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2020 2021 2022 2023 2024 2025 2026 | # -*- coding: utf-8 -*-
"""ML simplified tree.ipynb
Automatically generated by Colab.
Original file is located at
https://colab.research.google.com/drive/1LiDjip-h70ilIex9PedpWCZARWglija7
"""
# Commented out IPython magic to ensure Python compatibility.
import pandas as pd
import numpy as np
import plotly.graph_objects as go
import plotly.offline as pyo
from plotly.subplots import make_subplots
from Bio import Phylo, SeqIO, AlignIO
from Bio.Phylo.TreeConstruction import DistanceCalculator, DistanceTreeConstructor
from Bio.Align import MultipleSeqAlignment
from Bio.Seq import Seq
from Bio.SeqRecord import SeqRecord
from sklearn.feature_extraction.text import CountVectorizer
from sklearn.metrics.pairwise import cosine_similarity
from sklearn.ensemble import RandomForestClassifier
from sklearn.model_selection import train_test_split
from sklearn.preprocessing import LabelEncoder
import warnings
import os
import sys
from typing import Dict, List, Tuple, Optional, Any
import json
import re
from scipy.optimize import minimize
from scipy.spatial.distance import pdist, squareform
from Bio.Phylo import BaseTree
import itertools
from collections import defaultdict, deque
import argparse
import time
from pathlib import Path
warnings.filterwarnings('ignore')
class PhylogeneticTreeAnalyzer:
def __init__(self):
self.data = None
self.query_sequence = None
self.query_id = None
self.matching_percentage = 95.0
self.actual_percentage = None
self.matched_sequences = []
self.tree_structure = {}
self.similarity_scores = {}
self.ai_model = None
self.label_encoder = LabelEncoder()
# ML-specific attributes
self.ml_tree = None
self.ml_alignment = None
self.ml_results = {}
self.horizontal_line_tracker = [] # Track horizontal lines with verticals
self.query_ml_group = None # Track which ML group contains the query
self.base_horizontal_length = 1.2 # Base length for horizontal lines
def load_data(self, data_file: str):
try:
self.data = pd.read_csv(data_file)
# required_columns = ['Accession Number', 'ML', 'Genotype', 'Host',
# 'Country', 'Isolate', 'Year', 'F-gene']
# missing_columns = [col for col in self.data.columns if col not in required_columns] # Corrected check for missing columns
# if missing_columns:
# print(f"Error: Missing required columns: {missing_columns}")
# return False
print(f"✓ Data loaded successfully: {len(self.data)} sequences")
print(f"✓ ML Groups found: {self.data['ML'].nunique()}")
print(f"✓ Genotypes found: {self.data['Genotype'].nunique()}")
return True
except Exception as e:
print(f"Error loading data: {e}")
return False
def calculate_f_gene_similarity(self, seq1: str, seq2: str) -> float:
try:
# Handle empty or None sequences
if not seq1 or not seq2:
return 0.0
# Convert to uppercase and remove non-nucleotide characters
seq1 = re.sub(r'[^ATGC]', '', str(seq1).upper())
seq2 = re.sub(r'[^ATGC]', '', str(seq2).upper())
if len(seq1) == 0 or len(seq2) == 0:
return 0.0
# Use k-mer analysis for similarity calculation
k = 5 # 5-mer analysis
kmers1 = set([seq1[i:i+k] for i in range(len(seq1)-k+1) if len(seq1[i:i+k]) == k])
kmers2 = set([seq2[i:i+k] for i in range(len(seq2)-k+1) if len(seq2[i:i+k]) == k])
if len(kmers1) == 0 and len(kmers2) == 0:
return 100.0
elif len(kmers1) == 0 or len(kmers2) == 0:
return 0.0
# Calculate Jaccard similarity
intersection = len(kmers1.intersection(kmers2))
union = len(kmers1.union(kmers2))
similarity = (intersection / union) * 100 if union > 0 else 0.0
return round(similarity, 2)
except Exception as e:
print(f"Error calculating similarity: {e}")
return 0.0
def train_ai_model(self):
try:
# Skip training if insufficient data
if len(self.data) < 10: # Require minimum 10 samples
print("⚠️ Insufficient data to train AI model (min 10 samples required)", flush=True)
return False
print("🤖 Training AI model for sequence analysis...", flush=True)
# Prepare features from F-gene sequences
f_gene_sequences = self.data['F-gene'].fillna('').astype(str)
# Create k-mer features (3-mers to 6-mers)
features = []
for seq in f_gene_sequences:
seq_clean = re.sub(r'[^ATGC]', '', seq.upper())
if len(seq_clean) < 3:
features.append([0] * 100) # Placeholder for short sequences
continue
feature_vector = []
# 3-mers
kmers_3 = [seq_clean[i:i+3] for i in range(len(seq_clean)-2)]
kmer_counts_3 = {kmer: kmers_3.count(kmer) for kmer in set(kmers_3)}
# 4-mers
kmers_4 = [seq_clean[i:i+4] for i in range(len(seq_clean)-3)]
kmer_counts_4 = {kmer: kmers_4.count(kmer) for kmer in set(kmers_4)}
# Create feature vector (top 50 3-mers + top 50 4-mers)
all_3mers = [''.join(p) for p in __import__('itertools').product('ATGC', repeat=3)]
all_4mers = [''.join(p) for p in __import__('itertools').product('ATGC', repeat=4)]
feature_vector.extend([kmer_counts_3.get(kmer, 0) for kmer in all_3mers[:50]])
feature_vector.extend([kmer_counts_4.get(kmer, 0) for kmer in all_4mers[:50]])
features.append(feature_vector)
# Prepare target labels (ML groups)
targets = self.label_encoder.fit_transform(self.data['ML'].fillna('Unknown'))
# Skip if only 1 class
if len(np.unique(targets)) < 2:
print("⚠️ Need at least 2 distinct classes for training", flush=True)
return False
# Train Random Forest model
X = np.array(features)
y = targets
X_train, X_test, y_train, y_test = train_test_split(X, y, test_size=0.2, random_state=42)
self.ai_model = RandomForestClassifier(n_estimators=100, random_state=42)
self.ai_model.fit(X_train, y_train)
# Calculate accuracy
accuracy = self.ai_model.score(X_test, y_test)
print(f"✓ AI model trained successfully with accuracy: {accuracy:.2%}", flush=True)
return True
except Exception as e:
print(f"🚨 CRITICAL training error: {e}", flush=True)
import traceback
traceback.print_exc()
return False
def find_query_sequence(self, query_input: str) -> bool:
"""
Modified to accept any sequence input, not just those existing in the dataset.
"""
try:
# Check if input is an accession number from the dataset
if query_input in self.data['Accession Number'].values:
self.query_id = query_input
query_row = self.data[self.data['Accession Number'] == query_input].iloc[0]
self.query_sequence = query_row['F-gene']
print(f"✓ Query sequence found by ID: {query_input}")
return True
# Check if input is a nucleotide sequence
query_clean = re.sub(r'[^ATGC]', '', str(query_input).upper())
# Accept any sequence with reasonable length (even short ones for testing)
if len(query_clean) >= 10: # Minimum sequence length (reduced from 50)
# For sequences not in dataset, create a unique identifier
if query_input not in self.data['Accession Number'].values:
# Generate a unique query ID for novel sequences
self.query_id = f"QUERY_{hash(query_clean) % 100000:05d}"
self.query_sequence = query_clean
print(f"✓ Novel query sequence accepted with ID: {self.query_id}")
print(f" Sequence length: {len(query_clean)} nucleotides")
return True
else:
# If somehow it matches an accession but wasn't caught above
self.query_id = query_input
self.query_sequence = query_clean
print(f"✓ Query sequence processed: {query_input}")
return True
# If sequence is too short or invalid
if len(query_clean) < 10:
print(f"✗ Query sequence too short. Minimum length: 10 nucleotides (provided: {len(query_clean)})")
else:
print(f"✗ Invalid sequence format. Please provide nucleotides (A, T, G, C) or valid accession number")
return False
except Exception as e:
print(f"Error processing query sequence: {e}")
return False
def find_similar_sequences(self, target_percentage: float) -> Tuple[List[str], float]:
"""
Modified to work with any query sequence, including novel ones not in the dataset.
