workbench 0.8.162__py3-none-any.whl → 0.8.220__py3-none-any.whl

workbench/model_scripts/custom_models/chem_info/local_utils.py

@@ -1,769 +0,0 @@
-"""Local utilities for models that work with chemical information."""
-
-import logging
-import pandas as pd
-import numpy as np
-from typing import List, Optional
-
-# Molecular Descriptor Imports
-from rdkit import Chem
-from rdkit.Chem import Mol, Descriptors, rdFingerprintGenerator
-from rdkit.ML.Descriptors import MoleculeDescriptors
-from rdkit.Chem.MolStandardize.rdMolStandardize import TautomerEnumerator
-from rdkit.Chem import rdCIPLabeler
-from rdkit.Chem.rdMolDescriptors import CalcNumHBD, CalcExactMolWt
-from rdkit import RDLogger
-from rdkit.Chem import FunctionalGroups as FG
-from mordred import Calculator as MordredCalculator
-from mordred import AcidBase, Aromatic, Polarizability, RotatableBond
-
-# Load functional group hierarchy once during initialization
-fgroup_hierarchy = FG.BuildFuncGroupHierarchy()
-
-# Set RDKit logger to only show errors or critical messages
-lg = RDLogger.logger()
-lg.setLevel(RDLogger.ERROR)
-
-# Set up the logger
-log = logging.getLogger("workbench")
-
-
-def remove_disconnected_fragments(mol: Chem.Mol) -> Chem.Mol:
-    """
-    Remove disconnected fragments from a molecule, keeping the fragment with the most heavy atoms.
-
-    Args:
-        mol (Mol): RDKit molecule object.
-
-    Returns:
-        Mol: The fragment with the most heavy atoms, or None if no such fragment exists.
-    """
-    if mol is None or mol.GetNumAtoms() == 0:
-        return None
-    fragments = Chem.GetMolFrags(mol, asMols=True)
-    return max(fragments, key=lambda frag: frag.GetNumHeavyAtoms()) if fragments else None
-
-
-def contains_heavy_metals(mol: Mol) -> bool:
-    """
-    Check if a molecule contains any heavy metals (broad filter).
-
-    Args:
-        mol: RDKit molecule object.
-
-    Returns:
-        bool: True if any heavy metals are detected, False otherwise.
-    """
-    heavy_metals = {"Zn", "Cu", "Fe", "Mn", "Co", "Pb", "Hg", "Cd", "As"}
-    return any(atom.GetSymbol() in heavy_metals for atom in mol.GetAtoms())
-
-
-def halogen_toxicity_score(mol: Mol) -> (int, int):
-    """
-    Calculate the halogen count and toxicity threshold for a molecule.
-
-    Args:
-        mol: RDKit molecule object.
-
-    Returns:
-        Tuple[int, int]: (halogen_count, halogen_threshold), where the threshold
-        scales with molecule size (minimum of 2 or 20% of atom count).
-    """
-    # Define halogens and count their occurrences
-    halogens = {"Cl", "Br", "I", "F"}
-    halogen_count = sum(1 for atom in mol.GetAtoms() if atom.GetSymbol() in halogens)
-
-    # Define threshold: small molecules tolerate fewer halogens
-    # Threshold scales with molecule size to account for reasonable substitution
-    molecule_size = mol.GetNumAtoms()
-    halogen_threshold = max(2, int(molecule_size * 0.2))  # Minimum 2, scaled by 20% of molecule size
-
-    return halogen_count, halogen_threshold
-
-
-def toxic_elements(mol: Mol) -> Optional[List[str]]:
-    """
-    Identifies toxic elements or specific forms of elements in a molecule.
-
-    Args:
-        mol: RDKit molecule object.
-
-    Returns:
-        Optional[List[str]]: List of toxic elements or specific forms if found, otherwise None.
-
-    Notes:
-        Halogen toxicity logic integrates with `halogen_toxicity_score` and scales thresholds
-        based on molecule size.
