PluginBench
Skill
Pass
Audit score 90

arboreto

k-dense-ai/scientific-agent-skills

How to install arboreto

npx skills add https://github.com/k-dense-ai/scientific-agent-skills --skill arboreto
Claude Code
Cursor
Windsurf
Cline
Full instructions (SKILL.md)

Source of truth, from k-dense-ai/scientific-agent-skills.


name: arboreto description: Infer gene regulatory networks (GRNs) from gene expression data using scalable algorithms (GRNBoost2, GENIE3). Use when analyzing transcriptomics data (bulk RNA-seq, single-cell RNA-seq) to identify transcription factor-target gene relationships and regulatory interactions. Supports distributed computation for large-scale datasets. license: BSD-3-Clause license metadata: {"version": "1.0", "skill-author": "K-Dense Inc."}

Arboreto

Overview

Arboreto is a Python library from Aerts Lab for inferring gene regulatory networks (GRNs) from gene expression data. It parallelizes tree-based ensemble regression (GRNBoost2, GENIE3) with Dask across local cores or remote clusters.

Core capability: Identify which transcription factors (TFs) regulate which target genes based on expression patterns across observations (cells, samples, conditions).

Upstream: PyPI 0.1.6 (2021-02-09, latest). Docs: arboreto.readthedocs.io. Primary downstream consumer: pySCENIC.

Quick Start

Install arboreto:

uv pip install arboreto

Basic GRN inference:

import pandas as pd
from arboreto.algo import grnboost2

if __name__ == '__main__':
    # Load expression data (genes as columns)
    expression_matrix = pd.read_csv('expression_data.tsv', sep='\t')

    # Infer regulatory network
    network = grnboost2(expression_data=expression_matrix)

    # Save results (TF, target, importance)
    network.to_csv('network.tsv', sep='\t', index=False, header=False)

Critical: Always use if __name__ == '__main__': guard because Dask spawns new processes.

Core Capabilities

1. Basic GRN Inference

For standard GRN inference workflows including:

  • Input data preparation (Pandas DataFrame or NumPy array)
  • Running inference with GRNBoost2 or GENIE3
  • Filtering by transcription factors
  • Output format and interpretation

See: references/basic_inference.md

Use the ready-to-run script: scripts/basic_grn_inference.py for standard inference tasks:

python scripts/basic_grn_inference.py expression_data.tsv output_network.tsv --tf-file tfs.txt --seed 777 --limit 5000

2. Algorithm Selection

Arboreto provides two algorithms:

GRNBoost2 (Recommended):

  • Fast gradient boosting-based inference
  • Optimized for large datasets (10k+ observations)
  • Default choice for most analyses

GENIE3:

  • Random Forest-based inference
  • Original multiple regression approach
  • Use for comparison or validation

Quick comparison:

from arboreto.algo import grnboost2, genie3

# Fast, recommended
network_grnboost = grnboost2(expression_data=matrix)

# Classic algorithm
network_genie3 = genie3(expression_data=matrix)

For detailed algorithm comparison, parameters, and selection guidance: references/algorithms.md

3. Distributed Computing

Scale inference from local multi-core to cluster environments:

Local (default) - Uses all available cores automatically:

network = grnboost2(expression_data=matrix)

Custom local client - Control resources:

from distributed import LocalCluster, Client

local_cluster = LocalCluster(n_workers=10, memory_limit='8GB')
client = Client(local_cluster)

network = grnboost2(expression_data=matrix, client_or_address=client)

client.close()
local_cluster.close()

Cluster computing - Connect to remote Dask scheduler:

from distributed import Client

client = Client('tcp://scheduler:8786')
network = grnboost2(expression_data=matrix, client_or_address=client)

For cluster setup, performance optimization, and large-scale workflows: references/distributed_computing.md

Installation

uv pip install arboreto

Conda (Bioconda):

conda install -c bioconda arboreto

Dependencies (from upstream requirements.txt): dask[complete], distributed, numpy, pandas, scikit-learn, scipy

Input formats: pandas DataFrame, dense numpy.ndarray, or sparse scipy.sparse.csc_matrix (rows = observations, columns = genes). For array/matrix inputs, pass gene_names explicitly.

Common Use Cases

Single-Cell RNA-seq Analysis

import pandas as pd
from arboreto.algo import grnboost2

if __name__ == '__main__':
    # Load single-cell expression matrix (cells x genes)
    sc_data = pd.read_csv('scrna_counts.tsv', sep='\t')

    # Infer cell-type-specific regulatory network
    network = grnboost2(expression_data=sc_data, seed=42)

    # Filter high-confidence links
    high_confidence = network[network['importance'] > 0.5]
    high_confidence.to_csv('grn_high_confidence.tsv', sep='\t', index=False)

Bulk RNA-seq with TF Filtering

from arboreto.utils import load_tf_names
from arboreto.algo import grnboost2

if __name__ == '__main__':
    # Load data
    expression_data = pd.read_csv('rnaseq_tpm.tsv', sep='\t')
    tf_names = load_tf_names('human_tfs.txt')

    # Infer with TF restriction
    network = grnboost2(
        expression_data=expression_data,
        tf_names=tf_names,
        seed=123
    )

    network.to_csv('tf_target_network.tsv', sep='\t', index=False)

