Notre avis
Appelle les variants germinaux (SNP et petits indels) à partir d'alignements de séquençage longues lectures (ONT ou PacBio HiFi) en utilisant les modèles d'apprentissage profond de Clair3.
Points forts
- Haute précision pour l'appel de variants sur longues lectures
- Support des plateformes ONT et PacBio HiFi avec modèles spécifiques
- Options pour l'appel par régions, sortie gVCF et phasage
- Utilisable sur génomes humains et non humains
Limites
- Nécessite l'installation préalable de Clair3 et des modèles appropriés
- Non adapté au PacBio CLR (ancienne plateforme)
- Exige des ressources de calcul élevées (32 threads recommandés)
Lorsque vous avez besoin d'appels de variants précis à partir de données de séquençage longues lectures ONT ou PacBio HiFi pour des applications cliniques ou de recherche.
En présence de données PacBio CLR (utiliser PEPPER-Margin-DeepVariant) ou lorsque des outils pour courtes lectures suffisent.
Analyse de sécurité
SûrThe skill runs standard bioinformatics command-line tools (run_clair3.sh, bcftools) for variant calling, with no destructive, exfiltrating, or obfuscated actions. It uses run_shell_command but only in the context of legitimate data processing. No external downloads, piping to shell, or disabling of safety measures are instructed.
Aucun point d'attention détecté
Exemples
Run Clair3 to call SNPs and indels from an ONT alignment file sample.bam against reference reference.fasta with 32 threads.Run Clair3 with gVCF output on sample.bam for ONT data, using reference.fasta, and output to clair3_gvcf.Run Clair3 restricted to target_regions.bed from sample.bam with ont platform.name: bio-long-read-sequencing-clair3-variants 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. tool_type: cli primary_tool: Clair3 measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools:
- read_file
- run_shell_command
Clair3 Variant Calling
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
| Platform | Model | Recommended Coverage | |----------|-------|---------------------| | ONT R10 | r1041_e82_400bps_sup_v430 | 30-60x | | ONT R9 | r941_prom_sup_g5014 | 30-60x | | PacBio HiFi | hifi | 20-40x | | 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
| Parameter | Description | |-----------|-------------| | --platform | ont, hifi, or ilmn | | --model_path | Path to trained model | | --bed_fn | Restrict calling to regions | | --include_all_ctgs | Call on all contigs (not just chr1-22,X,Y) | | --no_phasing_for_fa | Disable phasing | | --gvcf | Output gVCF format | | --qual | Minimum 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
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
| Caller | Best For | Speed | Accuracy | |--------|----------|-------|----------| | Clair3 | ONT/HiFi germline | Fast | High | | DeepVariant | HiFi, Illumina | Medium | Very high | | PEPPER-DV | ONT (integrated) | Slow | Very high | | Longshot | ONT SNPs | Fast | Good |
Troubleshooting
| Issue | Solution | |-------|----------| | Missing model | Download from Clair3 releases or use conda models | | Low call rate | Check coverage; increase --qual threshold | | Slow performance | Reduce --threads or use --bed_fn for targeted calling | | Wrong variants on non-human | Use --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
Ingénierie de Prompts
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Bonnes pratiques et templates de prompt engineering pour maximiser les résultats IA.
Visualisation de Données
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Génère des visualisations de données et graphiques adaptés à vos données.
Architecture RAG
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Guide de configuration d'architectures RAG (Retrieval-Augmented Generation).