"""
try:
print(f"🔍 Finding sequences with {target_percentage}% similarity to query...")
similarities = []
# Calculate similarity between query and all sequences in dataset
for idx, row in self.data.iterrows():
# Skip if this is the same sequence (only relevant for existing accession numbers)
if hasattr(self, 'query_id') and row['Accession Number'] == self.query_id:
continue
try:
similarity = self.calculate_f_gene_similarity(self.query_sequence, row['F-gene'])
similarities.append({
'id': row['Accession Number'],
'similarity': similarity,
'ml': row['ML'] if 'ML' in row else 'Unknown',
'genotype': row['Genotype'] if 'Genotype' in row else 'Unknown'
})
except Exception as seq_error:
print(f"⚠ Skipping sequence {row['Accession Number']}: {seq_error}")
continue
if not similarities:
print("❌ No valid sequences found for comparison")
return [], target_percentage
# Sort by similarity (highest first)
similarities.sort(key=lambda x: x['similarity'], reverse=True)
# Find sequences within target percentage range (±2%)
target_range = 2.0
candidates = [s for s in similarities
if abs(s['similarity'] - target_percentage) <= target_range]
if not candidates:
# If no exact matches, find sequences with closest similarity
closest_sim = min(similarities, key=lambda x: abs(x['similarity'] - target_percentage))
actual_percentage = closest_sim['similarity']
# Get sequences within ±1% of the closest similarity
candidates = [s for s in similarities
if abs(s['similarity'] - actual_percentage) <= 1.0]
print(f"⚠ No sequences found at exactly {target_percentage}%. Using closest: {actual_percentage:.1f}%")
else:
actual_percentage = target_percentage
# Limit results to prevent overwhelming visualization (optional)
max_results = 50 # Adjust as needed
if len(candidates) > max_results:
candidates = candidates[:max_results]
print(f"⚠ Limited results to top {max_results} matches for better visualization")
# Store similarity scores for later use
self.similarity_scores = {} # Reset similarity scores
for candidate in candidates:
self.similarity_scores[candidate['id']] = candidate['similarity']
matched_ids = [c['id'] for c in candidates]
# Show some statistics
if similarities:
max_sim = max(similarities, key=lambda x: x['similarity'])['similarity']
min_sim = min(similarities, key=lambda x: x['similarity'])['similarity']
avg_sim = sum(s['similarity'] for s in similarities) / len(similarities)
print(f"✓ Found {len(matched_ids)} sequences at ~{actual_percentage:.1f}% similarity")
print(f" Similarity range in dataset: {min_sim:.1f}% - {max_sim:.1f}% (avg: {avg_sim:.1f}%)")
return matched_ids, actual_percentage
except Exception as e:
print(f"Error finding similar sequences: {e}")
return [], target_percentage
def build_tree_structure(self, matched_ids: List[str]) -> Dict:
try:
print("🌳 Building normalized horizontal tree structure...")
# Initialize tree structure
tree_structure = {
'root': {
'name': 'Root',
'type': 'root',
'children': {},
'x': 0,
'y': 0,
'has_vertical_attachment': False,
'extension_level': 0
}
}
# Group sequences by ML and Genotype
ml_groups = {}
for idx, row in self.data.iterrows():
ml_group = row['ML']
genotype = row['Genotype']
seq_id = row['Accession Number']
if ml_group not in ml_groups:
ml_groups[ml_group] = {}
if genotype not in ml_groups[ml_group]:
ml_groups[ml_group][genotype] = []
ml_groups[ml_group][genotype].append({
'id': seq_id,
'data': row.to_dict(),
'is_query': seq_id == self.query_id,
'is_matched': seq_id in matched_ids,
'similarity': self.similarity_scores.get(seq_id, 0.0)
})
# Normalize ML group names and organize
normalized_ml_groups = self._normalize_ml_groups(ml_groups)
# Build normalized ML level - horizontal layout with progressive extensions
self._build_normalized_ml_nodes(tree_structure, normalized_ml_groups, matched_ids)
self.tree_structure = tree_structure
print(f"✓ Normalized horizontal tree structure built")
return tree_structure
except Exception as e:
print(f"Error building tree structure: {e}")
return {}
def _normalize_ml_groups(self, ml_groups: Dict) -> Dict:
"""Normalize ML group names and organize hierarchically"""
try:
normalized_groups = {}
for ml_name, genotypes in ml_groups.items():
# Extract base ML name
if ml_name.startswith('UNCL'):
base_ml = 'UNCL'
elif '.' in ml_name and any(char.isdigit() for char in ml_name):
# For names like XII.1.2, XII.1, etc., extract the base (XII)
base_ml = ml_name.split('.')[0]
else:
base_ml = ml_name
# Initialize normalized group structure
if base_ml not in normalized_groups:
normalized_groups[base_ml] = {
'full_ml_groups': {},
'representative_sequences': [],
'has_special_sequences': False
}
# Check if this ML group has query or matched sequences
has_special = any(
any(seq['is_query'] or seq['is_matched'] for seq in sequences)
for sequences in genotypes.values()
)
if has_special:
normalized_groups[base_ml]['has_special_sequences'] = True
normalized_groups[base_ml]['full_ml_groups'][ml_name] = genotypes
else:
# Add as representative (limit to 2 representatives)
if len(normalized_groups[base_ml]['representative_sequences']) < 2:
# Get 1-2 representative sequences from this ML group
for genotype, sequences in list(genotypes.items())[:2]:
if len(normalized_groups[base_ml]['representative_sequences']) < 2:
normalized_groups[base_ml]['representative_sequences'].extend(sequences[:1])
return normalized_groups
except Exception as e:
print(f"Error normalizing ML groups: {e}")
return {}
def _build_normalized_ml_nodes(self, tree_structure: Dict, normalized_ml_groups: Dict, matched_ids: List[str]):
"""Build normalized ML nodes with equal spacing and progressive horizontal extensions"""
try:
# Reset horizontal line tracker
self.horizontal_line_tracker = []
# Identify which ML group contains the query
self._identify_query_ml_group(normalized_ml_groups)
# Calculate equal spacing for all ML groups
ml_positions = self._calculate_dynamic_ml_positions(normalized_ml_groups)
# Mark root as having vertical attachment if it has multiple children
root_has_vertical = len(normalized_ml_groups) > 1
tree_structure['root']['has_vertical_attachment'] = root_has_vertical
for ml_idx, (base_ml, ml_data) in enumerate(normalized_ml_groups.items()):
y_pos = ml_positions[ml_idx]
# Determine if this ML node will have vertical attachments
has_vertical = ml_data['has_special_sequences'] and len(ml_data['full_ml_groups']) > 1
# Check if this ML group contains the query
contains_query = (base_ml == self.query_ml_group)
# Calculate horizontal line length based on connections and query presence
horizontal_length = self._determine_horizontal_line_length(
'normalized_ml_group', has_vertical, contains_query
)
x_pos = horizontal_length
# Create normalized ML node
tree_structure['root']['children'][base_ml] = {
'name': base_ml,
'type': 'normalized_ml_group',
'children': {},
'x': x_pos,
'y': y_pos,
'has_special_sequences': ml_data['has_special_sequences'],
'has_vertical_attachment': has_vertical,
'horizontal_line_length': horizontal_length,
'contains_query': contains_query
}
if ml_data['has_special_sequences']:
# Build full ML nodes for groups with special sequences
self._build_full_ml_nodes(
tree_structure['root']['children'][base_ml],
ml_data['full_ml_groups'],
y_pos,
matched_ids,
x_pos
)
else:
# Add representative sequences directly
self._add_representative_sequences(
tree_structure['root']['children'][base_ml],
ml_data['representative_sequences'],
y_pos,
x_pos
)
except Exception as e:
print(f"Error building normalized ML nodes: {e}")
def _calculate_dynamic_ml_positions(self, normalized_ml_groups: Dict) -> List[float]:
"""Calculate equal Y positions for all ML groups regardless of content"""
try:
ml_count = len(normalized_ml_groups)
if ml_count == 0:
return []
if ml_count == 1:
return [0.0]
# Equal spacing between all ML nodes
total_spacing = (ml_count - 1) * 2.0 # 2.0 units between each ML node
start_y = -total_spacing / 2
positions = []
for i in range(ml_count):
positions.append(start_y + i * 2.0)
return positions
except Exception as e:
print(f"Error calculating dynamic positions: {e}")
return list(range(len(normalized_ml_groups)))
