Agent skill · Code Review & Quality

fastp-fastq-preprocessing

All-in-one FASTQ QC and adapter trimming. Auto-detects Illumina adapters, filters low-quality reads, corrects paired-end overlaps, emits HTML+JSON QC in one pass. 3-10x faster than Trim Galore/Trimmomatic. First step before STAR, BWA-MEM2, or Salmon.

BioTender-maxgithub.com/BioTender-maxGitHub ↗
claude-codeNOASSERTION
Install
npx skills add BioTender-max/awesome-bio-agent-skills --skill fastp-fastq-preprocessing --agent claude-code

Same command for any agent — swap --agent for codex, cursor, copilot.

Facts
Files in the skill folder: 1
SKILL.md size: 13 KB
Bundled scripts: none
Path: skills/sciagent/fastp-fastq-preprocessing/SKILL.md
Open the folder on GitHub →
Where it comes from
Stars: 135
Language: Python

Weekly change comes from our own snapshots, not the repository page — it measures attention, not adoption.

From the SKILL.md

# fastp — Fast FASTQ Quality Control and Adapter Trimming ## Overview fastp performs adapter trimming, quality filtering, and QC reporting for Illumina FASTQ files in a single multi-threaded pass. It automatically detects adapter sequences from paired-end read overlaps — eliminating the need to specify adapters manually. fastp corrects mismatches in paired-end overlap regions, filters reads by quality score and length, removes polyX tails (polyA for RNA-seq), and generates interactive HTML and machine-readable JSON QC reports. Being 3–10× faster than Trim Galore and Trimmomatic while providing comparable or better results, fastp has become the standard preprocessing step before alignment in WGS, RNA-seq, and ChIP-seq pipelines. ## When to Use - Trimming Illumina adapters and low-quality bases before alignment in any NGS pipeline (RNA-seq, WGS, WES, ChIP-seq, ATAC-seq) - Generating per-sample QC reports (HTML + JSON) as the first step of a pipeline, before MultiQC aggregation - Processing paired-end reads where adapter auto-detection from overlap is preferred over manual adapter specification - Removing polyA tails from RNA-seq reads from 3′ end-enriched protocols (Smart-seq, QuantS

What's inside
Steps it walks through
  1. Overview
  2. When to Use
  3. Prerequisites
  4. Quick Start
  5. Workflow
  6. Step 1: Single-End Adapter Trimming
  7. Step 2: Paired-End Adapter Trimming
  8. Step 3: Quality Filtering and Read Length Trimming
  9. Step 4: RNA-seq polyA Tail Removal
  10. Step 5: Parse QC Report JSON for Pipeline Monitoring
  11. Step 6: Batch Preprocessing Pipeline
  12. Key Parameters
  13. Common Recipes
  14. Recipe 1: Integrate fastp into a Snakemake Pipeline
Commands it runs
Install with conda
conda install -c bioconda fastp
Or download pre-compiled binary (Linux)
wget https://github.com/OpenGene/fastp/releases/download/v0.24.0/fastp
chmod +x fastp
fastp 0.24.0
Verify
fastp --version
Paired-end adapter trimming with QC report
fastp \
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About this skill
What does the fastp-fastq-preprocessing skill do?

All-in-one FASTQ QC and adapter trimming. Auto-detects Illumina adapters, filters low-quality reads, corrects paired-end overlaps, emits HTML+JSON QC in one pass. 3-10x faster than Trim Galore/Trimmomatic. First step before STAR, BWA-MEM2, or Salmon.

How do I install it?

Run `npx skills add BioTender-max/awesome-bio-agent-skills --skill fastp-fastq-preprocessing --agent claude-code` — it drops the skill into your project so the agent can pick it up. Swap the --agent value for codex, cursor or copilot if you use one of those.

Where does this skill come from?

From BioTender-max/awesome-bio-agent-skills, a repository with 135 stars. We read it straight from the repository tree rather than a submitted listing, so what you see here is what is actually published.

Is a popular skill a good skill?

Not necessarily. Stars measure attention, not adoption — a repository can trend for a week and be abandoned. That is why we show the weekly change from our own snapshots next to the total, instead of a single flattering number.

Keep going