Data & ReproBioinformatics & GenomicsFreedomIntelligence/OpenClaw-Medical-SkillsData & Reproduction
BI

bio-workflows-fastq-to-variants

Maintainer FreedomIntelligence · Last updated April 1, 2026

Complete FASTQ → alignment → variant calling pipeline.

OpenClawNanoClawAnalysisReproductionbio-workflows-fastq-to-variants🧠 bioos extended suitebioos extended bioinformatics suitecomplete

Original source

FreedomIntelligence/OpenClaw-Medical-Skills

https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills/tree/main/skills/bio-workflows-fastq-to-variants

Maintainer
FreedomIntelligence
License
MIT
Last updated
April 1, 2026

Skill Snapshot

Key Details From SKILL.md

2 min

Key Notes

  • Complete pipeline from raw DNA sequencing FASTQ files to filtered variant calls.
  • fastp -i sample_R1.fastq.gz -I sample_R2.fastq.gz \ -o sample_R1.trimmed.fq.gz -O sample_R2.trimmed.fq.gz \ --detect_adapter_for_pe \ --qualified_quality_phred 20 \ --length_required 50 \ --html sample_fastp.html.

Source Doc

Excerpt From SKILL.md

Batch processing

for sample in sample1 sample2 sample3; do fastp -i ${sample}_R1.fastq.gz -I ${sample}_R2.fastq.gz
-o trimmed/${sample}_R1.fq.gz -O trimmed/${sample}_R2.fq.gz
--detect_adapter_for_pe
--html qc/${sample}_fastp.html done


**QC Checkpoint 1:** Check fastp reports
- Q30 bases >85% (DNA typically higher quality than RNA)
- Adapter content <1%
- No unusual GC distribution

## Index reference (once)

bwa-mem2 index reference.fa

## Align with read group info

for sample in sample1 sample2 sample3; do
    bwa-mem2 mem -t 8 \
        -R "@RG\tID:${sample}\tSM:${sample}\tPL:ILLUMINA\tLB:lib1" \
        reference.fa \
        trimmed/${sample}_R1.fq.gz \
        trimmed/${sample}_R2.fq.gz \
    | samtools view -bS - > aligned/${sample}.bam
done
bash
samtools flagstat aligned/${sample}.bam
  • Mapped reads >95%
  • Properly paired >90%

Use cases

  • Use bio-workflows-fastq-to-variants for genomics and bioinformatics workflows.
  • Apply bio-workflows-fastq-to-variants to sequencing, variant, or omics analysis tasks.

Not for

  • Do not rely on this catalog entry alone for installation or maintenance details.

Upstream Related Skills

  • read-qc/fastp-workflow - Detailed QC options
  • read-alignment/bwa-alignment - BWA-MEM2 parameters
  • alignment-files/duplicate-handling - Duplicate marking details
  • variant-calling/variant-calling - bcftools calling options
  • variant-calling/gatk-variant-calling - GATK HaplotypeCaller details
  • variant-calling/filtering-best-practices - Advanced filtering strategies

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