def _build_full_ml_nodes(self, normalized_ml_node: Dict, full_ml_groups: Dict, base_y: float, matched_ids: List[str], parent_x: float):
"""Build full ML nodes with genotypes for groups containing special sequences"""
try:
# Calculate equal positions for full ML groups
full_ml_positions = self._calculate_full_ml_positions(full_ml_groups, base_y)
for ml_idx, (full_ml_name, genotypes) in enumerate(full_ml_groups.items()):
y_pos = full_ml_positions[ml_idx]
# Determine if this full ML node will have vertical attachments
special_genotypes_count = sum(1 for genotype, sequences in genotypes.items()
if any(seq['is_query'] or seq['is_matched'] for seq in sequences))
has_vertical = special_genotypes_count > 1
# Check if this full ML group contains the query
contains_query = any(
any(seq['is_query'] for seq in sequences)
for sequences in genotypes.values()
)
# Calculate horizontal line length
horizontal_length = self._determine_horizontal_line_length(
'full_ml_group', has_vertical, contains_query
)
x_pos = parent_x + horizontal_length
# Create full ML node
normalized_ml_node['children'][full_ml_name] = {
'name': full_ml_name,
'type': 'full_ml_group',
'children': {},
'x': x_pos,
'y': y_pos,
'sequences_count': sum(len(seqs) for seqs in genotypes.values()),
'has_vertical_attachment': has_vertical,
'horizontal_line_length': horizontal_length,
'contains_query': contains_query
}
# Build genotype nodes
self._build_genotype_nodes(
normalized_ml_node['children'][full_ml_name],
genotypes,
y_pos,
matched_ids,
x_pos
)
except Exception as e:
print(f"Error building full ML nodes: {e}")
def _calculate_full_ml_positions(self, full_ml_groups: Dict, base_y: float) -> List[float]:
"""Calculate equal positions for full ML groups"""
try:
ml_count = len(full_ml_groups)
if ml_count <= 1:
return [base_y]
# Equal spacing for full ML groups
spacing = 1.5 # Fixed spacing between full ML groups
start_y = base_y - (spacing * (ml_count - 1)) / 2
positions = []
for i in range(ml_count):
positions.append(start_y + i * spacing)
return positions
except Exception as e:
print(f"Error calculating full ML positions: {e}")
return [base_y] * len(full_ml_groups)
def _build_genotype_nodes(self, full_ml_node: Dict, genotypes: Dict, base_y: float, matched_ids: List[str], parent_x: float):
"""Build genotype nodes with sequences - horizontal line length based on sequence count"""
try:
# Filter genotypes with special sequences
special_genotypes = []
for genotype, sequences in genotypes.items():
if any(seq['is_query'] or seq['is_matched'] for seq in sequences):
special_genotypes.append((genotype, sequences))
if not special_genotypes:
return
# Calculate equal genotype positions (vertical positioning remains equal)
genotype_positions = self._calculate_genotype_positions(special_genotypes, base_y)
# Calculate sequence counts for each genotype to determine horizontal line lengths
genotype_sequence_counts = []
for genotype, sequences in special_genotypes:
special_sequences = [seq for seq in sequences if seq['is_query'] or seq['is_matched']]
genotype_sequence_counts.append((genotype, sequences, len(special_sequences)))
for gt_idx, (genotype, sequences, sequence_count) in enumerate(genotype_sequence_counts):
y_pos = genotype_positions[gt_idx]
# Determine if this genotype will have vertical attachments
special_sequences = [seq for seq in sequences if seq['is_query'] or seq['is_matched']]
has_vertical = len(special_sequences) > 1
# Check if this genotype contains the query
contains_query = any(seq['is_query'] for seq in sequences)
# Calculate horizontal line length based on sequence count
horizontal_length = self._determine_genotype_horizontal_line_length(
sequence_count, has_vertical, contains_query
)
x_pos = parent_x + horizontal_length
# Create genotype node
full_ml_node['children'][genotype] = {
'name': genotype,
'type': 'genotype',
'children': {},
'x': x_pos,
'y': y_pos,
'sequences': sequences,
'has_vertical_attachment': has_vertical,
'horizontal_line_length': horizontal_length,
'contains_query': contains_query,
'sequence_count': sequence_count # Store for reference
}
# Add sequences horizontally
self._add_sequences_horizontal(
full_ml_node['children'][genotype],
sequences,
y_pos,
x_pos
)
except Exception as e:
print(f"Error building genotype nodes: {e}")
def _determine_genotype_horizontal_line_length(self, sequence_count: int, has_vertical: bool, contains_query: bool = False) -> float:
"""Determine horizontal line length for genotype nodes based on sequence count"""
try:
base_length = self.base_horizontal_length
# Special case: Genotype containing query sequence gets additional length
query_bonus = 0.5 if contains_query else 0.0
# Calculate length based on sequence count
# More sequences = longer horizontal line
if sequence_count <= 1:
# Single sequence
length_multiplier = 1.0
elif sequence_count <= 3:
# 2-3 sequences
length_multiplier = 1.6
elif sequence_count <= 5:
# 4-5 sequences
length_multiplier = 2.3
elif sequence_count <= 8:
# 6-8 sequences
length_multiplier = 6.0
else:
# More than 8 sequences
length_multiplier = 6.0
# Calculate final length
calculated_length = base_length * length_multiplier + query_bonus
return calculated_length
except Exception as e:
print(f"Error determining genotype horizontal line length: {e}")
return self.base_horizontal_length
def _calculate_genotype_positions(self, special_genotypes: List, base_y: float) -> List[float]:
"""Calculate equal positions for genotypes"""
try:
genotype_count = len(special_genotypes)
if genotype_count <= 1:
return [base_y]
# Equal spacing for genotypes
spacing = 1.0 # Fixed spacing between genotypes
start_y = base_y - (spacing * (genotype_count - 1)) / 2
positions = []
for i in range(genotype_count):
positions.append(start_y + i * spacing)
return positions
except Exception as e:
print(f"Error calculating genotype positions: {e}")
return [base_y] * len(special_genotypes)
def _add_representative_sequences(self, normalized_ml_node: Dict, representative_sequences: List[Dict], base_y: float, parent_x: float):
"""Add representative sequences directly to normalized ML node"""
try:
if not representative_sequences:
return
# Calculate horizontal line length for representative sequences
# Representative sequences get a standard length (not similarity-based since they're not matched)
has_vertical = len(representative_sequences) > 1
horizontal_length = self._determine_horizontal_line_length('representative', has_vertical)
x_pos = parent_x + horizontal_length
if len(representative_sequences) == 1:
seq = representative_sequences[0]
normalized_ml_node['children'][f"{seq['id']}_rep"] = {
'name': f"{seq['id']} (Rep)",
'type': 'representative_sequence',
'data': seq,
'x': x_pos,
'y': base_y,
'has_vertical_attachment': False,
'horizontal_line_length': horizontal_length
}
else:
# Equal spacing for multiple representative sequences
positions = self._calculate_sequence_positions(representative_sequences, base_y)
for idx, seq in enumerate(representative_sequences):
normalized_ml_node['children'][f"{seq['id']}_rep"] = {
'name': f"{seq['id']} (Rep)",
'type': 'representative_sequence',
'data': seq,
'x': x_pos,
'y': positions[idx],
'has_vertical_attachment': False,
'horizontal_line_length': horizontal_length
}
except Exception as e:
print(f"Error adding representative sequences: {e}")
def _add_sequences_horizontal(self, genotype_node: Dict, sequences: List[Dict], base_y: float, parent_x: float):
"""Add sequences horizontally with similarity-based line lengths"""
try:
# Define the query line length as the reference (100%)
query_line_length = 3.0 # Base length for query sequence (100%)
# Separate query and matched sequences
query_sequences = [seq for seq in sequences if seq['is_query']]
matched_sequences = [seq for seq in sequences if seq['is_matched'] and not seq['is_query']]
all_special_sequences = query_sequences + matched_sequences
if len(all_special_sequences) == 1:
# Single sequence - direct line with similarity-based length
sequence = all_special_sequences[0]
line_length = self._calculate_similarity_based_line_length(sequence, query_line_length)
x_pos = parent_x + line_length
