Hypothesis Generation
spacering-net/codeg
Structured hypothesis formulation from observations. An agent skill from spacering-net/codeg.
Runs all-in-one FASTQ preprocessing with fastp in a single pass - adapter trimming via paired-end overlap analysis, quality/length filtering, 2-color poly-G removal, base correction, optional…
$ npx skills add GPTomics/bioSkills --skill bio-read-qc-fastp-workflow -a claude-codeProject install by default; add -g for ~/.claude/skills/.
$ gh skill install GPTomics/bioSkills bio-read-qc-fastp-workflow --agent claude-codeProject scope by default; add --scope user for a personal install. Needs GitHub CLI 2.90.0 or later (public preview).
$ git clone --depth 1 https://github.com/GPTomics/bioSkills.git skills-src && mkdir -p .claude/skills && cp -r skills-src/read-qc/fastp-workflow .claude/skills/bio-read-qc-fastp-workflow && rm -rf skills-srcUse ~/.claude/skills/ instead of .claude/skills for a personal install. The folder must contain SKILL.md.
Claude Code skills documentation · loads skills from .claude/skills/
Install the "bio-read-qc-fastp-workflow" agent skill from https://github.com/GPTomics/bioSkills/tree/main/read-qc/fastp-workflow into .claude/skills/bio-read-qc-fastp-workflow/ in this project. Copy the whole folder (SKILL.md and every file beside it), keep the folder name "bio-read-qc-fastp-workflow", then confirm the skill loads.Claude Code copies the folder itself, the same result as the manual copy. Check what it changed before you commit it.
$skill-installer install https://github.com/GPTomics/bioSkills/tree/main/read-qc/fastp-workflowType this inside Codex. $skill-installer <name> installs a curated skill from openai/skills. The installer writes to $CODEX_HOME/skills (default ~/.codex/skills). Restart Codex if the skill does not show up.
$ npx skills add GPTomics/bioSkills --skill bio-read-qc-fastp-workflow -a codexProject install goes to .agents/skills/; add -g for ~/.codex/skills/.
$ gh skill install GPTomics/bioSkills bio-read-qc-fastp-workflow --agent codexProject scope by default (.agents/skills/); add --scope user for a personal install.
$ git clone --depth 1 https://github.com/GPTomics/bioSkills.git skills-src && mkdir -p .agents/skills && cp -r skills-src/read-qc/fastp-workflow .agents/skills/bio-read-qc-fastp-workflow && rm -rf skills-srcUse ~/.agents/skills/ instead of .agents/skills for a personal install.
Codex skills documentation · loads skills from .agents/skills/
Install the "bio-read-qc-fastp-workflow" agent skill from https://github.com/GPTomics/bioSkills/tree/main/read-qc/fastp-workflow into .agents/skills/bio-read-qc-fastp-workflow/ in this project. Copy the whole folder (SKILL.md and every file beside it), keep the folder name "bio-read-qc-fastp-workflow", then confirm the skill loads.Codex copies the folder itself, the same result as the manual copy. Check what it changed before you commit it.
$ npx skills add GPTomics/bioSkills --skill bio-read-qc-fastp-workflow -a cursorProject install goes to .agents/skills/; add -g for ~/.cursor/skills/.
$ gh skill install GPTomics/bioSkills bio-read-qc-fastp-workflow --agent cursorProject scope by default (.agents/skills/); add --scope user for a personal install.
$ git clone --depth 1 https://github.com/GPTomics/bioSkills.git skills-src && mkdir -p .cursor/skills && cp -r skills-src/read-qc/fastp-workflow .cursor/skills/bio-read-qc-fastp-workflow && rm -rf skills-srcUse ~/.cursor/skills/ instead of .cursor/skills for a personal install.
