This skill performs protein-mediated regulatory community analysis from ChIA-PET datasets and provide a way for visualizing the communities. Use this skill when you have a annotated peak file (in BED format) from ChIA-PET experiment and you want to identify the protein-mediated regulatory community according to the BED and BEDPE file from ChIA-PET.
Scanned 5/31/2026
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---
name: regulatory-community-analysis-ChIA-PET
description: This skill performs protein-mediated regulatory community analysis from ChIA-PET datasets and provide a way for visualizing the communities. Use this skill when you have a annotated peak file (in BED format) from ChIA-PET experiment and you want to identify the protein-mediated regulatory community according to the BED and BEDPE file from ChIA-PET.
---
# Protein-Mediated Regulatory Community Analysis from ChIA-PET
## 1. Overview
Main steps include:
- Refer to the **Inputs & Outputs** section to check available inputs and design the output structure.
- Standardize the information contained in the BED format peak file.
- Build a chromatin interaction network where:
- nodes = protein binding sites (peaks)
- edges = protein-mediated loops.
- Detect regulatory communities (3D modules) using graph clustering.
- Prioritize hub anchors using network centrality.
- Visualize the largest regulatory communities.
Tools called in this skill:
- `mcp__igraph-tools__build_chromatin_network`
- `mcp__igraph-tools__analyze_chromatin_network`
- `mcp__igraph-tools__plot_chromatin_communities`
---
## 2. When to use this skill
Use this skill when you have ChIA-PET data in BEDPE and BED format and you want to:
- Reveal **regulatory communities** (3D modules) formed by:
- promoters
- enhancers
- other regulatory elements
- Identify **hub anchors** (peaks involved in many interactions) for a particular protein.
- Study **protein-mediated rewiring** of chromatin structure between conditions by comparing networks.
- Generate interpretable **network visualizations** for specific communities or loci.
Typical biological questions:
- Which promoters act as 3D regulatory hubs for my ChIA-PET factor (e.g., RNAPII, CTCF)?
- Which enhancers cluster with a given gene in 3D?
- Do disease-associated loci participate in specific regulatory communities?
- How does the chromatin interaction network structure change under perturbation (e.g., KO, treatment)?
---
## Inputs & Outputs
### Inputs
```bash
<sample>.bedpe # ChIA-PET loops: chr1 start1 end1 chr2 start2 end2 PET_count [optional extra fields...]
<sample>.bed # Tab-delimited file with at least 3 columns: chr, start, end
```
### Outputs
```bash
ChIA_PET_community/
communities/
${sample}_communities_membership.tsv # Network membership table
${sample}.graphml
plots/
${sample}_communities.pdf # Community network plots
temp/
... # other temp files
```
---
## Decision tree
### Step 1: Standardize the information contained in the BED format peak file
- Check whether the <peak_id> and <type> (e.g. promoter or other annotations) information if provided in the BED file.
- If not provided, assign "peak_${i}" as the <peak_id> column and "others" as the <type> column.
- Make sure that order of the information in the BED file is:
- 'chr' 'start' 'end' 'peak_id' 'type'
### Step 2: Build the Chromatin Interaction Network
Call:
- `mcp__igraph-tools__build_chromatin_network`
with:
- `loops_file`: path to BEDPE-like loops file.
- `peaks_file`: path to annotated peaks BED file.
- `proj_dir`: project directory (e.g. `ChIA_PET_community`).
- `graph_name` (optional): output GraphML filename.
- `min_pet` (optional): filter on PET counts (default `1`).
This tool will:
- Reads the loops and peaks files.
- Builds an **undirected igraph**:
- Saves the graph as:
- `${sample}.graphml` (GraphML)
---
### Step 2: Detect Communities and Compute Network Centrality
Call:
- `mcp__igraph-tools__analyze_chromatin_network`
with:
- `graph_path`: GraphML file from Step 1 (e.g. `${sample}.graphml`).
- `proj_dir`: same project directory.
- `membership_name` (optional): output TSV name, (e.g. `${sample}_communities_membership.tsv`).
- `weight_attr` (optional): edge weight attribute, default `"weight"`.
- `seed` (optional): random seed for community detection, default `1`.
This tool will:
- Load the GraphML network.
- Run **Louvain (multilevel)** community detection
- Compute centralities
- Export a **membership table**:
`${sample}_communities_membership.tsv` with columns
- Update the GraphML file with the new vertex attributes (community & centralities).
### Step 3 — Visualize Top Regulatory Communities
Call:
- `mcp__igraph-tools__plot_chromatin_communities`
with:
- `graph_path`: GraphML file with community attributes (from Step 2).
- `proj_dir`: project directory.
- `pdf_name` (optional): output PDF filename (e.g. `${sample}_communities.pdf`).
- `top_n` (optional): number of largest communities to plot, default `12`.
- `size_attr` (optional): vertex attribute for node size, default `"degree"`.
- `community_attr` (optional): vertex attribute containing community IDs, default `"community"`.
This tool will:
- Load the graph and verify that `community_attr` is present.
- Compute **plot aesthetics**
- Identify the **largest communities** (by vertex count), up to `top_n`.
- For each community:
- Create an induced subgraph.
- Compute a **Fruchterman–Reingold** layout.
- Draw nodes + edges + labels into a separate page of a multi-page PDF.
- Save the PDF as:
- `${sample}_communities.pdf`
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