bio-variant-calling-deepvariant — independently scanned and version-tracked by SaferSkills.
SaferSkills independently audited bio-variant-calling-deepvariant (Agent Skill) and scored it 100/100 (green). The audit ran 55 deterministic rules across Security, Supply Chain, Maintenance, Transparency, and Community; it found 0 high-severity and 0 lower-severity findings. The full rule-by-rule trace and per-finding evidence are below. Free, methodology-open.
Findings & checks · 0 flagged
Every scanned point with the score it earned and what moved between them.
First recorded scan — no prior version to compare against.
The primary manifest — the file an agent reads to learn what this artifact does.
docker pull google/deepvariant:1.6.1
# Or with GPU support
docker pull google/deepvariant:1.6.1-gpusingularity pull docker://google/deepvariant:1.6.1docker run -v "${PWD}:/input" -v "${PWD}/output:/output" \
google/deepvariant:1.6.1 \
/opt/deepvariant/bin/run_deepvariant \
--model_type=WGS \
--ref=/input/reference.fa \
--reads=/input/sample.bam \
--output_vcf=/output/sample.vcf.gz \
--output_gvcf=/output/sample.g.vcf.gz \
--num_shards=16| Model | Data Type | Use Case |
|---|---|---|
WGS | Illumina WGS | Whole genome sequencing |
WES | Illumina WES | Whole exome/targeted |
PACBIO | PacBio HiFi | Long-read HiFi |
ONT_R104 | ONT R10.4 | Oxford Nanopore |
HYBRID_PACBIO_ILLUMINA | Mixed | Hybrid assemblies |
For more control, run each step separately:
docker run -v "${PWD}:/data" google/deepvariant:1.6.1 \
/opt/deepvariant/bin/make_examples \
--mode calling \
--ref /data/reference.fa \
--reads /data/sample.bam \
--examples /data/examples.tfrecord.gz \
--gvcf /data/gvcf.tfrecord.gzdocker run -v "${PWD}:/data" google/deepvariant:1.6.1 \
/opt/deepvariant/bin/call_variants \
--outfile /data/call_variants.tfrecord.gz \
--examples /data/examples.tfrecord.gz \
--checkpoint /opt/models/wgs/model.ckptdocker run -v "${PWD}:/data" google/deepvariant:1.6.1 \
/opt/deepvariant/bin/postprocess_variants \
--ref /data/reference.fa \
--infile /data/call_variants.tfrecord.gz \
--outfile /data/output.vcf.gz \
--gvcf_outfile /data/output.g.vcf.gz \
--nonvariant_site_tfrecord_path /data/gvcf.tfrecord.gzdocker run --gpus all -v "${PWD}:/data" \
google/deepvariant:1.6.1-gpu \
/opt/deepvariant/bin/run_deepvariant \
--model_type=WGS \
--ref=/data/reference.fa \
--reads=/data/sample.bam \
--output_vcf=/data/output.vcf.gz \
--num_shards=16docker run -v "${PWD}:/data" google/deepvariant:1.6.1 \
/opt/deepvariant/bin/run_deepvariant \
--model_type=PACBIO \
--ref=/data/reference.fa \
--reads=/data/hifi_aligned.bam \
--output_vcf=/data/hifi_variants.vcf.gz \
--num_shards=16docker run -v "${PWD}:/data" google/deepvariant:1.6.1 \
/opt/deepvariant/bin/run_deepvariant \
--model_type=ONT_R104 \
--ref=/data/reference.fa \
--reads=/data/ont_aligned.bam \
--output_vcf=/data/ont_variants.vcf.gz \
--num_shards=16docker run -v "${PWD}:/data" google/deepvariant:1.6.1 \
/opt/deepvariant/bin/run_deepvariant \
--model_type=WES \
--ref=/data/reference.fa \
--reads=/data/exome.bam \
--regions=/data/targets.bed \
--output_vcf=/data/exome_variants.vcf.gz \
--num_shards=8For multi-sample cohorts, use gVCFs with GLnexus:
# Generate gVCFs for each sample
for bam in *.bam; do
sample=$(basename $bam .bam)
docker run -v "${PWD}:/data" google/deepvariant:1.6.1 \
/opt/deepvariant/bin/run_deepvariant \
--model_type=WGS \
--ref=/data/reference.fa \
--reads=/data/$bam \
--output_vcf=/data/${sample}.vcf.gz \
--output_gvcf=/data/${sample}.g.vcf.gz \
--num_shards=16
done
# Joint genotyping with GLnexus
docker run -v "${PWD}:/data" quay.io/mlin/glnexus:v1.4.1 \
/usr/local/bin/glnexus_cli \
--config DeepVariantWGS \
/data/*.g.vcf.gz \
| bcftools view - -Oz -o cohort.vcf.gz| Config | Use Case |
|---|---|
DeepVariantWGS | Illumina WGS |
DeepVariantWES | Illumina exome |
DeepVariant_unfiltered | Keep all variants |
# Variant statistics
bcftools stats output.vcf.gz > stats.txt
# Filter by quality
bcftools view -i 'QUAL>20 && FMT/GQ>20' output.vcf.gz -Oz -o filtered.vcf.gz
# Ti/Tv ratio (expect ~2.0-2.1 for WGS)
bcftools stats output.vcf.gz | grep TSTV# Using hap.py for GIAB benchmarking
docker run -v "${PWD}:/data" jmcdani20/hap.py:latest \
/opt/hap.py/bin/hap.py \
/data/HG002_GRCh38_truth.vcf.gz \
/data/deepvariant_output.vcf.gz \
-r /data/reference.fa \
-o /data/benchmark \
--threads 16#!/bin/bash
set -euo pipefail
BAM=$1
REFERENCE=$2
OUTPUT_PREFIX=$3
MODEL_TYPE=${4:-WGS}
THREADS=${5:-16}
echo "=== DeepVariant: ${MODEL_TYPE} mode ==="
docker run -v "${PWD}:/data" google/deepvariant:1.6.1 \
/opt/deepvariant/bin/run_deepvariant \
--model_type=${MODEL_TYPE} \
--ref=/data/${REFERENCE} \
--reads=/data/${BAM} \
--output_vcf=/data/${OUTPUT_PREFIX}.vcf.gz \
--output_gvcf=/data/${OUTPUT_PREFIX}.g.vcf.gz \
--intermediate_results_dir=/data/${OUTPUT_PREFIX}_tmp \
--num_shards=${THREADS}
echo "=== Indexing ==="
bcftools index -t ${OUTPUT_PREFIX}.vcf.gz
bcftools index -t ${OUTPUT_PREFIX}.g.vcf.gz
echo "=== Statistics ==="
bcftools stats ${OUTPUT_PREFIX}.vcf.gz > ${OUTPUT_PREFIX}_stats.txt
echo "=== Complete ==="
echo "VCF: ${OUTPUT_PREFIX}.vcf.gz"
echo "gVCF: ${OUTPUT_PREFIX}.g.vcf.gz"| Caller | Speed | Accuracy | Best For |
|---|---|---|---|
| DeepVariant | Moderate | Highest | Production, benchmarking |
| GATK HaplotypeCaller | Moderate | High | GATK ecosystem |
| bcftools | Fast | Good | Quick analysis |
| Clair3 | Fast | High | Long reads |
| Data Type | Memory | CPU Time (30x WGS) |
|---|---|---|
| WGS | 64 GB | ~4-6 hours |
| WES | 32 GB | ~30 min |
| With GPU | 32 GB | ~1-2 hours (WGS) |
~30 seconds. Free. No account. Every finding cites a rule and a line of evidence.