Cursor skills documentation · loads skills from .cursor/skills/, .agents/skills/, .claude/skills/, .codex/skills/
Install the "bio-read-qc-fastp-workflow" agent skill from https://github.com/GPTomics/bioSkills/tree/main/read-qc/fastp-workflow into .cursor/skills/bio-read-qc-fastp-workflow/ in this project. Copy the whole folder (SKILL.md and every file beside it), keep the folder name "bio-read-qc-fastp-workflow", then confirm the skill loads.Cursor copies the folder itself, the same result as the manual copy. Check what it changed before you commit it.
$ gemini skills install https://github.com/GPTomics/bioSkills.git --path read-qc/fastp-workflow--scope user (default) or --scope workspace; --path is the subfolder of the repo that holds the skill; --consent skips the security confirmation prompt.
$ npx skills add GPTomics/bioSkills --skill bio-read-qc-fastp-workflow -a gemini-cliProject install goes to .agents/skills/; add -g for ~/.gemini/skills/.
$ gh skill install GPTomics/bioSkills bio-read-qc-fastp-workflow --agent gemini-cliProject scope by default (.agents/skills/); add --scope user for a personal install.
$ git clone --depth 1 https://github.com/GPTomics/bioSkills.git skills-src && mkdir -p .gemini/skills && cp -r skills-src/read-qc/fastp-workflow .gemini/skills/bio-read-qc-fastp-workflow && rm -rf skills-srcUse ~/.gemini/skills/ instead of .gemini/skills for a personal install, then run /skills reload.
Gemini CLI skills documentation · loads skills from .gemini/skills/, .agents/skills/
Install the "bio-read-qc-fastp-workflow" agent skill from https://github.com/GPTomics/bioSkills/tree/main/read-qc/fastp-workflow into .gemini/skills/bio-read-qc-fastp-workflow/ in this project. Copy the whole folder (SKILL.md and every file beside it), keep the folder name "bio-read-qc-fastp-workflow", then confirm the skill loads.Gemini CLI copies the folder itself, the same result as the manual copy. Check what it changed before you commit it.
$ gh skill install GPTomics/bioSkills bio-read-qc-fastp-workflowInstalls for Copilot at project scope by default; add --scope user for a personal install. Preview a skill first with gh skill preview. Needs GitHub CLI 2.90.0 or later (public preview).
$ npx skills add GPTomics/bioSkills --skill bio-read-qc-fastp-workflow -a github-copilotProject install goes to .agents/skills/; add -g for ~/.copilot/skills/.
$ git clone --depth 1 https://github.com/GPTomics/bioSkills.git skills-src && mkdir -p .github/skills && cp -r skills-src/read-qc/fastp-workflow .github/skills/bio-read-qc-fastp-workflow && rm -rf skills-srcUse ~/.copilot/skills/ instead of .github/skills for a personal install. Commit .github/skills so cloud agent and code review can use it.
GitHub Copilot skills documentation · loads skills from .github/skills/, .claude/skills/, .agents/skills/
Install the "bio-read-qc-fastp-workflow" agent skill from https://github.com/GPTomics/bioSkills/tree/main/read-qc/fastp-workflow into .github/skills/bio-read-qc-fastp-workflow/ in this project. Copy the whole folder (SKILL.md and every file beside it), keep the folder name "bio-read-qc-fastp-workflow", then confirm the skill loads.GitHub Copilot copies the folder itself, the same result as the manual copy. Check what it changed before you commit it.
$ npx skills add GPTomics/bioSkills --skill bio-read-qc-fastp-workflow -a opencodeOpenCode documents no install command of its own. Project install goes to .agents/skills/; add -g for ~/.config/opencode/skills/.
$ gh skill install GPTomics/bioSkills bio-read-qc-fastp-workflow --agent opencodeProject scope by default (.agents/skills/); add --scope user for a personal install.
$ git clone --depth 1 https://github.com/GPTomics/bioSkills.git skills-src && mkdir -p .opencode/skills && cp -r skills-src/read-qc/fastp-workflow .opencode/skills/bio-read-qc-fastp-workflow && rm -rf skills-srcUse ~/.config/opencode/skills/ instead of .opencode/skills for a personal install.
