+        df["prediction_std"] = df[f"{first_target}_pred_std"]
 
     return df
 
@@ -454,13 +481,18 @@ if __name__ == "__main__":
     """Training script for ChemProp MPNN model"""
 
     # Template Parameters
-    target = TEMPLATE_PARAMS["target"]
+    target_columns = TEMPLATE_PARAMS["targets"]  # List of target columns
     model_type = TEMPLATE_PARAMS["model_type"]
     feature_list = TEMPLATE_PARAMS["feature_list"]
+    id_column = TEMPLATE_PARAMS["id_column"]
     model_metrics_s3_path = TEMPLATE_PARAMS["model_metrics_s3_path"]
-    train_all_data = TEMPLATE_PARAMS["train_all_data"]
     hyperparameters = TEMPLATE_PARAMS["hyperparameters"]
-    validation_split = 0.2
+
+    # Validate target_columns
+    if not target_columns or not isinstance(target_columns, list) or len(target_columns) == 0:
+        raise ValueError("'targets' must be a non-empty list of target column names")
+    n_targets = len(target_columns)
+    print(f"Target columns ({n_targets}): {target_columns}")
 
     # Get the SMILES column name from feature_list (user defines this, so we use their exact name)
     smiles_column = find_smiles_column(feature_list)
@@ -502,21 +534,29 @@ if __name__ == "__main__":
 
     check_dataframe(all_df, "training_df")
 
-    # Drop rows with missing SMILES or target values
+    # Drop rows with missing SMILES or all target values
     initial_count = len(all_df)
-    all_df = all_df.dropna(subset=[smiles_column, target])
+    all_df = all_df.dropna(subset=[smiles_column])
+    # Keep rows that have at least one non-null target (works for single and multi-task)
+    has_any_target = all_df[target_columns].notna().any(axis=1)
+    all_df = all_df[has_any_target]
     dropped = initial_count - len(all_df)
     if dropped > 0:
-        print(f"Dropped {dropped} rows with missing SMILES or target values")
+        print(f"Dropped {dropped} rows with missing SMILES or all target values")
 
-    print(f"Target: {target}")
+    print(f"Target columns: {target_columns}")
     print(f"Data Shape after cleaning: {all_df.shape}")
+    for tc in target_columns:
+        n_valid = all_df[tc].notna().sum()
+        print(f"  {tc}: {n_valid} samples with values")
 
-    # Set up label encoder for classification
+    # Set up label encoder for classification (single-target only)
     label_encoder = None
     if model_type == "classifier":
+        if n_targets > 1:
+            raise ValueError("Multi-task classification is not supported. Use regression for multi-task.")
         label_encoder = LabelEncoder()
-        all_df[target] = label_encoder.fit_transform(all_df[target])
+        all_df[target_columns[0]] = label_encoder.fit_transform(all_df[target_columns[0]])
         num_classes = len(label_encoder.classes_)
         print(
             f"Classification task with {num_classes} classes: {label_encoder.classes_}"
@@ -528,10 +568,10 @@ if __name__ == "__main__":
     print(f"Hyperparameters: {hyperparameters}")
     task = "classification" if model_type == "classifier" else "regression"
     n_extra = len(extra_feature_cols) if use_extra_features else 0
-    max_epochs = hyperparameters.get("max_epochs", 50)
-    patience = hyperparameters.get("patience", 10)
-    n_folds = hyperparameters.get("n_folds", 1)  # Number of CV folds (default: 1 = no CV)
-    batch_size = hyperparameters.get("batch_size", min(64, max(16, len(all_df) // 16)))
+    max_epochs = hyperparameters.get("max_epochs", 400)
+    patience = hyperparameters.get("patience", 40)
+    n_folds = hyperparameters.get("n_folds", 5)  # Number of CV folds (default: 5)
+    batch_size = hyperparameters.get("batch_size", 16)
 
     # Check extra feature columns exist
     if use_extra_features:
@@ -540,60 +580,108 @@ if __name__ == "__main__":
             raise ValueError(f"Missing extra feature columns in training data: {missing_cols}")
 
