nf 技能测试
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- 作者仓库 PantheonOS
nf-core Pipelines Skills
nf-core is a community-driven collection of 143+ curated Nextflow pipelines for bioinformatics. All pipelines are open-source (MIT), rigorously tested, and run portably on laptops, HPCs, and cloud platforms with automated dependency management via Docker, Singularity, or Conda.
Available Skills
Getting Started & Usage
Installation, configuration, and common usage patterns for running any nf-core pipeline on local machines, HPC clusters, or cloud environments.
Skill file: nfcore_usage.md
When to use:
- First time setting up Nextflow and nf-core
- Configuring pipelines for your HPC cluster or cloud environment
- Understanding resource management, resume, and offline execution
- Looking up nf-core CLI tool commands
Single-Cell & Bulk RNA-seq Pipelines
Pipelines for processing single-cell RNA-seq (10x, Drop-seq, Smart-seq) and bulk RNA-seq data from raw FASTQs to count matrices.
Skill file: nfcore_transcriptomics.md
When to use:
- Processing 10x Chromium, Drop-seq, or Smart-seq scRNA-seq data
- Running downstream single-cell analysis (doublet removal, integration, annotation)
- Processing bulk RNA-seq with STAR, HISAT2, Salmon, or Kallisto
- Generating gene/transcript count matrices and QC reports
Spatial Omics Pipelines
Pipelines for spatial transcriptomics platforms including Visium, Xenium, MERSCOPE, CosMX, and molecular cartography.
Skill file: nfcore_spatial.md
When to use:
- Processing 10x Visium or Visium HD data
- Analyzing Xenium in situ data with cell segmentation
- Running technology-agnostic spatial pipelines (sopa)
- Processing Resolve Bioscience Molecular Cartography data
Epigenomics Pipelines
Pipelines for chromatin accessibility, histone modification, protein-DNA interaction, and DNA methylation profiling.
Skill file: nfcore_epigenomics.md
When to use:
- Processing ATAC-seq data (bulk)
- Analyzing ChIP-seq experiments with peak calling
- Running CUT&Run or CUT&Tag with spike-in normalization
- Processing bisulfite sequencing or TAPS methylation data
Variant Calling Pipeline (Sarek)
Germline and somatic variant detection from WGS, WES, or targeted sequencing data with 16+ variant callers.
Skill file: nfcore_variant_calling.md
When to use:
- Detecting germline or somatic SNVs, indels, SVs, and CNVs
- Processing tumor/normal pairs or tumor-only samples
- Running multi-caller consensus variant analysis
- Annotating variants with SnpEff or VEP
Hi-C Chromatin Conformation Pipeline
Pipeline for processing Hi-C chromosome conformation capture data to study 3D genome organization: contact maps, TADs, and A/B compartments.
Skill file: nfcore_hic.md
When to use:
- Processing Hi-C data (digestion or DNase protocol)
- Generating multi-resolution contact maps (.cool/.mcool)
- Calling TADs and A/B compartments
- Studying 3D genome organization and chromatin interactions
Dynamic Pipeline Discovery (All 143+ Pipelines)
Meta-skill for dynamically discovering and using any nf-core pipeline, including those not covered by the skill files above. Teaches the agent how to fetch pipeline documentation, parameters, and samplesheet formats on-the-fly from standardized nf-core URLs and schemas.
Skill file: nfcore_dynamic_discovery.md
When to use:
- User asks about a pipeline not covered in the detailed skill files above
- Exploring what pipelines are available for a specific data type
- Need to look up parameters or samplesheet format for any nf-core pipeline
- Pipeline has been updated and you need the latest information
[!TIP] The detailed skill files above cover the most commonly used pipelines with full parameter tables and examples. For all other pipelines, use the dynamic discovery skill to fetch information on-the-fly from nf-co.re.
