scientific-epigenomics-chromatin

Integrate multi-omics epigenomics analyses into a unified Python pipeline.

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

SYSTEM DOCUMENTATION & REQUIREMENTS

What problem does it solve?

Provides an integrated computational epigenomics pipeline that consolidates ChIP-seq peak calling, ATAC-seq accessibility, DNA methylation analysis, ChromHMM chromatin-state modeling, Hi-C 3D genome structure inference, and motif enrichment into a single workflow, enabling coherent regulatory interpretation from multi-omics data.

Core Features & Use Cases

  • ChIP-seq peak calling with MACS2/MACS3
  • ATAC-seq nucleosome-free region detection
  • DNA methylation pattern analysis (WGBS/RRBS)
  • ChromHMM-based chromatin-state modeling
  • Hi-C contact maps and TAD detection
  • Transcription factor motif enrichment
  • Differential binding analysis with DiffBind
  • ToolUniverse integration via ChIP-Atlas
  • Use Case: multi-omics datasets across samples to annotate regulatory landscapes and compare chromatin states.

Quick Start

Run the integrated epigenomics workflow on ChIP-seq and ATAC-seq data to produce peaks, methylation profiles, chromatin-state annotations, and 3D genome features.

Frequently Asked Questions about scientific-epigenomics-chromatin

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

FAQPage Schema
How do I integrate ChIP-seq and ATAC-seq data for chromatin-state annotation in a multi-omics pipeline?

You can unify multi-omics epigenomics analyses by integrating ChIP-seq peak calling and ATAC-seq accessibility into a single workflow to annotate chromatin states. This pipeline leverages MACS2/MACS3 and ChromHMM to produce coherent regulatory interpretations from multi-omics datasets.

What is the best way to detect differential binding and transcription factor motif enrichment across multi-omics samples?

To detect differential binding and motif enrichment across samples, you can utilize DiffBind for differential binding analysis alongside integrated transcription factor motif enrichment tools. This workflow enables coherent comparison of chromatin states and regulatory landscapes across experimental conditions.

Can I use ChromHMM and DiffBind with Hi-C contact maps for 3D genome structure inference?

Yes, you can use ChromHMM for chromatin-state modeling and DiffBind for differential binding while simultaneously processing Hi-C data for contact maps and TAD detection. This modular Python-based implementation integrates these distinct epigenomics analyses into a unified regulatory interpretation.

Does the epigenomics pipeline support DNA methylation pattern analysis for WGBS and RRBS data?

Yes, the epigenomics pipeline supports DNA methylation pattern analysis for both WGBS and RRBS data. It integrates this methylation data with ChIP-seq and ATAC-seq workflows to provide a comprehensive view of the regulatory landscape and chromatin accessibility.

How do I run an integrated epigenomics workflow using ChIP-Atlas ToolUniverse integration?

You can run the integrated epigenomics workflow by utilizing ToolUniverse integrations like ChIP-Atlas to process ChIP-seq and ATAC-seq data. This produces peaks, methylation profiles, chromatin-state annotations, and 3D genome features in a unified Python-based pipeline.