     # =========================================================================
-    # SINGLE MODEL TRAINING (n_folds=1) - uses train/val split
+    # UNIFIED TRAINING: Works for n_folds=1 (single model) or n_folds>1 (K-fold CV)
     # =========================================================================
+    print(f"Training {'single model' if n_folds == 1 else f'{n_folds}-fold cross-validation ensemble'}...")
+
+    # Prepare extra features and validate SMILES upfront
+    all_extra_features = None
+    col_means = None
+    if use_extra_features:
+        all_extra_features = all_df[extra_feature_cols].values.astype(np.float32)
+        col_means = np.nanmean(all_extra_features, axis=0)
+        for i in range(all_extra_features.shape[1]):
+            all_extra_features[np.isnan(all_extra_features[:, i]), i] = col_means[i]
+
+    # Prepare target array: always 2D (n_samples, n_targets)
+    all_targets = all_df[target_columns].values.astype(np.float32)
+
+    # Filter invalid SMILES from the full dataset
+    _, valid_indices = create_molecule_datapoints(
+        all_df[smiles_column].tolist(), all_targets, all_extra_features
+    )
+    all_df = all_df.iloc[valid_indices].reset_index(drop=True)
+    all_targets = all_targets[valid_indices]
+    if all_extra_features is not None:
+        all_extra_features = all_extra_features[valid_indices]
+    print(f"Data after SMILES validation: {all_df.shape}")
+
+    # Compute dynamic task weights for multi-task regression
+    # Weight = inverse of sample count (normalized so min weight = 1.0)
+    # This gives higher weight to targets with fewer samples
+    task_weights = None
+    if n_targets > 1 and model_type != "classifier":
+        sample_counts = np.array([np.sum(~np.isnan(all_targets[:, t])) for t in range(n_targets)])
+        # Inverse weighting: fewer samples = higher weight
+        inverse_counts = 1.0 / sample_counts
+        # Normalize so minimum weight is 1.0
+        task_weights = inverse_counts / inverse_counts.min()
+        print(f"Task weights (inverse sample count):")
+        for t_idx, t_name in enumerate(target_columns):
+            print(f"  {t_name}: {task_weights[t_idx]:.3f} (n={sample_counts[t_idx]})")
+
+    # Create fold splits
     if n_folds == 1:
-        print("Training single model (no cross-validation)...")
-
-        # Split data
-        if train_all_data:
-            print("Training on ALL of the data")
-            df_train = all_df.copy()
-            df_val = all_df.copy()
-        elif "training" in all_df.columns:
+        # Single fold: use train/val split from "training" column or random split
+        if "training" in all_df.columns:
             print("Found training column, splitting data based on training column")
-            df_train = all_df[all_df["training"]].copy()
-            df_val = all_df[~all_df["training"]].copy()
+            train_idx = np.where(all_df["training"])[0]
+            val_idx = np.where(~all_df["training"])[0]
         else:
-            print("WARNING: No training column found, splitting data with random state=42")
-            df_train, df_val = train_test_split(
-                all_df, test_size=validation_split, random_state=42
-            )
+            print("WARNING: No training column found, splitting data with random 80/20 split")
+            indices = np.arange(len(all_df))
+            train_idx, val_idx = train_test_split(indices, test_size=0.2, random_state=42)
+        folds = [(train_idx, val_idx)]
+    else:
+        # K-Fold CV
+        if model_type == "classifier":
+            kfold = StratifiedKFold(n_splits=n_folds, shuffle=True, random_state=42)
+            split_target = all_df[target_columns[0]]
+        else:
+            kfold = KFold(n_splits=n_folds, shuffle=True, random_state=42)
+            split_target = None
+        folds = list(kfold.split(all_df, split_target))
+
+    # Initialize storage for out-of-fold predictions: always 2D (n_samples, n_targets)
+    oof_predictions = np.full((len(all_df), n_targets), np.nan, dtype=np.float64)
+    if model_type == "classifier" and num_classes and num_classes > 1:
+        oof_proba = np.full((len(all_df), num_classes), np.nan, dtype=np.float64)
+    else:
+        oof_proba = None
 