-    """
-    # Always toxic elements (heavy metals and known toxic single elements)
-    always_toxic = {"Pb", "Hg", "Cd", "As", "Be", "Tl", "Sb"}
-    toxic_found = set()
-
-    for atom in mol.GetAtoms():
-        symbol = atom.GetSymbol()
-        formal_charge = atom.GetFormalCharge()
-
-        # Check for always toxic elements
-        if symbol in always_toxic:
-            toxic_found.add(symbol)
-
-        # Conditionally toxic nitrogen (positively charged)
-        if symbol == "N" and formal_charge > 0:
-            # Exclude benign quaternary ammonium (e.g., choline-like structures)
-            if mol.HasSubstructMatch(Chem.MolFromSmarts("[N+](C)(C)(C)C")):  # Example benign structure
-                continue
-            toxic_found.add("N+")
-
-        # Halogen toxicity: Uses halogen_toxicity_score to flag excessive halogenation
-        if symbol in {"Cl", "Br", "I", "F"}:
-            halogen_count, halogen_threshold = halogen_toxicity_score(mol)
-            if halogen_count > halogen_threshold:
-                toxic_found.add(symbol)
-
-    return list(toxic_found) if toxic_found else None
-
-
-# Precompiled SMARTS patterns for custom toxic functional groups
-toxic_smarts_patterns = [
-    ("C(=S)N"),  # Dithiocarbamate
-    ("P(=O)(O)(O)O"),  # Phosphate Ester
-    ("[As](=O)(=O)-[OH]"),  # Arsenic Oxide
-    ("[C](Cl)(Cl)(Cl)"),  # Trichloromethyl
-    ("[Cr](=O)(=O)=O"),  # Chromium(VI)
-    ("[N+](C)(C)(C)(C)"),  # Quaternary Ammonium
-    ("[Se][Se]"),  # Diselenide
-    ("c1c(Cl)c(Cl)c(Cl)c1"),  # Trichlorinated Aromatic Ring
-    ("[CX3](=O)[CX4][Cl,Br,F,I]"),  # Halogenated Carbonyl
-    ("[P+](C*)(C*)(C*)(C*)"),  # Phosphonium Group
-    ("NC(=S)c1c(Cl)cccc1Cl"),  # Chlorobenzene Thiocarbamate
-    ("NC(=S)Nc1ccccc1"),  # Phenyl Thiocarbamate
-    ("S=C1NCCN1"),  # Thiourea Derivative
-]
-compiled_toxic_smarts = [Chem.MolFromSmarts(smarts) for smarts in toxic_smarts_patterns]
-
-# Precompiled SMARTS patterns for exemptions
-exempt_smarts_patterns = [
-    "c1ccc(O)c(O)c1",  # Phenols
-]
-compiled_exempt_smarts = [Chem.MolFromSmarts(smarts) for smarts in exempt_smarts_patterns]
-
-
-def toxic_groups(mol: Chem.Mol) -> Optional[List[str]]:
-    """
-    Check if a molecule contains known toxic functional groups using RDKit's functional groups and SMARTS patterns.
-
-    Args:
-        mol (rdkit.Chem.Mol): The molecule to evaluate.
-
-    Returns:
-        Optional[List[str]]: List of SMARTS patterns for toxic groups if found, otherwise None.
-    """
-    toxic_smarts_matches = []
-
-    # Use RDKit's functional group definitions
-    toxic_group_names = ["Nitro", "Azide", "Alcohol", "Aldehyde", "Halogen", "TerminalAlkyne"]
-    for group_name in toxic_group_names:
-        group_node = next(node for node in fgroup_hierarchy if node.label == group_name)
-        if mol.HasSubstructMatch(Chem.MolFromSmarts(group_node.smarts)):
-            toxic_smarts_matches.append(group_node.smarts)  # Use group_node's SMARTS directly
-
-    # Check for custom precompiled toxic SMARTS patterns
-    for smarts, compiled in zip(toxic_smarts_patterns, compiled_toxic_smarts):
-        if mol.HasSubstructMatch(compiled):  # Use precompiled SMARTS
-            toxic_smarts_matches.append(smarts)
-
-    # Special handling for N+
-    if mol.HasSubstructMatch(Chem.MolFromSmarts("[N+]")):
-        if not mol.HasSubstructMatch(Chem.MolFromSmarts("C[N+](C)(C)C")):  # Exclude benign
-            toxic_smarts_matches.append("[N+]")  # Append as SMARTS
-
-    # Exempt stabilizing functional groups using precompiled patterns
-    for compiled in compiled_exempt_smarts:
-        if mol.HasSubstructMatch(compiled):
-            return None
-
-    return toxic_smarts_matches if toxic_smarts_matches else None
-
-
-def contains_metalloenzyme_relevant_metals(mol: Mol) -> bool:
-    """
-    Check if a molecule contains metals relevant to metalloenzymes.
