Agent skill

bio-epidemiological-genomics-transmission-inference

Infer pathogen transmission networks and identify likely transmission pairs using TransPhylo and outbreak reconstruction algorithms. Estimate who-infected-whom from genomic and epidemiological data. Use when investigating outbreak transmission chains or identifying superspreaders.

Stars 2,009
Forks 275

Install this agent skill to your Project

npx add-skill https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills/tree/main/skills/bio-epidemiological-genomics-transmission-inference

SKILL.md

Version Compatibility

Reference examples tested with: BioPython 1.83+, TreeTime 0.11+, matplotlib 3.8+, numpy 1.26+, pandas 2.2+, scanpy 1.10+

Before using code patterns, verify installed versions match. If versions differ:

  • Python: pip show <package> then help(module.function) to check signatures
  • R: packageVersion('<pkg>') then ?function_name to verify parameters

If code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.

Transmission Inference

"Infer who infected whom in my outbreak" → Reconstruct transmission networks from genomic and epidemiological data to identify transmission pairs, superspreaders, and unsampled cases.

  • R: TransPhylo::inferTTree() for Bayesian transmission tree inference

TransPhylo in R

r
library(TransPhylo)
library(ape)

# Load dated phylogeny (from BEAST/TreeTime)
tree <- read.nexus('dated_tree.nexus')

# Convert to TransPhylo format
ptree <- ptreeFromPhylo(tree, dateLastSample = 2020.5)

# Estimate transmission tree
# Uses MCMC to sample from posterior distribution
res <- inferTTree(
    ptree,
    mcmcIterations = 100000,
    startNeg = 0.1,      # Initial within-host effective population
    startOff.r = 2,      # Initial R0 estimate
    startOff.p = 0.5,    # Initial sampling probability
    startPi = 0.9,       # Initial probability of being sampled
    dateT = 2020.6       # End of outbreak observation
)

# Extract consensus transmission tree
ttree <- extractTTree(res)

# Get transmission pairs
pairs <- ttree$ttree[, c('infector', 'infectee', 'time')]

Prepare Data

python
def prepare_for_transphylo(dated_tree_file, sample_dates, output_prefix):
    '''Prepare inputs for TransPhylo analysis

    Requirements:
    - Time-scaled phylogeny (from TreeTime or BEAST)
    - Sample collection dates
    - Tips must have matching names

    TransPhylo estimates:
    - Who infected whom
    - Unsampled cases in the transmission chain
    - R0 and generation time
    '''
    from Bio import Phylo
    import pandas as pd

    tree = Phylo.read(dated_tree_file, 'nexus')

    # Verify all tips have dates
    dates_df = pd.read_csv(sample_dates, sep='\t')
    tip_names = {clade.name for clade in tree.get_terminals()}
    dated_names = set(dates_df['name'])

    missing = tip_names - dated_names
    if missing:
        print(f'Warning: {len(missing)} tips without dates: {missing}')

    return {'tree': dated_tree_file, 'dates': sample_dates}

Interpret Results

r
# Analyze TransPhylo output

# Get median transmission tree
med_tree <- medTTree(res)

# Plot transmission tree
plot(med_tree)

# Get R0 estimate
r0_samples <- res$record[, 'off.r']
cat('R0 estimate:', median(r0_samples), '\n')
cat('95% CI:', quantile(r0_samples, c(0.025, 0.975)), '\n')

# Identify superspreaders
# Count number infected by each case
infections_per_case <- table(med_tree$ttree[, 'infector'])
superspreaders <- names(infections_per_case[infections_per_case > 3])

Python Alternative: outbreaker2 Wrapper

Goal: Infer likely transmission pairs from genomic distance and collection dates without requiring a dated phylogeny.

Approach: For each pair of samples, check that the potential infector was sampled earlier, that the time interval is compatible with the generation time, and that the SNP distance is consistent with direct transmission.

python
def infer_transmission_simple(distance_matrix, dates, generation_time=5):
    '''Simplified transmission inference

    Uses genomic distance and collection dates to infer likely
    transmission pairs. Less sophisticated than TransPhylo but
    doesn't require dated phylogeny.

    Criteria for transmission pair (A -> B):
    1. A collected before B
    2. Genomic distance consistent with direct transmission
    3. Time difference compatible with generation time
    '''
    import pandas as pd
    import numpy as np

    n = len(dates)
    transmission_pairs = []

    for i in range(n):
        for j in range(n):
            if i == j:
                continue

            time_diff = dates[j] - dates[i]  # Days between collection

            # Potential infector must be sampled first
            if time_diff <= 0:
                continue

            # Check if time difference is compatible
            # Generation time: time between infection of case and infection of secondary
            # Serial interval: time between symptom onset (often used as proxy)
            if time_diff > generation_time * 3:  # Too much time
                continue

            # Check genomic distance
            snp_diff = distance_matrix[i, j]

            # Expected SNPs = rate * time
            # For most pathogens, direct transmission = 0-5 SNP difference
            expected_snps = (time_diff / 365) * 10  # Rough estimate

            if snp_diff <= max(5, expected_snps * 2):
                transmission_pairs.append({
                    'infector': i,
                    'infectee': j,
                    'snp_distance': snp_diff,
                    'days_between': time_diff,
                    'confidence': 'high' if snp_diff <= 2 else 'moderate'
                })

    return pd.DataFrame(transmission_pairs)

Network Visualization

Goal: Visualize the inferred transmission chain as a directed network graph showing who infected whom.

