--> --- name: bio-alignment-msa-statistics description: Calculate alignment statistics including sequence identity, conservation scores, substitution matrices, and similarity metrics. Use when comparing alignment quality, measuring sequence divergence, and analyzing evolutionary patterns. tool_type: python primary_tool: Bio.Align measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools: - read_file - run_shell_command --- Calculate sequence id...
Scanned 9/8/2026
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---
name: bio-alignment-msa-statistics
description: Calculate alignment statistics including sequence identity, conservation scores, substitution matrices, and similarity metrics. Use when comparing alignment quality, measuring sequence divergence, and analyzing evolutionary patterns.
tool_type: python
primary_tool: Bio.Align
measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes.
allowed-tools:
- read_file
- run_shell_command
---
# MSA Statistics
Calculate sequence identity, conservation scores, substitution counts, and other alignment metrics.
## Required Import
```python
from Bio import AlignIO
from Bio.Align import substitution_matrices
from collections import Counter
import numpy as np
import math
```
## Pairwise Identity
### Calculate Identity Between Two Sequences
```python
def pairwise_identity(seq1, seq2):
matches = sum(a == b and a != '-' for a, b in zip(seq1, seq2))
aligned_positions = sum(a != '-' or b != '-' for a, b in zip(seq1, seq2))
return matches / aligned_positions if aligned_positions > 0 else 0
alignment = AlignIO.read('alignment.fasta', 'fasta')
seq1, seq2 = str(alignment[0].seq), str(alignment[1].seq)
identity = pairwise_identity(seq1, seq2)
print(f'Identity: {identity * 100:.1f}%')
```
### Identity Matrix for All Sequences
```python
def identity_matrix(alignment):
n = len(alignment)
matrix = np.zeros((n, n))
for i in range(n):
for j in range(i, n):
seq_i = str(alignment[i].seq)
seq_j = str(alignment[j].seq)
ident = pairwise_identity(seq_i, seq_j)
matrix[i, j] = matrix[j, i] = ident
return matrix
alignment = AlignIO.read('alignment.fasta', 'fasta')
mat = identity_matrix(alignment)
seq_ids = [r.id for r in alignment]
print('Pairwise Identity Matrix:')
print(f'{"":>10}', ' '.join(f'{s[:8]:>8}' for s in seq_ids))
for i, row in enumerate(mat):
print(f'{seq_ids[i][:10]:>10}', ' '.join(f'{v*100:>7.1f}%' for v in row))
```
## Conservation Score
### Per-Column Conservation
```python
def column_conservation(alignment, col_idx, ignore_gaps=True):
column = alignment[:, col_idx]
if ignore_gaps:
column = column.replace('-', '')
if not column:
return 0.0
counts = Counter(column)
most_common_count = counts.most_common(1)[0][1]
return most_common_count / len(column)
alignment = AlignIO.read('alignment.fasta', 'fasta')
for i in range(min(20, alignment.get_alignment_length())):
cons = column_conservation(alignment, i)
print(f'Column {i}: {cons*100:.0f}% conserved')
```
### Average Conservation Across Alignment
```python
def average_conservation(alignment, ignore_gaps=True):
scores = []
for col_idx in range(alignment.get_alignment_length()):
scores.append(column_conservation(alignment, col_idx, ignore_gaps))
return sum(scores) / len(scores)
avg_cons = average_conservation(alignment)
print(f'Average conservation: {avg_cons*100:.1f}%')
```
### Conservation Profile
```python
def conservation_profile(alignment, window=10):
profile = []
for i in range(alignment.get_alignment_length()):
start = max(0, i - window // 2)
end = min(alignment.get_alignment_length(), i + window // 2)
scores = [column_conservation(alignment, j) for j in range(start, end)]
profile.append(sum(scores) / len(scores))
return profile
profile = conservation_profile(alignment, window=10)
```
## Substitution Counts
### Count Substitutions from Alignment
```python
def substitution_counts(alignment):
from collections import defaultdict
counts = defaultdict(int)
for col_idx in range(alignment.get_alignment_length()):
column = alignment[:, col_idx]
chars = [c for c in column if c != '-']
for i, c1 in enumerate(chars):
for c2 in chars[i+1:]:
if c1 != c2:
pair = tuple(sorted([c1, c2]))
counts[pair] += 1
return dict(counts)
subs = substitution_counts(alignment)
print('Substitution counts:')
for pair, count in sorted(subs.items(), key=lambda x: -x[1])[:10]:
print(f' {pair[0]}<->{pair[1]}: {count}')
```
### Build Substitution Matrix from MSA
```python
def build_substitution_matrix(alignment):
from collections import defaultdict
matrix = defaultdict(lambda: defaultdict(int))
for col_idx in range(alignment.get_alignment_length()):
column = alignment[:, col_idx]
chars = [c for c in column if c != '-']
for c1 in chars:
for c2 in chars:
matrix[c1][c2] += 1
return {k: dict(v) for k, v in matrix.items()}
sub_matrix = build_substitution_matrix(alignment)
```
### Using Alignment.substitutions (Pairwise Alignments)
For pairwise alignments created with `PairwiseAligner`, use the built-in `.substitutions` property:
```python
from Bio.Align import PairwiseAligner
aligner = PairwiseAligner(mode='global', match_score=1, mismatch_score=-1)