OpenCode skills documentation · loads skills from .opencode/skills/, .claude/skills/, .agents/skills/
Install the "bio-read-qc-fastp-workflow" agent skill from https://github.com/GPTomics/bioSkills/tree/main/read-qc/fastp-workflow into .opencode/skills/bio-read-qc-fastp-workflow/ in this project. Copy the whole folder (SKILL.md and every file beside it), keep the folder name "bio-read-qc-fastp-workflow", then confirm the skill loads.OpenCode copies the folder itself, the same result as the manual copy. Check what it changed before you commit it.
bio-read-qc-fastp-workflowRuns all-in-one FASTQ preprocessing with fastp in a single pass - adapter trimming via paired-end overlap analysis, quality/length filtering, 2-color poly-G removal, base correction, optional…
Bio Read Qc Fastp Workflow is an agent skill from GPTomics/bioSkills. Runs all-in-one FASTQ preprocessing with fastp in a single pass - adapter trimming via paired-end overlap analysis, quality/length filtering, 2-color poly-G removal, base correction, optional dedup/UMI/merge, and HTML/JSON reports. Use when preprocessing bulk Illumina data and wanting one fast tool instead of separate Cutadapt, Trimmomatic, and FastQC steps. For precise small-RNA/amplicon adapters use adapter-trimming; for molecule-accurate UMI dedup use umi-processing.
Its SKILL.md is about 2.3k tokens, which your agent loads only when the skill is triggered. The skill folder holds 3 other files (for example `examples/fastp_pipeline.sh` and `usage-guide.md`).
It sits in Research & Science. The repository describes itself as: a set of SKILLS.md for doing bioinformatics with agents like claude code. The licence is MIT.
3 steps, taken from the first numbered list in SKILL.md.
Read from SKILL.md and the folder at commit d91ed3d. It shows what the files ask for, not the result of running them.
Pre-approves nothing: there is no allowed-tools line, so your agent's usual permission prompts apply.
From allowed-tools in the SKILL.md frontmatter.
Ships script files (Shell), which the agent can run.
Shell commands in SKILL.md call:
pipFrom the folder's file list and the shell code blocks in SKILL.md.
No URLs in SKILL.md. Its commands use pip, which can reach the network depending on how they are called.
From URLs in SKILL.md, links to its own repository left out.
Names no API keys, tokens, secrets or passwords.
From names ending in _API_KEY, _TOKEN, _SECRET, _KEY or _PASSWORD in SKILL.md.
Bio Read Qc Fastp Workflow loads about 2.3k tokens when it runs. Until then it costs about 125 tokens; SKILL.md has 740 words of instructions outside code blocks.
Estimates: characters ÷ 4, the usual rule of thumb; real counts depend on the model's tokenizer. Scripts and assets cost tokens only if the agent reads them.
The automated check found no risky patterns in SKILL.md.
Automated static check — not a guarantee. Review scripts before installing. It scans the text of SKILL.md for risky patterns (piping downloads into a shell, reading credential files, hidden Unicode, destructive commands); files beside SKILL.md are not scanned.
The full file from GPTomics/bioSkills at commit d91ed3d, republished under its MIT licence (© GPTomics). 740 words, ~2,348 tokens.
.claude/skills/bio-read-qc-fastp-workflow/SKILL.md (or your agent's skills folder). This skill also uses 2 other files; get the full folder from GitHub.Reference examples tested with: fastp 0.23+, FastQC 0.12+, MultiQC 1.21+
Before using code patterns, verify installed versions match. If versions differ:
<tool> --version then <tool> --help to confirm flagspip show <package> then help(module.function) to check signaturesIf code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.
Run adapter trimming, quality/length filtering, poly-G removal, and reporting in a single fast pass.
