ColiFormer-ui / evaluate_optimizer.py
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import sys
"""
File: evaluate_optimizer.py
---------------------------
Evaluate ColiFormer with enhanced capabilities:
1) DNAChisel post-processing for sequence polishing
2) Optional multi-objective generation (Pareto-style filtering)
3) Enhanced beam search with multiple candidates
4) Comprehensive metrics and optional ablation studies
"""
import argparse
import json
import os
import warnings
from typing import Dict, List, Tuple, Any
import numpy as np
import pandas as pd
import torch
from CAI import CAI, relative_adaptiveness
from tqdm import tqdm
from CodonTransformer.CodonData import (
download_codon_frequencies_from_kazusa,
get_codon_frequencies,
)
from CodonTransformer.CodonPrediction import (
load_model,
predict_dna_sequence,
get_high_frequency_choice_sequence_optimized,
)
from CodonTransformer.CodonEvaluation import (
calculate_dtw_distance,
calculate_homopolymer_runs,
calculate_tAI,
count_negative_cis_elements,
get_GC_content,
get_ecoli_tai_weights,
get_min_max_profile,
get_sequence_similarity,
scan_for_restriction_sites,
calculate_ENC,
calculate_CPB,
calculate_SCUO,
)
from CodonTransformer.CodonPostProcessing import (
polish_sequence_with_dnachisel,
)
from CodonTransformer.CodonUtils import DNASequencePrediction
def translate_dna_to_protein(dna_sequence: str) -> str:
"""Translate DNA sequence to protein sequence."""
codon_table = {
'TTT': 'F', 'TTC': 'F', 'TTA': 'L', 'TTG': 'L',
'TCT': 'S', 'TCC': 'S', 'TCA': 'S', 'TCG': 'S',
'TAT': 'Y', 'TAC': 'Y', 'TAA': '*', 'TAG': '*',
'TGT': 'C', 'TGC': 'C', 'TGA': '*', 'TGG': 'W',
'CTT': 'L', 'CTC': 'L', 'CTA': 'L', 'CTG': 'L',
'CCT': 'P', 'CCC': 'P', 'CCA': 'P', 'CCG': 'P',
'CAT': 'H', 'CAC': 'H', 'CAA': 'Q', 'CAG': 'Q',
'CGT': 'R', 'CGC': 'R', 'CGA': 'R', 'CGG': 'R',
'ATT': 'I', 'ATC': 'I', 'ATA': 'I', 'ATG': 'M',
'ACT': 'T', 'ACC': 'T', 'ACA': 'T', 'ACG': 'T',
'AAT': 'N', 'AAC': 'N', 'AAA': 'K', 'AAG': 'K',
'AGT': 'S', 'AGC': 'S', 'AGA': 'R', 'AGG': 'R',
'GTT': 'V', 'GTC': 'V', 'GTA': 'V', 'GTG': 'V',
'GCT': 'A', 'GCC': 'A', 'GCA': 'A', 'GCG': 'A',
'GAT': 'D', 'GAC': 'D', 'GAA': 'E', 'GAG': 'E',
'GGT': 'G', 'GGC': 'G', 'GGA': 'G', 'GGG': 'G'
}
protein = ""
for i in range(0, len(dna_sequence), 3):
codon = dna_sequence[i:i+3].upper()
if len(codon) == 3:
aa = codon_table.get(codon, 'X')
if aa == '*': # Stop codon
break
protein += aa
return protein
def evaluate_with_enhancements(
protein_sequence: str,
model,
tokenizer,
device,
cai_weights: Dict[str, float],
tai_weights: Dict[str, float],
codon_frequencies: Dict,
reference_profile: List[float],
args,
) -> Dict[str, Any]:
"""
Evaluate a protein sequence with enhanced generation techniques.