-        print(f"TRAIN: {df_train.shape}")
-        print(f"VALIDATION: {df_val.shape}")
+    ensemble_models = []
 
-        # Extract and prepare extra features
-        train_extra_features = None
-        val_extra_features = None
-        col_means = None
+    for fold_idx, (train_idx, val_idx) in enumerate(folds):
+        print(f"\n{'='*50}")
+        print(f"Training Fold {fold_idx + 1}/{len(folds)}")
+        print(f"{'='*50}")
 
-        if use_extra_features:
-            train_extra_features = df_train[extra_feature_cols].values.astype(np.float32)
-            val_extra_features = df_val[extra_feature_cols].values.astype(np.float32)
-            col_means = np.nanmean(train_extra_features, axis=0)
-            for i in range(train_extra_features.shape[1]):
-                train_extra_features[np.isnan(train_extra_features[:, i]), i] = col_means[i]
-                val_extra_features[np.isnan(val_extra_features[:, i]), i] = col_means[i]
-
-        # Create ChemProp datasets
-        train_datapoints, train_valid_idx = create_molecule_datapoints(
-            df_train[smiles_column].tolist(), df_train[target].tolist(), train_extra_features
+        # Split data for this fold
+        df_train = all_df.iloc[train_idx].reset_index(drop=True)
+        df_val = all_df.iloc[val_idx].reset_index(drop=True)
+        train_targets = all_targets[train_idx]
+        val_targets = all_targets[val_idx]
+
+        train_extra = all_extra_features[train_idx] if all_extra_features is not None else None
+        val_extra = all_extra_features[val_idx] if all_extra_features is not None else None
+
+        print(f"Fold {fold_idx + 1} - Train: {len(df_train)}, Val: {len(df_val)}")
+
+        # Create ChemProp datasets for this fold
+        train_datapoints, _ = create_molecule_datapoints(
+            df_train[smiles_column].tolist(), train_targets, train_extra
         )
-        val_datapoints, val_valid_idx = create_molecule_datapoints(
-            df_val[smiles_column].tolist(), df_val[target].tolist(), val_extra_features
+        val_datapoints, _ = create_molecule_datapoints(
+            df_val[smiles_column].tolist(), val_targets, val_extra
         )
 
-        df_train = df_train.iloc[train_valid_idx].reset_index(drop=True)
-        df_val = df_val.iloc[val_valid_idx].reset_index(drop=True)
-
         train_dataset = data.MoleculeDataset(train_datapoints)
         val_dataset = data.MoleculeDataset(val_datapoints)
 
-        # Save raw validation features for predictions later
-        val_extra_raw = val_extra_features[val_valid_idx] if val_extra_features is not None else None
+        # Save raw val features for prediction
+        val_extra_raw = val_extra.copy() if val_extra is not None else None
 
-        # Scale features and targets
+        # Scale features and targets for this fold
         x_d_transform = None
         if use_extra_features:
             feature_scaler = train_dataset.normalize_inputs("X_d")
@@ -601,7 +689,7 @@ if __name__ == "__main__":
             x_d_transform = nn.ScaleTransform.from_standard_scaler(feature_scaler)
 
         output_transform = None
-        if model_type == "regressor":
+        if model_type in ["regressor", "uq_regressor"]:
             target_scaler = train_dataset.normalize_targets()
             val_dataset.normalize_targets(target_scaler)
             output_transform = nn.UnscaleTransform.from_standard_scaler(target_scaler)
@@ -609,17 +697,18 @@ if __name__ == "__main__":
         train_loader = data.build_dataloader(train_dataset, batch_size=batch_size, shuffle=True)
         val_loader = data.build_dataloader(val_dataset, batch_size=batch_size, shuffle=False)
 
