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bio-long-read-sequencing-clair3-variants

Use Clair3 to detect inherited single-base changes and small insertions or deletions from aligned ONT or PacBio HiFi long reads. Select platform models, restrict analysis to target regions, and filter variant files by quality.

OriginalShow the original description

Deep learning-based variant calling from long reads using Clair3 for SNPs and small indels. Use when calling germline variants from ONT or PacBio alignments, particularly when high accuracy is needed for clinical or research applications.

Works withDocker

Run score Not tested

See how to install

Good for

  • Detect variants from aligned ONT or PacBio HiFi reads
  • Limit variant detection to regions specified in a BED file
  • Filter variant results by quality or variant type
  • Analyze all contigs in a non-human genome

Files included (3)

  • SKILL.md7.2 KB
  • examples/clair3_workflow.sh1.8 KB
  • usage-guide.md2.3 KB

SKILL.md (original)

Review the instructions the agent will receive before you install.

Version Compatibility

Reference examples tested with: DeepVariant 1.6+, Entrez Direct 21.0+, bcftools 1.19+, minimap2 2.26+

Before using code patterns, verify installed versions match. If versions differ:

  • Python: pip show <package> then help(module.function) to check signatures
  • CLI: <tool> --version then <tool> --help to confirm flags

If code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.

Clair3 Variant Calling

"Call variants from my long-read data" → Use deep learning to identify germline SNPs and small indels from ONT or PacBio aligned reads with high accuracy.

  • CLI: run_clair3.sh --bam_fn=sample.bam --ref_fn=ref.fa --platform=ont

Basic Usage

# ONT variant calling
run_clair3.sh \
    --bam_fn=sample.bam \
    --ref_fn=reference.fasta \
    --threads=32 \
    --platform=ont \
    --model_path=${CONDA_PREFIX}/bin/models/ont \
    --output=clair3_output

# PacBio HiFi variant calling
run_clair3.sh \
    --bam_fn=sample.bam \
    --ref_fn=reference.fasta \
    --threads=32 \
    --platform=hifi \
    --model_path=${CONDA_PREFIX}/bin/models/hifi \
    --output=clair3_output

# Output: clair3_output/merge_output.vcf.gz

Platform-Specific Models

PlatformModelRecommended Coverage
ONT R10r1041_e82_400bps_sup_v43030-60x
ONT R9r941_prom_sup_g501430-60x
PacBio HiFihifi20-40x
PacBio CLR-Use PEPPER-Margin-DeepVariant
# List available models
ls ${CONDA_PREFIX}/bin/models/

# Specify exact model
run_clair3.sh \
    --bam_fn=sample.bam \
    --ref_fn=reference.fasta \
    --model_path=${CONDA_PREFIX}/bin/models/r1041_e82_400bps_sup_v430 \
    --output=clair3_out \
    --threads=32

Key Parameters

ParameterDescription
--platformont, hifi, or ilmn
--model_pathPath to trained model
--bed_fnRestrict calling to regions
--include_all_ctgsCall on all contigs (not just chr1-22,X,Y)
--no_phasing_for_faDisable phasing
--gvcfOutput gVCF format
--qualMinimum variant quality (default: 2)

Region-Specific Calling

# Call variants in specific regions
run_clair3.sh \
    --bam_fn=sample.bam \
    --ref_fn=reference.fasta \
    --bed_fn=target_regions.bed \
    --threads=32 \
    --platform=ont \
    --model_path=${CONDA_PREFIX}/bin/models/ont \
    --output=clair3_targeted

# Call on non-human genomes (all contigs)
run_clair3.sh \
    --bam_fn=sample.bam \
    --ref_fn=reference.fasta \
    --include_all_ctgs \
    --threads=32 \
    --platform=hifi \
    --model_path=${CONDA_PREFIX}/bin/models/hifi \
    --output=clair3_all_contigs

gVCF Output

# Generate gVCF for joint calling
run_clair3.sh \
    --bam_fn=sample.bam \
    --ref_fn=reference.fasta \
    --gvcf \
    --threads=32 \
    --platform=ont \
    --model_path=${CONDA_PREFIX}/bin/models/ont \
    --output=clair3_gvcf