"Preprocess my reads with fastp" -> Trim adapters from the read overlap, filter low-quality reads, remove 2-color poly-G, and emit an HTML/JSON report.
fastp -i R1.fq.gz -I R2.fq.gz -o c_R1.fq.gz -O c_R2.fq.gz -h report.html -j report.jsonScope: this skill OWNS general-purpose single-pass Illumina preprocessing. Precise small-RNA/amplicon/anchored adapters -> read-qc/adapter-trimming. Molecule-accurate UMI dedup/consensus -> read-qc/umi-processing. DNA coordinate dedup -> alignment-files/duplicate-handling. OUT OF SCOPE: transcriptome QC (read-qc/rnaseq-qc).
fastp trims paired-end adapters by OVERLAP ANALYSIS, needing no adapter sequence at all. It aligns R1 against the reverse complement of R2, finds the insert-derived overlap, and trims whatever extends past it (the read-through region) -- so it can trim adapter down to a SINGLE trailing base, where sequence-matching tools need at least 3. The same overlap drives --correction (-c): where the mates disagree and one base is high-quality and the other very low, fastp overwrites the low-quality base with the high-quality call. This overlap machinery is why fastp is the default bulk PE preprocessor and why it needs no --adapter_sequence for standard libraries.
--dedup is SEQUENCE-identity deduplication at the FASTQ level -- no coordinates, no UMI -- so it removes BIOLOGICAL duplicates too. It cannot tell a PCR duplicate from a highly expressed transcript's fragment or a targeted amplicon. NEVER use --dedup for RNA-seq quantification, amplicon, or any assay where identical reads are genuine signal. For molecule-accurate removal use UMIs (read-qc/umi-processing); for DNA variant calling use coordinate-based dedup AFTER alignment (alignment-files/duplicate-handling). fastp --dedup is for the narrow case of removing exact-duplicate reads from a non-UMI library where that is known to be safe.
Poly-G trimming auto-enables for 2-color instruments (NextSeq/NovaSeq) from the machine ID, because G is the no-signal call. Leave it on; a high-quality poly-G tail is invisible to the quality filter. One fast pass does adapter + quality + poly-G + filtering + QC report, and the JSON feeds MultiQC -- but fastp does NOT replace cutadapt's precision for small-RNA 3' adapters, amplicon primers, or anchored/linked adapters.
| Need | Use fastp? | Alternative |
|---|---|---|
| Bulk PE WGS/WES/RNA/cfDNA preprocessing | Yes (default) | -- |
| One pass: trim + filter + poly-G + QC report | Yes | -- |
| Small-RNA 3' adapter + tight length gate | No | cutadapt (read-qc/adapter-trimming) |
| Amplicon / anchored / linked primers | No | cutadapt |
| Molecule counting / ctDNA consensus | Extract only | umi_tools / fgbio (read-qc/umi-processing) |
| RNA-seq molecule dedup | No (--dedup is wrong) | UMIs, or do not dedup |
# Single-end and paired-end basics
fastp -i in.fq.gz -o out.fq.gz
fastp -i R1.fq.gz -I R2.fq.gz -o c_R1.fq.gz -O c_R2.fq.gz
# Adapter: PE overlap is automatic; --detect_adapter_for_pe ADDS sequence-based detection on top
fastp -i R1.fq.gz -I R2.fq.gz -o c_R1.fq.gz -O c_R2.fq.gz --detect_adapter_for_pe
# Manual adapter sequences (SE auto-detects from data by default)
fastp -i in.fq.gz -o out.fq.gz --adapter_sequence AGATCGGAAGAGCACACGTCTGAACTCCAGTCA
# Quality FILTER (per-read): base <Q20 unqualified; drop if >40% unqualified or >5 Ns
fastp -i in.fq.gz -o out.fq.gz -q 20 -u 40 -n 5
# Quality TRIM (sliding window from 3', SLIDINGWINDOW analogue) + length gate
fastp -i in.fq.gz -o out.fq.gz --cut_right --cut_window_size 4 --cut_mean_quality 20 -l 36
