Bio Long Read Sequencing Clair3 Variants

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

# 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

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

Troubleshooting

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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