-
-    Args:
-        mol: RDKit molecule object.
-
-    Returns:
-        bool: True if metalloenzyme-relevant metals are detected, False otherwise.
-    """
-    metalloenzyme_metals = {"Zn", "Cu", "Fe", "Mn", "Co"}
-    return any(atom.GetSymbol() in metalloenzyme_metals for atom in mol.GetAtoms())
-
-
-def contains_salts(mol: Mol) -> bool:
-    """
-    Check if a molecule contains common salts or counterions.
-
-    Args:
-        mol: RDKit molecule object.
-
-    Returns:
-        bool: True if salts are detected, False otherwise.
-    """
-    # Define common inorganic salt fragments (SMARTS patterns)
-    salt_patterns = ["[Na+]", "[K+]", "[Cl-]", "[Mg+2]", "[Ca+2]", "[NH4+]", "[SO4--]"]
-    for pattern in salt_patterns:
-        if mol.HasSubstructMatch(Chem.MolFromSmarts(pattern)):
-            return True
-    return False
-
-
-def is_druglike_compound(mol: Mol) -> bool:
-    """
-    Filter for drug-likeness and QSAR relevance based on Lipinski's Rule of Five.
-    Returns False for molecules unlikely to be orally bioavailable.
-
-    Args:
-        mol: RDKit molecule object.
-
-    Returns:
-        bool: True if the molecule is drug-like, False otherwise.
-    """
-
-    # Lipinski's Rule of Five
-    mw = Descriptors.MolWt(mol)
-    logp = Descriptors.MolLogP(mol)
-    hbd = Descriptors.NumHDonors(mol)
-    hba = Descriptors.NumHAcceptors(mol)
-    if mw > 500 or logp > 5 or hbd > 5 or hba > 10:
-        return False
-
-    # Allow exceptions for linear molecules that meet strict RO5 criteria
-    if mol.GetRingInfo().NumRings() == 0:
-        if mw <= 300 and logp <= 3 and hbd <= 3 and hba <= 3:
-            pass  # Allow small, non-cyclic druglike compounds
-        else:
-            return False
-
-    return True
-
-
-def add_compound_tags(df, mol_column="molecule") -> pd.DataFrame:
-    """
-    Adds a 'tags' column to a DataFrame, tagging compounds based on their properties.
-
-    Args:
-        df (pd.DataFrame): Input DataFrame containing molecular data.
-        mol_column (str): Column name containing RDKit molecule objects.
-
-    Returns:
-        pd.DataFrame: Updated DataFrame with a 'tags' column.