# 2-color poly-G (auto for NextSeq/NovaSeq); poly-X for 3' poly-A etc.
fastp -i in.fq.gz -o out.fq.gz --trim_poly_g # --poly_g_min_len 10 default
fastp -i in.fq.gz -o out.fq.gz --trim_poly_x
# Overlap base correction (PE only; high-Q mate fixes low-Q base)
fastp -i R1.fq.gz -I R2.fq.gz -o c_R1.fq.gz -O c_R2.fq.gz --correction
# Merge overlapping pairs (short inserts: cfDNA, small-RNA, aDNA). Produces THREE streams:
# the merged file is single-end (full insert) and un_R1/un_R2 stay paired -- align them separately
# (merged as SE, un_R1/un_R2 as PE) and combine the BAMs.
fastp -i R1.fq.gz -I R2.fq.gz --merge --merged_out merged.fq.gz -o un_R1.fq.gz -O un_R2.fq.gz
# UMI extraction: fastp moves the inline UMI out of the read before trimming; molecule-accurate
# dedup/consensus still happens AFTER alignment (umi_tools/fgbio), not in fastp
fastp -i R1.fq.gz -I R2.fq.gz -o c_R1.fq.gz -O c_R2.fq.gz --umi --umi_loc read1 --umi_len 8Key flags: -q qualified quality (default 15), -u unqualified percent limit (40), -n N limit (5), -e average-quality filter (0=off), -l length required (15), --length_limit (0=off), --cut_right/--cut_front/--cut_tail window cut modes (off by default), --cut_window_size (4), --cut_mean_quality (Q20), --thread/-w (default 3), -h/-j HTML/JSON report.
# Standard Illumina PE (4-color: HiSeq/MiSeq)
fastp -i raw_R1.fq.gz -I raw_R2.fq.gz -o clean_R1.fq.gz -O clean_R2.fq.gz \
--detect_adapter_for_pe --cut_right --cut_window_size 4 --cut_mean_quality 20 \
-q 20 -l 36 -w 8 -h sample.html -j sample.json
# NovaSeq / NextSeq (2-color): add poly-G (auto, but explicit for clarity)
fastp -i raw_R1.fq.gz -I raw_R2.fq.gz -o clean_R1.fq.gz -O clean_R2.fq.gz \
--detect_adapter_for_pe --trim_poly_g \
--cut_right --cut_window_size 4 --cut_mean_quality 20 -q 20 -l 36 -w 8 \
-h sample.html -j sample.json
# RNA-seq: light trim only (aligner soft-clips; do NOT --dedup), longer min length
fastp -i raw_R1.fq.gz -I raw_R2.fq.gz -o clean_R1.fq.gz -O clean_R2.fq.gz \
--detect_adapter_for_pe -q 20 -l 50 -w 8 -h sample.html -j sample.jsonimport json
with open('sample.json') as f:
report = json.load(f)
after = report['summary']['after_filtering']
print(f"reads kept: {after['total_reads']}, Q30: {after['q30_rate']:.2%}")
print(f"duplication: {report['duplication']['rate']:.2%}") # diagnostic only -- do not auto-dedupMultiQC parses fastp JSON directly: multiqc . over a directory of *.json builds the cohort report (read-qc/quality-reports).
| Symptom | Cause | Solution |
|---|---|---|
| RNA-seq counts deflated after fastp | Used --dedup (sequence dedup removes biological dups) | Drop --dedup for RNA-seq; never sequence-dedup expression data |
| Adapter not trimmed (SE) | SE has no overlap; relies on data auto-detect | Pass --adapter_sequence explicitly for SE |
| Poly-G remains | 4-color run, or auto-detect missed the instrument | Add --trim_poly_g explicitly |
| Small-RNA results poor | fastp overlap is not precise enough for ~22 nt inserts | Use cutadapt with --discard-untrimmed (read-qc/adapter-trimming) |
| Over-trimmed RNA-seq | Aggressive --cut_right quality | Light trim only; aligner soft-clips (read-qc/quality-filtering) |
| UMI dedup expected but none happened | --umi only EXTRACTS; dedup is post-alignment | Extract here, dedup with umi_tools/fgbio after mapping (read-qc/umi-processing) |
Chen S, Zhou Y, Chen Y, Gu J. 2018. fastp: an ultra-fast all-in-one FASTQ preprocessor. Bioinformatics 34(17):i884-i890. Chen S. 2023. Ultrafast one-pass FASTQ data preprocessing, quality control, and deduplication using fastp. iMeta 2(2):e107. Ewels P, Magnusson M, Lundin S, Kaller M. 2016. MultiQC: summarize analysis results for multiple tools and samples in a single report. Bioinformatics 32(19):3047-3048.