Using Skills
- Start with usage guide: Read
nfcore_usage.mdfor installation and configuration - Select pipeline skill: Choose the skill matching your data type
- Pipeline not listed? Use
nfcore_dynamic_discovery.mdto fetch docs on-the-fly - Follow samplesheet format: Each pipeline requires a specific CSV samplesheet
- Test first: Always run with
-profile test,dockerbefore real data - Use
-resume: Re-run failed pipelines without recomputing successful steps
- 流狐分类
- 工程开发
- 作者声明 Agent
- 未找到明确声明;不据此推断已兼容或已测试
- 静态检查
- 88 / 100 · 启发式扫描,不代表运行安全
- 作者 / 版本 / 许可
- @aristoteleo · 未声明 license
- 流狐 Token 估算
- 低消耗
- 流狐接入估算
- 需手动接入
- 是否需要外部 API Key
- 未发现要求
- 检测到的系统要求
- Docker
- 底层运行要求
- Docker
- 检测到的文件与系统行为
-
- 只读
- Shell 执行
- 检测到的网络行为
- 允许外网请求
- 安装命令数
- 无(仅作为资料)
档案由构建时根据 SKILL.md 与安装命令自动衍生,可能与作者实际意图存在差异。
需要注意: 未限定 allowed-tools,默认拥有全部工具权限。
作者没有在当前 SKILL.md 中定义固定输出样例。 Available Skills
Installation, configuration, and common usage patterns for running any nf-core pipeline on local machines, HPC clusters, or cloud environments. Skill file: nfcoreusage.md
Pipelines for processing single-cell RNA-seq (10x, Drop-seq, Smart-seq) and bulk RNA-seq data from raw FASTQs to count matrices. Skill file: nfcoretranscriptomics.md
Pipelines for spatial transcriptomics platforms including Visium, Xenium, MERSCOPE, CosMX, and molecular cartography. Skill file: nfcorespatial.md
Pipelines for chromatin accessibility, histone modification, protein-DNA interaction, and DNA methylation profiling. Skill file: nfcoreepigenomics.md
Germline and somatic variant detection from WGS, WES, or targeted sequencing data with 16+ variant callers. Skill file: nfcorevariantcalling.md
# nf-core Pipelines Skills
[nf-core](https://nf-co.re/) is a community-driven collection of **143+ curated
Nextflow pipelines** for bioinformatics. All pipelines are open-source (MIT),
rigorously tested, and run portably on laptops, HPCs, and cloud platforms with
automated dependency management via Docker, Singularity, or Conda.
## Available Skills
### Getting Started & Usage
Installation, configuration, and common usage patterns for running any
nf-core pipeline on local machines, HPC clusters, or cloud environments.
**Skill file**: [nfcore_usage.md](./nfcore_usage.md)
**When to use**:
- First time setting up Nextflow and nf-core
- Configuring pipelines for your HPC cluster or cloud environment
- Understanding resource management, resume, and offline execution
- Looking up nf-core CLI tool commands
---
### Single-Cell & Bulk RNA-seq Pipelines
Pipelines for processing single-cell RNA-seq (10x, Drop-seq, Smart-seq)
and bulk RNA-seq data from raw FASTQs to count matrices.
**Skill file**: [nfcore_transcriptomics.md](./nfcore_transcriptomics.md)
**When to use**:
- Processing 10x Chromium, Drop-seq, or Smart-seq scRNA-seq data
- Running downstream single-cell analysis (doublet removal, integration, annotation)
- Processing bulk RNA-seq with STAR, HISAT2, Salmon, or Kallisto
- Generating gene/transcript count matrices and QC reports
---
### Spatial Omics Pipelines
Pipelines for spatial transcriptomics platforms including Visium, Xenium,
MERSCOPE, CosMX, and molecular cartography.
**Skill file**: [nfcore_spatial.md](./nfcore_spatial.md)
**When to use**:
- Processing 10x Visium or Visium HD data
- Analyzing Xenium in situ data with cell segmentation
- Running technology-agnostic spatial pipelines (sopa)
- Processing Resolve Bioscience Molecular Cartography data
… 作者原文负责流程事实;流狐只索引当前章节、要点、文件与命令。
章节 -> Available Skills → Getting Started & Usage → Single-Cell & Bulk RNA-seq Pipelines → Spatial Omics Pipelines → Epigenomics Pipelines → Variant Calling Pipeline (Sarek)
要点 -> Skill file · When to use · any · Start with usage guide · Select pipeline skill · Pipeline not listed? · Follow samplesheet format · Test first
文件/命令 -> nfcoreusage.md · nfcoredynamicdiscovery.md · -profile test,docker · -resume
内容 SHA-256 -> 59f803a92cd7
原文结构
适用与边界
原文中的明确线索
nfcoreusage.md、nfcoredynamicdiscovery.md、-profile test,docker、-resume