-    """
-    # Initialize the tags column
-    df["tags"] = [[] for _ in range(len(df))]
-    df["meta"] = [{} for _ in range(len(df))]
-
-    # Process each molecule in the DataFrame
-    for idx, row in df.iterrows():
-        mol = row[mol_column]
-        tags = []
-
-        # Check for salts
-        if contains_salts(mol):
-            tags.append("salt")
-
-        # Check for fragments (should be done after salt check)
-        fragments = Chem.GetMolFrags(mol, asMols=True)
-        if len(fragments) > 1:
-            tags.append("frag")
-
-        # Check for heavy metals
-        if contains_heavy_metals(mol):
-            tags.append("heavy_metals")
-
-        # Check for toxic elements
-        te = toxic_elements(mol)
-        if te:
-            tags.append("toxic_element")
-            df.at[idx, "meta"]["toxic_elements"] = te
-
-        # Check for toxic groups
-        tg = toxic_groups(mol)
-        if tg:
-            tags.append("toxic_group")
-            df.at[idx, "meta"]["toxic_groups"] = tg
-
-        # Check for metalloenzyme-relevant metals
-        if contains_metalloenzyme_relevant_metals(mol):
-            tags.append("metalloenzyme")
-
-        # Check for drug-likeness
-        if is_druglike_compound(mol):
-            tags.append("druglike")
-
-        # Update tags
-        df.at[idx, "tags"] = tags
-
-    return df
-
-
-def compute_molecular_descriptors(df: pd.DataFrame, tautomerize=True) -> pd.DataFrame:
-    """Compute and add all the Molecular Descriptors
-
-    Args:
-        df (pd.DataFrame): Input DataFrame containing SMILES strings.
-        tautomerize (bool): Whether to tautomerize the SMILES strings.
-
-    Returns:
-        pd.DataFrame: The input DataFrame with all the RDKit Descriptors added
-    """
-
-    # Check for the smiles column (any capitalization)
-    smiles_column = next((col for col in df.columns if col.lower() == "smiles"), None)
-    if smiles_column is None:
-        raise ValueError("Input DataFrame must have a 'smiles' column")
-
-    # Compute/add all the Molecular Descriptors
-    log.info("Computing Molecular Descriptors...")
-
-    # Convert SMILES to RDKit molecule objects (vectorized)
-    log.info("Converting SMILES to RDKit Molecules...")
-    df["molecule"] = df[smiles_column].apply(Chem.MolFromSmiles)
-
-    # Make sure our molecules are not None
-    failed_smiles = df[df["molecule"].isnull()][smiles_column].tolist()
-    if failed_smiles:
-        log.error(f"Failed to convert the following SMILES to molecules: {failed_smiles}")
-    df = df.dropna(subset=["molecule"])
-
-    # If we have fragments in our compounds, get the largest fragment before computing descriptors
-    df["molecule"] = df["molecule"].apply(remove_disconnected_fragments)
-
-    # Tautomerize the molecules if requested
-    if tautomerize:
-        log.info("Tautomerizing molecules...")
-        tautomer_enumerator = TautomerEnumerator()
-        df["molecule"] = df["molecule"].apply(tautomer_enumerator.Canonicalize)
-
-    # Now get all the RDKIT Descriptors
-    all_descriptors = [x[0] for x in Descriptors._descList]
-
-    # There's an overflow issue that happens with the IPC descriptor, so we'll remove it
-    # See: https://github.com/rdkit/rdkit/issues/1527
-    if "Ipc" in all_descriptors:
-        all_descriptors.remove("Ipc")
-
-    # Make sure we don't have duplicates
-    all_descriptors = list(set(all_descriptors))
-
-    # RDKit Molecular Descriptor Calculator Class
-    log.info("Computing RDKit Descriptors...")
-    calc = MoleculeDescriptors.MolecularDescriptorCalculator(all_descriptors)
-    descriptor_values = [calc.CalcDescriptors(m) for m in df["molecule"]]
-
-    # Lowercase the column names
-    column_names = [name.lower() for name in calc.GetDescriptorNames()]
-    rdkit_features_df = pd.DataFrame(descriptor_values, columns=column_names)
-
-    # Now compute Mordred Features
-    log.info("Computing Mordred Descriptors...")