Approach: Build a directed NetworkX graph from transmission pairs and render it with spring layout, directional arrows, and labeled nodes.

python
def plot_transmission_network(pairs_df, metadata=None):
    '''Visualize transmission network

    Uses networkx to create directed graph of transmissions.
    '''
    import networkx as nx
    import matplotlib.pyplot as plt

    G = nx.DiGraph()

    for _, row in pairs_df.iterrows():
        G.add_edge(row['infector'], row['infectee'],
                   weight=row.get('confidence', 1))

    # Layout
    pos = nx.spring_layout(G)

    # Draw
    plt.figure(figsize=(12, 8))
    nx.draw(G, pos, with_labels=True, node_color='lightblue',
            node_size=500, arrows=True, arrowsize=20)

    plt.title('Transmission Network')
    return plt.gcf()

Superspreader Analysis

python
def identify_superspreaders(transmission_pairs, threshold=3):
    '''Identify superspreading events

    Superspreader: Individual who infected many others
    Threshold typically 80/20 rule: 20% of cases cause 80% of transmission

    Common threshold: >3 secondary cases
    '''
    from collections import Counter

    infector_counts = Counter(transmission_pairs['infector'])

    superspreaders = {k: v for k, v in infector_counts.items() if v >= threshold}

    total_transmissions = sum(infector_counts.values())
    ss_transmissions = sum(superspreaders.values())

    print(f'Superspreaders (>{threshold} secondary cases):')
    for ss, count in sorted(superspreaders.items(), key=lambda x: -x[1]):
        print(f'  Case {ss}: {count} secondary infections')

    print(f'\nSuperspreading contribution: {ss_transmissions/total_transmissions:.1%}')

    return superspreaders

Related Skills

  • epidemiological-genomics/phylodynamics - Generate dated trees
  • epidemiological-genomics/pathogen-typing - Identify outbreak clones
  • data-visualization/interactive-visualization - Visualize transmission

Expand your agent's capabilities with these related and highly-rated skills.

FreedomIntelligence/OpenClaw-Medical-Skills

vcf-annotator

Annotate VCF variants with VEP, ClinVar, gnomAD frequencies, and ancestry-aware context. Generates prioritised variant reports.

2,009 275
Explore
FreedomIntelligence/OpenClaw-Medical-Skills

chemist-analyst

Analyzes events through chemistry lens using molecular structure, reaction mechanisms, thermodynamics, kinetics, and analytical techniques (spectroscopy, chromatography, mass spectrometry). Provides insights on chemical processes, material properties, reaction pathways, synthesis, and analytical methods. Use when: Chemical reactions, material analysis, synthesis planning, process optimization, environmental chemistry. Evaluates: Molecular structure, reaction mechanisms, yield, selectivity, safety, environmental impact.

2,009 275
Explore
FreedomIntelligence/OpenClaw-Medical-Skills

bio-alignment-io

Read, write, and convert multiple sequence alignment files using Biopython Bio.AlignIO. Supports Clustal, PHYLIP, Stockholm, FASTA, Nexus, and other alignment formats for phylogenetics and conservation analysis. Use when reading, writing, or converting alignment file formats.

2,009 275
Explore
FreedomIntelligence/OpenClaw-Medical-Skills

sleep-analyzer

分析睡眠数据、识别睡眠模式、评估睡眠质量,并提供个性化睡眠改善建议。支持与其他健康数据的关联分析。

2,009 275
Explore
FreedomIntelligence/OpenClaw-Medical-Skills

metabolomics-workbench-database

Access NIH Metabolomics Workbench via REST API (4,200+ studies). Query metabolites, RefMet nomenclature, MS/NMR data, m/z searches, study metadata, for metabolomics and biomarker discovery.

2,009 275
Explore
FreedomIntelligence/OpenClaw-Medical-Skills

bio-hi-c-analysis-matrix-operations

Balance, normalize, and transform Hi-C contact matrices using cooler and cooltools. Apply iterative correction (ICE), compute expected values, and generate observed/expected matrices. Use when normalizing or transforming Hi-C matrices.

2,009 275
Explore

Didn't find tool you were looking for?

Be as detailed as possible for better results