alignments = aligner.align(seq1, seq2)
substitutions = alignments[0].substitutions
# Returns Array with substitution counts
print(substitutions)
```
## Information Content
### Shannon Entropy Per Column
```python
import math
def shannon_entropy(column, ignore_gaps=True):
if ignore_gaps:
column = column.replace('-', '')
if not column:
return 0.0
counts = Counter(column)
total = len(column)
entropy = 0.0
for count in counts.values():
p = count / total
if p > 0:
entropy -= p * math.log2(p)
return entropy
alignment = AlignIO.read('alignment.fasta', 'fasta')
for i in range(min(20, alignment.get_alignment_length())):
column = alignment[:, i]
ent = shannon_entropy(column)
print(f'Column {i}: entropy = {ent:.2f} bits')
```
### Information Content (Max Entropy - Observed Entropy)
```python
def information_content(column, alphabet_size=4):
max_entropy = math.log2(alphabet_size) # 4 for DNA, 20 for protein
observed_entropy = shannon_entropy(column)
return max_entropy - observed_entropy
# DNA alignment
for i in range(min(20, alignment.get_alignment_length())):
column = alignment[:, i]
ic = information_content(column, alphabet_size=4)
print(f'Column {i}: IC = {ic:.2f} bits')
```
## Gap Statistics
### Gap Fraction Per Column
```python
def gap_profile(alignment):
profile = []
for col_idx in range(alignment.get_alignment_length()):
column = alignment[:, col_idx]
gap_fraction = column.count('-') / len(alignment)
profile.append(gap_fraction)
return profile
gaps = gap_profile(alignment)
avg_gaps = sum(gaps) / len(gaps)
print(f'Average gap fraction: {avg_gaps*100:.1f}%')
```
### Gap Statistics Summary
```python
def gap_statistics(alignment):
num_seqs = len(alignment)
num_cols = alignment.get_alignment_length()
total_positions = num_seqs * num_cols
total_gaps = sum(str(r.seq).count('-') for r in alignment)
gaps_per_seq = [str(r.seq).count('-') for r in alignment]
gaps_per_col = [alignment[:, i].count('-') for i in range(num_cols)]
return {
'total_gaps': total_gaps,
'gap_fraction': total_gaps / total_positions,
'gappiest_seq': max(range(num_seqs), key=lambda i: gaps_per_seq[i]),
'gappiest_col': max(range(num_cols), key=lambda i: gaps_per_col[i]),
'gap_free_cols': sum(1 for g in gaps_per_col if g == 0),
}
stats = gap_statistics(alignment)
print(f"Total gaps: {stats['total_gaps']}")
print(f"Gap fraction: {stats['gap_fraction']*100:.1f}%")
print(f"Gap-free columns: {stats['gap_free_cols']}")
```
## Alignment Quality Metrics
### Overall Alignment Score
```python
def alignment_score(alignment, match=1, mismatch=-1, gap=-2):
total_score = 0
for col_idx in range(alignment.get_alignment_length()):
column = alignment[:, col_idx]
for i, c1 in enumerate(column):
for c2 in column[i+1:]:
if c1 == '-' or c2 == '-':
total_score += gap
elif c1 == c2:
total_score += match
else:
total_score += mismatch
return total_score
score = alignment_score(alignment)
print(f'Alignment score: {score}')
```
### Sum of Pairs Score
```python
def sum_of_pairs(alignment, substitution_matrix=None):
if substitution_matrix is None:
substitution_matrix = substitution_matrices.load('BLOSUM62')
total = 0
for col_idx in range(alignment.get_alignment_length()):
column = alignment[:, col_idx]
for i, c1 in enumerate(column):
for c2 in column[i+1:]:
if c1 != '-' and c2 != '-':
total += substitution_matrix.get((c1, c2), 0)
return total
```
## Position-Specific Score Matrix (PSSM)
```python
def position_specific_score_matrix(alignment):
pssm = []
for col_idx in range(alignment.get_alignment_length()):
column = alignment[:, col_idx]
counts = Counter(column)
if '-' in counts:
del counts['-']
pssm.append(dict(counts))
return pssm
alignment = AlignIO.read('alignment.fasta', 'fasta')
pssm = position_specific_score_matrix(alignment)
for i, row in enumerate(pssm[:10]):
print(f'Position {i}: {row}')
```
## Note on Bio.Align.AlignInfo
The `AlignInfo.SummaryInfo` class is **deprecated** in recent Biopython versions. Use the custom functions in this skill instead:
- For PSSM: use `position_specific_score_matrix()` above
- For information content: use `information_content()` function earlier in this skill
- For consensus: see msa-parsing skill
## Quick Reference: Metrics
| Metric | Description | Range |
|--------|-------------|-------|
| Identity | Fraction of identical residues | 0-1 |
| Conservation | Most common residue frequency | 0-1 |
| Shannon Entropy | Variability measure | 0 to log2(alphabet) |
| Information Content | Max entropy - observed entropy | 0 to log2(alphabet) |
| Gap Fraction | Proportion of gaps | 0-1 |
## Common Errors
| Error | Cause | Solution |
|-------|-------|----------|
| `ZeroDivisionError` | Empty column after gap removal | Check for gap-only columns |
| `KeyError` | Character not in substitution matrix | Handle gaps separately |
| Negative IC | Wrong alphabet size | Use 4 for DNA, 20 for protein |
## Related Skills
- msa-parsing - Parse and manipulate alignments
- alignment-io - Read/write alignment files
- pairwise-alignment - Create and score pairwise alignments
- sequence-manipulation/sequence-properties - Sequence-level statistics
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