Datasets:
Formats:
parquet
Languages:
English
Size:
10M - 100M
Tags:
biology
chemistry
drug-discovery
clinical-trials
protein-protein-interaction
gene-essentiality
License:
File size: 11,811 Bytes
6d1bbc7 | 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 100 101 102 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 119 120 121 122 123 124 125 126 127 128 129 130 131 132 133 134 135 136 137 138 139 140 141 142 143 144 145 146 147 148 149 150 151 152 153 154 155 156 157 158 159 160 161 162 163 164 165 166 167 168 169 170 171 172 173 174 175 176 177 178 179 180 181 182 183 184 185 186 187 188 189 190 191 192 193 194 195 196 197 198 199 200 201 202 203 204 205 206 207 208 209 210 211 212 213 214 215 216 217 218 219 220 221 222 223 224 225 226 227 228 229 230 231 232 233 234 235 236 237 238 239 240 241 242 243 244 245 246 247 248 249 250 251 252 253 254 255 256 257 258 259 260 261 262 263 264 265 266 267 268 269 270 271 272 273 274 275 276 277 278 279 280 281 282 283 284 285 286 287 288 289 290 291 292 293 294 295 296 297 298 299 300 301 302 303 304 305 306 307 308 309 310 311 312 313 314 315 316 317 318 319 320 | #!/usr/bin/env python3
"""Analyze PPI-L4 contamination gap vs protein popularity (study depth).
Addresses expert panel review findings R4-4 and R1-5:
Is the L4 temporal contamination gap (pre-2015 vs post-2020) driven by
genuine memorization, or confounded with protein study depth / popularity?
Approach:
1. Load L4 dataset with gene symbols and temporal groups
2. Map gene symbols → network degree (from PPI DB protein_protein_pairs)
3. Load predictions from each model
4. Stratify accuracy by temporal_group × degree_bin (high/low median split)
5. If pre-2015 advantage persists in both degree bins → true contamination
If advantage only in high-degree → popularity confound
Output: Markdown table to stdout and results/ppi_llm/contamination_vs_popularity.md
Usage:
PYTHONPATH=src python scripts_ppi/analyze_ppi_contamination.py \\
--db-path data/negbiodb_ppi.db \\
--results-dir results/ppi_llm/
"""
from __future__ import annotations
import argparse
import json
import re
from pathlib import Path
import numpy as np
PROJECT_ROOT = Path(__file__).resolve().parent.parent
DEFAULT_DB = PROJECT_ROOT / "data" / "negbiodb_ppi.db"
DEFAULT_RESULTS = PROJECT_ROOT / "results" / "ppi_llm"
DATASET_PATH = PROJECT_ROOT / "exports" / "ppi_llm" / "ppi_l4_dataset.jsonl"
def load_l4_dataset(dataset_path: Path) -> list[dict]:
"""Load L4 dataset records."""
records = []
with open(dataset_path) as f:
for line in f:
records.append(json.loads(line))
return records
def load_protein_degrees(db_path: Path) -> dict[str, float]:
"""Load gene_symbol → network degree from PPI pairs parquet (fast).
Falls back to DB query if parquet is unavailable.
"""
parquet_path = db_path.parent.parent / "exports" / "ppi" / "negbiodb_ppi_pairs.parquet"
if parquet_path.exists():
import pandas as pd
df = pd.read_parquet(
parquet_path,
columns=["gene_symbol_1", "protein1_degree"],
)
df = df.dropna(subset=["gene_symbol_1", "protein1_degree"])
degrees = df.groupby("gene_symbol_1")["protein1_degree"].max().to_dict()
return degrees
# Fallback: slow DB query (~160s on 2.2M rows)
import sqlite3
conn = sqlite3.connect(str(db_path))
try:
rows = conn.execute("""
SELECT p.gene_symbol, MAX(pp.protein1_degree)
FROM proteins p
JOIN protein_protein_pairs pp ON p.protein_id = pp.protein1_id
WHERE p.gene_symbol IS NOT NULL AND pp.protein1_degree IS NOT NULL
GROUP BY p.gene_symbol
""").fetchall()
finally:
conn.close()
return {row[0]: row[1] for row in rows}
def load_predictions(results_dir: Path) -> dict[str, dict[str, str]]:
"""Load predictions for all L4 runs.