read-qc/adapter-trimming - Precise adapter/primer control for small-RNA and amplicon read-qc/quality-filtering - Detailed quality/length filtering options and the trim-light evidence base read-qc/quality-reports - Aggregate fastp JSON across samples with MultiQC read-qc/umi-processing - Molecule-accurate UMI dedup and consensus after alignment alignment-files/duplicate-handling - Coordinate-based duplicate marking for DNA variant calling
© GPTomics, MIT. Rendered from Markdown: HTML in the file is shown as text, images as links, and headings moved down two levels. Raw file
SKILL.md and 2 other files in read-qc/fastp-workflow of GPTomics/bioSkills.
Open the folder on GitHubat commit d91ed3d
We found 1 copy of this SKILL.md (exact, near-identical or edited) in other folders, from 1 other GitHub owner. This page covers the copy in GPTomics/bioSkills, which our catalogue first saw on October 7, 2026.
Bio Read Qc Fastp Workflow next to the 5 skills that share the most tags, products or categories with it. Stars are the repository's; “used in” counts other GitHub owners with a copy.
| Skill | Stars | Used in | Tokens | Auto-check | Licence | Repo updated |
|---|---|---|---|---|---|---|
| Bio Read Qc Fastp Workflow this skillGPTomics/bioSkills | 1.2k | 1 repos | ~2.3k | Automated safety check: Pass | MIT | |
| Hypothesis Generationspacering-net/codeg | 3.9k | 14 repos | ~3.6k | Automated safety check: Notes | MIT | |
| GitHub Deep Researchbytedance/deer-flow | 84k | 4 repos | ~1.3k | Automated safety check: Pass | MIT | |
| Nature Paper CardYuan1z0825/nature-skills | 47k | 2 repos | ~2.1k | Automated safety check: Pass | Apache-2.0 | |
| Content Research Writerweapp-tailwindcss/weapp-tailwindcss | 1.9k | 25 repos | ~3.5k | Automated safety check: Pass | MIT | |
| Last30daysmvanhorn/last30days-skill | 64k | — | ~7.9k | Automated safety check: Notes | MIT |
spacering-net/codeg
Structured hypothesis formulation from observations. An agent skill from spacering-net/codeg.
bytedance/deer-flow
Researches a GitHub repository over four rounds using the GitHub API and web search, then writes a structured markdown report with timeline, metrics and Mermaid diagrams.
Yuan1z0825/nature-skills
Builds a structured deep-reading card for one scientific paper, covering methods, how experiments support claims, limitations and research ideas, with a script to prepare the source.
weapp-tailwindcss/weapp-tailwindcss
Assists in writing high-quality content by conducting research, adding citations, improving hooks, iterating on outlines, and providing real-time feedback on each section.
mvanhorn/last30days-skill
Research what people actually say about any topic in the last 30 days.
spacering-net/codeg
Structured manuscript/grant review with checklist-based evaluation.
GPTomics/bioSkills
Read, write, and convert multiple sequence alignment files using Biopython Bio.AlignIO.
GPTomics/bioSkills
Installs the bioSkills collection of 425 bioinformatics skills in one step, or only chosen categories, so sequencing, RNA-seq, single-cell and variant tasks get specialized help.