-    descriptor_choice = [AcidBase, Aromatic, Polarizability, RotatableBond]
-    calc = MordredCalculator()
-    for des in descriptor_choice:
-        calc.register(des)
-    mordred_df = calc.pandas(df["molecule"], nproc=1)
-
-    # Lowercase the column names
-    mordred_df.columns = [col.lower() for col in mordred_df.columns]
-
-    # Compute stereochemistry descriptors
-    stereo_df = compute_stereochemistry_descriptors(df)
-
-    # Combine the DataFrame with the RDKit and Mordred Descriptors added
-    # Note: This will overwrite any existing columns with the same name. This is a good thing
-    #       since we want computed descriptors to overwrite anything in the input dataframe
-    output_df = stereo_df.combine_first(mordred_df).combine_first(rdkit_features_df)
-
-    # Ensure no duplicate column names
-    output_df = output_df.loc[:, ~output_df.columns.duplicated()]
-
-    # Reorder the columns to have all the ones in the input df first and then the descriptors
-    input_columns = df.columns.tolist()
-    output_df = output_df[input_columns + [col for col in output_df.columns if col not in input_columns]]
-
-    # Drop the intermediate 'molecule' column
-    del output_df["molecule"]
-
-    # Return the DataFrame with the RDKit and Mordred Descriptors added
-    return output_df
-
-
-def compute_stereochemistry_descriptors(df: pd.DataFrame) -> pd.DataFrame:
-    """Compute stereochemistry descriptors for molecules in a DataFrame.
-
-    This function analyzes the stereochemical properties of molecules, including:
-    - Chiral centers (R/S configuration)
-    - Double bond stereochemistry (E/Z configuration)
-
-    Args:
-        df (pd.DataFrame): Input DataFrame with RDKit molecule objects in 'molecule' column
-
-    Returns:
-        pd.DataFrame: DataFrame with added stereochemistry descriptors
-    """
-    if "molecule" not in df.columns:
-        raise ValueError("Input DataFrame must have a 'molecule' column")
-
-    log.info("Computing stereochemistry descriptors...")
-    output_df = df.copy()
-
-    # Create helper functions to process a single molecule
-    def process_molecule(mol):
-        if mol is None:
-            log.warning("Found a None molecule, skipping...")
-            return {
-                "chiral_centers": 0,
-                "r_cnt": 0,
-                "s_cnt": 0,
-                "db_stereo": 0,
-                "e_cnt": 0,
-                "z_cnt": 0,
-                "chiral_fp": 0,
-                "db_fp": 0,
-            }
-
-        try:
-            # Use the more accurate CIP labeling algorithm (Cahn-Ingold-Prelog rules)
-            # This assigns R/S to chiral centers and E/Z to double bonds based on
-            # the priority of substituents (atomic number, mass, etc.)
-            rdCIPLabeler.AssignCIPLabels(mol)
-
-            # Find all potential stereochemistry sites in the molecule
-            stereo_info = Chem.FindPotentialStereo(mol)
-
-            # Initialize counters
-            specified_centers = 0  # Number of chiral centers with defined stereochemistry
-            r_cnt = 0  # Count of R configured centers
-            s_cnt = 0  # Count of S configured centers
-            stereo_atoms = []  # List to store atom indices and their R/S configuration
-
-            specified_bonds = 0  # Number of double bonds with defined stereochemistry
-            e_cnt = 0  # Count of E (trans) configured double bonds
-            z_cnt = 0  # Count of Z (cis) configured double bonds
-            stereo_bonds = []  # List to store bond indices and their E/Z configuration
-
-            # Process all stereo information found in the molecule
-            for element in stereo_info:
-                # Handle tetrahedral chiral centers
-                if element.type == Chem.StereoType.Atom_Tetrahedral:
-                    atom_idx = element.centeredOn
-
-                    # Only count centers where stereochemistry is explicitly defined
-                    if element.specified == Chem.StereoSpecified.Specified:
-                        specified_centers += 1
-                        if element.descriptor == Chem.StereoDescriptor.Tet_CCW:
-                            r_cnt += 1
-                            stereo_atoms.append((atom_idx, "R"))