Returns:
Dict mapping run_name → {question_id: prediction_text}
"""
all_preds = {}
for run_dir in sorted(results_dir.iterdir()):
if not run_dir.is_dir():
continue
if not run_dir.name.startswith("ppi-l4_"):
continue
pred_file = run_dir / "predictions.jsonl"
if not pred_file.exists():
continue
preds = {}
with open(pred_file) as f:
for line in f:
rec = json.loads(line)
qid = rec.get("question_id")
pred = rec.get("prediction", "")
if qid:
preds[qid] = pred
all_preds[run_dir.name] = preds
return all_preds
def parse_l4_prediction(text: str) -> str | None:
"""Parse L4 prediction to 'tested' or 'untested'."""
if not text:
return None
low = text.strip().lower()
if "tested" in low and "untested" not in low and "not tested" not in low:
return "tested"
if "untested" in low or "not tested" in low:
return "untested"
return None
def parse_run_name(name: str) -> tuple[str, str] | None:
"""Extract (model, config) from run name."""
m = re.match(r"ppi-l4_(.+?)_(zero-shot|3-shot)(?:_fs\d+)?$", name)
if m:
return m.group(1), m.group(2)
return None
def analyze(
dataset: list[dict],
degrees: dict[str, float],
all_preds: dict[str, dict[str, str]],
) -> str:
"""Run the contamination vs popularity analysis."""
lines = ["# Contamination vs Protein Popularity Analysis (PPI-L4)", ""]
lines.append("**Question:** Is the temporal contamination gap driven by "
"memorization or protein popularity?")
lines.append("")
# Enrich dataset with degree info
tested_records = [r for r in dataset if r.get("temporal_group") in ("pre_2015", "post_2020")]
pair_degrees = []
for rec in tested_records:
meta = rec.get("metadata", {})
g1 = meta.get("gene_symbol_1", "")
g2 = meta.get("gene_symbol_2", "")
d1 = degrees.get(g1, 0)
d2 = degrees.get(g2, 0)
pair_degrees.append((d1 + d2) / 2.0)
if not pair_degrees:
return "\n".join(lines + ["No tested records with degree data found."])
median_deg = float(np.median(pair_degrees))
lines.append(f"**Median pair degree:** {median_deg:.1f}")
lines.append(f"**Tested records with temporal group:** {len(tested_records)}")
lines.append("")
# Per-model analysis
header = "| Model | Config | Pre-2015 High | Pre-2015 Low | Post-2020 High | Post-2020 Low | Gap High | Gap Low |"
sep = "|---|---|---|---|---|---|---|---|"
lines.extend([header, sep])
for run_name, preds in sorted(all_preds.items()):
parsed = parse_run_name(run_name)
if not parsed:
continue
model, config = parsed
# Compute accuracy in 4 cells: temporal_group × degree_bin
cells = {}
for group in ["pre_2015", "post_2020"]:
for deg_bin in ["high", "low"]:
cells[(group, deg_bin)] = {"correct": 0, "total": 0}
for rec, avg_deg in zip(tested_records, pair_degrees):
qid = rec["question_id"]
pred_text = preds.get(qid)
if pred_text is None:
continue
parsed_pred = parse_l4_prediction(pred_text)
if parsed_pred is None:
continue
group = rec["temporal_group"]
deg_bin = "high" if avg_deg >= median_deg else "low"
cells[(group, deg_bin)]["total"] += 1
if parsed_pred == rec["gold_answer"]:
cells[(group, deg_bin)]["correct"] += 1
def acc(g: str, d: str) -> float | None:
c = cells[(g, d)]
return c["correct"] / c["total"] if c["total"] > 0 else None
pre_h = acc("pre_2015", "high")
pre_l = acc("pre_2015", "low")
post_h = acc("post_2020", "high")
post_l = acc("post_2020", "low")
gap_h = (pre_h - post_h) if pre_h is not None and post_h is not None else None
gap_l = (pre_l - post_l) if pre_l is not None and post_l is not None else None
def fmt(v: float | None) -> str:
return f"{v:.3f}" if v is not None else "—"
lines.append(
f"| {model} | {config} | {fmt(pre_h)} | {fmt(pre_l)} | "
f"{fmt(post_h)} | {fmt(post_l)} | {fmt(gap_h)} | {fmt(gap_l)} |"
)