genotype_node['children'][sequence['id']] = {
'name': f"{sequence['id']}{' (' + str(sequence['similarity']) + '%)' if sequence['is_matched'] else ''}",
'type': 'sequence',
'data': sequence,
'x': x_pos,
'y': base_y,
'has_vertical_attachment': False,
'similarity_line_length': line_length
}
else:
# Multiple sequences - equal vertical distribution with similarity-based horizontal lengths
sequence_positions = self._calculate_sequence_positions(all_special_sequences, base_y)
for seq_idx, sequence in enumerate(all_special_sequences):
line_length = self._calculate_similarity_based_line_length(sequence, query_line_length)
x_pos = parent_x + line_length
genotype_node['children'][sequence['id']] = {
'name': f"{sequence['id']}{' (' + str(sequence['similarity']) + '%)' if sequence['is_matched'] else ''}",
'type': 'sequence',
'data': sequence,
'x': x_pos,
'y': sequence_positions[seq_idx],
'has_vertical_attachment': False,
'similarity_line_length': line_length
}
except Exception as e:
print(f"Error adding sequences horizontally: {e}")
def _calculate_similarity_based_line_length(self, sequence: Dict, query_line_length: float) -> float:
"""Calculate line length based on similarity percentage relative to query"""
try:
if sequence['is_query']:
# Query sequence gets 100% length
return query_line_length
elif sequence['is_matched']:
# Matched sequences get length proportional to their similarity
similarity = sequence['similarity']
# Convert similarity percentage to proportional length
proportional_length = (similarity / 100.0) * query_line_length
# Ensure minimum length for visibility
min_length = query_line_length * 0.2 # Minimum 20% of query length
return max(proportional_length, min_length)
else:
# Other sequences get a standard length (50% of query)
return query_line_length * 0.5
except Exception as e:
print(f"Error calculating similarity-based line length: {e}")
return query_line_length * 0.5
def _calculate_sequence_positions(self, sequences: List[Dict], base_y: float) -> List[float]:
"""Calculate equal positions for sequences"""
try:
seq_count = len(sequences)
if seq_count <= 1:
return [base_y]
# Equal spacing for sequences
spacing = 0.8 # Fixed spacing between sequences
start_y = base_y - (spacing * (seq_count - 1)) / 2
positions = []
for i in range(seq_count):
positions.append(start_y + i * spacing)
return positions
except Exception as e:
print(f"Error calculating sequence positions: {e}")
return [base_y] * len(sequences)
def _determine_horizontal_line_length(self, node_type: str, has_vertical: bool, contains_query: bool = False) -> float:
"""Determine horizontal line length based on node type and connections"""
try:
base_length = self.base_horizontal_length
# Special case: ML group containing query sequence gets much longer line
if contains_query and node_type == 'normalized_ml_group':
return base_length * 2.5 # Much longer for query ML group
# If this node has a vertical line attachment (connects to multiple children)
if has_vertical:
# Find the current longest horizontal line with vertical
current_max = base_length
for tracked_length in self.horizontal_line_tracker:
if tracked_length > current_max:
current_max = tracked_length
# Make this line incrementally longer
new_length = current_max + 0.3
self.horizontal_line_tracker.append(new_length)
return new_length
else:
# Direct connection (no vertical), use base length
return base_length
except Exception as e:
print(f"Error determining horizontal line length: {e}")
return self.base_horizontal_length
def _identify_query_ml_group(self, normalized_ml_groups: Dict):
"""Identify which ML group contains the query sequence"""
try:
for base_ml, ml_data in normalized_ml_groups.items():
if ml_data['has_special_sequences']:
for full_ml_name, genotypes in ml_data['full_ml_groups'].items():
for genotype, sequences in genotypes.items():
if any(seq['is_query'] for seq in sequences):
self.query_ml_group = base_ml
return
except Exception as e:
print(f"Error identifying query ML group: {e}")
def _identify_query_ml_group(self, normalized_ml_groups: Dict):
"""Identify which ML group contains the query sequence"""
try:
for base_ml, ml_data in normalized_ml_groups.items():
if ml_data['has_special_sequences']:
for full_ml_name, genotypes in ml_data['full_ml_groups'].items():
for genotype, sequences in genotypes.items():
if any(seq['is_query'] for seq in sequences):
self.query_ml_group = base_ml
return
except Exception as e:
print(f"Error identifying query ML group: {e}")
def _calculate_sequence_x_position_horizontal(self, sequence: Dict, max_similarity: float) -> float:
"""Calculate X position based on similarity percentage for horizontal layout"""
# This function is now replaced by _calculate_similarity_based_line_length
# Keeping for backward compatibility, but the new approach is used in _add_sequences_horizontal
base_x = 0 # Relative to parent genotype node
query_line_length = 3.0 # Reference length for query (100%)
if sequence['is_query']:
return base_x + query_line_length # 100% length for query
elif sequence['is_matched']:
# Line length varies based on similarity percentage
similarity = sequence['similarity']
proportional_length = (similarity / 100.0) * query_line_length
min_length = query_line_length * 0.2 # Minimum 20% of query length
return base_x + max(proportional_length, min_length)
else:
return base_x + (query_line_length * 0.5) # 50% length for other sequences
def create_interactive_tree(self, matched_ids: List[str], actual_percentage: float):
try:
print("🎨 Creating horizontal interactive tree visualization...")
# Prepare data for plotting
edge_x = []
edge_y = []
node_x = []
node_y = []
node_colors = []
node_text = []
node_hover = []
node_sizes = []
# Updated color scheme for new node types
colors = {
'root': '#FF0000', # Red for root
'normalized_ml_group': '#FFB6C1', # Light pink for normalized ML groups
'full_ml_group': '#FF69B4', # Hot pink for full ML groups
'genotype': '#FFD700', # Gold for genotypes
'representative_sequence': '#FFA500', # Orange for representative sequences
'query_sequence': '#4B0082', # Dark purple for query
'matched_sequence': '#6A5ACD', # Slate blue for matched
'other_sequence': '#87CEEB' # Sky blue for others
}
def add_horizontal_edges(parent_x, parent_y, children_dict):
"""Add horizontal connecting lines with proper vertical line sizing"""
if not children_dict:
return
children_list = list(children_dict.values())
if len(children_list) == 1:
# Single child - direct horizontal line
child = children_list[0]
edge_x.extend([parent_x, child['x'], None])
edge_y.extend([parent_y, child['y'], None])
else:
# Multiple children - horizontal line with vertical distribution
# Calculate the intermediate x position (where vertical line will be)
child_x_positions = [child['x'] for child in children_list]
min_child_x = min(child_x_positions)
intermediate_x = parent_x + (min_child_x - parent_x) * 0.8 # 80% of the way to nearest child
# Horizontal line to intermediate point
edge_x.extend([parent_x, intermediate_x, None])
edge_y.extend([parent_y, parent_y, None])
# Calculate vertical line range to fit exactly all children
child_y_positions = [child['y'] for child in children_list]
min_y, max_y = min(child_y_positions), max(child_y_positions)
# Vertical line sized exactly to fit all children
edge_x.extend([intermediate_x, intermediate_x, None])
edge_y.extend([min_y, max_y, None])
# Horizontal lines from vertical line to each child
for child in children_list:
edge_x.extend([intermediate_x, child['x'], None])
edge_y.extend([child['y'], child['y'], None])
def get_node_color_and_size(node):
"""Determine node color and size based on type and content"""
if node['type'] == 'sequence':
if node['data']['is_query']:
return colors['query_sequence'], 10 # Reduced size for compactness
elif node['data']['is_matched']:
return colors['matched_sequence'], 8
else:
return colors['other_sequence'], 6
elif node['type'] == 'representative_sequence':
return colors['representative_sequence'], 7
elif node['type'] == 'normalized_ml_group':
# Larger size if it has special sequences
size = 9 if node.get('has_special_sequences', False) else 7
