nextflow-development
Run nf-core bioinformatics pipelines (rnaseq, sarek, atacseq) on sequencing data.
Skill by necboy-eng
Install
Works with Claude Code, Claude apps, Codex, Cursor, Gemini CLI, GitHub Copilot, VS Code, OpenCode, Goose, Windsurf. Read the repository before you give any tool access to your data.
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About
Use cases: data, research
Reviews
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What this skill can do and what it asks for, from its SKILL.md. Checked Oct 25, 2026.
- Tools
- No tools found
- Secrets
- None asked for
- Install scripts
- None found
- Runs as
- Python package
Network hosts it talks to 1
codeload.github.com· found in install command
Files it touches
~/.claude/skills/nextflow-development
What's inside
- Skill name
nextflow-development- Description
- Run nf-core bioinformatics pipelines (rnaseq, sarek, atacseq) on sequencing data. Use when analyzing RNA-seq, WGS/WES, or ATAC-seq data—either local FASTQs or public datasets from GEO/SRA. Triggers on nf-core, Nextflow, FASTQ analysis, variant calling, gene expression, differential expression, GEO reanalysis, GSE/GSM/SRR accessions, or samplesheet creation.
- License
- MIT
- Instructions
- 287 lines in SKILL.md · view on GitHub
Before installing
- Ships executable scripts
- Instructions call the network
Files (22)
- LICENSE.txt
- SKILL.md
- geo-sra-acquisition.md · references/
- installation.md · references/
- atacseq.md · references/pipelines/
- rnaseq.md · references/pipelines/
- sarek.md · references/pipelines/
- troubleshooting.md · references/
- check_environment.py · scripts/
- genomes.yaml · scripts/config/
- atacseq.yaml · scripts/config/pipelines/
- rnaseq.yaml · scripts/config/pipelines/
- sarek.yaml · scripts/config/pipelines/
- detect_data_type.py · scripts/
- generate_samplesheet.py · scripts/
- manage_genomes.py · scripts/
- sra_geo_fetch.py · scripts/
- __init__.py · scripts/utils/
- file_discovery.py · scripts/utils/
- ncbi_utils.py · scripts/utils/
- sample_inference.py · scripts/utils/
- validators.py · scripts/utils/
SKILL.md (first lines)
# nf-core Pipeline Deployment Run nf-core bioinformatics pipelines on local or public sequencing data. **Target users:** Bench scientists and researchers without specialized bioinformatics training who need to run large-scale omics analyses—differential expression, variant calling, or chromatin accessibility analysis. ## Workflow Checklist ``` - [ ] Step 0: Acquire data (if from GEO/SRA) - [ ] Step 1: Environment check (MUST pass) - [ ] Step 2: Select pipeline (confirm with user) - [ ] Step 3: Run test profile (MUST pass) - [ ] Step 4: Create samplesheet - [ ] Step 5: Configure & run (confirm genome with user) - [ ] Step 6: Verify outputs ``` --- ## Step 0: Acquire Data (GEO/SRA Only) **Skip this step if user has local FASTQ files.** For public datasets, fetch from GEO/SRA first. See [references/geo-sra-acquisition.md](references/geo-sra-acquisition.md) for the full workflow. **Quick start:** ```bash # 1. Get study info python scripts/sra_geo_fetch.py info GSE110004 # 2. Download (interactive mode) python scripts/sra_geo_fetch.py download GSE110004 -o ./fastq -i # 3. Generate samplesheet python scripts/sra_geo_fetch.py samplesheet GSE110004 --fastq-dir ./fastq -o samplesheet.csv ``` **DECISION POINT:** After fetching study info, confirm with user: - Which sample subset to download (if multiple data types) - Suggested genome and pipeline Then continue to Step 1. --- ## Step 1: Environment Check **Run first. Pipeline will fail without passing environment.** ```bash python scripts/check_environment.py ``` All critical checks must pass. If any fail, provide fix instructions: ### Docker issues | Problem | Fix | |---------|-----| | Not installed | Install from https://docs.docker.com/get-docker/ | | Permission denied | `sudo usermod -aG docker $USER` then re-login | | Daemon not running | `sudo systemctl start docker` | ### Nextflow issues | Problem | Fix | |---------|-----| | Not installed | `curl -s https://get.nextflow.io \| bash && mv nextflow ~/bin/` | | Version < 23.04 | `nextflow self-update` | ### Java issues | Problem | Fix | |---------|-----| | Not installed / < 11 | `sudo apt install openjdk-11-jdk` | **Do not proceed until all checks pass.** For HPC/Singularity, see [references/troubleshooting.md](references/troubleshooting.md). --- ## Step 2: Select Pipeline **DECISION POINT: Confirm with user before proceeding.** | Data Type | Pipeline | Version | Goal | |-----------|----------|---------|------| | RNA-seq | `rnaseq` | 3.22.2 | Gene expression | | WGS/WES | `sarek` | 3.7.1 | Variant calling | | ATAC-seq | `atacseq` | 2.1.2 | Chromatin accessibility | Auto-detect from data: ```bash python scripts/detect_data_type.py /path/to/data ``` For pipeline-specific details: - [references/pipelines/rnaseq.md](references/pipelines/rnaseq.md) - [references/pipelines/sarek.md](references/pipelines/sarek.md) - [references/pipelines/atacseq.md](references/pipelines/atacseq.md) --- ## Step 3: Run Test Profile **Validates environment with small data. MUST pass before real data.** ```bash nextflow run nf-core/<pipeline> -r <version> -profile test,docker --outdir test_output ``` | Pipeline | Command | |----------|---------| | rnaseq | `nextflow run nf-core/rnaseq -r 3.22.2 -profile test,docker --outdir test_rnaseq` | | sarek | `nextflow run nf-core/sarek -r 3.7.1 -profile test,docker --outdir test_sarek` | | atacseq | `nextflow run nf-core/atacseq -r 2.1.2 -profile test,docker --outdir test_atacseq` | Verify:
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Signals
- Stars
- 1
- Forks
- 0
- Open issues
- 0
- Last commit (this folder)
- Feb 23, 2026 (8 months ago)
From GitHub (fetched Oct 24, 2026).
Details
- License
- MIT
- Repository
- github.com/necboy-eng/MantisBot
- First seen
- Oct 24, 2026
- Last checked
- Oct 24, 2026
- Source
- GitHubgithub-graphql
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Cite this page
nextflow-development skill. Agent Mart. https://agentmart.dev/skills/necboy-eng-nextflow-development (last updated 2026-10-24)