Workflow for amplicon microbiome analysis including denoising, taxonomy assignment, diversity analysis, and differential abundance.
Scanned 9/4/2026
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---
name: microbiome-amplicon
description: Workflow for amplicon microbiome analysis including denoising, taxonomy assignment, diversity analysis, and differential abundance.
tool_type: mixed
primary_tool: QIIME2-style
---
# Microbiome Amplicon
## Version Compatibility
Reference examples assume recent stable releases of the preferred tools, especially `QIIME2-style` and the other tools listed below.
Before using code or command patterns, verify installed versions match the environment:
- Python: `python -c "import <module>; print(<module>.__version__)"`
- CLI: `<tool> --version`
- If signatures differ, inspect the installed help or API and adapt the pattern instead of retrying unchanged.
## Overview
Workflow for amplicon microbiome analysis including denoising, taxonomy assignment, diversity analysis, and differential abundance.
## When To Use This Skill
- use when the task is 16S, ITS, or other amplicon-based microbiome profiling
- use when denoising, taxonomy assignment, and diversity metrics are required
- use when the user needs cohort-level differential abundance or community structure summaries
## Quick Route
- If the input is raw or minimally processed data, start with validation and QC before any modeling.
- If the input is already processed, skip directly to the first workflow step that matches the user goal.
- If the user asks for a biological conclusion, always produce at least one QC or confidence artifact alongside the final result.
## Progressive Disclosure
- Read `references/technical_reference.md` when you need deeper tool-selection rules, environment adaptation notes, or extra validation guidance.
- Keep `SKILL.md` as the main execution path and load the reference file only when the task or failure mode needs the extra detail.
## Default Rules
- Prefer Python-first workflows unless the task explicitly requires something else.
- Keep intermediate and final outputs separated.
- Record software versions, reference builds, and key parameters when they affect interpretation.
- Favor reproducible tables and figures over one-off interactive-only outputs.
## Expected Inputs
- amplicon FASTQ files
- sample metadata
- taxonomy database
## Expected Outputs
- ASV or OTU tables
- taxonomy assignments
- diversity and differential abundance summaries
## Preferred Tools
- QIIME2-style workflows
- pandas
- scikit-bio
- seaborn
## Starter Pattern
```text
Preferred starting point: QIIME2-style
Inputs: amplicon FASTQ files, sample metadata, taxonomy database
Outputs: ASV or OTU tables, taxonomy assignments, diversity and differential abundance summaries
```
## Workflow
### 1. Preprocess reads
Trim primers or adapters and denoise reads into ASVs or OTUs.
### 2. Assign taxonomy
Use a suitable taxonomy model or reference database for the marker type.
### 3. Compute diversity
Calculate alpha and beta diversity with metadata-aware comparisons.
### 4. Compare groups
Run differential abundance with methods matched to compositional data constraints.
### 5. Export community reports
Save tables, ordinations, and taxonomy summaries.
## Output Artifacts
- Recommended output layout:
- `results/` for final tables and serialized objects
- `figures/` for plots and static visual exports
- `qc/` for checks that justify downstream interpretation
- Minimum expected outputs for this skill:
- `ASV or OTU tables`
- `taxonomy assignments`
- `diversity and differential abundance summaries`
## Quality Review
- Confirm identifiers and metadata join correctly before modeling or summarizing.
- Generate at least one QC artifact before final biological interpretation.
- Keep raw or minimally processed inputs separate from transformed outputs.
- Review sample contamination, depth differences, and database choice before comparing communities.
- State clearly whether outputs are relative abundance, counts, or derived functions.
## Anti-Patterns
- treating relative abundance changes as absolute shifts without context
- using a taxonomy database mismatched to the marker region
- running differential abundance without accounting for compositional effects
## Related Skills
- `Metagenomics`
- `Pathogen Epidemiological Genomics`
- `Phylogenetics`
## Optional Supplements
- `scikit-bio`
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