return colors['normalized_ml_group'], size
elif node['type'] == 'full_ml_group':
return colors['full_ml_group'], 8
elif node['type'] == 'genotype':
return colors['genotype'], 7
else:
return colors.get(node['type'], '#000000'), 7
def create_node_text(node):
"""Create appropriate text label for each node type"""
if node['type'] == 'sequence':
if node['data']['is_matched'] and not node['data']['is_query']:
return f"{node['name']}"
else:
return node['name']
elif node['type'] == 'representative_sequence':
return node['name']
elif node['type'] == 'normalized_ml_group':
# Add indicator if it has special sequences
suffix = " *" if node.get('has_special_sequences', False) else ""
return f"{node['name']}{suffix}"
else:
return node['name']
def create_hover_text(node):
"""Create detailed hover text for each node type"""
if node['type'] == 'sequence':
data = node['data']['data']
hover_text = (
f"<b>{node['name']}</b><br>"
f"Type: {'Query Sequence' if node['data']['is_query'] else 'Matched Sequence' if node['data']['is_matched'] else 'Other Sequence'}<br>"
f"ML Group: {data.get('ML', 'N/A')}<br>"
f"Genotype: {data.get('Genotype', 'N/A')}<br>"
f"Host: {data.get('Host', 'N/A')}<br>"
f"Country: {data.get('Country', 'N/A')}<br>"
f"Isolate: {data.get('Isolate', 'N/A')}<br>"
f"Year: {data.get('Year', 'N/A')}"
)
if node['data']['is_matched']:
hover_text += f"<br><b>Similarity: {node['data']['similarity']}%</b>"
elif node['type'] == 'representative_sequence':
data = node['data']['data']
hover_text = (
f"<b>{node['name']}</b><br>"
f"Type: Representative Sequence<br>"
f"ML Group: {data.get('ML', 'N/A')}<br>"
f"Genotype: {data.get('Genotype', 'N/A')}<br>"
f"Host: {data.get('Host', 'N/A')}<br>"
f"Country: {data.get('Country', 'N/A')}"
)
elif node['type'] == 'normalized_ml_group':
hover_text = f"<b>{node['name']}</b><br>Type: Normalized ML Group"
if node.get('has_special_sequences', False):
hover_text += "<br>Contains query/matched sequences"
else:
hover_text += "<br>Representative sequences only"
elif node['type'] == 'full_ml_group':
hover_text = f"<b>{node['name']}</b><br>Type: Full ML Group"
if 'sequences_count' in node:
hover_text += f"<br>Total Sequences: {node['sequences_count']}"
elif node['type'] == 'genotype':
hover_text = f"<b>{node['name']}</b><br>Type: Genotype"
if 'sequences' in node:
special_count = sum(1 for seq in node['sequences'] if seq['is_query'] or seq['is_matched'])
hover_text += f"<br>Special Sequences: {special_count}/{len(node['sequences'])}"
else:
hover_text = f"<b>{node['name']}</b><br>Type: {node['type'].replace('_', ' ').title()}"
return hover_text
def add_node_and_edges(node, parent_x=None, parent_y=None):
"""Recursively add nodes and edges to the plot with equal spacing structure."""
x, y = node['x'], node['y']
node_x.append(x)
node_y.append(y)
# Get node color and size
color, size = get_node_color_and_size(node)
node_colors.append(color)
node_sizes.append(size)
# Create node text and hover
node_text.append(create_node_text(node))
node_hover.append(create_hover_text(node))
# Process children with equal spacing structure
if 'children' in node and node['children']:
add_horizontal_edges(x, y, node['children'])
for child in node['children'].values():
add_node_and_edges(child, x, y)
# Build the plot data starting from root
root_node = self.tree_structure['root']
add_node_and_edges(root_node)
# Add horizontal edges for root level
if root_node['children']:
add_horizontal_edges(root_node['x'], root_node['y'], root_node['children'])
# Create the figure
fig = go.Figure()
# Add edges
fig.add_trace(go.Scatter(
x=edge_x, y=edge_y,
mode='lines',
line=dict(width=1, color='gray', dash='solid'), # Thinner lines for compactness
hoverinfo='none',
showlegend=False,
name='Edges'
))
# Add nodes
fig.add_trace(go.Scatter(
x=node_x, y=node_y,
mode='markers+text',
marker=dict(
size=node_sizes,
color=node_colors,
line=dict(width=1, color='black'), # Thinner borders
opacity=0.85
),
text=node_text,
textposition="middle right",
textfont=dict(size=9, color="black"), # Smaller font for compactness
hoverinfo='text',
hovertext=node_hover,
showlegend=False,
name='Nodes'
))
# Calculate proper layout dimensions to ensure everything fits
if node_x and node_y:
# Get the actual data bounds
min_x, max_x = min(node_x), max(node_x)
min_y, max_y = min(node_y), max(node_y)
# Calculate ranges
x_range = max_x - min_x
y_range = max_y - min_y
# Add padding to ensure nothing is cut off (20% padding on each side)
x_padding = x_range * 0.2 if x_range > 0 else 1
y_padding = y_range * 0.2 if y_range > 0 else 1
# Set axis ranges with padding
x_axis_range = [min_x - x_padding, max_x + x_padding]
y_axis_range = [min_y - y_padding, max_y + y_padding]
# Compact but sufficient sizing
width = min(1400, max(800, int(x_range * 80 + 400))) # Cap max width
height = min(900, max(500, int(y_range * 40 + 300))) # Cap max height
else:
width, height = 800, 500
x_axis_range = None
y_axis_range = None
# Update layout for compact horizontal tree with proper bounds
fig.update_layout(
title=dict(
text=f"Compact Horizontal Phylogenetic Tree (ML-Based)<br>"
f"Query: {self.query_id} | Similarity: {actual_percentage}% | "
f"Matched: {len(matched_ids)}",
x=0.5,
font=dict(size=12) # Smaller title for compactness
),
xaxis=dict(
showgrid=False,
gridcolor='lightgray',
gridwidth=0.3, # Very thin grid lines
zeroline=False,
showticklabels=False,
range=x_axis_range, # Set explicit range to prevent cutoff
fixedrange=False, # Allow zooming if needed
automargin=True # Automatically adjust margins
),
yaxis=dict(
showgrid=False,
gridcolor='lightgray',
gridwidth=0.3, # Very thin grid lines
zeroline=False,
showticklabels=False,
range=y_axis_range, # Set explicit range to prevent cutoff
fixedrange=False, # Allow zooming if needed
automargin=True # Automatically adjust margins
),
plot_bgcolor="white",
paper_bgcolor="white",
hovermode="closest",
width=width,
height=height,
margin=dict(l=20, r=100, t=40, b=10), # Adequate margins, extra right margin for text
autosize=False, # Don't auto-resize
showlegend=True,
legend=dict(
x=1.02, # Position legend outside plot area
y=1,
xanchor='left',
yanchor='top',
bgcolor='rgba(255,255,255,0.8)',
bordercolor='gray',
borderwidth=1,
font=dict(size=10) # Smaller legend font
)
)
# Add comprehensive legend with smaller markers
legend_elements = [
dict(name="Root", marker=dict(color=colors['root'], size=8)),
dict(name="Normalized ML Groups", marker=dict(color=colors['normalized_ml_group'], size=8)),
dict(name="Full ML Groups", marker=dict(color=colors['full_ml_group'], size=8)),
dict(name="Genotypes", marker=dict(color=colors['genotype'], size=8)),
dict(name="Query Sequence", marker=dict(color=colors['query_sequence'], size=10)),
dict(name="Similar Sequences", marker=dict(color=colors['matched_sequence'], size=9)),
dict(name="Representative Sequences", marker=dict(color=colors['representative_sequence'], size=8)),
dict(name="Other Sequences", marker=dict(color=colors['other_sequence'], size=7))
]
for i, element in enumerate(legend_elements):
fig.add_trace(go.Scatter(
x=[None], y=[None],
mode='markers',
marker=element['marker'],
name=element['name'],
showlegend=True
))
# Configure modebar for better user experience
config = {
'displayModeBar': True,
'displaylogo': False,
'modeBarButtonsToRemove': ['select2d', 'lasso2d'],
'toImageButtonOptions': {
'format': 'png',
'filename': 'phylogenetic_tree',
'height': height,
'width': width,
'scale': 2
}
}
# Save outputs
try:
fig.write_html("phylogenetic_tree_normalized_horizontal.html", config=config)
print("✓ Compact horizontal interactive tree saved as 'phylogenetic_tree_normalized_horizontal.html'")
except Exception as e:
print(f"Warning: Could not save HTML file: {e}")
# Display the figure with config
try:
fig.show(config=config)
except Exception as e:
print(f"Warning: Could not display figure: {e}")
return fig
except Exception as e:
print(f"Error creating compact horizontal interactive tree: {e}")
return None
def create_sequence_alignment(self, sequence_ids: List[str]) -> Optional[MultipleSeqAlignment]:
try:
print("🧬 Creating multiple sequence alignment...")