-        # Build and train single model
-        pl.seed_everything(42)
+        # Build and train model for this fold
+        pl.seed_everything(42 + fold_idx)
         mpnn = build_mpnn_model(
-            hyperparameters, task=task, num_classes=num_classes,
+            hyperparameters, task=task, num_classes=num_classes, n_targets=n_targets,
             n_extra_descriptors=n_extra, x_d_transform=x_d_transform, output_transform=output_transform,
+            task_weights=task_weights,
         )
 
         callbacks = [
             pl.callbacks.EarlyStopping(monitor="val_loss", patience=patience, mode="min"),
             pl.callbacks.ModelCheckpoint(
-                dirpath=args.model_dir, filename="best_model_0",
+                dirpath=args.model_dir, filename=f"best_model_{fold_idx}",
                 monitor="val_loss", mode="min", save_top_k=1,
             ),
         ]
@@ -636,201 +725,95 @@ if __name__ == "__main__":
             mpnn.load_state_dict(checkpoint["state_dict"])
 
         mpnn.eval()
-        ensemble_models = [mpnn]
+        ensemble_models.append(mpnn)
 
-        # Make predictions on validation set
+        # Make out-of-fold predictions using raw features
         val_datapoints_raw, _ = create_molecule_datapoints(
-            df_val[smiles_column].tolist(), df_val[target].tolist(), val_extra_raw
+            df_val[smiles_column].tolist(), val_targets, val_extra_raw
         )
         val_dataset_raw = data.MoleculeDataset(val_datapoints_raw)
         val_loader_pred = data.build_dataloader(val_dataset_raw, batch_size=batch_size, shuffle=False)
 
         with torch.inference_mode():
-            val_predictions = trainer.predict(mpnn, val_loader_pred)
-        preds = np.concatenate([p.numpy() for p in val_predictions], axis=0)
-        if preds.ndim == 3 and preds.shape[1] == 1:
-            preds = preds.squeeze(axis=1)
-
-        preds_std = None
-        y_validate = df_val[target].values
-
-    # =========================================================================
-    # K-FOLD CROSS-VALIDATION (n_folds > 1) - trains n_folds models
-    # =========================================================================
-    else:
-        print(f"Training {n_folds}-fold cross-validation ensemble...")
-
-        # Validate all SMILES upfront and filter invalid ones
-        all_extra_features = None
-        if use_extra_features:
-            all_extra_features = all_df[extra_feature_cols].values.astype(np.float32)
-            col_means = np.nanmean(all_extra_features, axis=0)
-            for i in range(all_extra_features.shape[1]):
-                all_extra_features[np.isnan(all_extra_features[:, i]), i] = col_means[i]
+            fold_predictions = trainer.predict(mpnn, val_loader_pred)
+        fold_preds = np.concatenate([p.numpy() for p in fold_predictions], axis=0)
+        if fold_preds.ndim == 3 and fold_preds.shape[1] == 1:
+            fold_preds = fold_preds.squeeze(axis=1)
+
+        # Store out-of-fold predictions
+        if model_type == "classifier" and fold_preds.ndim == 2:
+            # Store class index in first column for classification
+            oof_predictions[val_idx, 0] = np.argmax(fold_preds, axis=1)
+            if oof_proba is not None:
+                oof_proba[val_idx] = fold_preds
         else:
-            col_means = None
+            # Regression: fold_preds shape is (n_val, n_targets) or (n_val,)
+            if fold_preds.ndim == 1:
+                fold_preds = fold_preds.reshape(-1, 1)
+            oof_predictions[val_idx] = fold_preds
 
-        # Filter invalid SMILES from the full dataset
-        _, valid_indices = create_molecule_datapoints(
-            all_df[smiles_column].tolist(), all_df[target].tolist(), all_extra_features
-        )
-        all_df = all_df.iloc[valid_indices].reset_index(drop=True)
-        if all_extra_features is not None:
-            all_extra_features = all_extra_features[valid_indices]
-        print(f"Data after SMILES validation: {all_df.shape}")
+        print(f"Fold {fold_idx + 1} complete!")
 
