scientific-bioinformatics

Coordinates multi-omics bioinformatics workflows including scRNA-seq, genome, PPI, and metabolomics analyses.

3|1|Updated Feb 11, 2026
One-click install
npx skills add https://github.com/nahisaho/satori --skill scientific-bioinformatics
Or copy as Structured Prompt for Agent
Please help me install this Agent Skill.
Skill: scientific-bioinformatics
Source: https://github.com/nahisaho/satori/tree/main/src/.github/skills/scientific-bioinformatics
Command: npx skills add https://github.com/nahisaho/satori --skill scientific-bioinformatics

SYSTEM DOCUMENTATION & REQUIREMENTS

What problem does it solve?

Provides unified, reusable pipelines for major bioinformatics tasks (scRNA-seq, genome analysis, PPI networks, and metabolomics preprocessing), helping researchers standardize workflows and reproduce results.

Core Features & Use Cases

  • Integrates four primary workflows: scRNA-seq QC/normalization/ clustering/ DEG, genome sequence alignment and phylogeny, PPI network construction and centrality analysis, and metabolomics preprocessing (imputation, log transformation, scaling).
  • Use Cases: Exp-01, Exp-04, Exp-07, Exp-09 patterns; can adapt to new datasets and tools; supports cross-omics analysis.
  • Example scenario: A data scientist applies the SciBioinformatics pipelines to preprocess RNA data, assemble PPIs, and prepare metabolomics data for downstream modeling.

Quick Start

Run the scRNA-seq pipeline on your dataset using Scanpy.

Frequently Asked Questions about scientific-bioinformatics

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

FAQPage Schema
How do I build reproducible bioinformatics pipelines for multi-omics data?

You can run standardized pipelines for scRNA-seq, genome analysis, PPI networks, and metabolomics to ensure reproducible results across multi-omics research projects. It provides parameterized steps and modular components with explicit dependencies.

How do I run scRNA-seq QC, normalization, and clustering using Scanpy?

The scRNA-seq pipeline processes datasets using Scanpy to perform quality control, normalization, clustering, and differential gene expression analysis within a standardized, parameterized workflow.

What is the best way to preprocess metabolomics data for downstream modeling?

Preprocess metabolomics data by applying pipeline steps for imputation, log transformation, and scaling, preparing the dataset for downstream modeling and cross-omics analysis.

Can I use this pipeline for genome sequence alignment and phylogeny analysis?

Yes, the integrated bioinformatics workflows include genome sequence alignment and phylogeny analysis, allowing you to process genomic sequences within standardized, reproducible pipelines.

Does this workflow support PPI network construction and centrality analysis?

Yes, the pipelines support PPI network construction and centrality analysis, enabling you to assemble protein-protein interaction networks and calculate node importance for multi-omics research.

Do I need specific dependencies to run cross-omics analysis with these pipelines?

No external dependencies are required to run the workflows, as the modular components feature explicit dependencies and resource references internally, supporting cross-omics analysis and adaptation to new datasets.