#!/usr/bin/env python3 """ caption_v2.py — disease/lesion-centric caption generator (caption v2). A PURE FUNCTION of a manifest row -> specificity-tiered caption rows. Used to REGENERATE captions from existing *_images_v1.parquet WITHOUT re-running extraction (same idea as regen_oct_captions.py), so it works uniformly for the private, public-fundus and public-OCT cohorts. Schema (EyeDiff-aligned): {modality}, {region}, {diagnosis[+severity]}, {lesions...} Tiers (Brack et al. 2025 — vary SPECIFICITY, not wording): short : {modality}, {diagnosis} (no region / severity / lesion) medium : {modality}, {region}, {diagnosis+severity} dense : {modality}, {region}, {diagnosis+severity}, {lesions} Identical tiers are de-duplicated (a normal, lesion-free image collapses to one short caption). The ~10% empty-caption dropout for classifier-free guidance is a TRAINING-loader concern and is intentionally NOT stored as data rows. Acquisition metadata (device, dataset name, quality score, slice index, bbox, exact µm thickness, eye laterality) stays in the image parquet — it is deliberately kept OUT of the prompt text. Region rule: emitted for OCT / SLO (macula vs optic disc matters); omitted for color fundus (inherently posterior-pole, EyeDiff-style "color fundus, "). """ import disease_dict as dd CAP_COLS = ["caption_id", "image_id", "level", "prompt_text", "language", "generator", "grounded_in"] def _get(row, k, default=None): if hasattr(row, "get"): return row.get(k, default) return getattr(row, k, default) def _as_list(x): if x is None: return [] if isinstance(x, (list, tuple)): return list(x) if hasattr(x, "tolist"): try: return list(x.tolist()) except Exception: pass return [x] def caption_rows_for(row): """row: dict-like with modality, anatomy, diagnosis_group, severity, lesion_tags, image_id. Returns a list of caption-row dicts (CAP_COLS).""" image_id = _get(row, "image_id") mod = _get(row, "modality") anat = _get(row, "anatomy") or "macula" sev = _get(row, "severity") raw_dx = _as_list(_get(row, "diagnosis_group")) raw_les = _as_list(_get(row, "lesion_tags")) # Normalize old-mapping diagnosis tokens through the v2 dictionary # (CNV -> nAMD + lesion CNV; DRUSEN -> AMD + lesion drusen; CSR -> CSC; ...) codes, lesions = [], [] for t in raw_dx: c, _s, l = dd.normalize_diagnosis(t) codes += c lesions += l for lt in raw_les: cc = dd.normalize_lesion(lt) if cc: lesions.append(cc) codes = list(dict.fromkeys(codes)) # dedup, keep order lesions = list(dict.fromkeys(lesions)) # CONFIRMED normal only when there is no diagnosis AND severity says 'none'. is_normal = (len(raw_dx) == 0 and str(sev) == "none") mod_s = dd.modality_phrase(mod) region_s = dd.anatomy_phrase(anat) if mod in ("oct_bscan", "slo_gray") else None dx_short = dd.compose_disease_segment(codes, None, [], include_lesions=False, is_normal=is_normal) dx_med = dd.compose_disease_segment(codes, sev, lesions, include_lesions=False, is_normal=is_normal) dx_dense = dd.compose_disease_segment(codes, sev, lesions, include_lesions=True, is_normal=is_normal) def join(parts): return ", ".join([p for p in parts if p]) tiers = [ ("short", join([mod_s] + dx_short)), ("medium", join([mod_s, region_s] + dx_med)), ("dense", join([mod_s, region_s] + dx_dense)), ] out, seen = [], set() for lvl, txt in tiers: # first (least specific) wins on dup if not txt or txt in seen: continue seen.add(txt) out.append({"caption_id": f"{image_id}_{lvl}", "image_id": image_id, "level": lvl, "prompt_text": txt, "language": "en", "generator": "caption_v2", "grounded_in": "manifest_fields"}) return out # --------------------------------------------------------------------------- # # preview: sample real manifest rows and print v2 captions (no writes) # # --------------------------------------------------------------------------- # if __name__ == "__main__": import argparse import pandas as pd ap = argparse.ArgumentParser() ap.add_argument("--manifest", required=True) ap.add_argument("--n-per-group", type=int, default=2) ap.add_argument("--group-col", default="cohort") args = ap.parse_args() df = pd.read_parquet(args.manifest) print(f"loaded {len(df)} rows from {args.manifest}\n") # show a spread: a few rows per (cohort) and ensure disease variety shown = 0 for _, g in df.groupby(args.group_col): # prefer rows with a diagnosis, fall back to any nz = g[g["diagnosis_group"].apply(lambda x: x is not None and len(_as_list(x)) > 0)] pick = pd.concat([nz.head(args.n_per_group), g.head(1)]).drop_duplicates("image_id") for _, r in pick.head(args.n_per_group).iterrows(): dxs = _as_list(r.get("diagnosis_group")) print(f"[{r.get('cohort')}] modality={r.get('modality')} anat={r.get('anatomy')} " f"dx={dxs} sev={r.get('severity')} les={_as_list(r.get('lesion_tags'))}") for c in caption_rows_for(r): print(f" {c['level']:6s}| {c['prompt_text']}") shown += 1 print() print(f"shown {shown} sample images")