Delegate independent tasks to specialized agents working concurrently with isolated context.
Ancestral Sequence Reconstruction
bio-comparative-genomics-ancestral-reconstruction
Reconstruct ancestral sequences at phylogenetic nodes using PAML and IQ-TREE marginal likelihood methods. Infer ancient protein sequences and trace evolutionary trajectories through sequence history. Use when inferring ancestral states for protein resurrection or tracing evolutionary history.
SKILL.md
Full skill instructions
Ancestral Sequence Reconstruction
PAML Ancestral Reconstruction
'''Ancestral sequence reconstruction with PAML codeml/baseml'''
import subprocess
import re
from Bio import SeqIO
from Bio.Seq import Seq
def create_asr_control(alignment, tree, output_dir, seq_type='protein'):
'''Create control file for ancestral reconstruction
RateAncestor = 1: Enable ancestral reconstruction
Generates RST file with ancestral sequences
For codons: Use codeml with seqtype = 1
For amino acids: Use codeml with seqtype = 2
For nucleotides: Use baseml
'''
if seq_type == 'protein':
ctl = f'''
seqfile = {alignment}
treefile = {tree}
outfile = {output_dir}/asr.mlc
seqtype = 2
model = 3
aaRatefile = wag.dat
RateAncestor = 1
cleandata = 0
'''
else: # codon
ctl = f'''
seqfile = {alignment}
treefile = {tree}
outfile = {output_dir}/asr.mlc
seqtype = 1
CodonFreq = 2
model = 0
NSsites = 0
RateAncestor = 1
cleandata = 0
'''
ctl_file = f'{output_dir}/asr.ctl'
with open(ctl_file, 'w') as f:
f.write(ctl)
return ctl_file
def parse_rst_file(rst_file):
'''Parse PAML RST file for ancestral sequences
RST contains:
- Tree with node numbers
- Ancestral sequences at each node
- Posterior probabilities for each site
Node numbering: Extant sequences first, then internal nodes
'''
ancestors = {}
current_node = None
current_seq = []
with open(rst_file) as f:
content = f.read()
# Find ancestral sequence section
if 'Ancestral reconstruction by' in content:
sections = content.split('Ancestral reconstruction by')
for section in sections[1:]:
lines = section.strip().split('\n')
for line in lines:
if line.startswith('node #'):
if current_node and current_seq:
ancestors[current_node] = ''.join(current_seq)
match = re.search(r'node #(\d+)', line)
if match:
current_node = f'Node_{match.group(1)}'
current_seq = []
elif current_node and line.strip() and not line.startswith(' '):
# Sequence line
seq_part = ''.join(line.split()[1:]) if len(line.split()) > 1 else ''
current_seq.append(seq_part)
if current_node and current_seq:
ancestors[current_node] = ''.join(current_seq)
return ancestors
def extract_marginal_probabilities(rst_file):
'''Extract site-wise posterior probabilities
High confidence: P > 0.95 (commonly used threshold)
Moderate confidence: P > 0.80
Low confidence: P < 0.80 (consider alternatives)
Report ambiguous sites for experimental validation
'''
site_probs = []
with open(rst_file) as f:
in_probs = False
for line in f:
if 'Prob of best state' in line:
in_probs = True
continue
if in_probs and line.strip():
parts = line.split()
if len(parts) >= 3:
try:
site = int(parts[0])
state = parts[1]
prob = float(parts[2])
site_probs.append({
'site': site,
'state': state,
'probability': prob,
'confidence': 'high' if prob > 0.95 else 'moderate' if prob > 0.8 else 'low'
})
except ValueError:
in_probs = False
return site_probs
IQ-TREE Ancestral Reconstruction
def run_iqtree_asr(alignment, tree=None, model='LG+G4', output_prefix='asr'):
'''Run IQ-TREE for ancestral sequence reconstruction
IQ-TREE provides:
- Marginal reconstruction (default)
- Joint reconstruction (-asr-joint)
- State file (.state) with probabilities
Advantages over PAML:
