bioinformatics

Fetch domain-specific bioinformatics skills and reference materials from bioSkills and ClawBio.

1|Updated Mar 22, 2026
One-click install
npx skills add https://github.com/nelohenriq/hermes-agent-plus --skill bioinformatics-nelohenriq
Or copy as Structured Prompt for Agent
Please help me install this Agent Skill.
Skill: bioinformatics
Source: https://github.com/nelohenriq/hermes-agent-plus/tree/main/optional-skills/research/bioinformatics
Command: npx skills add https://github.com/nelohenriq/hermes-agent-plus --skill bioinformatics-nelohenriq

SYSTEM DOCUMENTATION & REQUIREMENTS

What problem does it solve?

This Skill bundles access to two expansive open-source knowledge bases for bioinformatics, enabling fast discovery of domain-specific guidance without duplicating content.

Core Features & Use Cases

  • Domain-wide access: Provides a gateway to bioSkills and ClawBio libraries, surfacing relevant reference material and runnable pipelines on demand.
  • Curated domain coverage: Covers genomics, transcriptomics, single-cell analysis, variant calling, pharmacogenomics, metagenomics, and more, helping researchers locate authoritative guidance quickly.
  • Use Case: When starting a new bioinformatics analysis, fetch the appropriate SKILL.md topic to understand recommended tools, parameters, and best practices.

Quick Start

Clone and read the domain-specific SKILL.md files from bioSkills and ClawBio repositories to begin.

Frequently Asked Questions about bioinformatics

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

FAQPage Schema
How do I find recommended tools and parameters for genomics and transcriptomics workflows?

To find recommended tools and parameters for genomics and transcriptomics workflows, this Skill fetches domain-specific reference materials and runnable pipelines from the bioSkills and ClawBio open-source knowledge bases. It indexes and retrieves authoritative guidance on demand.

What is the best way to access open-source reference materials for single-cell analysis?

The best way to access open-source reference materials for single-cell analysis is through this Skill, which serves as a gateway to 400+ bioinformatics skills. It surfaces curated domain coverage and best practices directly from the bioSkills and ClawBio libraries.

Can I retrieve variant calling and pharmacogenomics pipelines without duplicating content?

Yes, you can retrieve variant calling and pharmacogenomics pipelines without duplicating content. This Skill bundles access to bioSkills and ClawBio, enabling fast discovery of domain-specific computational biology guidance while respecting licensing and reproducibility considerations.

Does this bioinformatics knowledge fetcher cover metagenomics research contexts?

Yes, this bioinformatics knowledge fetcher covers metagenomics research contexts. It provides curated domain coverage across computational biology workflows, fetching relevant reference material and runnable pipelines on demand for various biological research applications.

How do I start a new computational biology analysis using fetched SKILL.md files?

To start a new computational biology analysis using fetched SKILL.md files, clone and read the domain-specific files from the bioSkills and ClawBio repositories. This allows you to understand recommended tools, parameters, and best practices for your specific research task.