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SKILL verified MIT Self-run

Chip Seq

skill-cheatthegod-biohermes-chip-seq · by cheatthegod

ChIP-seq peak calling and downstream interpretation with MACS3, signal track export, annotation, motif analysis, and differential binding review.

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Install

$ agentstack add skill-cheatthegod-biohermes-chip-seq

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Security review

✓ Passed

No issues found. Passed automated security review. · v0.1.0 How review works →

  • Prompt-injection patterns
  • Secret / credential exfiltration
  • Dangerous shell & filesystem operations
  • Untrusted network calls
  • Known-malicious package signatures

What it can access

  • Network access No
  • Filesystem access No
  • Shell / process execution No
  • Environment & secrets No
  • Dynamic code execution No

From automated source analysis of v0.1.0. “Used” means the capability is present in the source — more access means more to trust, not that it’s unsafe.

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Reliability & compatibility

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About

ChIP Seq

Version Compatibility

Reference examples assume:

  • macs3 3.0+
  • samtools 1.18+
  • deepTools 3.5+

Before using commands, verify the installed environment:

  • CLI: macs3 --version, samtools --version, bamCoverage --version
  • If flags differ, inspect --help and adapt rather than forcing the example unchanged.

Overview

Use this skill for:

  • narrow or broad peak calling
  • input-normalized signal tracks
  • peak annotation
  • motif follow-up
  • differential binding review when replicates exist

When To Use This Skill

  • the user has aligned ChIP and optional input BAM files
  • the deliverable includes peaks, browser tracks, or motif results
  • the assay is TF ChIP or histone-mark ChIP and needs standard peak-centric processing

Quick Route

  • TF or narrow marks: use narrow peak mode first.
  • H3K27me3, H3K36me3, or other broad marks: use --broad.
  • Paired-end BAM: prefer -f BAMPE.
  • No input control: still possible, but report the limitation explicitly.

Progressive Disclosure

  • Read [technicalreference.md](technicalreference.md) for QC gates, narrow-versus-broad logic, and replicate handling.
  • Read [commandsandthresholds.md](commandsandthresholds.md) for MACS3 commands, parameter defaults, and output file conventions.

Prerequisites

| Requirement | Narrow TF-style | Broad histone-style | |---|---:|---:| | usable uniquely mapped reads | >= 10M | >= 20M | | matched input recommended | yes | yes | | biological replicates recommended | >= 2 | >= 2 |

Expected Inputs

  • chip.bam
  • input.bam when available
  • reference genome build
  • chromosome sizes if bigWig export is needed

Expected Outputs

  • results/peaks/sample_peaks.narrowPeak or .broadPeak
  • results/peaks/sample_summits.bed
  • results/tracks/sample_treat_pileup.bw
  • results/annotation/peak_annotation.tsv
  • qc/chip_qc_summary.tsv

Starter Pattern

macs3 callpeak \
  -t chip.bam \
  -c input.bam \
  -f BAMPE \
  -g hs \
  -n sample \
  -q 0.01 \
  --outdir results/peaks

Key Parameters

| Parameter | Typical value | Meaning | |---|---|---| | -f | BAM or BAMPE | paired-end should use BAMPE | | -g | hs, mm, or numeric | effective genome size | | -q | 0.01 or 0.05 | FDR cutoff for narrow peaks | | --broad | broad marks only | broad peak mode | | --broad-cutoff | 0.1 | broad-peak FDR cutoff | | -B --SPMR | enabled for tracks | bedGraph for normalized signal |

Workflow

1. Validate BAMs and replicate structure

Check:

  • mapped read counts
  • duplicate burden
  • whether input control exists
  • whether the mark is narrow or broad

2. Call peaks with MACS3

  • narrow marks: -q 0.01 is a good starting point
  • broad marks: use --broad --broad-cutoff 0.1
  • paired-end: -f BAMPE

3. Export signal tracks

Use -B --SPMR, sort the resulting bedGraph, then convert to bigWig for browser use.

4. Annotate and inspect peaks

Map peaks to promoters, gene bodies, or distal intervals and review top loci in a genome browser or track plot.

5. Run motif or differential follow-up

Only after peak quality looks credible and replicate structure supports the downstream question.

Output Artifacts

results/
├── peaks/
│   ├── sample_peaks.narrowPeak
│   ├── sample_summits.bed
│   └── sample_model.r
├── tracks/
│   ├── sample_treat_pileup.bdg
│   └── sample_treat_pileup.bw
└── annotation/
    └── peak_annotation.tsv
qc/
└── chip_qc_summary.tsv

Quality Review

  • TF ChIP-seq FRiP:
  • 0.05 generally solid
  • Histone broad-mark FRiP often differs; compare within assay type rather than against TF expectations.
  • Use replicate concordance when available. Do not trust a single noisy replicate just because peaks were called.
  • Check that top peaks occur in plausible loci and not only blacklisted or artifactual regions.

Anti-Patterns

  • treating broad and narrow marks with the same peak-calling setup
  • calling peaks on unsorted or low-quality BAMs
  • presenting motif hits without showing peak quality
  • hiding that no input control was available

Related Skills

  • ATAC Seq
  • Methylation Analysis
  • Gene Regulatory Networks

Optional Supplements

  • deeptools
  • pysam

Source & license

This open-source skill is cataloged on AgentStack and links to its original source — we do not rehost the code.

Install and usage instructions live in the source repository linked above.

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Versions

  • v0.1.0 Imported from the upstream source.