Comparative Analysis (Multiple Conditions)

from arboreto.algo import grnboost2

if __name__ == '__main__':
    # Infer networks for different conditions
    conditions = ['control', 'treatment_24h', 'treatment_48h']

    for condition in conditions:
        data = pd.read_csv(f'{condition}_expression.tsv', sep='\t')
        network = grnboost2(expression_data=data, seed=42)
        network.to_csv(f'{condition}_network.tsv', sep='\t', index=False)

Output Interpretation

Arboreto returns a DataFrame with regulatory links:

ColumnDescription
TFTranscription factor (regulator)
targetTarget gene
importanceRegulatory importance score (higher = stronger)

Filtering strategy:

  • limit=N at inference time (return top N links globally)
  • Post-hoc importance threshold (e.g., > 0.5)
  • Top links per target via groupby('target')
  • Statistical significance testing (permutation tests, external tools)

Integration with pySCENIC

Arboreto powers the GRN inference step in pySCENIC. pySCENIC 0.11+ passes sparse expression matrices to grnboost2 / genie3; pySCENIC 0.12+ defaults to arboreto_with_multiprocessing.py (no Dask) for compatibility — use standalone arboreto when you need Dask scaling.

# Standalone: infer co-expression modules before pySCENIC cisTarget pruning
from arboreto.algo import grnboost2

network = grnboost2(expression_data=expression_df, tf_names=tf_list, limit=5000)

# Downstream: pySCENIC ctx pruning, regulon definition, AUCell (see pySCENIC docs)

Convert AnnData to a DataFrame for arboreto directly:

expression_df = adata.to_df()  # cells x genes

Reproducibility

Always set a seed for reproducible results:

network = grnboost2(expression_data=matrix, seed=777)

Run multiple seeds for robustness analysis:

from distributed import LocalCluster, Client

if __name__ == '__main__':
    client = Client(LocalCluster())

    seeds = [42, 123, 777]
    networks = []

    for seed in seeds:
        net = grnboost2(expression_data=matrix, client_or_address=client, seed=seed)
        networks.append(net)

    # Consensus: links recurring across runs (example: mean importance per TF-target pair)
    import pandas as pd
    combined = pd.concat(networks)
    consensus = (
        combined.groupby(['TF', 'target'], as_index=False)['importance']
        .mean()
        .query('importance > 0.5')
    )

Troubleshooting

Memory errors: Reduce dataset size by filtering low-variance genes or use distributed computing

Slow performance: Use GRNBoost2 instead of GENIE3, enable distributed client, filter TF list

Dask errors: Ensure if __name__ == '__main__': guard is present in scripts (required on Windows/macOS with spawn-based multiprocessing)

Empty results: Check data format (genes as columns), verify TF names match column names in the expression matrix

Sparse data: Use scipy.sparse.csc_matrix and pass matching gene_names; supported since arboreto 0.1.6 / pySCENIC 0.11

Related skills

More from k-dense-ai/scientific-agent-skills and the wider catalog.

ASastropy logo

astropy

k-dense-ai/scientific-agent-skills

Core Python library for astronomy and astrophysics workflows that need Astropy APIs, including units/quantities, coordinates, FITS I/O, tables, time systems, WCS, and cosmology. Use when implementing or debugging astronomical data analysis code with Astropy.

668 installsAudited
BEbenchling-integration logo

benchling-integration

k-dense-ai/scientific-agent-skills

Benchling Python SDK and REST API integration for registry entities, inventory, ELN entries, workflows, Benchling Apps, and Data Warehouse queries. Use when automating lab data with benchling-sdk or the v2 API.

671 installsAudited
BGbgpt-paper-search logo

bgpt-paper-search

k-dense-ai/scientific-agent-skills

Search scientific papers and retrieve structured experimental data extracted from full-text studies via the BGPT MCP server. Returns 25+ fields per paper including methods, results, sample sizes, quality scores, and conclusions. Use for literature reviews, evidence synthesis, and finding experimental details not available in abstracts alone.

770 installs
BIbiopython logo

biopython

k-dense-ai/scientific-agent-skills

Comprehensive molecular biology toolkit. Use for sequence manipulation, file parsing (FASTA/GenBank/PDB), phylogenetics, and programmatic NCBI/PubMed access (Bio.Entrez). Best for batch processing, custom bioinformatics pipelines, BLAST automation. For quick lookups use gget; for multi-service integration use bioservices.

697 installsAudited
BIbioservices logo

bioservices

k-dense-ai/scientific-agent-skills

Unified Python interface to 40+ bioinformatics services. Use when querying multiple databases (UniProt, KEGG, ChEMBL, Reactome) in a single workflow with consistent API. Best for cross-database analysis, ID mapping across services. For quick single-database lookups use gget; for sequence/file manipulation use biopython.

686 installsAudited
CEcellxgene-census logo

cellxgene-census

k-dense-ai/scientific-agent-skills

Query the CZ CELLxGENE Census programmatically for versioned public single-cell and spatial transcriptomics data. Use when you need population-scale cell metadata, gene expression slices, Census summary counts, source H5AD URIs/downloads, embeddings, spatial Census data, or reference atlas comparisons across organisms, tissues, diseases, assays, and cell types. For analyzing your own local single-cell data use scanpy, anndata, or scvi-tools.

669 installsAudited