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

bio-read-qc-quality-reports

Maintainer FreedomIntelligence · Last updated April 1, 2026

Generate and interpret quality reports from FASTQ files using FastQC and MultiQC. Assess per-base quality, adapter content, GC bias, duplication levels, and overrepresented sequences. Use when performing initial QC on raw sequencing data or validating preprocessing results.

OpenClawNanoClawAnalysisReproductionbio-read-qc-quality-reports🧬 bioinformatics (gptomics bio-* suite)bioinformatics — sequencing & read qcgenerate

Original source

FreedomIntelligence/OpenClaw-Medical-Skills

https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills/tree/main/skills/bio-read-qc-quality-reports

Maintainer
FreedomIntelligence
License
MIT
Last updated
April 1, 2026

Skill Snapshot

Key Details From SKILL.md

2 min

Key Notes

  • CLI: fastqc *.fastq.gz then multiqc.
  • Generate quality reports for FASTQ files using FastQC and aggregate multiple reports with MultiQC.
  • Run quality control on FASTQ files" → Generate per-base quality, adapter content, and duplication plots, then aggregate across samples. CLI: fastqc *.fastq.gz then multiqc.
  • fastqc -o qc_reports/ sample_R1.fastq.gz sample_R2.fastq.gz.

Source Doc

Excerpt From SKILL.md

Output Files

FastQC produces two files per input:

  • sample_fastqc.html - Interactive HTML report
  • sample_fastqc.zip - Data files and images

Key Modules

ModuleWhat It ShowsWarning Signs
Per base sequence qualityQuality scores across readDrop below Q20 at 3' end
Per sequence qualityQuality score distributionBimodal distribution
Per base sequence contentNucleotide compositionImbalance at start (normal)
Per sequence GC contentGC distributionSecondary peak (contamination)
Per base N contentUnknown basesHigh N content
Sequence length distributionRead lengthsUnexpected variation
Sequence duplicationDuplicate readsHigh duplication (PCR)
Overrepresented sequencesCommon sequencesAdapter contamination
Adapter contentAdapter sequencesVisible adapter curves

Get per-base quality

cat sample_fastqc/fastqc_data.txt | grep -A 50 ">>Per base sequence quality"

Use cases

  • Use when performing initial QC on raw sequencing data or validating preprocessing results.

Not for

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

Upstream Related Skills

  • adapter-trimming - Remove adapters detected by FastQC
  • fastp-workflow - All-in-one QC and trimming
  • sequence-io/read-sequences - FASTQ file reading/writing

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