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维护者 FreedomIntelligence · 最近更新 2026年4月1日
Call accessible chromatin regions from ATAC-seq data using MACS3 with ATAC-specific parameters. Use when identifying open chromatin regions from aligned ATAC-seq BAM files, different from ChIP-seq peak calling.
原始来源
https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills/tree/main/skills/bio-atac-seq-atac-peak-calling
技能摘要
原始文档
Goal: Identify open chromatin regions from ATAC-seq data using ATAC-specific peak calling parameters.
Approach: Run MACS3 in paired-end mode with Tn5 shift correction, no model building, and duplicate retention since ATAC-seq generates natural duplicates at accessible sites.
## Explained parameters
macs3 callpeak \
-t sample.bam \ # Treatment BAM
-f BAMPE \ # Paired-end BAM (uses fragment size)
-g hs \ # Genome size: hs (human), mm (mouse)
-n sample \ # Output name prefix
--nomodel \ # Don't build shifting model
--shift -75 \ # Shift reads to center on Tn5 cut site
--extsize 150 \ # Extend reads to this size
--keep-dup all \ # Keep duplicates (ATAC has natural duplicates)
-B \ # Generate bedGraph for visualization
--call-summits # Call peak summits
| Parameter | Reason |
|---|---|
| --nomodel | ATAC doesn't have control, can't build model |
| --shift -75 | Centers on Tn5 insertion site |
| --extsize 150 | Smooths signal around cut sites |
| --keep-dup all | Tn5 creates duplicate cuts at accessible sites |
| -f BAMPE | Uses actual fragment size from paired-end |
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