epitranscriptomics

Detect and interpret RNA modification signals from MeRIP-seq sequencing data.

25|5|Updated Mar 22, 2026
One-click install
npx skills add https://github.com/zongtingwei/Bioclaw_Skills_Hub --skill epitranscriptomics
Or copy as Structured Prompt for Agent
Please help me install this Agent Skill.
Skill: epitranscriptomics
Source: https://github.com/zongtingwei/Bioclaw_Skills_Hub/tree/main/skills/epigenomics-and-regulation/epitranscriptomics
Command: npx skills add https://github.com/zongtingwei/Bioclaw_Skills_Hub --skill epitranscriptomics

SYSTEM DOCUMENTATION & REQUIREMENTS

💡 This Skill includes references (resource) components.

What problem does it solve?

Workflow for RNA modification analysis such as m6A peak calling, differential modification, and transcript-level visualization.

Core Features & Use Cases

  • RNA modification analysis: m6A peak calling, differential modification assessment, and transcript-level visualization.
  • Broad applicability: suitable for MeRIP-seq experiments and transcriptome-wide modification studies.
  • Use Case: researchers compare conditions to find differential RNA modification patterns and visualize modifications on representative transcripts.

Quick Start

Provide modification-enriched reads, input reads, and transcript annotations to start the workflow.

Frequently Asked Questions about epitranscriptomics

High-intent search queries and answers about installing and using this skill.

FAQPage Schema
How do I perform m6A peak calling from MeRIP-seq data?

To perform m6A peak calling from MeRIP-seq data, you provide modification-enriched reads, input reads, and transcript annotations to start the workflow. This enables detection of transcriptome-wide RNA modification signals.

What is differential modification analysis for RNA modification studies?

Differential modification analysis compares RNA modification patterns across different experimental conditions. Researchers use it to identify significant changes in modification levels like m6A from normalized MeRIP-seq data.

Can I visualize RNA modification context within specific transcripts?

Yes, you can visualize RNA modification context within specific transcripts. The workflow generates visualization outputs that map detected modification signals directly onto representative transcript structures.

Do I need input reads and transcript annotations to start RNA modification analysis?

Yes, you need modification-enriched reads, input reads, and transcript annotations to start RNA modification analysis. These inputs are required for data normalization and accurate peak-calling.

Are reproducibility notes included when detecting transcriptome-wide RNA modifications?

Yes, reproducibility notes are included when detecting transcriptome-wide RNA modifications. The workflow provides visualization outputs with clear provenance to ensure data normalization results are traceable.