# Joint genotyping multiple samples
bcftools merge sample1.g.vcf.gz sample2.g.vcf.gz -o cohort.vcf.gz

Phased Variant Calling

# With phasing information (requires haplotagged BAM)
run_clair3.sh \
    --bam_fn=haplotagged.bam \
    --ref_fn=reference.fasta \
    --enable_phasing \
    --longphase_for_phasing \
    --threads=32 \
    --platform=ont \
    --model_path=${CONDA_PREFIX}/bin/models/ont \
    --output=clair3_phased

Quality Filtering

# Filter by quality score
bcftools view -i 'QUAL>20' clair3_output/merge_output.vcf.gz -Oz -o filtered.vcf.gz

# Filter by genotype quality
bcftools view -i 'GQ>30' clair3_output/merge_output.vcf.gz -Oz -o high_gq.vcf.gz

# SNPs only
bcftools view -v snps clair3_output/merge_output.vcf.gz -Oz -o snps.vcf.gz

# Indels only
bcftools view -v indels clair3_output/merge_output.vcf.gz -Oz -o indels.vcf.gz

Python Wrapper

Goal: Run Clair3 variant calling and quality filtering from Python with platform-specific model auto-detection.

Approach: Build the Clair3 command dynamically from parameters, execute via subprocess, then filter the output VCF with bcftools.

import subprocess
from pathlib import Path

def run_clair3(bam, reference, output_dir, platform='ont', model_path=None,
               threads=32, bed=None, gvcf=False, include_all_ctgs=False):
    if model_path is None:
        import os
        conda_prefix = os.environ.get('CONDA_PREFIX', '')
        model_path = f'{conda_prefix}/bin/models/{platform}'

    cmd = [
        'run_clair3.sh',
        f'--bam_fn={bam}',
        f'--ref_fn={reference}',
        f'--threads={threads}',
        f'--platform={platform}',
        f'--model_path={model_path}',
        f'--output={output_dir}'
    ]

    if bed:
        cmd.append(f'--bed_fn={bed}')
    if gvcf:
        cmd.append('--gvcf')
    if include_all_ctgs:
        cmd.append('--include_all_ctgs')

    subprocess.run(cmd, check=True)
    return Path(output_dir) / 'merge_output.vcf.gz'

def filter_variants(vcf, output, min_qual=20, variant_type=None):
    cmd = ['bcftools', 'view', '-i', f'QUAL>{min_qual}']
    if variant_type:
        cmd.extend(['-v', variant_type])
    cmd.extend([vcf, '-Oz', '-o', output])
    subprocess.run(cmd, check=True)
    subprocess.run(['bcftools', 'index', '-t', output], check=True)
    return output

# Example
vcf = run_clair3('sample.bam', 'ref.fa', 'clair3_out', platform='hifi', threads=48)
snps = filter_variants(str(vcf), 'snps_q20.vcf.gz', min_qual=20, variant_type='snps')

Comparison with Other Callers

CallerBest ForSpeedAccuracy
Clair3ONT/HiFi germlineFastHigh
DeepVariantHiFi, IlluminaMediumVery high
PEPPER-DVONT (integrated)SlowVery high
LongshotONT SNPsFastGood

Troubleshooting

IssueSolution
Missing modelDownload from Clair3 releases or use conda models
Low call rateCheck coverage; increase --qual threshold
Slow performanceReduce --threads or use --bed_fn for targeted calling
Wrong variants on non-humanUse --include_all_ctgs

Docker Usage

# Using Docker
docker run -v /data:/data \
    hkubal/clair3:latest \
    /opt/bin/run_clair3.sh \
    --bam_fn=/data/sample.bam \
    --ref_fn=/data/reference.fasta \
    --threads=32 \
    --platform=ont \
    --model_path=/opt/models/ont \
    --output=/data/clair3_output

# Singularity
singularity exec clair3.sif run_clair3.sh \
    --bam_fn=sample.bam \
    --ref_fn=reference.fasta \
    --threads=32 \
    --platform=ont \
    --model_path=/opt/models/ont \
    --output=clair3_output

Related Skills

  • variant-calling/bcftools-basics - VCF manipulation
  • variant-calling/filtering-best-practices - Quality filtering
  • long-read-sequencing/long-read-qc - Input quality control
  • long-read-sequencing/long-read-alignment - Mapping with minimap2

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