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Maintainer FreedomIntelligence · Last updated April 1, 2026
Complete FASTQ → alignment → variant calling pipeline.
Original source
https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills/tree/main/skills/bio-workflows-fastq-to-variants
Skill Snapshot
Source Doc
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
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