Args:
protein_sequence: Input protein sequence
model: Fine-tuned model
tokenizer: Model tokenizer
device: PyTorch device
cai_weights: CAI weights dictionary
tai_weights: tAI weights dictionary
codon_frequencies: Codon frequencies dictionary
reference_profile: Reference profile for DTW calculation
args: Command line arguments
Returns:
Dict containing evaluation results for all methods
"""
results = {}
# 1. Original fine-tuned model (baseline)
try:
original_output = predict_dna_sequence(
protein=protein_sequence,
organism="Escherichia coli general",
device=device,
model=model,
deterministic=True,
match_protein=True,
use_constrained_search=args.use_constrained_search,
gc_bounds=tuple(args.gc_bounds),
beam_size=args.beam_size,
length_penalty=args.length_penalty,
diversity_penalty=args.diversity_penalty,
)
if isinstance(original_output, list):
original_dna = original_output[0].predicted_dna
else:
original_dna = original_output.predicted_dna
results['fine_tuned_original'] = {
'dna_sequence': original_dna,
'method': 'fine_tuned_original',
'enhancement': 'none',
}
except Exception as e:
print(f"Warning: Original fine-tuned generation failed: {str(e)}")
results['fine_tuned_original'] = {
'dna_sequence': '',
'method': 'fine_tuned_original',
'enhancement': 'none',
'error': str(e),
}
# 2. Enhanced sequence generation (DNAChisel + Pareto filtering)
if args.use_enhanced_generation:
try:
enhanced_dna, generation_report = enhanced_sequence_generation(
protein_sequence=protein_sequence,
model=model,
tokenizer=tokenizer,
device=device,
beam_size=args.enhanced_beam_size,
gc_bounds=(args.gc_bounds[0] * 100, args.gc_bounds[1] * 100),
use_dnachisel_polish=args.use_dnachisel,
use_pareto_filtering=args.use_pareto_filtering,
cai_weights=cai_weights,
tai_weights=tai_weights,
codon_frequencies=codon_frequencies,
reference_profile=reference_profile,
)
results['fine_tuned_enhanced'] = {
'dna_sequence': enhanced_dna,
'method': 'fine_tuned_enhanced',
'enhancement': 'dnachisel+pareto',
'generation_report': generation_report,
}
except Exception as e:
print(f"Warning: Enhanced generation failed: {str(e)}")
results['fine_tuned_enhanced'] = {
'dna_sequence': '',
'method': 'fine_tuned_enhanced',
'enhancement': 'dnachisel+pareto',
'error': str(e),
}
# 3. DNAChisel post-processing only (ablation study)
if args.use_dnachisel and 'fine_tuned_original' in results and results['fine_tuned_original']['dna_sequence']:
try:
dnachisel_dna, polish_report = polish_sequence_with_dnachisel(
dna_sequence=results['fine_tuned_original']['dna_sequence'],
protein_sequence=protein_sequence,
gc_bounds=(args.gc_bounds[0] * 100, args.gc_bounds[1] * 100),
maximize_cai=True,
seed=42,
)
results['fine_tuned_dnachisel'] = {
'dna_sequence': dnachisel_dna,
'method': 'fine_tuned_dnachisel',
'enhancement': 'dnachisel_only',
'polish_report': polish_report,
}
except Exception as e:
print(f"Warning: DNAChisel post-processing failed: {str(e)}")
results['fine_tuned_dnachisel'] = {
'dna_sequence': '',
'method': 'fine_tuned_dnachisel',
'enhancement': 'dnachisel_only',
'error': str(e),
}
return results
def calculate_comprehensive_metrics(
dna_sequence: str,
protein_sequence: str,
cai_weights: Dict[str, float],
tai_weights: Dict[str, float],
codon_frequencies: Dict,
reference_profile: List[float],
ref_sequences: List[str],
) -> Dict[str, float]:
"""Calculate comprehensive metrics for a DNA sequence."""
if not dna_sequence:
return {
'cai': 0.0,
'tai': 0.0,
'gc_content': 0.0,
'restriction_sites': float('inf'),
'neg_cis_elements': float('inf'),
'homopolymer_runs': float('inf'),
'dtw_distance': float('inf'),
'enc': 0.0,
'cpb': 0.0,
'scuo': 0.0,
}
return calculate_sequence_metrics(
dna_sequence=dna_sequence,
protein_sequence=protein_sequence,
cai_weights=cai_weights,
tai_weights=tai_weights,
codon_frequencies=codon_frequencies,
reference_profile=reference_profile,
)
def run_ablation_study(results_df: pd.DataFrame) -> pd.DataFrame:
"""
Run ablation study to compare different enhancement methods.
