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Jj

Jujutsu (jj) version control system - a Git-compatible VCS with novel features. Use when working with jj repositories, managing stacked/dependent commits, needing automatic rebasing with first-class conflict handling, using revsets to select commits, or wanting enhanced Git workflows. Triggers on mentions of 'jj', 'jujutsu', change IDs, operation log, or jj-specific commands.

dashed

Core Features

Ready to Use

Quick integration into your workflow with minimal setup

Community Verified

Active open-source community with continuous updates

Completely Free

MIT/Apache licensed for commercial and personal use

Flexible Extension

Customizable and extendable based on your needs

How to Use

1Get Skill File

Download or copy the skill file from the source repository

2Install to Claude

Place the skill file in Claude's skills directory (usually ~/.claude/skills/)。

3Start Using

Restart Claude or run the reload command to load the skill

Tip: Read the documentation and code carefully before first use to understand functionality and permission requirements

Related Tags

#backend#documentation#git

Technical Information

Author
dashed
Category
Development
File Size
8.74 KB
Source Repository
dashed__claude-marketplace
Metadata
Includes YAML metadata
License
MIT

All Skills from open-source community, preserving original authors' copyrights

dashed__claude-marketplace/plugins/jj/skill.md

Why Choose This Skill

Proven benefits and measurable impact

5x

Faster variant analysis

Reduce manual variant interpretation time from hours to minutes

30%

Improved diagnostic accuracy

Leverage curated ClinVar data to reduce variant misclassification rates

50%

Streamlined VCF processing

Automate annotation tasks to cut bioinformatics pipeline runtime

Use Cases

Perfect for these scenarios

🧬

Variant pathogenicity check

Clinicians quickly verify genetic variant clinical significance for diagnosis

💻

VCF file annotation

Bioinformaticians annotate VCFs with ClinVar data for research pipelines

🔬

Gene-specific variant search

Researchers query variants by gene or position for targeted studies

📊

Clinical report generation

Generate variant interpretation reports with ClinVar classifications for patients

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