Skip to content
Back to skills

Functional Profiling

ASecurity

Profile functional potential of metagenomes using HUMAnN3 and similar tools. Use when obtaining pathway abundances, gene family counts, or functional annotations from metagenomic data.

  • 666 stars
  • 0 votes
  • 0 copies
  • 3 views
  • Added February 8, 2026
datapythongobashdatabase

Works with

  • cli

Security analysis

A100/100

Scanned February 12, 2026

npx -y skills add majiayu000/claude-skill-registry --skill functional-profiling --agent claude-code

Installs into .claude/skills of the current project.

Are you the author of Functional Profiling?

Add the live security badge to your README. It updates with every re-scan.

Security grade badge for Functional Profiling
[![Security: A — Skills Directory](https://www.skillsdirectory.com/api/skills/majiayu000-functional-profiling/badge)](https://www.skillsdirectory.com/skills/majiayu000-functional-profiling)

More formats (shields.io, HTML) on the badges page. Keep it an A: scan every change in CI with Pro.

Download with Pro
SKILL.md
---
name: bio-metagenomics-functional-profiling
description: Profile functional potential of metagenomes using HUMAnN3 and similar tools. Use when obtaining pathway abundances, gene family counts, or functional annotations from metagenomic data.
tool_type: cli
primary_tool: humann
---

# Functional Profiling

Profile the functional potential of metagenomic samples using HUMAnN3 to get pathway and gene family abundances.

## HUMAnN3 Workflow

### Installation

```bash
# Install via conda (recommended)
conda create -n humann -c bioconda humann
conda activate humann

# Download databases
humann_databases --download chocophlan full /path/to/databases
humann_databases --download uniref uniref90_diamond /path/to/databases

# Update config with database paths
humann_config --update database_folders nucleotide /path/to/databases/chocophlan
humann_config --update database_folders protein /path/to/databases/uniref
```

### Basic Usage

```bash
# Run HUMAnN3 on a single sample
humann --input sample.fastq.gz --output sample_humann

# With MetaPhlAn taxonomic profile (faster)
humann --input sample.fastq.gz \
       --taxonomic-profile sample_metaphlan.txt \
       --output sample_humann

# Paired-end reads (concatenate first)
cat sample_R1.fq.gz sample_R2.fq.gz > sample_concat.fq.gz
humann --input sample_concat.fq.gz --output sample_humann
```

### Output Files

```
sample_humann/
├── sample_genefamilies.tsv     # Gene family abundances (UniRef90)
├── sample_pathabundance.tsv    # MetaCyc pathway abundances
├── sample_pathcoverage.tsv     # Pathway coverage (0-1)
└── sample_humann_temp/         # Intermediate files
```

## Output Format

### Gene Families

```
# Gene Family   sample_Abundance-RPKs
UniRef90_A0A000|g__Bacteroides.s__Bacteroides_vulgatus   123.45
UniRef90_A0A001|unclassified                              67.89
UNMAPPED                                                  1000.0
```

### Pathway Abundance

```
# Pathway                                    sample_Abundance
PWY-5100: pyruvate fermentation              456.78
PWY-5100|g__Bacteroides.s__Bacteroides_vulgatus  234.56
PWY-5100|unclassified                        222.22
```

## Batch Processing

```bash
# Process multiple samples
for fq in *.fastq.gz; do
    sample=$(basename $fq .fastq.gz)
    humann --input $fq --output ${sample}_humann --threads 8
done

# Join tables across samples
humann_join_tables -i . -o merged_genefamilies.tsv --file_name genefamilies
humann_join_tables -i . -o merged_pathabundance.tsv --file_name pathabundance
```

## Normalization

```bash
# Normalize to relative abundance
humann_renorm_table -i merged_genefamilies.tsv \
                    -o genefamilies_relab.tsv \
                    -u relab

# Normalize to copies per million (CPM)
humann_renorm_table -i merged_pathabundance.tsv \
                    -o pathabundance_cpm.tsv \
                    -u cpm
```