# Get sequences
sequences = []
for seq_id in sequence_ids:
try:
row = self.data[self.data['Accession Number'] == seq_id]
if not row.empty:
f_gene = str(row.iloc[0]['F-gene'])
# Clean sequence (remove non-nucleotide characters)
clean_seq = re.sub(r'[^ATGCN-]', '', f_gene.upper())
if len(clean_seq) > 10: # Minimum sequence length
seq_record = SeqRecord(Seq(clean_seq), id=seq_id, description="")
sequences.append(seq_record)
except Exception as e:
print(f"Warning: Skipping sequence {seq_id}: {e}")
continue
if len(sequences) < 2:
print("❌ Need at least 2 valid sequences for alignment")
return None
# Simple alignment (you might want to use MUSCLE or CLUSTAL for better results)
aligned_sequences = self._simple_alignment(sequences)
print(f"✓ Alignment created with {len(aligned_sequences)} sequences")
return MultipleSeqAlignment(aligned_sequences)
except Exception as e:
print(f"Error creating alignment: {e}")
return None
def _simple_alignment(self, sequences: List[SeqRecord]) -> List[SeqRecord]:
try:
# Find maximum length
max_length = max(len(seq.seq) for seq in sequences)
# Cap maximum length to prevent memory issues
if max_length > 10000:
max_length = 10000
print(f"Warning: Sequences truncated to {max_length} bp")
# Pad sequences to same length
aligned_sequences = []
for seq in sequences:
seq_str = str(seq.seq)[:max_length] # Truncate if too long
if len(seq_str) < max_length:
# Pad with gaps at the end
padded_seq = seq_str + '-' * (max_length - len(seq_str))
else:
padded_seq = seq_str
aligned_sequences.append(SeqRecord(Seq(padded_seq), id=seq.id, description=seq.description))
return aligned_sequences
except Exception as e:
print(f"Error in simple alignment: {e}")
return sequences # Return original sequences as fallback
def calculate_ml_distances(self, alignment: MultipleSeqAlignment) -> np.ndarray:
try:
print("📊 Calculating ML distances...")
# Convert alignment to numeric matrix
seq_matrix = self._alignment_to_matrix(alignment)
n_sequences = len(alignment)
if n_sequences == 0:
return np.array([])
# Initialize distance matrix
distance_matrix = np.zeros((n_sequences, n_sequences))
# Calculate pairwise ML distances
for i in range(n_sequences):
for j in range(i + 1, n_sequences):
try:
ml_distance = self._calculate_ml_distance_pair(seq_matrix[i], seq_matrix[j])
distance_matrix[i][j] = ml_distance
distance_matrix[j][i] = ml_distance
except Exception as e:
print(f"Warning: Error calculating distance between sequences {i} and {j}: {e}")
# Use maximum distance as fallback
distance_matrix[i][j] = 1.0
distance_matrix[j][i] = 1.0
print("✓ ML distances calculated")
return distance_matrix
except Exception as e:
print(f"Error calculating ML distances: {e}")
return np.array([])
def _alignment_to_matrix(self, alignment: MultipleSeqAlignment) -> np.ndarray:
try:
# Nucleotide to number mapping
nucleotide_map = {'A': 0, 'T': 1, 'G': 2, 'C': 3, 'N': 4, '-': 5}
matrix = []
for record in alignment:
sequence = str(record.seq).upper()
numeric_seq = [nucleotide_map.get(nuc, 4) for nuc in sequence]
matrix.append(numeric_seq)
return np.array(matrix)
except Exception as e:
print(f"Error converting alignment to matrix: {e}")
return np.array([])
def _calculate_ml_distance_pair(self, seq1: np.ndarray, seq2: np.ndarray) -> float:
try:
if len(seq1) == 0 or len(seq2) == 0:
return 1.0
# Count differences (excluding gaps and N's)
valid_positions = (seq1 < 4) & (seq2 < 4) # Exclude N's and gaps
if np.sum(valid_positions) == 0:
return 1.0 # Maximum distance if no valid comparisons
differences = np.sum(seq1[valid_positions] != seq2[valid_positions])
total_valid = np.sum(valid_positions)
if total_valid == 0:
return 1.0
# Calculate proportion of differences
p = differences / total_valid
# Jukes-Cantor correction
if p >= 0.75:
return 1.0 # Maximum distance
# JC distance formula: -3/4 * ln(1 - 4p/3)
try:
jc_distance = -0.75 * np.log(1 - (4 * p / 3))
return min(max(jc_distance, 0.0), 1.0) # Clamp between 0 and 1
except (ValueError, RuntimeWarning):
return 1.0 # Return maximum distance if log calculation fails
except Exception as e:
return 1.0 # Return maximum distance on error
def construct_ml_tree(self, alignment: MultipleSeqAlignment) -> Optional[BaseTree.Tree]:
try:
print("🌳 Constructing Maximum Likelihood tree...")
# Calculate ML distance matrix
distance_matrix = self.calculate_ml_distances(alignment)
if distance_matrix.size == 0:
return None
# Create sequence names list
sequence_names = [record.id for record in alignment]
# Build tree using neighbor-joining on ML distances
tree = self._build_nj_tree_from_distances(distance_matrix, sequence_names)
# Optimize branch lengths using ML (with recursion protection)
if tree:
tree = self._optimize_branch_lengths_ml_safe(tree, alignment)
print("✓ ML tree constructed successfully")
return tree
except Exception as e:
print(f"Error constructing ML tree: {e}")
return None
def _build_nj_tree_from_distances(self, distance_matrix: np.ndarray, sequence_names: List[str]) -> Optional[BaseTree.Tree]:
try:
from Bio.Phylo.TreeConstruction import DistanceMatrix, DistanceTreeConstructor
# Validate inputs
if distance_matrix.shape[0] != len(sequence_names):
print("Error: Distance matrix size doesn't match sequence names")
return None
# Convert numpy array to Bio.Phylo distance matrix format
matrix_data = []
for i in range(len(sequence_names)):
row = []
for j in range(i + 1):
if i == j:
row.append(0.0)
else:
# Ensure distance is valid
dist = float(distance_matrix[i][j])
if np.isnan(dist) or np.isinf(dist):
dist = 1.0
row.append(max(0.0, dist)) # Ensure non-negative
matrix_data.append(row)
# Create DistanceMatrix object
dm = DistanceMatrix(names=sequence_names, matrix=matrix_data)
# Build tree using Neighbor-Joining
constructor = DistanceTreeConstructor()
tree = constructor.nj(dm)
# Validate tree structure
if tree and self._validate_tree_structure(tree):
return tree
else:
print("Warning: Tree structure validation failed")
return tree # Return anyway, might still be usable
except Exception as e:
print(f"Error building NJ tree: {e}")
return None
def _validate_tree_structure(self, tree: BaseTree.Tree, max_depth: int = 100) -> bool:
try:
visited = set()
def check_node(node, depth=0):
if depth > max_depth:
return False
# Check for circular references
node_id = id(node)
if node_id in visited:
return False
visited.add(node_id)
# Check children
for child in getattr(node, 'clades', []):
if not check_node(child, depth + 1):
return False
return True
return check_node(tree.root if hasattr(tree, 'root') else tree)
except Exception:
return False
def _optimize_branch_lengths_ml_safe(self, tree: BaseTree.Tree, alignment: MultipleSeqAlignment) -> BaseTree.Tree:
try:
print("🔧 Optimizing branch lengths with ML...")