Args:
results_df: DataFrame with evaluation results
Returns:
DataFrame with ablation study results
"""
# Group by protein and calculate improvements
ablation_results = []
for protein in results_df['protein_sequence'].unique():
protein_results = results_df[results_df['protein_sequence'] == protein]
# Get baseline (original fine-tuned)
baseline = protein_results[protein_results['method'] == 'fine_tuned_original']
if baseline.empty:
continue
baseline_metrics = baseline.iloc[0]
# Compare each enhancement method
for method in protein_results['method'].unique():
if method == 'fine_tuned_original':
continue
method_results = protein_results[protein_results['method'] == method]
if method_results.empty:
continue
method_metrics = method_results.iloc[0]
# Calculate improvements
improvements = {
'protein': protein,
'method': method,
'enhancement': method_metrics['enhancement'],
'cai_improvement': method_metrics['cai'] - baseline_metrics['cai'],
'tai_improvement': method_metrics['tai'] - baseline_metrics['tai'],
'gc_improvement': abs(method_metrics['gc_content'] - 52) - abs(baseline_metrics['gc_content'] - 52),
'restriction_sites_improvement': baseline_metrics['restriction_sites'] - method_metrics['restriction_sites'],
'neg_cis_improvement': baseline_metrics['neg_cis_elements'] - method_metrics['neg_cis_elements'],
'homopolymer_improvement': baseline_metrics['homopolymer_runs'] - method_metrics['homopolymer_runs'],
'dtw_improvement': baseline_metrics['dtw_distance'] - method_metrics['dtw_distance'],
'composite_score_improvement': (
(method_metrics['cai'] - baseline_metrics['cai']) * 0.3 +
(method_metrics['tai'] - baseline_metrics['tai']) * 0.3 +
(abs(baseline_metrics['gc_content'] - 52) - abs(method_metrics['gc_content'] - 52)) * 0.2 +
(baseline_metrics['restriction_sites'] - method_metrics['restriction_sites']) * 0.1 +
(baseline_metrics['neg_cis_elements'] - method_metrics['neg_cis_elements']) * 0.1
),
}
ablation_results.append(improvements)
return pd.DataFrame(ablation_results)
def main(args):
"""Main function to run the enhanced evaluation."""
print("=== Enhanced CodonTransformer Evaluation ===")
# Setup device
device = torch.device("cuda" if torch.cuda.is_available() and args.use_gpu else "cpu")
print(f"Using device: {device}")
# Load test data
with open(args.test_data_path, "r") as f:
first = f.read(1)
f.seek(0)
if first == "[":
test_set = json.load(f)
else:
test_set = [json.loads(line) for line in f if line.strip()]
# Limit test set size if requested
if args.max_test_proteins > 0:
test_set = test_set[:args.max_test_proteins]
print(f"Loaded {len(test_set)} proteins from the test set.")
# Load models
print("Loading models...")
finetuned_model = load_model(model_path=args.checkpoint_path, device=device)
print(f"Fine-tuned model loaded from {args.checkpoint_path}")
# Load tokenizer
from transformers import AutoTokenizer
tokenizer = AutoTokenizer.from_pretrained("adibvafa/CodonTransformer")
# Load base model if comparison requested
base_model = None
if args.compare_with_base:
base_model = load_model(device=device)
print("Base model loaded from Hugging Face")
# Prepare evaluation utilities
print("Preparing evaluation utilities...")
