Design armored CAR-T cells with cytokine payloads and resistance mechanisms.
bio-chipseq-super-enhancers
维护者 FreedomIntelligence · 最近更新 2026年4月1日
Identifies super-enhancers from H3K27ac ChIP-seq data using ROSE and related tools. Use when studying cell identity genes, cancer-associated regulatory elements, or master transcription factor binding regions that cluster into large enhancer domains.
原始来源
FreedomIntelligence/OpenClaw-Medical-Skills
https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills/tree/main/skills/bio-chipseq-super-enhancers
- 维护者
- FreedomIntelligence
- 许可
- MIT
- 最近更新
- 2026年4月1日
技能摘要
来自 SKILL.md 的关键信息
核心说明
- CLI:ROSE_main.py -g hg38 -i peaks.gff -r chip.bam -c input.bam。
- Identify super-enhancers ,面向 H3K27ac ChIP-seq" → Stitch nearby enhancer peaks 、 rank by signal to find large regulatory domains controlling cell identity genes. CLI:ROSE_main.py -g hg38 -i peaks.gff -r chip.bam -c input.bam。
- Identify super-enhancers (SEs) - large clusters of enhancers that control cell identity genes。
- Large clusters of enhancer regions。
- Marked by H3K27ac,Med1,BRD4。
原始文档
SKILL.md 摘录
Installation
git clone https://github.com/stjude/ROSE.git
cd ROSE
## Input Requirements
1. **BAM file** - H3K27ac ChIP-seq aligned reads
2. **Peak file** - Called peaks (BED or GFF)
3. **Genome annotation** - TSS annotations
## Run ROSE
**Goal:** Identify super-enhancers by stitching nearby enhancer peaks and ranking by H3K27ac signal.
**Approach:** Run ROSE_main.py with a GFF peak file, ChIP-seq BAM, and optional input control to stitch enhancers within 12.5 kb, rank by signal, and identify the inflection point separating super-enhancers from typical enhancers.
```bash
适用场景
- 适合在studying cell identity genes,cancer-associated regulatory elements,或 master transcription factor binding regions that cluster into large enhancer domains时使用。
不适用场景
- Do not rely on this catalog entry alone ,用于 installation 或 maintenance details。
上游相关技能
- chip-seq/peak-calling - Call H3K27ac peaks first
- chip-seq/peak-annotation - Annotate SE to genes
- chip-seq/differential-binding - Compare SE between conditions
- data-visualization/genome-tracks - Visualize SE regions
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