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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.
Original source
https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills/tree/main/skills/bio-read-qc-quality-reports
Skill Snapshot
Source Doc
FastQC produces two files per input:
sample_fastqc.html - Interactive HTML reportsample_fastqc.zip - Data files and images| Module | What It Shows | Warning Signs |
|---|---|---|
| Per base sequence quality | Quality scores across read | Drop below Q20 at 3' end |
| Per sequence quality | Quality score distribution | Bimodal distribution |
| Per base sequence content | Nucleotide composition | Imbalance at start (normal) |
| Per sequence GC content | GC distribution | Secondary peak (contamination) |
| Per base N content | Unknown bases | High N content |
| Sequence length distribution | Read lengths | Unexpected variation |
| Sequence duplication | Duplicate reads | High duplication (PCR) |
| Overrepresented sequences | Common sequences | Adapter contamination |
| Adapter content | Adapter sequences | Visible adapter curves |
cat sample_fastqc/fastqc_data.txt | grep -A 50 ">>Per base sequence quality"
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