# CAI weights
natural_csv = args.natural_sequences_path
natural_df = pd.read_csv(natural_csv)
ref_sequences = natural_df['dna_sequence'].tolist()
cai_weights = relative_adaptiveness(sequences=ref_sequences)
print("CAI weights generated")
# tAI weights
tai_weights = get_ecoli_tai_weights()
print("tAI weights loaded")
# Codon frequencies
try:
codon_frequencies = download_codon_frequencies_from_kazusa(taxonomy_id=83333)
print("Codon frequencies loaded from Kazusa")
except Exception as e:
print(f"Warning: Kazusa download failed ({e}). Using local frequencies.")
codon_frequencies = get_codon_frequencies(
ref_sequences, organism="Escherichia coli general"
)
# Reference profile for DTW
reference_profiles = [
get_min_max_profile(seq, codon_frequencies) for seq in ref_sequences[:100]
]
valid_profiles = [p for p in reference_profiles if p and not all(v is None for v in p)]
if valid_profiles:
max_len = max(len(p) for p in valid_profiles)
padded_profiles = [
np.pad(
np.array([v for v in p if v is not None]),
(0, max_len - len([v for v in p if v is not None])),
"constant",
constant_values=np.nan,
)
for p in valid_profiles
]
avg_reference_profile = np.nanmean(padded_profiles, axis=0).tolist()
else:
avg_reference_profile = []
print("Reference profile generated")
# Run evaluation
all_results = []
evaluation_reports = []
print("Starting enhanced evaluation...")
for i, item in enumerate(tqdm(test_set, desc="Evaluating proteins")):
# Get protein sequence
if "protein_sequence" in item:
protein_sequence = item["protein_sequence"]
else:
dna_sequence = item["codons"]
protein_sequence = translate_dna_to_protein(dna_sequence)
# Skip if protein is too short or too long
if len(protein_sequence) < 10 or len(protein_sequence) > 1000:
continue
# Evaluate with enhancements
protein_results = evaluate_with_enhancements(
protein_sequence=protein_sequence,
model=finetuned_model,
tokenizer=tokenizer,
device=device,
cai_weights=cai_weights,
tai_weights=tai_weights,
codon_frequencies=codon_frequencies,
reference_profile=avg_reference_profile,
args=args,
)
# Add base model comparison if requested
if base_model:
try:
base_output = predict_dna_sequence(
protein=protein_sequence,
organism="Escherichia coli general",
device=device,
model=base_model,
deterministic=True,
match_protein=True,
)
base_dna = base_output.predicted_dna if not isinstance(base_output, list) else base_output[0].predicted_dna
protein_results['base_model'] = {
'dna_sequence': base_dna,
'method': 'base_model',
'enhancement': 'none',
}
except Exception as e:
print(f"Warning: Base model generation failed: {str(e)}")
# Add naive baseline
try:
naive_dna = get_high_frequency_choice_sequence_optimized(
protein=protein_sequence, codon_frequencies=codon_frequencies
)
protein_results['naive_hfc'] = {
'dna_sequence': naive_dna,
'method': 'naive_hfc',
'enhancement': 'none',
}
except Exception as e:
print(f"Warning: Naive HFC generation failed: {str(e)}")
# Calculate metrics for each method
for method_name, method_result in protein_results.items():
if 'error' in method_result:
continue
dna_seq = method_result['dna_sequence']
if not dna_seq:
continue
metrics = calculate_comprehensive_metrics(
dna_sequence=dna_seq,
protein_sequence=protein_sequence,
cai_weights=cai_weights,
tai_weights=tai_weights,
codon_frequencies=codon_frequencies,
reference_profile=avg_reference_profile,
ref_sequences=ref_sequences,
)
# Combine results
result_row = {
'protein_id': i,
'protein_sequence': protein_sequence,
'protein_length': len(protein_sequence),
'method': method_name,
'enhancement': method_result['enhancement'],
'dna_sequence': dna_seq,
'dna_length': len(dna_seq),
**metrics,
}
# Add generation reports if available
if 'generation_report' in method_result:
result_row['generation_report'] = str(method_result['generation_report'])
if 'polish_report' in method_result:
result_row['polish_report'] = str(method_result['polish_report'])