-        # Set up K-Fold
-        if model_type == "classifier":
-            kfold = StratifiedKFold(n_splits=n_folds, shuffle=True, random_state=42)
-            split_target = all_df[target]
-        else:
-            kfold = KFold(n_splits=n_folds, shuffle=True, random_state=42)
-            split_target = None
+    print(f"\nTraining complete! Trained {len(ensemble_models)} model(s).")
 
-        # Initialize storage for out-of-fold predictions
-        oof_predictions = np.full(len(all_df), np.nan, dtype=np.float64)
-        if model_type == "classifier" and num_classes and num_classes > 1:
-            oof_proba = np.full((len(all_df), num_classes), np.nan, dtype=np.float64)
-        else:
-            oof_proba = None
-
-        ensemble_models = []
-
-        for fold_idx, (train_idx, val_idx) in enumerate(kfold.split(all_df, split_target)):
-            print(f"\n{'='*50}")
-            print(f"Training Fold {fold_idx + 1}/{n_folds}")
-            print(f"{'='*50}")
-
-            # Split data for this fold
-            df_train = all_df.iloc[train_idx].reset_index(drop=True)
-            df_val = all_df.iloc[val_idx].reset_index(drop=True)
-
-            train_extra = all_extra_features[train_idx] if all_extra_features is not None else None
-            val_extra = all_extra_features[val_idx] if all_extra_features is not None else None
-
-            print(f"Fold {fold_idx + 1} - Train: {len(df_train)}, Val: {len(df_val)}")
-
-            # Create ChemProp datasets for this fold
-            train_datapoints, _ = create_molecule_datapoints(
-                df_train[smiles_column].tolist(), df_train[target].tolist(), train_extra
-            )
-            val_datapoints, _ = create_molecule_datapoints(
-                df_val[smiles_column].tolist(), df_val[target].tolist(), val_extra
-            )
-
-            train_dataset = data.MoleculeDataset(train_datapoints)
-            val_dataset = data.MoleculeDataset(val_datapoints)
-
-            # Save raw val features for prediction
-            val_extra_raw = val_extra.copy() if val_extra is not None else None
-
-            # Scale features and targets for this fold
-            x_d_transform = None
-            if use_extra_features:
-                feature_scaler = train_dataset.normalize_inputs("X_d")
-                val_dataset.normalize_inputs("X_d", feature_scaler)
-                x_d_transform = nn.ScaleTransform.from_standard_scaler(feature_scaler)
-
-            output_transform = None
-            if model_type == "regressor":
-                target_scaler = train_dataset.normalize_targets()
-                val_dataset.normalize_targets(target_scaler)
-                output_transform = nn.UnscaleTransform.from_standard_scaler(target_scaler)
-
-            train_loader = data.build_dataloader(train_dataset, batch_size=batch_size, shuffle=True)
-            val_loader = data.build_dataloader(val_dataset, batch_size=batch_size, shuffle=False)
-
-            # Build and train model for this fold
-            pl.seed_everything(42 + fold_idx)
-            mpnn = build_mpnn_model(
-                hyperparameters, task=task, num_classes=num_classes,
-                n_extra_descriptors=n_extra, x_d_transform=x_d_transform, output_transform=output_transform,
-            )
-
-            callbacks = [
-                pl.callbacks.EarlyStopping(monitor="val_loss", patience=patience, mode="min"),
-                pl.callbacks.ModelCheckpoint(
-                    dirpath=args.model_dir, filename=f"best_model_{fold_idx}",
-                    monitor="val_loss", mode="min", save_top_k=1,
-                ),
-            ]
-
-            trainer = pl.Trainer(
-                accelerator="auto", max_epochs=max_epochs, callbacks=callbacks,
-                logger=False, enable_progress_bar=True,
-            )
-
-            trainer.fit(mpnn, train_loader, val_loader)
-
-            if trainer.checkpoint_callback and trainer.checkpoint_callback.best_model_path:
-                checkpoint = torch.load(trainer.checkpoint_callback.best_model_path, weights_only=False)
-                mpnn.load_state_dict(checkpoint["state_dict"])
-
-            mpnn.eval()
-            ensemble_models.append(mpnn)
-
-            # Make out-of-fold predictions using raw features
-            val_datapoints_raw, _ = create_molecule_datapoints(
-                df_val[smiles_column].tolist(), df_val[target].tolist(), val_extra_raw
-            )
-            val_dataset_raw = data.MoleculeDataset(val_datapoints_raw)
-            val_loader_pred = data.build_dataloader(val_dataset_raw, batch_size=batch_size, shuffle=False)
+    # Use out-of-fold predictions for metrics
+    # For n_folds=1, we only have predictions for val_idx, so filter to those rows
+    if n_folds == 1:
+        # oof_predictions is always 2D now: check if any column has a value
+        val_mask = ~np.isnan(oof_predictions).all(axis=1)
+        preds = oof_predictions[val_mask]
+        df_val = all_df[val_mask].copy()
+        y_validate = all_targets[val_mask]
+        if oof_proba is not None:
+            oof_proba = oof_proba[val_mask]
+        val_extra_features = all_extra_features[val_mask] if all_extra_features is not None else None
+    else:
+        preds = oof_predictions
+        df_val = all_df.copy()
+        y_validate = all_targets
+        val_extra_features = all_extra_features
+
+    # Compute prediction_std by running all ensemble models on validation data
+    # For n_folds=1, std will be 0 (only one model). For n_folds>1, std shows ensemble disagreement.
+    preds_std = None
+    if model_type in ["regressor", "uq_regressor"] and len(ensemble_models) > 0:
+        print("Computing prediction_std from ensemble predictions on validation data...")
+        val_datapoints_for_std, _ = create_molecule_datapoints(
+            df_val[smiles_column].tolist(),
+            y_validate,
+            val_extra_features
+        )
+        val_dataset_for_std = data.MoleculeDataset(val_datapoints_for_std)
+        val_loader_for_std = data.build_dataloader(val_dataset_for_std, batch_size=batch_size, shuffle=False)
 