# Model-averaged summary (aggregate 3-shot fs0/fs1/fs2 → mean)
from collections import defaultdict
model_gaps: dict[str, dict[str, list[float]]] = defaultdict(lambda: defaultdict(list))
for run_name, preds in sorted(all_preds.items()):
parsed = parse_run_name(run_name)
if not parsed:
continue
model, config = parsed
cells_local: dict[tuple[str, str], dict[str, int]] = {}
for group in ["pre_2015", "post_2020"]:
for deg_bin in ["high", "low"]:
cells_local[(group, deg_bin)] = {"correct": 0, "total": 0}
for rec, avg_deg in zip(tested_records, pair_degrees):
qid = rec["question_id"]
pred_text = preds.get(qid)
if pred_text is None:
continue
parsed_pred = parse_l4_prediction(pred_text)
if parsed_pred is None:
continue
group = rec["temporal_group"]
deg_bin = "high" if avg_deg >= median_deg else "low"
cells_local[(group, deg_bin)]["total"] += 1
if parsed_pred == rec["gold_answer"]:
cells_local[(group, deg_bin)]["correct"] += 1
def acc_local(g: str, d: str) -> float | None:
c = cells_local[(g, d)]
return c["correct"] / c["total"] if c["total"] > 0 else None
gh = acc_local("pre_2015", "high")
gl = acc_local("pre_2015", "low")
ph = acc_local("post_2020", "high")
pl = acc_local("post_2020", "low")
if gh is not None and ph is not None:
model_gaps[model]["gap_high"].append(gh - ph)
if gl is not None and pl is not None:
model_gaps[model]["gap_low"].append(gl - pl)
lines.extend(["", "## Model-Averaged Summary", ""])
lines.append("| Model | Avg Gap High | Avg Gap Low | Verdict |")
lines.append("|---|---|---|---|")
for model in sorted(model_gaps.keys()):
gh_vals = model_gaps[model]["gap_high"]
gl_vals = model_gaps[model]["gap_low"]
avg_gh = float(np.mean(gh_vals)) if gh_vals else None
avg_gl = float(np.mean(gl_vals)) if gl_vals else None
if avg_gh is not None and avg_gl is not None:
if avg_gh > 0.15 and avg_gl > 0.15:
if avg_gl >= avg_gh:
verdict = "True contamination (stronger for obscure)"
else:
verdict = "True contamination"
elif avg_gh > 0.15:
verdict = "Popularity confound"
else:
verdict = "No significant gap"
else:
verdict = "Insufficient data"
fmt_gh = f"{avg_gh:.3f}" if avg_gh is not None else "—"
fmt_gl = f"{avg_gl:.3f}" if avg_gl is not None else "—"
lines.append(f"| {model} | {fmt_gh} | {fmt_gl} | {verdict} |")
# Interpretation
lines.extend(["", "## Interpretation Guide", ""])
lines.append("- **Gap High > 0.15 AND Gap Low > 0.15:** True contamination "
"(memorization persists regardless of protein popularity)")
lines.append("- **Gap High > 0.15 BUT Gap Low ≈ 0:** Popularity confound "
"(well-studied proteins drive the gap)")
lines.append("- **Gap Low > Gap High:** Contamination stronger for "
"obscure proteins (pure memorization signal)")
return "\n".join(lines)
def main():
parser = argparse.ArgumentParser(description="PPI-L4 contamination vs popularity")
parser.add_argument("--db-path", type=Path, default=DEFAULT_DB)
parser.add_argument("--results-dir", type=Path, default=DEFAULT_RESULTS)
parser.add_argument("--dataset", type=Path, default=DATASET_PATH)
args = parser.parse_args()
print("Loading L4 dataset...")
dataset = load_l4_dataset(args.dataset)
print(f" {len(dataset)} records")
print("Loading protein degrees from DB...")
degrees = load_protein_degrees(args.db_path)
print(f" {len(degrees)} proteins with degree data")
print("Loading predictions...")
all_preds = load_predictions(args.results_dir)
print(f" {len(all_preds)} L4 runs found")
result = analyze(dataset, degrees, all_preds)
print(f"\n{result}")
out_path = args.results_dir / "contamination_vs_popularity.md"
out_path.parent.mkdir(parents=True, exist_ok=True)
with open(out_path, "w") as f:
f.write(result)
print(f"\nSaved: {out_path}")
if __name__ == "__main__":
main()
|