all_results.append(result_row)
# Create results DataFrame
results_df = pd.DataFrame(all_results)
# Save detailed results
os.makedirs(os.path.dirname(args.output_path), exist_ok=True)
results_df.to_csv(args.output_path, index=False)
print(f"Detailed results saved to {args.output_path}")
# Run ablation study
if args.run_ablation_study:
ablation_df = run_ablation_study(results_df)
ablation_path = args.output_path.replace('.csv', '_ablation.csv')
ablation_df.to_csv(ablation_path, index=False)
print(f"Ablation study results saved to {ablation_path}")
# Print summary statistics
print("\n=== ABLATION STUDY SUMMARY ===")
for method in ablation_df['method'].unique():
method_results = ablation_df[ablation_df['method'] == method]
print(f"\n{method.upper()}:")
print(f" CAI improvement: {method_results['cai_improvement'].mean():.4f} ± {method_results['cai_improvement'].std():.4f}")
print(f" tAI improvement: {method_results['tai_improvement'].mean():.4f} ± {method_results['tai_improvement'].std():.4f}")
print(f" GC improvement: {method_results['gc_improvement'].mean():.4f} ± {method_results['gc_improvement'].std():.4f}")
print(f" Restriction sites improvement: {method_results['restriction_sites_improvement'].mean():.2f} ± {method_results['restriction_sites_improvement'].std():.2f}")
print(f" Composite score improvement: {method_results['composite_score_improvement'].mean():.4f} ± {method_results['composite_score_improvement'].std():.4f}")
# Print final summary
print("\n=== EVALUATION COMPLETE ===")
print(f"Total proteins evaluated: {len(results_df['protein_id'].unique())}")
print(f"Total sequences generated: {len(results_df)}")
print(f"Results saved to: {args.output_path}")
if __name__ == "__main__":
parser = argparse.ArgumentParser(description="Enhanced CodonTransformer Evaluation")
# Input/Output paths
parser.add_argument("--checkpoint_path", type=str, default="models/ecoli-codon-optimizer/finetune_best.ckpt",
help="Path to fine-tuned model checkpoint")
parser.add_argument("--test_data_path", type=str, default="data/test_set.json",
help="Path to test dataset")
parser.add_argument("--natural_sequences_path", type=str, default="data/ecoli_processed_genes.csv",
help="Path to natural E. coli sequences for CAI calculation")
parser.add_argument("--output_path", type=str, default="results/enhanced_evaluation_results.csv",
help="Path to save evaluation results")
# Model parameters
parser.add_argument("--use_gpu", action="store_true", help="Use GPU if available")
parser.add_argument("--compare_with_base", action="store_true", help="Compare with base model")
# Generation parameters
parser.add_argument("--use_constrained_search", action="store_true",
help="Use constrained beam search")
parser.add_argument("--gc_bounds", type=float, nargs=2, default=[0.50, 0.54],
help="GC content bounds (min max)")
parser.add_argument("--beam_size", type=int, default=10,
help="Beam size for standard generation")
parser.add_argument("--length_penalty", type=float, default=1.2,
help="Length penalty for beam search")
parser.add_argument("--diversity_penalty", type=float, default=0.1,
help="Diversity penalty for beam search")
# Enhancement parameters
parser.add_argument("--use_enhanced_generation", action="store_true",
help="Use enhanced generation with DNAChisel and Pareto filtering")
parser.add_argument("--enhanced_beam_size", type=int, default=20,
help="Beam size for enhanced generation")
parser.add_argument("--use_dnachisel", action="store_true",
help="Use DNAChisel post-processing")
parser.add_argument("--use_pareto_filtering", action="store_true",
help="Use Pareto frontier filtering")
# Evaluation parameters
parser.add_argument("--max_test_proteins", type=int, default=0,
help="Maximum number of proteins to test (0 for all)")
parser.add_argument("--run_ablation_study", action="store_true",
help="Run ablation study comparing methods")
args = parser.parse_args()
main(args)