-                        elif element.descriptor == Chem.StereoDescriptor.Tet_CW:
-                            s_cnt += 1
-                            stereo_atoms.append((atom_idx, "S"))
-
-                # Handle double bond stereochemistry
-                elif element.type == Chem.StereoType.Bond_Double:
-                    bond_idx = element.centeredOn
-
-                    # Only count bonds where stereochemistry is explicitly defined
-                    if element.specified == Chem.StereoSpecified.Specified:
-                        specified_bonds += 1
-                        if element.descriptor == Chem.StereoDescriptor.Bond_Trans:
-                            e_cnt += 1
-                            stereo_bonds.append((bond_idx, "E"))
-                        elif element.descriptor == Chem.StereoDescriptor.Bond_Cis:
-                            z_cnt += 1
-                            stereo_bonds.append((bond_idx, "Z"))
-
-            # Calculate chiral center fingerprint - unique bit vector for stereochemical configuration
-            chiral_fp = 0
-            if stereo_atoms:
-                for i, (idx, stereo) in enumerate(sorted(stereo_atoms, key=lambda x: x[0])):
-                    bit_val = 1 if stereo == "R" else 0
-                    chiral_fp += bit_val << i  # Shift bits to create a unique fingerprint
-
-            # Calculate double bond fingerprint - bit vector for E/Z configurations
-            db_fp = 0
-            if stereo_bonds:
-                for i, (idx, stereo) in enumerate(sorted(stereo_bonds, key=lambda x: x[0])):
-                    bit_val = 1 if stereo == "E" else 0
-                    db_fp += bit_val << i  # Shift bits to create a unique fingerprint
-
-            return {
-                "chiral_centers": specified_centers,
-                "r_cnt": r_cnt,
-                "s_cnt": s_cnt,
-                "db_stereo": specified_bonds,
-                "e_cnt": e_cnt,
-                "z_cnt": z_cnt,
-                "chiral_fp": chiral_fp,
-                "db_fp": db_fp,
-            }
-
-        except Exception as e:
-            log.warning(f"Error processing stereochemistry: {str(e)}")
-            return {
-                "chiral_centers": 0,
-                "r_cnt": 0,
-                "s_cnt": 0,
-                "db_stereo": 0,
-                "e_cnt": 0,
-                "z_cnt": 0,
-                "chiral_fp": 0,
-                "db_fp": 0,
-            }
-
-    # Process all molecules and collect results
-    results = []
-    for mol in df["molecule"]:
-        results.append(process_molecule(mol))
-
-    # Add all descriptors to the output dataframe
-    for key in results[0].keys():
-        output_df[key] = [r[key] for r in results]
-
-    # Boolean flag indicating if the molecule has any stereochemistry defined
-    output_df["has_stereo"] = (output_df["chiral_centers"] > 0) | (output_df["db_stereo"] > 0)
-
-    return output_df
-
-
-def compute_morgan_fingerprints(df: pd.DataFrame, radius=2, n_bits=2048, counts=True) -> pd.DataFrame:
-    """Compute and add Morgan fingerprints to the DataFrame.
-
-    Args:
-        df (pd.DataFrame): Input DataFrame containing SMILES strings.
-        radius (int): Radius for the Morgan fingerprint.
-        n_bits (int): Number of bits for the fingerprint.
-        counts (bool): Count simulation for the fingerprint.
-
-    Returns:
-        pd.DataFrame: The input DataFrame with the Morgan fingerprints added as bit strings.
-
-    Note:
-        See: https://greglandrum.github.io/rdkit-blog/posts/2021-07-06-simulating-counts.html
-    """
-    delete_mol_column = False
-
-    # Check for the SMILES column (case-insensitive)
-    smiles_column = next((col for col in df.columns if col.lower() == "smiles"), None)
-    if smiles_column is None:
-        raise ValueError("Input DataFrame must have a 'smiles' column")
-
-    # Sanity check the molecule column (sometimes it gets serialized, which doesn't work)
-    if "molecule" in df.columns and df["molecule"].dtype == "string":
-        log.warning("Detected serialized molecules in 'molecule' column. Removing...")
-        del df["molecule"]
-
-    # Convert SMILES to RDKit molecule objects (vectorized)
-    if "molecule" not in df.columns:
-        log.info("Converting SMILES to RDKit Molecules...")