## Regroup Gene Families

```bash
# Regroup to different functional categories
# EC numbers
humann_regroup_table -i genefamilies.tsv \
                     -g uniref90_level4ec \
                     -o genefamilies_ec.tsv

# KEGG Orthologs
humann_regroup_table -i genefamilies.tsv \
                     -g uniref90_ko \
                     -o genefamilies_ko.tsv

# GO terms
humann_regroup_table -i genefamilies.tsv \
                     -g uniref90_go \
                     -o genefamilies_go.tsv

# Pfam domains
humann_regroup_table -i genefamilies.tsv \
                     -g uniref90_pfam \
                     -o genefamilies_pfam.tsv
```

## Stratification

### Split by Organism

```bash
# Unstratify (remove organism info, sum across species)
humann_split_stratified_table -i merged_pathabundance.tsv \
                               -o .

# Creates: merged_pathabundance_unstratified.tsv
#          merged_pathabundance_stratified.tsv
```

### Species Contributions

```python
import pandas as pd

df = pd.read_csv('merged_pathabundance.tsv', sep='\t', index_col=0)

unstratified = df[~df.index.str.contains('\\|')]
stratified = df[df.index.str.contains('\\|')]

def get_species_contrib(pathway, df):
    '''Get species contributions to a pathway'''
    mask = df.index.str.startswith(pathway + '|')
    return df[mask]

contrib = get_species_contrib('PWY-5100', stratified)
```

## Quality Control

```bash
# Check unmapped and unintegrated
humann_barplot -i merged_pathabundance.tsv \
               -o pathabundance_barplot.png \
               --focal-feature UNMAPPED
```

### Key QC Metrics

| Metric | Good | Concerning |
|--------|------|------------|
| UNMAPPED (gene families) | <30% | >50% |
| UNINTEGRATED (pathways) | <40% | >60% |
| Pathway coverage | >0.5 | <0.3 |

## Differential Analysis

### LEfSe Format

```bash
# Format for LEfSe
humann_join_tables -i . -o merged.tsv --file_name pathabundance
humann_renorm_table -i merged.tsv -o merged_relab.tsv -u relab
```

### Python Analysis

```python
import pandas as pd
from scipy import stats

df = pd.read_csv('pathabundance_cpm.tsv', sep='\t', index_col=0)
metadata = pd.read_csv('metadata.tsv', sep='\t', index_col=0)

group1 = metadata[metadata['condition'] == 'healthy'].index
group2 = metadata[metadata['condition'] == 'disease'].index

results = []
for pathway in df.index:
    if '|' not in pathway and pathway != 'UNMAPPED':
        vals1 = df.loc[pathway, group1]
        vals2 = df.loc[pathway, group2]
        stat, pval = stats.mannwhitneyu(vals1, vals2)
        fc = vals2.mean() / (vals1.mean() + 1e-10)
        results.append({'pathway': pathway, 'pvalue': pval, 'fold_change': fc})

results_df = pd.DataFrame(results)
results_df['padj'] = stats.false_discovery_control(results_df['pvalue'])
```

## Visualization

```python
import matplotlib.pyplot as plt
import seaborn as sns

df = pd.read_csv('pathabundance_relab.tsv', sep='\t', index_col=0)
df = df[~df.index.str.contains('\\|')]
df = df.drop(['UNMAPPED', 'UNINTEGRATED'], errors='ignore')
top = df.mean(axis=1).nlargest(20).index

plt.figure(figsize=(12, 8))
sns.heatmap(df.loc[top].T, cmap='viridis', xticklabels=True)
plt.tight_layout()
plt.savefig('pathway_heatmap.png')
```

## Related Skills

- metagenomics/metaphlan-profiling - Taxonomic profiling (input for HUMAnN)
- metagenomics/kraken-classification - Alternative taxonomy
- metagenomics/metagenome-visualization - Visualization methods
- pathway-analysis/kegg-pathways - KEGG pathway interpretation

Attribution

Is this your skill, or is something wrong with this listing? Request removal or report an issue. Author removals are honored within 72 hours.

Comments

Loading comments…

Newsletter

Get the weekly list of safe new skills, and the ones we pulled.