GPTomics/bioSkills
Write biological sequences to files (FASTA, FASTQ, GenBank, EMBL) using Biopython Bio.SeqIO.
GPTomics/bioSkills
Soft- or hard-clips PCR primer footprints from aligned amplicon BAMs so primer bases stop masquerading as confirmed reference sequence.
GPTomics/bioSkills
Filters BAM alignments by FLAG bits, mapping quality and regions with samtools view or pysam, with recipes for common keep and drop cases.
GPTomics/bioSkills
Create and use BAI/CSI indices for BAM/CRAM files using samtools and pysam.
Categories
Runs all-in-one FASTQ preprocessing with fastp in a single pass - adapter trimming via paired-end overlap analysis, quality/length filtering, 2-color poly-G removal, base correction, optional…. Bio Read Qc Fastp Workflow is an agent skill from GPTomics/bioSkills. Runs all-in-one FASTQ preprocessing with fastp in a single pass - adapter trimming via paired-end overlap analysis, quality/length filtering, 2-color poly-G removal, base correction, optional dedup/UMI/merge, and HTML/JSON reports.
Bio Read Qc Fastp Workflow fits situations like: preprocessing bulk Illumina data and wanting one fast tool instead of separate Cutadapt.
Run `npx skills add GPTomics/bioSkills --skill bio-read-qc-fastp-workflow -a claude-code`. Or copy the skill folder (read-qc/fastp-workflow in GPTomics/bioSkills) into .claude/skills/bio-read-qc-fastp-workflow in your project. Claude Code loads it when a task matches its description.
Run `npx skills add GPTomics/bioSkills --skill bio-read-qc-fastp-workflow -a codex`. Or copy the skill folder (read-qc/fastp-workflow in GPTomics/bioSkills) into .agents/skills/bio-read-qc-fastp-workflow in your project. Codex loads it when a task matches its description.
Cursor, Gemini CLI, GitHub Copilot and OpenCode also load SKILL.md folders. With the skills CLI, run `npx skills add GPTomics/bioSkills --skill bio-read-qc-fastp-workflow -a cursor` (or -a gemini-cli, github-copilot or opencode for the others). To copy it by hand, put the folder in .cursor/skills/bio-read-qc-fastp-workflow, .gemini/skills/bio-read-qc-fastp-workflow, .github/skills/bio-read-qc-fastp-workflow and .opencode/skills/bio-read-qc-fastp-workflow in your project.
Going by SKILL.md and its folder, Bio Read Qc Fastp Workflow needs a shell for the scripts in its folder and the command-line tools its instructions call (pip). Our summary lists: Python 3; A Bash shell.
SKILL.md contains no URLs. Its commands use pip, which can reach the network depending on how they are called. This is read from the text; nothing was executed.
Our automated static check of SKILL.md found no risky patterns, such as piping downloads into a shell, reading credential files or hidden Unicode. It is not a guarantee. Review the folder before installing.
Bio Read Qc Fastp Workflow is published under the MIT licence (the repository's licence). It allows redistribution, so the full SKILL.md is shown on this page.
About 2.3k tokens (SKILL.md is roughly 9.4k characters). Agents keep only the skill's name and description in context until a task matches; then they load SKILL.md in full.
Skills that share tags, products or a category with Bio Read Qc Fastp Workflow: Hypothesis Generation (spacering-net/codeg, 3.9k stars), GitHub Deep Research (bytedance/deer-flow, 84k stars), Nature Paper Card (Yuan1z0825/nature-skills, 47k stars) and Content Research Writer (weapp-tailwindcss/weapp-tailwindcss, 1.9k stars). The comparison table on this page puts their stars, adoption, token cost, safety result and licence side by side.
GPTomics (a GitHub organization) maintains it in GPTomics/bioSkills, which has 1,218 GitHub stars. The repository holds 559 skills in this directory. The repository was last updated on August 15, 2026.
Source: GPTomics/bioSkills on GitHub. Facts on this page come from the repository at the commit we read; the author's words are quoted as theirs.