pipeline-atacseq
CommunityProcess chromatin accessibility data from FASTQ to peaks.
Content & Communication#bioinformatics#genomics#nextflow#atac-seq#peak calling#chromatin accessibility#ENCODE standards
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 requiredComponents
scriptsreferencesassets
💻 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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