-        delete_mol_column = True
-        df["molecule"] = df[smiles_column].apply(Chem.MolFromSmiles)
-        # Make sure our molecules are not None
-        failed_smiles = df[df["molecule"].isnull()][smiles_column].tolist()
-        if failed_smiles:
-            log.error(f"Failed to convert the following SMILES to molecules: {failed_smiles}")
-        df = df.dropna(subset=["molecule"])
-
-    # If we have fragments in our compounds, get the largest fragment before computing fingerprints
-    largest_frags = df["molecule"].apply(remove_disconnected_fragments)
-
-    # Create a Morgan fingerprint generator
-    if counts:
-        n_bits *= 4  # Multiply by 4 to simulate counts
-    morgan_generator = rdFingerprintGenerator.GetMorganGenerator(radius=radius, fpSize=n_bits, countSimulation=counts)
-
-    # Compute Morgan fingerprints (vectorized)
-    fingerprints = largest_frags.apply(
-        lambda mol: (morgan_generator.GetFingerprint(mol).ToBitString() if mol else pd.NA)
-    )
-
-    # Add the fingerprints to the DataFrame
-    df["fingerprint"] = fingerprints
-
-    # Drop the intermediate 'molecule' column if it was added
-    if delete_mol_column:
-        del df["molecule"]
-    return df
-
-
-def fingerprints_to_matrix(fingerprints, dtype=np.uint8):
-    """
-    Convert bitstring fingerprints to numpy matrix.
-
-    Args:
-        fingerprints: pandas Series or list of bitstring fingerprints
-        dtype: numpy data type (uint8 is default: np.bool_ is good for Jaccard computations
-
-    Returns:
-        dense numpy array of shape (n_molecules, n_bits)
-    """
-
-    # Dense matrix representation (we might support sparse in the future)
-    return np.array([list(fp) for fp in fingerprints], dtype=dtype)
-
-
-def canonicalize(df: pd.DataFrame, remove_mol_col: bool = True) -> pd.DataFrame:
-    """
-    Generate RDKit's canonical SMILES for each molecule in the input DataFrame.
-
-    Args:
-        df (pd.DataFrame): Input DataFrame containing a column named 'SMILES' (case-insensitive).
-        remove_mol_col (bool): Whether to drop the intermediate 'molecule' column. Default is True.
-
-    Returns:
-        pd.DataFrame: A DataFrame with an additional 'smiles_canonical' column and,
-                      optionally, the 'molecule' column.
-    """
-    # Identify the SMILES column (case-insensitive)
-    smiles_column = next((col for col in df.columns if col.lower() == "smiles"), None)
-    if smiles_column is None:
-        raise ValueError("Input DataFrame must have a 'SMILES' column")
-
-    # Convert SMILES to RDKit molecules
-    df["molecule"] = df[smiles_column].apply(Chem.MolFromSmiles)
-
-    # Log invalid SMILES
-    invalid_indices = df[df["molecule"].isna()].index
-    if not invalid_indices.empty:
-        log.critical(f"Invalid SMILES strings at indices: {invalid_indices.tolist()}")
-
-    # Drop rows where SMILES failed to convert to molecule
-    df.dropna(subset=["molecule"], inplace=True)
-
-    # Remove disconnected fragments (keep the largest fragment)
-    df["molecule"] = df["molecule"].apply(lambda mol: remove_disconnected_fragments(mol) if mol else None)
-
-    # Convert molecules to canonical SMILES (preserving isomeric information)
-    df["smiles_canonical"] = df["molecule"].apply(
-        lambda mol: Chem.MolToSmiles(mol, isomericSmiles=True) if mol else None
-    )
-
-    # Drop intermediate RDKit molecule column if requested
-    if remove_mol_col:
-        df.drop(columns=["molecule"], inplace=True)
-
-    return df
-
-
-def custom_tautomer_canonicalization(mol: Mol) -> str:
-    """Domain-specific processing of a molecule to select the canonical tautomer.
-
-    This function enumerates all possible tautomers for a given molecule and applies
-    custom logic to select the canonical form.
-
-    Args:
-        mol (Mol): The RDKit molecule for which the canonical tautomer is to be determined.
-
-    Returns:
-        str: The SMILES string of the selected canonical tautomer.
