Agent skill
bio-reference-operations
Install this agent skill to your Project
npx add-skill https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills/tree/main/skills/bio-reference-operations
SKILL.md
name: bio-reference-operations description: Generate consensus sequences and manage reference files using samtools. Use when creating consensus from alignments, indexing references, or creating sequence dictionaries. tool_type: cli primary_tool: samtools measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools:
- read_file
- run_shell_command
Reference Operations
Generate consensus sequences and manage reference files using samtools.
samtools faidx - Index Reference FASTA
Create index for random access to reference sequences.
Create Index
samtools faidx reference.fa
# Creates reference.fa.fai
Fetch Region from Reference
samtools faidx reference.fa chr1:1000-2000
Fetch Multiple Regions
samtools faidx reference.fa chr1:1000-2000 chr2:3000-4000
Fetch Entire Chromosome
samtools faidx reference.fa chr1
Output to File
samtools faidx reference.fa chr1:1000-2000 > region.fa
Reverse Complement
samtools faidx -i reference.fa chr1:1000-2000
FAI File Format
chr1 248956422 6 60 61
chr2 242193529 253404903 60 61
Columns: name, length, offset, line bases, line width
samtools dict - Create Sequence Dictionary
Create SAM header dictionary for reference (used by GATK, Picard).
Create Dictionary
samtools dict reference.fa -o reference.dict
With Assembly Info
samtools dict -a GRCh38 -s "Homo sapiens" reference.fa -o reference.dict
Dictionary Format
@HD VN:1.6 SO:unsorted
@SQ SN:chr1 LN:248956422 M5:6aef897c3d6ff0c78aff06ac189178dd UR:file:reference.fa
@SQ SN:chr2 LN:242193529 M5:f98db672eb0993dcfdabafe2a882905c UR:file:reference.fa
samtools consensus - Generate Consensus
Create consensus sequence from alignments.
Basic Consensus
samtools consensus input.bam -o consensus.fa
From Specific Region
samtools consensus -r chr1:1000-2000 input.bam -o region_consensus.fa
Output Formats
# FASTA (default)
samtools consensus -f fasta input.bam -o consensus.fa
# FASTQ (includes quality)
samtools consensus -f fastq input.bam -o consensus.fq
Quality Options
# Minimum depth to call base
samtools consensus -d 5 input.bam -o consensus.fa
# Call all positions (including low coverage)
samtools consensus -a input.bam -o consensus.fa
Ambiguity Handling
# Use IUPAC codes for heterozygous positions
samtools consensus --show-ins no --show-del no input.bam -o consensus.fa
pysam Python Alternative
Fetch from Indexed FASTA
import pysam
with pysam.FastaFile('reference.fa') as ref:
seq = ref.fetch('chr1', 999, 2000) # 0-based
print(seq)
Get Reference Lengths
with pysam.FastaFile('reference.fa') as ref:
for name in ref.references:
length = ref.get_reference_length(name)
print(f'{name}: {length:,} bp')
Fetch All Chromosomes
with pysam.FastaFile('reference.fa') as ref:
for chrom in ref.references:
seq = ref.fetch(chrom)
print(f'>{chrom}')
print(seq[:100] + '...')
Generate Simple Consensus
import pysam
from collections import Counter
def consensus_at_position(bam, chrom, pos):
bases = Counter()
for pileup in bam.pileup(chrom, pos, pos + 1, truncate=True):
if pileup.pos == pos:
for read in pileup.pileups:
if not read.is_del and not read.is_refskip:
bases[read.alignment.query_sequence[read.query_position]] += 1
if bases:
return bases.most_common(1)[0][0]
return 'N'
with pysam.AlignmentFile('input.bam', 'rb') as bam:
consensus = consensus_at_position(bam, 'chr1', 1000000)
print(f'Consensus at chr1:1000000 = {consensus}')
Build Consensus Sequence
import pysam
from collections import Counter
def build_consensus(bam_path, chrom, start, end, min_depth=3):
consensus = []
with pysam.AlignmentFile(bam_path, 'rb') as bam:
for pileup in bam.pileup(chrom, start, end, truncate=True):
bases = Counter()
for read in pileup.pileups:
if not read.is_del and not read.is_refskip:
base = read.alignment.query_sequence[read.query_position]
bases[base] += 1
if sum(bases.values()) >= min_depth:
consensus.append(bases.most_common(1)[0][0])
else:
consensus.append('N')
return ''.join(consensus)
seq = build_consensus('input.bam', 'chr1', 1000, 2000, min_depth=5)
print(f'>{chrom}:{start}-{end}')
print(seq)
Create Dictionary Header
import pysam
def create_dict_header(fasta_path):
header = {'HD': {'VN': '1.6', 'SO': 'unsorted'}, 'SQ': []}
with pysam.FastaFile(fasta_path) as ref:
for name in ref.references:
length = ref.get_reference_length(name)
header['SQ'].append({'SN': name, 'LN': length})
return header
header = create_dict_header('reference.fa')
for sq in header['SQ'][:5]:
print(f'{sq["SN"]}: {sq["LN"]:,} bp')
Reference Preparation Workflow
Prepare Reference for Analysis
# 1. Index FASTA for samtools/pysam
samtools faidx reference.fa
# 2. Create sequence dictionary for GATK/Picard
samtools dict reference.fa -o reference.dict
# 3. Index for BWA
bwa index reference.fa
# 4. Index for Bowtie2
bowtie2-build reference.fa reference
Check Reference Setup
# Verify FAI exists
ls -la reference.fa.fai
# Verify dict exists
head reference.dict
# Test fetch
samtools faidx reference.fa chr1:1-100
Common Operations
Extract Chromosome
samtools faidx reference.fa chr1 > chr1.fa
samtools faidx chr1.fa # Index the subset
Get Chromosome Sizes
cut -f1,2 reference.fa.fai > chrom.sizes
Subset Reference
samtools faidx reference.fa chr1 chr2 chr3 > subset.fa
samtools faidx subset.fa
Compare Consensus to Reference
# Generate consensus
samtools consensus input.bam -o consensus.fa
# Align consensus back to reference
minimap2 -a reference.fa consensus.fa > comparison.sam
Quick Reference
| Task | Command |
|---|---|
| Index FASTA | samtools faidx ref.fa |
| Fetch region | samtools faidx ref.fa chr1:1-1000 |
| Create dict | samtools dict ref.fa -o ref.dict |
| Build consensus | samtools consensus in.bam -o out.fa |
| Chrom sizes | cut -f1,2 ref.fa.fai |
Related Skills
- sam-bam-basics - Reference required for CRAM
- alignment-indexing - faidx for reference access
- pileup-generation - Pileup for consensus building
- variant-calling - bcftools consensus from VCF
- sequence-io/read-sequences - Parse FASTA with Biopython
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