kwp-bio-research-nextflow-development

Automate nf-core pipeline deployment and execution for genomic data analysis.

7|5|Updated May 7, 2026
One-click install
npx skills add https://github.com/14790897/MiQi --skill kwp-bio-research-nextflow-development
Or copy as Structured Prompt for Agent
Please help me install this Agent Skill.
Skill: kwp-bio-research-nextflow-development
Source: https://github.com/14790897/MiQi/tree/main/miqi/skills/kwp/bio-research/nextflow-development
Command: npx skills add https://github.com/14790897/MiQi --skill kwp-bio-research-nextflow-development

SYSTEM DOCUMENTATION & REQUIREMENTS

💡 This Skill requires docker, nextflow, openjdk-11-jdk, sra-tools, and includes scripts (resource) and references (resource) components.

What problem does it solve?

This skill removes the technical barrier for researchers needing to perform complex genomic analyses like RNA-seq or variant calling by automating the deployment of nf-core pipelines.

Core Features & Use Cases

  • Pipeline Automation: Orchestrates the execution of standard nf-core pipelines including rnaseq, sarek, and atacseq.
  • Data Management: Handles the acquisition of public datasets from GEO/SRA and generates necessary samplesheets automatically.
  • Environment Validation: Ensures all dependencies like Docker, Nextflow, and Java are correctly configured before execution to prevent runtime failures.

Quick Start

Use the kwp-bio-research-nextflow-development skill to analyze the RNA-seq data located in the current directory using the nf-core rnaseq pipeline.

Frequently Asked Questions about kwp-bio-research-nextflow-development

High-intent search queries and answers about installing and using this skill.

FAQPage Schema
How do I automate nf-core RNA-seq pipeline execution for genomic data analysis?

Automate nf-core RNA-seq pipeline execution by deploying workflows that orchestrate genomic data analysis, environment validation, and public dataset acquisition to ensure reproducible computational results.

What dependencies do I need to run nf-core pipelines for variant calling?

To run nf-core pipelines for variant calling, you need Docker, Nextflow, OpenJDK 11, and SRA-tools configured in your environment to ensure scalable and reproducible workflow execution.

Can I automatically acquire public datasets and generate samplesheets for Nextflow workflows?

Yes, you can automatically acquire public datasets from GEO/SRA and generate necessary samplesheets for Nextflow workflows, removing the manual data preparation barrier before running bioinformatics pipelines.

Does this approach support ATAC-seq and WGS workflows alongside RNA-seq analysis?

Yes, this approach supports ATAC-seq and WGS/WES workflows alongside RNA-seq analysis by orchestrating standard nf-core pipelines including rnaseq, sarek, and atacseq for comprehensive genomic data processing.

Why does my nf-core pipeline fail before execution starts?

nf-core pipeline execution fails before starting when dependencies like Docker, Nextflow, and Java are incorrectly configured, which is why environment validation is performed automatically before runtime to prevent failures.