pipeline-atacseq

Community

Process chromatin accessibility data from FASTQ to peaks.

Authorammawla
Version1.0.0
Installs0

System Documentation

What problem does it solve?

This Skill streamlines the analysis of ATAC-seq data by providing an automated pipeline from raw sequencing reads to high-confidence accessible chromatin peaks, enabling accurate epigenomic insights.

Core Features & Use Cases

  • Data Processing: Performs quality control, adapter trimming, alignment, and Tn5 offset correction on raw FASTQ files.
  • Peak Identification: Calls peaks on nucleosome-free fragments to identify open chromatin regions, suitable for TF binding analysis.
  • QC & Visualization: Provides comprehensive quality metrics including TSS enrichment, fragment size distributions, and signal tracks for downstream interpretation or publication.
  • Use Case: Researchers analyzing ENCODE ATAC-seq datasets or their own samples can utilize this pipeline to generate reproducible, publication-ready accessibility maps aligned with ENCODE standards.

Quick Start

Run the pipeline with your FASTQ files and reference genome to obtain peaks and QC reports for chromatin accessibility studies.

Dependency Matrix

Required Modules

None required

Components

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💻 Claude Code Installation

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Please help me install this Skill:
Name: pipeline-atacseq
Download link: https://github.com/ammawla/encode-toolkit/archive/main.zip#pipeline-atacseq

Please download this .zip file, extract it, and install it in the .claude/skills/ directory.
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