+        all_ensemble_preds_for_std = []
+        trainer_pred = pl.Trainer(accelerator="auto", logger=False, enable_progress_bar=False)
+        for ens_model in ensemble_models:
             with torch.inference_mode():
-                fold_predictions = trainer.predict(mpnn, val_loader_pred)
-            fold_preds = np.concatenate([p.numpy() for p in fold_predictions], axis=0)
-            if fold_preds.ndim == 3 and fold_preds.shape[1] == 1:
-                fold_preds = fold_preds.squeeze(axis=1)
-
-            # Store out-of-fold predictions
-            if model_type == "classifier" and fold_preds.ndim == 2:
-                oof_predictions[val_idx] = np.argmax(fold_preds, axis=1)
-                if oof_proba is not None:
-                    oof_proba[val_idx] = fold_preds
-            else:
-                oof_predictions[val_idx] = fold_preds.flatten()
-
-            print(f"Fold {fold_idx + 1} complete!")
-
-        print(f"\nCross-validation complete! Trained {len(ensemble_models)} models.")
-
-        # Use out-of-fold predictions for metrics
-        preds = oof_predictions
-        preds_std = None  # Will compute from ensemble at inference time
-        y_validate = all_df[target].values
-        df_val = all_df  # For saving predictions
+                ens_preds = trainer_pred.predict(ens_model, val_loader_for_std)
+            ens_preds = np.concatenate([p.numpy() for p in ens_preds], axis=0)
+            if ens_preds.ndim == 3 and ens_preds.shape[1] == 1:
+                ens_preds = ens_preds.squeeze(axis=1)
+            all_ensemble_preds_for_std.append(ens_preds)
+
+        # Stack ensemble predictions: shape (n_ensemble, n_samples, n_targets)
+        ensemble_preds_stacked = np.stack(all_ensemble_preds_for_std, axis=0)
+        preds_std = np.std(ensemble_preds_stacked, axis=0)
+        # Ensure 2D
+        if preds_std.ndim == 1:
+            preds_std = preds_std.reshape(-1, 1)
+        print(f"Ensemble prediction_std - mean per target: {np.nanmean(preds_std, axis=0)}")
 