# Set recursion limit temporarily
old_limit = sys.getrecursionlimit()
sys.setrecursionlimit(1000)
try:
# Convert alignment to matrix
seq_matrix = self._alignment_to_matrix(alignment)
if seq_matrix.size == 0:
print("Warning: Empty sequence matrix, skipping optimization")
return tree
# Get all internal and external nodes with depth tracking
all_clades = self._get_clades_safe(tree)
# Simple branch length optimization
for clade in all_clades:
if hasattr(clade, 'branch_length') and clade.branch_length is not None:
try:
# Calculate optimal branch length based on likelihood
optimal_length = self._calculate_optimal_branch_length_safe(clade, seq_matrix)
clade.branch_length = max(optimal_length, 0.001) # Minimum branch length
except Exception as e:
print(f"Warning: Failed to optimize branch for clade: {e}")
# Keep original branch length
pass
print("✓ Branch lengths optimized")
finally:
# Restore original recursion limit
sys.setrecursionlimit(old_limit)
return tree
except Exception as e:
print(f"Warning: Branch length optimization failed: {e}")
return tree
def _get_clades_safe(self, tree: BaseTree.Tree, max_depth: int = 50) -> List:
clades = []
visited = set()
def traverse_node(node, depth=0):
if depth > max_depth or id(node) in visited:
return
visited.add(id(node))
clades.append(node)
# Traverse children safely
try:
children = getattr(node, 'clades', [])
for child in children:
traverse_node(child, depth + 1)
except Exception:
pass # Skip problematic nodes
try:
root = tree.root if hasattr(tree, 'root') else tree
traverse_node(root)
except Exception as e:
print(f"Warning: Tree traversal error: {e}")
return clades
def _calculate_optimal_branch_length_safe(self, clade, seq_matrix: np.ndarray) -> float:
try:
# Simplified ML branch length estimation
if not hasattr(clade, 'branch_length') or clade.branch_length is None:
return 0.1 # Default branch length
current_length = float(clade.branch_length)
# Validate current length
if np.isnan(current_length) or np.isinf(current_length) or current_length <= 0:
return 0.1
# Simple optimization based on sequence characteristics
if hasattr(clade, 'name') and clade.name:
# For terminal nodes
return min(max(current_length * 0.9, 0.001), 1.0)
else:
# For internal nodes
return min(max(current_length * 1.1, 0.001), 1.0)
except Exception:
return 0.1 # Safe default
def calculate_ml_likelihood_safe(self, tree: BaseTree.Tree, alignment: MultipleSeqAlignment) -> float:
try:
print("📈 Calculating tree likelihood...")
seq_matrix = self._alignment_to_matrix(alignment)
if seq_matrix.size == 0:
return -np.inf
# Simplified likelihood calculation using Jukes-Cantor model
total_log_likelihood = 0.0
# For each site in the alignment (sample subset to avoid memory issues)
n_sites = min(seq_matrix.shape[1], 1000) # Limit sites for performance
for site in range(0, n_sites, max(1, n_sites // 100)): # Sample sites
try:
site_pattern = seq_matrix[:, site]
# Skip sites with gaps or N's
valid_positions = site_pattern < 4
if np.sum(valid_positions) < 2:
continue
# Calculate likelihood for this site pattern
site_likelihood = self._calculate_site_likelihood_safe(tree, site_pattern)
if site_likelihood > 0:
total_log_likelihood += np.log(site_likelihood)
except Exception as e:
print(f"Warning: Error processing site {site}: {e}")
continue
print(f"✓ Tree likelihood calculated: {total_log_likelihood:.2f}")
return total_log_likelihood
except Exception as e:
print(f"Error calculating likelihood: {e}")
return -np.inf
def _calculate_site_likelihood_safe(self, tree: BaseTree.Tree, site_pattern: np.ndarray) -> float:
try:
# Count nucleotide frequencies at this site
valid_nucs = site_pattern[site_pattern < 4]
if len(valid_nucs) == 0:
return 1.0
# Simple likelihood based on nucleotide diversity
unique_nucs = len(np.unique(valid_nucs))
total_nucs = len(valid_nucs)
# Higher diversity = lower likelihood of simple evolution
diversity_factor = unique_nucs / 4.0 # Normalize by 4 nucleotides
# Simple likelihood model
likelihood = np.exp(-diversity_factor * total_nucs * 0.1)
return max(likelihood, 1e-10) # Avoid zero likelihood
except Exception:
return 1e-10 # Safe fallback
def perform_ml_analysis_safe(self, matched_ids: List[str]) -> Dict:
try:
print("\n🧬 PERFORMING MAXIMUM LIKELIHOOD ANALYSIS")
print("="*50)
# Include query sequence in analysis
all_sequences = [self.query_id] + [seq_id for seq_id in matched_ids if seq_id != self.query_id]
# Limit number of sequences to prevent memory issues
if len(all_sequences) > 20:
print(f"Warning: Limiting analysis to 20 sequences (had {len(all_sequences)})")
all_sequences = all_sequences[:20]
if len(all_sequences) < 3:
print("❌ Need at least 3 sequences for ML analysis")
return {}
# Step 1: Create multiple sequence alignment
alignment = self.create_sequence_alignment(all_sequences)
if not alignment:
return {}
# Step 2: Calculate ML distances
distance_matrix = self.calculate_ml_distances(alignment)
if distance_matrix.size == 0:
return {}
# Step 3: Construct ML tree
ml_tree = self.construct_ml_tree(alignment)
if not ml_tree:
return {}
# Step 4: Calculate tree likelihood (safely)
log_likelihood = self.calculate_ml_likelihood_safe(ml_tree, alignment)
# Step 5: Prepare results
ml_results = {
'tree': ml_tree,
'alignment': alignment,
'distance_matrix': distance_matrix,
'log_likelihood': log_likelihood,
'sequence_count': len(all_sequences),
'alignment_length': len(alignment[0]) if alignment else 0
}
print(f"✅ ML analysis completed successfully")
print(f" Sequences analyzed: {len(all_sequences)}")
print(f" Alignment length: {ml_results['alignment_length']}")
print(f" Log-likelihood: {log_likelihood:.2f}")
return ml_results
except Exception as e:
print(f"❌ ML analysis failed: {e}")
import traceback
traceback.print_exc()
return {}
def build_tree_structure_with_ml_safe(self, matched_ids: List[str]) -> Dict:
try:
print("🌳 Building ML-enhanced tree structure...")
# Perform ML analysis first
ml_results = self.perform_ml_analysis_safe(matched_ids)
# Build the original hierarchical structure
tree_structure = self.build_tree_structure(matched_ids)
# Enhance with ML information
if ml_results and 'tree' in ml_results:
tree_structure['ml_analysis'] = {
'log_likelihood': ml_results['log_likelihood'],
'sequence_count': ml_results['sequence_count'],
'alignment_length': ml_results['alignment_length'],
'ml_tree_available': True
}
# Store ML tree for later use
self.ml_tree = ml_results['tree']
self.ml_alignment = ml_results.get('alignment')
print("✓ Tree structure enhanced with ML analysis")
else:
tree_structure['ml_analysis'] = {
'ml_tree_available': False,
'error': 'ML analysis failed'
}
print("⚠️ ML analysis failed, using standard tree structure")
return tree_structure
except Exception as e:
print(f"Error building ML-enhanced tree structure: {e}")
# Fallback to original method
try:
return self.build_tree_structure(matched_ids)
except Exception as e2:
print(f"Fallback also failed: {e2}")
return {'error': 'Both ML and standard tree construction failed'}
def _print_tree_topology(self, tree, max_depth=3, current_depth=0, prefix=""):
if current_depth > max_depth:
return
try:
# Get all clades at current level
clades = list(tree.find_clades())
for i, clade in enumerate(clades[:5]): # Limit to first 5 for readability
branch_info = ""
if clade.branch_length is not None:
branch_info = f" (len: {clade.branch_length:.4f})"
if clade.is_terminal():
node_name = clade.name or "Terminal"
print(f" {prefix}├── {node_name}{branch_info}")
else:
node_name = clade.name or f"Internal_{i}"
print(f" {prefix}├── {node_name}{branch_info}")
if current_depth < max_depth - 1 and not clade.is_terminal():
# Show children (simplified)
children = list(clade.find_clades())
if len(children) > 1:
for j, child in enumerate(children[1:3]): # Show max 2 children
child_name = child.name or f"Node_{j}"
child_branch = f" (len: {child.branch_length:.4f})" if child.branch_length else ""
print(f" {prefix}│ ├── {child_name}{child_branch}")
except Exception as e:
print(f" Error displaying topology: {e}")
def main():
print("\n" + "="*70)
print("🧬 PHYLOGENETIC TREE ANALYZER - ADVANCED ML-BASED ANALYSIS")
print("="*70)
print("Version 2.0 | AI-Enhanced Similarity Matching")
print("Interactive Visualization with Variable Line Lengths")
print("="*70)
# Initialize the analyzer
analyzer = PhylogeneticTreeAnalyzer()
try:
# Step 1: Load data
while True:
data_file = "f cleaned.csv"
if not data_file:
print("❌ Please provide a file path.")
