daa-diagnose

Diagnose microbiome count data sparsity, library size, and study design to recommend differential abundance analysis methods.

1|1|Updated Jan 30, 2026
One-click install
npx skills add https://github.com/shandley/composable-daa --skill daa-diagnose
Or copy as Structured Prompt for Agent
Please help me install this Agent Skill.
Skill: daa-diagnose
Source: https://github.com/shandley/composable-daa/tree/main/.claude/skills/daa-diagnose
Command: npx skills add https://github.com/shandley/composable-daa --skill daa-diagnose

SYSTEM DOCUMENTATION & REQUIREMENTS

What problem does it solve?

Diagnose microbiome/virome count data and identify the most suitable differential abundance analysis method.

Core Features & Use Cases

  • Diagnoses data characteristics (sparsity, library size, and study design) to guide method choice.
  • Recommends appropriate differential abundance analysis methods (LinDA, ZINB, Hurdle, LMM) based on data.
  • Use case: A researcher provides counts and metadata and receives a tailored method recommendation.

Quick Start

Provide counts and metadata files to receive an automated diagnosis and recommended DAA method.

Frequently Asked Questions about daa-diagnose

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

FAQPage Schema
How do I choose the right differential abundance analysis method for microbiome data?

Differential abundance analysis for microbiome data requires evaluating sparsity, library size, and study design. Diagnosing these characteristics recommends tailored methods like LinDA, ZINB, Hurdle, or LMM for accurate cross-sectional or longitudinal results.

What differential abundance method should I use for longitudinal microbiome studies?

Longitudinal microbiome studies often utilize Linear Mixed Models (LMM). Diagnosing your specific data characteristics confirms if LMM suits your study design compared to cross-sectional alternatives like LinDA or ZINB.

How do I diagnose microbiome count data before selecting a DAA method?

Diagnosing microbiome count data involves empirically profiling sparsity, library size, and study design. Providing counts and metadata files outputs a tailored differential abundance method recommendation for your dataset.

Does data sparsity affect which differential abundance method I should use?

Data sparsity directly impacts differential abundance method selection. High sparsity in microbiome count data often guides the recommendation toward zero-inflated methods like ZINB or Hurdle to handle excessive zeros accurately.

What is the best way to analyze differential abundance in highly sparse virome data?

Analyzing differential abundance in highly sparse virome data requires diagnosing sparsity and library size. This profiling typically recommends zero-inflated methods like ZINB or Hurdle to handle excessive zeros effectively.