     if model_type == "classifier":
-        # Classification metrics - handle multi-class output
-        # For CV mode, preds already contains class indices; for single model, preds are probabilities
-        if preds.ndim == 2 and preds.shape[1] > 1:
-            # Multi-class probabilities: (n_samples, n_classes), take argmax
-            class_preds = np.argmax(preds, axis=1)
-            has_proba = True
-        elif preds.ndim == 1:
-            # Either class indices (CV mode) or binary probabilities
-            if n_folds > 1:
-                # CV mode: preds are already class indices
-                class_preds = preds.astype(int)
-                has_proba = False
-            else:
-                # Single model: preds are probabilities
-                class_preds = (preds > 0.5).astype(int)
-                has_proba = False
-        else:
-            # Squeeze extra dimensions if needed
-            preds = preds.squeeze()
-            if preds.ndim == 2:
-                class_preds = np.argmax(preds, axis=1)
-                has_proba = True
-            else:
-                class_preds = (preds > 0.5).astype(int)
-                has_proba = False
+        # Classification metrics - preds contains class indices in first column from OOF predictions
+        class_preds = preds[:, 0].astype(int)
+        has_proba = oof_proba is not None
 
         print(f"class_preds shape: {class_preds.shape}")
 
-        # Decode labels for metrics
-        y_validate_decoded = label_encoder.inverse_transform(y_validate.astype(int))
+        # Decode labels for metrics (classification is single-target only)
+        target_name = target_columns[0]
+        y_validate_decoded = label_encoder.inverse_transform(y_validate[:, 0].astype(int))
         preds_decoded = label_encoder.inverse_transform(class_preds)
 
         # Calculate metrics
@@ -841,7 +824,7 @@ if __name__ == "__main__":
 
         score_df = pd.DataFrame(
             {
-                target: label_names,
+                target_name: label_names,
                 "precision": scores[0],
                 "recall": scores[1],
                 "f1": scores[2],
@@ -853,7 +836,7 @@ if __name__ == "__main__":
         metrics = ["precision", "recall", "f1", "support"]
         for t in label_names:
             for m in metrics:
-                value = score_df.loc[score_df[target] == t, m].iloc[0]
+                value = score_df.loc[score_df[target_name] == t, m].iloc[0]
                 print(f"Metrics:{t}:{m} {value}")
 
         # Confusion matrix
@@ -868,34 +851,61 @@ if __name__ == "__main__":
         # Save validation predictions
         df_val = df_val.copy()
         df_val["prediction"] = preds_decoded
-        if has_proba and preds.ndim == 2 and preds.shape[1] > 1:
-            df_val["pred_proba"] = [p.tolist() for p in preds]
+        if has_proba and oof_proba is not None:
+            df_val["pred_proba"] = [p.tolist() for p in oof_proba]
             df_val = expand_proba_column(df_val, label_names)
 