-    """
-    tautomer_enumerator = TautomerEnumerator()
-    enumerated_tautomers = tautomer_enumerator.Enumerate(mol)
-
-    # Example custom logic: prioritize based on use-case specific criteria
-    selected_tautomer = None
-    highest_score = float("-inf")
-
-    for taut in enumerated_tautomers:
-        # Compute custom scoring logic:
-        # 1. Prefer forms with fewer hydrogen bond donors (HBD) if membrane permeability is important
-        # 2. Penalize forms with high molecular weight for better drug-likeness
-        # 3. Incorporate known functional group preferences (e.g., keto > enol for binding)
-
-        hbd = CalcNumHBD(taut)  # Hydrogen Bond Donors
-        mw = CalcExactMolWt(taut)  # Molecular Weight
-        aromatic_rings = taut.GetRingInfo().NumAromaticRings()  # Favor aromaticity
-
-        # Example scoring: balance HBD, MW, and aromaticity
-        score = -hbd - 0.01 * mw + aromatic_rings * 2
-
-        # Update selected tautomer
-        if score > highest_score:
-            highest_score = score
-            selected_tautomer = taut
-
-    # Return the SMILES of the selected tautomer
-    return Chem.MolToSmiles(selected_tautomer)
-
-
-def standard_tautomer_canonicalization(mol: Mol) -> str:
-    """Standard processing of a molecule to select the canonical tautomer.
-
-    RDKit's `TautomerEnumerator` uses heuristics to select a canonical tautomer,
-    such as preferring keto over enol forms and minimizing formal charges.
-
-    Args:
-        mol (Mol): The RDKit molecule for which the canonical tautomer is to be determined.
-
-    Returns:
-        str: The SMILES string of the canonical tautomer.
-    """
-    tautomer_enumerator = TautomerEnumerator()
-    canonical_tautomer = tautomer_enumerator.Canonicalize(mol)
-    return Chem.MolToSmiles(canonical_tautomer)
-
-
-def tautomerize_smiles(df: pd.DataFrame) -> pd.DataFrame:
-    """
-    Perform tautomer enumeration and canonicalization on a DataFrame.
-
-    Args:
-        df (pd.DataFrame): Input DataFrame containing SMILES strings.
-
-    Returns:
-        pd.DataFrame: A new DataFrame with additional 'smiles_canonical' and 'smiles_tautomer' columns.
-    """
-    # Standardize SMILES strings and create 'molecule' column for further processing
-    df = canonicalize(df, remove_mol_col=False)
-
-    # Helper function to safely canonicalize a molecule's tautomer
-    def safe_tautomerize(mol):
-        """Safely canonicalize a molecule's tautomer, handling errors gracefully."""
-        if not mol:
-            return pd.NA
-        try:
-            # Use RDKit's standard Tautomer enumeration and canonicalization
-            # For custom logic, replace with custom_tautomer_canonicalization(mol)
-            return standard_tautomer_canonicalization(mol)
-        except Exception as e:
-            log.warning(f"Tautomerization failed: {str(e)}")
-            return pd.NA
-
-    # Apply tautomer canonicalization to each molecule
-    df["smiles_tautomer"] = df["molecule"].apply(safe_tautomerize)
-
-    # Drop intermediate RDKit molecule column to clean up the DataFrame
-    df.drop(columns=["molecule"], inplace=True)
-
-    # Now switch the smiles columns
-    df.rename(columns={"smiles": "smiles_orig", "smiles_tautomer": "smiles"}, inplace=True)
-
-    return df
-
-
-if __name__ == "__main__":
-
-    # Small set of tests
-    smiles = "O=C(CCl)c1ccc(Cl)cc1Cl"
-    mol = Chem.MolFromSmiles(smiles)
-
-    # Compute Molecular Descriptors
-    df = pd.DataFrame({"smiles": [smiles, smiles, smiles, smiles, smiles]})
-    md_df = compute_molecular_descriptors(df)
-    print(md_df)
-
-    # Compute Morgan Fingerprints
-    fp_df = compute_morgan_fingerprints(df)
-    print(fp_df)
-
-    # Perform Tautomerization
-    t_df = tautomerize_smiles(df)
-    print(t_df)