One-click install
npx skills add https://github.com/shushuzn/Rairos --skill gget-shushuzn
Or copy as Structured Prompt for Agent
Please help me install this Agent Skill.
Skill: gget
Source: https://github.com/shushuzn/Rairos/tree/main/skills/gget
Command: npx skills add https://github.com/shushuzn/Rairos --skill gget-shushuzn

SYSTEM DOCUMENTATION & REQUIREMENTS

💡 This Skill includes scripts (resource) and references (resource) components.

What problem does it solve?

gget eliminates slow, fragmented research lookups by providing a single, consistent interface to query multiple genomics, proteomics, structure, expression, and enrichment resources without switching tools or manually reformatting results.

Core Features & Use Cases

  • Unified multi-database queries: Retrieve gene references, gene/transcript metadata, sequences, and cross-resource identifiers through consistent CLI/Python APIs.
  • Integrated analysis tools: Run BLAST/BLAT, multiple sequence alignment, local protein alignment (DIAMOND), motif prediction (ELM), structure retrieval (PDB), and structure prediction (AlphaFold).
  • End-to-end research workflows: Support common pipelines like gene discovery → sequence/structure → expression/correlation → enrichment → disease/drug association exploration.
  • Use Case: If you have a gene list from your study, you can quickly fetch sequences, run enrichments, and pull candidate disease/drug links in one repeatable workflow.

Quick Start

Ask the AI to run: "Search for GABA-related genes in human with gget search -s human gaba gamma-aminobutyric and return the top results as JSON."

Frequently Asked Questions about gget

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

FAQPage Schema
How do I query multiple bioinformatics databases for gene sequences and annotations in one workflow?

Querying multiple bioinformatics databases for gene sequences and annotations is done through a unified interface that retrieves gene references, identifiers, sequences, and biological annotations across genomic and proteomic resources without switching tools.

Can I retrieve protein structures and run sequence alignment from a single CLI tool?

Yes, you can retrieve protein structures and run sequence alignment from a single CLI tool. The interface supports integrated BLAST/BLAT searches, multiple sequence alignment, local protein alignment via DIAMOND, and structure retrieval or prediction using PDB and AlphaFold.

What is the best way to run enrichment analysis and disease association queries on a gene list?

Running enrichment analysis and disease association queries on a gene list is best handled by an end-to-end research workflow that fetches sequences, executes enrichments, and pulls candidate disease and drug association links in one repeatable pipeline.

Does gene search and expression correlation require setting up dependencies for specific modules?

Gene search and expression correlation requires module-scoped dependency setup for specific resources. You must configure dependencies for AlphaFold, ELM, and cellxgene to enable structure prediction, motif prediction, and expression correlation respectively.

How do I serialize bioinformatics query results into JSON, CSV, FASTA, or PDB formats?

Serializing bioinformatics query results into JSON, CSV, FASTA, or PDB formats is handled natively by the deterministic CLI and Python interface. The interface provides output serialization options alongside species and assembly selection parameters.

Why use a unified local query tool instead of manually switching between genomic and proteomic resources?

Using a unified local query tool instead of manually switching between genomic and proteomic resources eliminates slow, fragmented research lookups by preventing manual result reformatting and providing a single consistent API across multiple databases.