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parquet
Languages:
English
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10M - 100M
Tags:
biology
chemistry
drug-discovery
clinical-trials
protein-protein-interaction
gene-essentiality
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File size: 6,131 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 | #!/usr/bin/env python3
"""Build GE-L2 extraction dataset for LLM benchmark.
Generates 500 evidence extraction records using constructed evidence descriptions
(DepMap publications don't reference individual gene-cell_line pairs in abstracts).
Each record contains a 1-3 gene essentiality finding per cell line.
Gold standard derived from database fields.
Split: 50 fewshot + 50 val + 400 test
Output: exports/ge_llm/ge_l2_dataset.jsonl
Usage:
PYTHONPATH=src python scripts_depmap/build_ge_l2_dataset.py
"""
from __future__ import annotations
import argparse
import logging
import sys
from pathlib import Path
import numpy as np
import pandas as pd
logging.basicConfig(level=logging.INFO, format="%(asctime)s %(levelname)s %(message)s")
logger = logging.getLogger(__name__)
PROJECT_ROOT = Path(__file__).resolve().parent.parent
OUTPUT_DIR = PROJECT_ROOT / "exports" / "ge_llm"
N_TOTAL = 500
GENES_PER_RECORD = [1, 1, 2, 2, 3] # ~40% 1-gene, ~40% 2-gene, ~20% 3-gene
def construct_multi_gene_evidence(rows: list[pd.Series]) -> tuple[str, dict]:
"""Build a multi-gene evidence summary and gold extraction.
Returns (evidence_text, gold_extraction_dict).
"""
cell_line = rows[0].get("ccle_name") or rows[0].get("model_id", "UNKNOWN")
lineage = rows[0].get("lineage", "unknown lineage")
lines = [
f"A genome-wide CRISPR-Cas9 knockout screen was performed in {cell_line} "
f"({lineage}) as part of the Cancer Dependency Map (DepMap) project.",
"",
"Gene-level essentiality results (Chronos algorithm):",
]
gold_genes = []
for row in rows:
gene = row.get("gene_symbol", "UNKNOWN")
effect = row.get("gene_effect_score")
dep_prob = row.get("dependency_probability")
evidence_type = row.get("evidence_type", "crispr_nonessential")
tier = row.get("confidence_tier", "bronze")
score_str = f"gene effect = {effect:.3f}" if effect is not None and not pd.isna(effect) else "score unavailable"
prob_str = f"dependency probability = {dep_prob:.3f}" if dep_prob is not None and not pd.isna(dep_prob) else ""
parts = [score_str]
if prob_str:
parts.append(prob_str)
lines.append(f"- {gene}: {', '.join(parts)} → classified as non-essential")
gold_genes.append({
"gene_name": gene,
"cell_line": cell_line,
"screen_method": "CRISPR" if "crispr" in evidence_type else "RNAi",
"essentiality_status": "non-essential",
"dependency_score": float(effect) if effect is not None and not pd.isna(effect) else None,
})
evidence_text = "\n".join(lines)
gold_extraction = {
"genes": gold_genes,
"total_genes_mentioned": len(gold_genes),
"cell_line": cell_line,
"screen_type": "CRISPR",
}
return evidence_text, gold_extraction
def main(argv: list[str] | None = None) -> int:
parser = argparse.ArgumentParser(description="Build GE-L2 extraction dataset.")
parser.add_argument("--db", type=Path, default=PROJECT_ROOT / "data" / "negbiodb_depmap.db")
parser.add_argument("--output", type=Path, default=OUTPUT_DIR / "ge_l2_dataset.jsonl")
parser.add_argument("--seed", type=int, default=42)
args = parser.parse_args(argv)
from negbiodb_depmap.depmap_db import get_connection
from negbiodb_depmap.llm_dataset import (
apply_max_per_gene,
assign_splits,
load_ge_candidate_pool,
write_dataset_metadata,
write_jsonl,
)
rng = np.random.RandomState(args.seed)
conn = get_connection(args.db)
try:
df = load_ge_candidate_pool(conn, min_confidence="silver")
finally:
conn.close()
df = apply_max_per_gene(df, max_per_gene=5, seed=args.seed)
df = df.sample(frac=1, random_state=rng).reset_index(drop=True)
# Build records with varying gene counts per record
records = []
idx = 0
record_count = 0
while record_count < N_TOTAL and idx < len(df):
n_genes = GENES_PER_RECORD[record_count % len(GENES_PER_RECORD)]
if idx + n_genes > len(df):
n_genes = 1
gene_rows = [df.iloc[idx + j] for j in range(n_genes)]
idx += n_genes
evidence_text, gold_extraction = construct_multi_gene_evidence(gene_rows)
rec = {
"question_id": f"GEL2-{record_count:04d}",
"task": "ge-l2",
"split": "test",
"difficulty": "medium",
"context_text": evidence_text,
"gold_answer": gold_extraction["genes"][0].get("gene_name", ""),
"gold_category": gene_rows[0].get("source_db", "depmap"),
"gold_extraction": gold_extraction,
"metadata": {
"n_genes": n_genes,
"source_db": gene_rows[0].get("source_db"),
"gene_symbols": [r.get("gene_symbol") for r in gene_rows],
"cell_line": gene_rows[0].get("ccle_name") or gene_rows[0].get("model_id"),
},
}
records.append(rec)
record_count += 1
logger.info("Built %d L2 records from %d gene rows", len(records), idx)
# Assign splits
records_df = pd.DataFrame({"idx": range(len(records))})
records_df = assign_splits(records_df, ratios={"train": 0.1, "val": 0.1, "test": 0.8})
records_df["split"] = records_df["split"].replace({"train": "fewshot"})
for i, (_, row) in enumerate(records_df.iterrows()):
if i < len(records):
records[i]["split"] = row["split"]
write_jsonl(records, args.output)
stats = {
"n_total": len(records),
"design": "constructed_evidence",
"gene_distribution": dict(pd.Series([r["metadata"]["n_genes"] for r in records]).value_counts()),
"split_distribution": dict(pd.Series([r["split"] for r in records]).value_counts()),
"seed": args.seed,
}
write_dataset_metadata(args.output.parent, "ge-l2", stats)
logger.info("GE-L2 dataset built: %d records", len(records))
return 0
if __name__ == "__main__":
sys.exit(main())
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