     else:
-        # Regression metrics
-        preds_flat = preds.flatten()
-        rmse = root_mean_squared_error(y_validate, preds_flat)
-        mae = mean_absolute_error(y_validate, preds_flat)
-        r2 = r2_score(y_validate, preds_flat)
-        print(f"RMSE: {rmse:.3f}")
-        print(f"MAE: {mae:.3f}")
-        print(f"R2: {r2:.3f}")
-        print(f"NumRows: {len(df_val)}")
-
+        # Regression metrics: compute per target (works for single or multi-task)
         df_val = df_val.copy()
-        df_val["prediction"] = preds_flat
+        print("\n--- Per-target metrics ---")
+        for t_idx, t_name in enumerate(target_columns):
+            # Get valid (non-NaN) indices for this target
+            target_valid_mask = ~np.isnan(y_validate[:, t_idx])
+            y_true = y_validate[target_valid_mask, t_idx]
+            y_pred = preds[target_valid_mask, t_idx]
+
+            if len(y_true) > 0:
+                rmse = root_mean_squared_error(y_true, y_pred)
+                mae = mean_absolute_error(y_true, y_pred)
+                medae = median_absolute_error(y_true, y_pred)
+                r2 = r2_score(y_true, y_pred)
+                spearman_corr = spearmanr(y_true, y_pred).correlation
+                support = len(y_true)
+                # Print metrics in format expected by SageMaker metric definitions
+                print(f"rmse: {rmse:.3f}")
+                print(f"mae: {mae:.3f}")
+                print(f"medae: {medae:.3f}")
+                print(f"r2: {r2:.3f}")
+                print(f"spearmanr: {spearman_corr:.3f}")
+                print(f"support: {support}")
+
+            # Store predictions in dataframe
+            df_val[f"{t_name}_pred"] = preds[:, t_idx]
+            if preds_std is not None:
+                df_val[f"{t_name}_pred_std"] = preds_std[:, t_idx]
+            else:
+                df_val[f"{t_name}_pred_std"] = 0.0
 
-        # Add prediction_std for ensemble models
-        if preds_std is not None:
-            df_val["prediction_std"] = preds_std.flatten()
-            print(f"Ensemble std - mean: {df_val['prediction_std'].mean():.4f}, max: {df_val['prediction_std'].max():.4f}")
+        # Add prediction/prediction_std aliases for first target
+        first_target = target_columns[0]
+        df_val["prediction"] = df_val[f"{first_target}_pred"]
+        df_val["prediction_std"] = df_val[f"{first_target}_pred_std"]
 
     # Save validation predictions to S3
-    output_columns = [target, "prediction"]
-    if "prediction_std" in df_val.columns:
-        output_columns.append("prediction_std")
+    # Include id_column if it exists in df_val
+    output_columns = []
+    if id_column in df_val.columns:
+        output_columns.append(id_column)
+    # Include all target columns and their predictions
+    output_columns += target_columns
+    output_columns += [f"{t}_pred" for t in target_columns]
+    output_columns += [f"{t}_pred_std" for t in target_columns]
+    output_columns += ["prediction", "prediction_std"]
+    # Add proba columns for classifiers
     output_columns += [col for col in df_val.columns if col.endswith("_proba")]
+    # Filter to only columns that exist
+    output_columns = [c for c in output_columns if c in df_val.columns]
     wr.s3.to_csv(
         df_val[output_columns],
         path=f"{model_metrics_s3_path}/validation_predictions.csv",
@@ -908,11 +918,20 @@ if __name__ == "__main__":
         models.save_model(model_path, ens_model)
         print(f"Saved model {model_idx + 1} to {model_path}")
 
+    # Clean up checkpoint files (not needed for inference, reduces artifact size)
+    for ckpt_file in glob.glob(os.path.join(args.model_dir, "best_model_*.ckpt")):
+        os.remove(ckpt_file)
+        print(f"Removed checkpoint: {ckpt_file}")
+
     # Save ensemble metadata (n_ensemble = number of models for inference)
     n_ensemble = len(ensemble_models)
-    ensemble_metadata = {"n_ensemble": n_ensemble, "n_folds": n_folds}
+    ensemble_metadata = {
+        "n_ensemble": n_ensemble,
+        "n_folds": n_folds,
+        "target_columns": target_columns,
+    }
     joblib.dump(ensemble_metadata, os.path.join(args.model_dir, "ensemble_metadata.joblib"))
-    print(f"Saved ensemble metadata (n_ensemble={n_ensemble}, n_folds={n_folds})")
+    print(f"Saved ensemble metadata (n_ensemble={n_ensemble}, n_folds={n_folds}, targets={target_columns})")
 
     # Save label encoder if classification
     if label_encoder is not None: