#!/usr/bin/env python """ Evaluate retrieval on MassSpecGym. Plan ยง5. Metrics: Recall@1/10/50, optional Tanimoto@1. Unfiltered and formula-filtered. """ from __future__ import annotations import argparse import json import sys from functools import lru_cache from pathlib import Path ROOT = Path(__file__).resolve().parents[1] if str(ROOT) not in sys.path: sys.path.insert(0, str(ROOT)) def parse_args(): p = argparse.ArgumentParser(description="Evaluate retrieval JSONL (from retrieve_generate.py)") p.add_argument("--pred-jsonl", required=True, help="JSONL: each line has smiles_gt, candidates list") p.add_argument("--report", default=None, help="Write metrics JSON here") p.add_argument("--tanimoto", action="store_true", help="Compute Tanimoto@1 (requires RDKit)") return p.parse_args() @lru_cache(maxsize=200000) def canonicalize_smiles(smiles: str) -> str: text = str(smiles or "").strip() if not text: return "" try: from rdkit import Chem except ImportError: return text mol = Chem.MolFromSmiles(text) if mol is None: return text return Chem.MolToSmiles(mol, canonical=True) def recall_at_k(candidates: list, gt_smiles: str, k: int) -> bool: """True if gt_smiles is in the first k candidates (by order).""" if not gt_smiles or not candidates: return False gt_canon = canonicalize_smiles(gt_smiles) smiles_list = [ canonicalize_smiles(c.get("smiles", c) if isinstance(c, dict) else c) for c in candidates[:k] ] return gt_canon in smiles_list def recall_at_k_rank(candidates: list, gt_smiles: str, k: int) -> int | None: """Rank (1-based) of gt_smiles in candidates, or None if not in top k.""" if not gt_smiles or not candidates: return None gt_canon = canonicalize_smiles(gt_smiles) for i, c in enumerate(candidates[:k]): smi = canonicalize_smiles(c.get("smiles", c) if isinstance(c, dict) else c) if smi == gt_canon: return i + 1 return None def tanimoto_at_1(candidates: list, gt_smiles: str) -> float | None: """Tanimoto similarity of top-1 candidate to gt_smiles. None if no RDKit or no candidates.""" try: from rdkit import Chem from rdkit.Chem import DataStructs from rdkit.Chem.AllChem import GetMorganFingerprintAsBitVect except ImportError: return None if not candidates or not gt_smiles: return None top = candidates[0] smi_pred = top.get("smiles", top) if isinstance(top, dict) else top mol_gt = Chem.MolFromSmiles(gt_smiles) mol_pred = Chem.MolFromSmiles(smi_pred) if mol_gt is None or mol_pred is None: return None fp_gt = GetMorganFingerprintAsBitVect(mol_gt, 2, nBits=2048) fp_pred = GetMorganFingerprintAsBitVect(mol_pred, 2, nBits=2048) return DataStructs.TanimotoSimilarity(fp_gt, fp_pred) def compute_metrics(rows: list, include_tanimoto: bool = False) -> dict: n = len(rows) if n == 0: return {"n": 0, "Recall@1": 0.0, "Recall@10": 0.0, "Recall@50": 0.0} metrics = { "n": n, "Recall@1": sum(1 for r in rows if recall_at_k(r.get("candidates", []), r.get("smiles_gt", ""), 1)) / n, "Recall@10": sum(1 for r in rows if recall_at_k(r.get("candidates", []), r.get("smiles_gt", ""), 10)) / n, "Recall@50": sum(1 for r in rows if recall_at_k(r.get("candidates", []), r.get("smiles_gt", ""), 50)) / n, } if include_tanimoto: tan_list = [] for r in rows: t = tanimoto_at_1(r.get("candidates", []), r.get("smiles_gt", "")) if t is not None: tan_list.append(t) if tan_list: metrics["Tanimoto@1_mean"] = sum(tan_list) / len(tan_list) metrics["Tanimoto@1_count"] = len(tan_list) return metrics def main(): args = parse_args() path = Path(args.pred_jsonl) if not path.exists(): raise SystemExit(f"Not found: {path}") rows = [] with open(path) as f: for line in f: line = line.strip() if not line: continue rows.append(json.loads(line)) if not rows: raise SystemExit("Empty JSONL") metrics = compute_metrics(rows, include_tanimoto=args.tanimoto) mode_groups = {} for row in rows: mode = row.get("retrieval_mode") if not mode: continue mode_groups.setdefault(str(mode), []).append(row) if mode_groups: metrics["by_retrieval_mode"] = { mode: compute_metrics(group_rows, include_tanimoto=args.tanimoto) for mode, group_rows in sorted(mode_groups.items()) } print("Metrics:", json.dumps(metrics, indent=2)) if args.report: with open(args.report, "w") as f: json.dump(metrics, f, indent=2) print(f"Wrote {args.report}") if __name__ == "__main__": main()