- Automatic model selection
- Better handling of gaps
- Faster for large datasets
'''
cmd = f'iqtree2 -s {alignment} -m {model} --ancestral -pre {output_prefix}'
if tree:
cmd += f' -te {tree}'
subprocess.run(cmd, shell=True)
return f'{output_prefix}.state'
def parse_iqtree_state(state_file):
'''Parse IQ-TREE .state file
Format: Node Site State Probability [other states and probs]
'''
ancestors = {}
with open(state_file) as f:
next(f) # Skip header
for line in f:
parts = line.strip().split('\t')
if len(parts) >= 4:
node = parts[0]
site = int(parts[1])
state = parts[2]
prob = float(parts[3])
if node not in ancestors:
ancestors[node] = {'sequence': [], 'probabilities': []}
ancestors[node]['sequence'].append(state)
ancestors[node]['probabilities'].append(prob)
# Convert to sequences
for node in ancestors:
ancestors[node]['sequence'] = ''.join(ancestors[node]['sequence'])
return ancestors
Alternative State Analysis
def get_alternative_states(site_probs, threshold=0.1):
'''Identify sites with plausible alternative ancestral states
Alternative states with P > 0.1 should be considered
for experimental validation (ancestral protein resurrection)
These sites may:
- Affect function differently
- Represent true ancestral ambiguity
- Be targets for directed evolution
'''
ambiguous_sites = []
for site_data in site_probs:
if 'alternatives' in site_data:
significant_alts = [
alt for alt in site_data['alternatives']
if alt['probability'] > threshold
]
if significant_alts:
ambiguous_sites.append({
'site': site_data['site'],
'best_state': site_data['state'],
'best_prob': site_data['probability'],
'alternatives': significant_alts
})
return ambiguous_sites
def calculate_sequence_confidence(site_probs):
'''Calculate overall confidence in ancestral sequence
Metrics:
- Mean posterior probability
- Fraction of high-confidence sites (P > 0.95)
- Number of ambiguous positions
'''
if not site_probs:
return None
probs = [s['probability'] for s in site_probs]
high_conf = sum(1 for p in probs if p > 0.95) / len(probs)
low_conf = sum(1 for p in probs if p < 0.8)
return {
'mean_probability': sum(probs) / len(probs),
'high_confidence_fraction': high_conf,
'low_confidence_sites': low_conf,
'total_sites': len(probs),
'overall_quality': 'high' if high_conf > 0.9 else 'moderate' if high_conf > 0.7 else 'low'
}
Ancestral Protein Resurrection
def design_asr_construct(ancestral_seq, extant_reference, ambiguous_sites):
'''Design constructs for ancestral protein resurrection
Strategy:
1. Use most probable state at each position
2. Create alternative constructs at ambiguous sites
3. Consider codon optimization for expression host
Validation:
- Test activity of resurrected proteins
- Compare to extant proteins
- Test alternative constructs at ambiguous positions
'''
constructs = [{'name': 'ASR_ML', 'sequence': ancestral_seq, 'description': 'Maximum likelihood ancestral'}]
# Create alternative constructs for ambiguous sites
for site in ambiguous_sites[:5]: # Limit to top 5 ambiguous
alt_seq = list(ancestral_seq)
best_alt = site['alternatives'][0]
alt_seq[site['site'] - 1] = best_alt['state']
constructs.append({
'name': f"ASR_alt_{site['site']}",
'sequence': ''.join(alt_seq),
'description': f"Alternative at position {site['site']}: {best_alt['state']}"
})
return constructs
Related Skills
- comparative-genomics/positive-selection - Selection analysis on ancestral branches
- comparative-genomics/ortholog-inference - Identify orthologs for reconstruction
- phylogenetics/modern-tree-inference - Generate trees for ASR
- alignment/pairwise-alignment - Prepare MSA for reconstruction
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