Agent skill

spatial-epigenomics-agent

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Forks 31

Install this agent skill to your Project

npx add-skill https://github.com/majiayu000/claude-skill-registry/tree/main/skills/data/spatial-epigenomics-agent

SKILL.md

---name: spatial-epigenomics-agent description: AI-powered spatial epigenomics analysis combining chromatin accessibility, histone modifications, and DNA methylation with spatial coordinates for tissue architecture mapping. license: MIT metadata: author: AI Group version: "1.0.0" created: "2026-01-19" compatibility:

  • system: Python 3.10+ allowed-tools:
  • run_shell_command
  • read_file
  • write_file

keywords:

  • spatial-epigenomics-agent
  • automation
  • biomedical measurable_outcome: execute task with >95% success rate. ---"

Spatial Epigenomics Agent

The Spatial Epigenomics Agent analyzes spatial epigenomic data combining chromatin accessibility (ATAC-seq), histone modifications (CUT&Tag), and DNA methylation with spatial coordinates. It maps regulatory landscapes across tissue architecture to understand cell-state regulation in spatial context.

When to Use This Skill

  • When analyzing spatial ATAC-seq data (Slide-seq + ATAC, DBiT-seq).
  • To map chromatin accessibility across tissue microenvironments.
  • For spatial profiling of histone modifications (H3K27ac, H3K4me3, H3K27me3).
  • When integrating spatial epigenomics with spatial transcriptomics.
  • To identify spatially-variable regulatory elements and enhancers.

Core Capabilities

  1. Spatial ATAC Analysis: Process spatial chromatin accessibility data to identify open chromatin regions with spatial coordinates.

  2. Spatial CUT&Tag: Analyze spatially-resolved histone modification profiles (H3K27ac for enhancers, H3K4me3 for promoters).

  3. Spatial Methylation: Map DNA methylation patterns across tissue sections using spatial bisulfite methods.

  4. Multi-Modal Integration: Combine spatial epigenomics with spatial transcriptomics for regulatory network inference.

  5. Regulatory Element Mapping: Identify spatially-variable enhancers, promoters, and silencers.

  6. 3D Chromatin Organization: Integrate with MERFISH/seqFISH+ for spatial chromatin organization.

Technologies Supported

Technology Epigenetic Mark Resolution Method
Spatial-ATAC-seq Open chromatin ~10-50μm Microfluidic barcoding
DBiT-seq ATAC + expression ~10μm Deterministic barcoding
Spatial-CUT&Tag Histone marks ~50μm Cleavage under targets
Spatial-MethylSeq DNA methylation Variable Bisulfite conversion
MERFISH + epigenetics 3D organization Single-cell Imaging-based

Workflow

  1. Input: Spatial epigenomics data (BAM files + spatial coordinates) or processed peak matrices.

  2. Preprocessing: Alignment, deduplication, peak calling with spatial awareness.

  3. Spatial Clustering: Identify spatial domains with similar epigenetic profiles.

  4. Peak Annotation: Map peaks to genomic features (promoters, enhancers, gene bodies).

  5. Motif Analysis: Identify transcription factor binding motifs in spatially-variable peaks.

  6. Integration: Combine with expression data for regulatory inference.

  7. Output: Spatial peak maps, regulatory networks, domain annotations.

Example Usage

User: "Analyze this spatial ATAC-seq dataset to identify spatially-variable regulatory elements in the tumor microenvironment."

Agent Action:

bash
python3 Skills/Genomics/Spatial_Epigenomics_Agent/spatial_epigenomics.py \
    --input spatial_atac_fragments.tsv.gz \
    --coordinates spot_coordinates.csv \
    --peaks macs2_peaks.bed \
    --spatial_variable true \
    --motif_db jaspar_2024 \
    --integrate_with spatial_rna.h5ad \
    --output spatial_epi_results/

Analysis Modules

1. Spatial Peak Calling

  • Adapted MACS2/Genrich for spatial data
  • Spatial autocorrelation of accessibility
  • Pseudo-bulk and single-spot approaches

2. Spatial Domain Detection

  • Graph-based clustering (Leiden, Louvain)
  • Hidden Markov Random Fields
  • Deep learning segmentation

3. Transcription Factor Analysis

  • ChromVAR for TF activity scores
  • SCENIC+ for spatial regulon inference
  • Motif enrichment in spatial domains

4. Enhancer-Gene Linking

  • Activity-by-contact (ABC) model adaptation
  • Spatial correlation of enhancer accessibility with gene expression
  • Chromatin loop integration

Integration with Spatial Transcriptomics

Spatial ATAC-seq          Spatial RNA-seq
      |                        |
      v                        v
  Peak Matrix            Expression Matrix
      |                        |
      +--------> Integration <-+
                     |
                     v
         Regulatory Network
         (Enhancer -> TF -> Gene)

Key Metrics

Metric Description Typical Range
TSS Enrichment Signal at transcription start sites >4 good quality
FRiP Fraction reads in peaks >30%
Spatial autocorrelation Moran's I for epigenetic features 0.2-0.8
Spots per gene Detection sensitivity 100-500

Prerequisites

  • Python 3.10+
  • SnapATAC2, ArchR for ATAC analysis
  • Squidpy, Scanpy for spatial analysis
  • MACS2/Genrich for peak calling

Related Skills

  • Spatial_Transcriptomics - For gene expression spatial mapping
  • Epigenomics_MethylGPT_Agent - For methylation analysis
  • Single_Cell - For non-spatial epigenomics

Applications

  1. Tumor Microenvironment: Map regulatory programs across tumor-stroma boundary
  2. Development: Track enhancer activation during tissue morphogenesis
  3. Neuroanatomy: Brain region-specific regulatory landscapes
  4. Disease Mechanisms: Spatial dysregulation in pathology

Author

AI Group - Biomedical AI Platform

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