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572 Usage Guide 5deb5784

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Complete alternative splicing analysis workflow from raw RNA-seq FASTQ files to differential splicing results and visualizations. Includes QC checkpoints and best practices.

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  • Added October 11, 2026
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Scanned October 11, 2026

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SKILL.md
# Splicing Pipeline - Usage Guide

## Overview
Complete alternative splicing analysis workflow from raw RNA-seq FASTQ files to differential splicing results and visualizations. Includes QC checkpoints and best practices.

## Prerequisites
```bash
# Core tools
conda install -c bioconda star rmats-turbo ggsashimi fastp rseqc

# Python dependencies
pip install pandas numpy matplotlib

# R packages (optional, for isoform switching)
BiocManager::install('IsoformSwitchAnalyzeR')
```

## Quick Start
Tell your AI agent what you want to do:
- "Run a complete splicing analysis from my FASTQ files"
- "Set up a splicing pipeline for my RNA-seq experiment"
- "Analyze differential splicing between my conditions"
- "Generate sashimi plots for my significant splicing events"

## Example Prompts

### Full Pipeline
> "I have RNA-seq FASTQs from 3 control and 3 treatment samples. Run a complete splicing analysis."

> "Set up STAR 2-pass alignment and rMATS differential splicing for my samples."

### Individual Steps
> "Align my samples with STAR 2-pass mode for optimal junction detection."

> "Run junction saturation QC to check if I have enough sequencing depth."

> "Visualize the top 20 differential splicing events with sashimi plots."

## What the Agent Will Do
1. Perform read QC and adapter trimming (fastp)
2. Align with STAR 2-pass mode for junction detection
3. Run junction saturation QC checkpoint
4. Perform differential splicing analysis (rMATS-turbo)
5. Filter significant events (FDR < 0.05, |deltaPSI| > 0.1)
6. Optionally analyze isoform switches
7. Generate sashimi plots for visualization

## Tips
- STAR 2-pass mode is essential for novel junction discovery
- Check junction saturation curves before trusting results
- Use `--outSJfilterOverhangMin 8 8 8 8` for stringent junction filtering
- rMATS-turbo combines quantification and differential testing
- Standard thresholds: |deltaPSI| > 0.1, FDR < 0.05
- Always require minimum junction reads (>= 10) for reliability

## Related Skills
- alternative-splicing/splicing-quantification - Quantification details
- alternative-splicing/differential-splicing - Analysis methods
- alternative-splicing/sashimi-plots - Visualization
- read-alignment/star-alignment - STAR alignment options

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