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"""
Verify JCVI Syn3.0 annotation results (Paper Figure 2A).
This script reproduces the key result from the paper: 39.6% (59/149) of genes
with unknown function in JCVI Syn3.0 minimal genome received confident
functional annotations at FDR α=0.1.
Required data files (see docs/INSTALLATION.md for download instructions):
- data/gene_unknown/unknown_aa_seqs.npy: Protein-Vec embeddings of 149 unknown genes
- data/gene_unknown/unknown_aa_seqs.fasta: FASTA sequences (for metadata)
- data/lookup_embeddings.npy: UniProt lookup embeddings (from Zenodo)
- data/lookup_embeddings_meta_data.tsv: UniProt metadata with Pfam annotations
- data/pfam_new_proteins.npy: Calibration data for Venn-Abers (from Zenodo)
Expected output:
- 59 hits out of 149 queries (39.6%) at FDR threshold λ ≈ 0.999980
Usage:
python scripts/verify_syn30.py
python scripts/verify_syn30.py --alpha 0.1 --output results/syn30_hits.csv
"""
import argparse
import sys
from pathlib import Path
import numpy as np
import pandas as pd
# Add parent directory to path for imports
sys.path.insert(0, str(Path(__file__).parent.parent))
from protein_conformal.util import (
read_fasta,
load_database,
query,
simplifed_venn_abers_prediction,
get_sims_labels,
)
def load_fdr_threshold(fdr_file: Path = None, alpha: float = 0.1) -> float:
"""
Load pre-computed FDR threshold or use hardcoded value from paper.
The FDR threshold is computed using Learn-Then-Test (LTT) calibration.
For α=0.1, the mean threshold across calibration runs is 0.999980225003127.
"""
if fdr_file and fdr_file.exists():
fdr_data = np.load(fdr_file, allow_pickle=True).item()
return np.mean(fdr_data['lhats'])
# Hardcoded value from paper/notebook for α=0.1
# This is the average threshold from 100 calibration trials
if alpha == 0.1:
return 0.999980225003127
else:
raise ValueError(
f"No pre-computed threshold for alpha={alpha}. "
"Please provide an FDR file or use alpha=0.1."
)
def verify_syn30(
query_embeddings_path: Path,
query_fasta_path: Path,
lookup_embeddings_path: Path,
lookup_metadata_path: Path,
calibration_data_path: Path,
fdr_threshold_path: Path = None,
alpha: float = 0.1,
output_csv: Path = None,
verbose: bool = True,
) -> dict:
"""
Run the JCVI Syn3.0 verification experiment.
Returns dict with:
- n_queries: Total number of query proteins
- n_hits: Number of proteins with confident hits
- hit_rate: Fraction of proteins with hits
- threshold: FDR threshold used
- hits_df: DataFrame with detailed hit information
"""
if verbose:
print("=" * 60)
print("JCVI Syn3.0 Annotation Verification")
print("=" * 60)
# Load query embeddings (149 unknown genes)
if verbose:
print(f"\nLoading query embeddings from {query_embeddings_path}...")
query_embeddings = np.load(query_embeddings_path)
n_queries = query_embeddings.shape[0]
if verbose:
print(f" Loaded {n_queries} query embeddings, shape: {query_embeddings.shape}")
# Load query FASTA for metadata
if verbose:
print(f"\nLoading query FASTA from {query_fasta_path}...")
query_fastas, query_metadata = read_fasta(str(query_fasta_path))
if verbose:
print(f" Loaded {len(query_fastas)} sequences")
# Load lookup database (UniProt with Pfam annotations)
if verbose:
print(f"\nLoading lookup embeddings from {lookup_embeddings_path}...")
embeddings = np.load(lookup_embeddings_path)
if verbose:
print(f" Loaded {embeddings.shape[0]} embeddings, shape: {embeddings.shape}")
if verbose:
print(f"\nLoading lookup metadata from {lookup_metadata_path}...")
lookup_proteins_meta = pd.read_csv(lookup_metadata_path, sep="\t")
if verbose:
print(f" Loaded metadata for {len(lookup_proteins_meta)} proteins")
# Filter to proteins with Pfam annotations
column = 'Pfam'
col_lookup = lookup_proteins_meta[~lookup_proteins_meta[column].isnull()]
col_lookup_embeddings = embeddings[col_lookup.index]
col_meta_data = col_lookup[column].values
if verbose:
print(f" {len(col_lookup)} proteins have Pfam annotations")
# Build FAISS index
if verbose:
print("\nBuilding FAISS index...")
lookup_database = load_database(col_lookup_embeddings)
# Query for nearest neighbors
if verbose:
print("Querying for nearest neighbors (k=1)...")
