star-alignment
CommunityAlign RNA-seq reads with STAR for novel junction discovery.
Authorpradyumnasagar
Version1.0.0
Installs0
System Documentation
What problem does it solve?
This Skill aligns RNA-seq reads with STAR, a powerful aligner for novel junction discovery, providing 2-pass mapping and genome-generation strategies.
Core Features & Use Cases
- Splice-aware Alignment: Aligns RNA-seq reads with high sensitivity to novel junctions.
- 2-pass Mapping: Offers 2-pass mapping for sensitive novel junction discovery.
- Genome Generation: Generates genome index for alignment.
- Use Case: Ideal for bulk RNA-seq with novel junction discovery, single-cell RNA-seq, chimeric/fusion detection, and long-read cDNA/ONT direct RNA.
Quick Start
Generate the genome index with 'STAR --runMode genomeGenerate' and align reads with 'STAR --runMode alignReads'.
Dependency Matrix
Required Modules
STARsamtools
Components
scriptsreferences
💻 Claude Code Installation
Recommended: Let Claude install automatically. Simply copy and paste the text below to Claude Code.
Please help me install this Skill: Name: star-alignment Download link: https://github.com/pradyumnasagar/open-research-skills/archive/main.zip#star-alignment Please download this .zip file, extract it, and install it in the .claude/skills/ directory.
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