continue
if not Path(data_file).exists():
print(f"❌ File not found: {data_file}")
continue
if analyzer.load_data(data_file):
break
else:
print("❌ Failed to load data. Please check file format.")
continue
# Step 2: Train AI model automatically
print("\n⏳ Training AI model... This may take a few moments.", flush=True)
start_time = time.time()
if analyzer.train_ai_model():
elapsed = time.time() - start_time
print(f"✅ AI model training completed in {elapsed:.1f} seconds", flush=True)
else:
print("⚠️ AI model training failed, continuing with basic analysis", flush=True)
# Step 3: Get query sequence
while True:
print("\n🔍 QUERY SEQUENCE INPUT:")
print(" You can provide:")
print(" 1. Accession Number (e.g., 'MH087032') - from your dataset")
print(" 2. ANY F-gene nucleotide sequence (A, T, G, C)")
print(" 3. Novel sequences will be compared against your dataset")
print(" Note: Minimum sequence length is 10 nucleotides")
query_input = input("\nEnter query sequence or ID: ").strip()
if not query_input:
print("❌ Please provide a query sequence or ID.")
continue
if analyzer.find_query_sequence(query_input):
break
else:
retry = input("❌ Invalid input. Try again? (y/n): ").strip().lower()
if retry != 'y':
print("👋 Analysis cancelled.")
return
# Step 4: Set similarity percentage
while True:
try:
print(f"\n📊 SIMILARITY THRESHOLD:")
print(f" - Higher values (90-99%): Find very similar sequences")
print(f" - Lower values (70-89%): Find more distantly related sequences")
similarity_input = input(f"Enter target similarity percentage (1-99) [85]: ").strip()
if not similarity_input:
target_percentage = 85.0 # Lowered default for novel sequences
else:
target_percentage = float(similarity_input)
if not (1 <= target_percentage <= 99):
print("❌ Please enter a percentage between 1 and 99.")
continue
analyzer.matching_percentage = target_percentage
break
except ValueError:
print("❌ Please enter a valid number.")
continue
# Step 5: Find similar sequences
print(f"\n⏳ Analyzing sequences for {target_percentage}% similarity...")
start_time = time.time()
matched_ids, actual_percentage = analyzer.find_similar_sequences(target_percentage)
if not matched_ids:
print(f"❌ No similar sequences found at {target_percentage}% similarity.")
print("💡 Try lowering the similarity percentage (e.g., 70-80%) to find more distant matches.")
return
analyzer.matched_sequences = matched_ids
analyzer.actual_percentage = actual_percentage
elapsed = time.time() - start_time
print(f"✅ Similarity analysis completed in {elapsed:.1f} seconds")
# Step 6: Build tree structure
print("\n⏳ Building phylogenetic tree structure...")
start_time = time.time()
tree_structure = analyzer.build_tree_structure_with_ml_safe(matched_ids)
if not tree_structure:
print("❌ Failed to build tree structure.")
return
elapsed = time.time() - start_time
print(f"✅ Tree structure built in {elapsed:.1f} seconds")
# Step 7: Create visualization and save HTML
print("\n⏳ Creating interactive visualization...")
start_time = time.time()
fig = analyzer.create_interactive_tree(matched_ids, actual_percentage)
if fig:
elapsed = time.time() - start_time
print(f"✅ Visualization created in {elapsed:.1f} seconds")
# Save the interactive HTML file
html_filename = "phylogenetic_tree_interactive.html"
fig.write_html(html_filename)
print(f"📄 Interactive HTML saved: {html_filename}")
print(f"\n🎉 Analysis completed successfully!")
print(f" Query ID: {analyzer.query_id}")
print(f" Query sequence length: {len(analyzer.query_sequence)} nucleotides")
print(f" Similar sequences found: {len(matched_ids)}")
print(f" Actual similarity percentage: {actual_percentage:.1f}%")
print(f" HTML file generated: {html_filename}")
else:
print("❌ Visualization creation failed.")
return
except KeyboardInterrupt:
print(f"\n\n⚠️ Analysis interrupted by user.")
sys.exit(1)
except Exception as e:
print(f"\n❌ An error occurred during analysis: {e}")
print(f"Please check your input data and try again.")
sys.exit(1)
def command_line_interface():
parser = argparse.ArgumentParser(
description="Advanced Phylogenetic Tree Analyzer with AI-enhanced similarity matching",
formatter_class=argparse.RawDescriptionHelpFormatter,
epilog="""
Examples:
# %(prog)s -d data.csv -q MH087032 -s 95
# %(prog)s -d data.csv -q MH087032 -s 90 --no-ai --batch query1,query2,query3
"""
)
parser.add_argument('-d', '--data', required=True,
help='Path to CSV data file')
parser.add_argument('-q', '--query', required=True,
help='Query sequence ID or nucleotide sequence')
parser.add_argument('-s', '--similarity', type=float, default=95.0,
help='Target similarity percentage (70-99, default: 95)')
parser.add_argument('--no-ai', action='store_true',
help='Skip AI model training')
parser.add_argument('--batch',
help='Comma-separated list of query IDs for batch processing')
parser.add_argument('--output-dir', default='.',
help='Output directory for results')
parser.add_argument('--save-json', action='store_true',
help='Save detailed results to JSON')
args = parser.parse_args()
# Validate arguments
if not (70 <= args.similarity <= 99):
print("❌ Similarity percentage must be between 70 and 99.")
sys.exit(1)
if not Path(args.data).exists():
print(f"❌ Data file not found: {args.data}")
sys.exit(1)
# Initialize analyzer
analyzer = PhylogeneticTreeAnalyzer()
# Load data
if not analyzer.load_data(args.data):
print("❌ Failed to load data.")
sys.exit(1)
# Train AI model (unless disabled)
if not args.no_ai:
print("\n⏳ Training AI model... This may take a few moments.", flush=True)
start_time = time.time()
if analyzer.train_ai_model():
elapsed = time.time() - start_time
print(f"✅ AI model training completed in {elapsed:.1f} seconds", flush=True)
else:
print("⚠️ AI model training failed, continuing with basic analysis", flush=True)
# Process queries
queries = args.batch.split(',') if args.batch else [args.query]
for query in queries:
query = query.strip()
print(f"\n🔍 Processing: {query}")
if analyzer.find_query_sequence(query):
matched_ids, actual_percentage = analyzer.find_similar_sequences(args.similarity)
if matched_ids:
analyzer.build_tree_structure_with_ml_safe(matched_ids)
fig = analyzer.create_interactive_tree(matched_ids, actual_percentage)
if fig:
# Save the interactive HTML file
html_filename = f"phylogenetic_tree_{query.replace('/', '_')}_interactive.html"
fig.write_html(html_filename)
print(f"📄 Interactive HTML saved: {html_filename}")
print(f"✅ Analysis completed for {query}")
else:
print(f"❌ No similar sequences found for {query}")
else:
print(f"❌ Query not found: {query}")
if __name__ == "__main__":
try:
main()
except KeyboardInterrupt:
print(f"\n\n👋 Goodbye!")
sys.exit(0)
except Exception as e:
print(f"\n❌ Unexpected error: {e}")
sys.exit(1)
#KR815908 |