k = 1
D, I = query(lookup_database, query_embeddings, k)
D_max = np.max(D, axis=1)
# Load FDR threshold
l_hat = load_fdr_threshold(fdr_threshold_path, alpha)
if verbose:
print(f"\nFDR threshold (α={alpha}): λ = {l_hat:.12f}")
# Count hits
hits_mask = D_max > l_hat
n_hits = hits_mask.sum()
hit_rate = n_hits / n_queries
if verbose:
print(f"\n{'=' * 60}")
print(f"RESULTS")
print(f"{'=' * 60}")
print(f"Total queries: {n_queries}")
print(f"Confident hits: {n_hits}")
print(f"Hit rate: {hit_rate:.1%} (expected: 39.6%)")
print(f"{'=' * 60}")
# Compute Venn-Abers probabilities for hits
if verbose and calibration_data_path.exists():
print("\nComputing Venn-Abers probabilities...")
data = np.load(calibration_data_path, allow_pickle=True)
n_calib = 100
np.random.seed(42) # For reproducibility
np.random.shuffle(data)
cal_data = data[:n_calib]
X_cal, y_cal = get_sims_labels(cal_data, partial=False)
X_cal = X_cal.flatten()
y_cal = y_cal.flatten()
p_s = []
for d in D:
p_0, p_1 = simplifed_venn_abers_prediction(X_cal, y_cal, d)
p_s.append((p_0 + p_1) / 2) # Point estimate
p_s = np.array(p_s)
print(f" Mean probability for hits: {np.mean(p_s[hits_mask]):.3f}")
else:
p_s = np.full(n_queries, np.nan)
# Build results DataFrame
results_data = {
'query_name': query_metadata,
'query_sequence': query_fastas,
'similarity': D_max,
'probability': p_s,
'is_hit': hits_mask,
}
# Add Pfam annotations for hits
filtered_I = I[hits_mask, 0]
pfam_annotations = np.array([''] * n_queries, dtype=object)
pfam_annotations[hits_mask] = col_meta_data[filtered_I]
results_data['pfam_annotation'] = pfam_annotations
results_df = pd.DataFrame(results_data)
hits_df = results_df[results_df['is_hit']].copy()
if output_csv:
if verbose:
print(f"\nSaving results to {output_csv}...")
hits_df.to_csv(output_csv, index=False)
return {
'n_queries': n_queries,
'n_hits': n_hits,
'hit_rate': hit_rate,
'threshold': l_hat,
'hits_df': hits_df,
'results_df': results_df,
}
def main():
parser = argparse.ArgumentParser(
description='Verify JCVI Syn3.0 annotation results (Paper Figure 2A)'
)
parser.add_argument(
'--data-dir',
type=Path,
default=Path(__file__).parent.parent / 'data',
help='Base data directory'
)
parser.add_argument(
'--alpha',
type=float,
default=0.1,
help='FDR level (default: 0.1)'
)
parser.add_argument(
'--output',
type=Path,
default=None,
help='Output CSV file for hit results'
)
parser.add_argument(
'--quiet',
action='store_true',
help='Suppress verbose output'
)
args = parser.parse_args()
data_dir = args.data_dir
# Define file paths
query_embeddings_path = data_dir / 'gene_unknown' / 'unknown_aa_seqs.npy'
query_fasta_path = data_dir / 'gene_unknown' / 'unknown_aa_seqs.fasta'
lookup_embeddings_path = data_dir / 'lookup_embeddings.npy'
lookup_metadata_path = data_dir / 'lookup_embeddings_meta_data.tsv'
calibration_data_path = data_dir / 'pfam_new_proteins.npy'
# Check for missing files
missing_files = []
for path in [query_embeddings_path, query_fasta_path,
lookup_embeddings_path, lookup_metadata_path]:
if not path.exists():
missing_files.append(path)
if missing_files:
print("ERROR: Missing required data files:")
for f in missing_files:
print(f" - {f}")
print("\nSee docs/INSTALLATION.md for download instructions.")
print("\nQuick fix for Syn3.0 data:")
print(" The unknown_aa_seqs.npy and .fasta files contain the 149 genes")
print(" from JCVI Syn3.0 with unknown function. These need to be")
print(" generated using the Protein-Vec embedding model.")
sys.exit(1)
# Run verification
results = verify_syn30(
query_embeddings_path=query_embeddings_path,
query_fasta_path=query_fasta_path,
lookup_embeddings_path=lookup_embeddings_path,
lookup_metadata_path=lookup_metadata_path,
calibration_data_path=calibration_data_path,
alpha=args.alpha,
output_csv=args.output,
verbose=not args.quiet,
)
# Verify expected result
expected_hits = 59
expected_rate = 0.396
if results['n_hits'] == expected_hits:
print(f"\n✓ VERIFICATION PASSED: {results['n_hits']} hits matches expected {expected_hits}")
else:
print(f"\n✗ VERIFICATION FAILED: Got {results['n_hits']} hits, expected {expected_hits}")
print(" This may be due to different calibration data or random seed.")
return results
if __name__ == '__main__':
main()
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