bio-comparative-genomics-ancestral-reconstruction
This skill reconstructs ancestral protein and nucleotide sequences at internal nodes of phylogenetic trees using PAML and IQ-TREE marginal likelihood methods. It infers ancient sequences by analyzing evolutionary relationships and posterior probabilities across alignment positions. Use this when resurrecting extinct proteins, tracing molecular evolution across deep time, or inferring functional states at specific evolutionary divergence points.
git clone --depth 1 https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills /tmp/bio-comparative-genomics-ancestral-reconstruction && cp -r /tmp/bio-comparative-genomics-ancestral-reconstruction/skills/bio-comparative-genomics-ancestral-reconstruction ~/.claude/skills/bio-comparative-genomics-ancestral-reconstructionSKILL.md
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---
name: bio-comparative-genomics-ancestral-reconstruction
description: 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.
tool_type: mixed
primary_tool: PAML
measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes.
allowed-tools:
- read_file
- run_shell_command
---
# Ancestral Sequence Reconstruction
## PAML Ancestral Reconstruction
```python
'''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
```python
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': []}
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