Evidence map›Paper›PMID 40848247›Full record

ArticleBioinformatics (Oxford, England)2025

CANA v1.0.0: efficient quantification of canalization in automata networks.

Austin M Marcus, Jordan Rozum, Herbert Sizek, Luis M Rocha

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Austin M MarcusCenter for Complex Biological Systems, University of California Irvine, Irvine, CA 92697, United States.
Jordan RozumSchool of Systems Science and Industrial Engineering, Binghamton University (State University of New York), Vestal, NY 13850, United States.ORCID 0000-0002-4356-9809
Herbert SizekDepartment of Informatics, Indiana University, Bloomington, IN 47405, United States.
Luis M RochaSchool of Systems Science and Industrial Engineering, Binghamton University (State University of New York), Vestal, NY 13850, United States.ORCID 0000-0001-9402-887X

Funding

Evidence-based Drug-Interaction Discovery: In-Vivo, In-Vitro and ClinicalR01LM011945 · NLM · INDIANA UNIVERSITY INDIANAPOLIS · PI LI, LANG, ROCHA, LUIS M · 2014 to 2017
$1.8M
Fundação para a Ciência e a Tecnologia 2022.09122.PTDCNIH National Library of Medicine Program 01LM011945-01NLM NIH HHS R01 LM011945
6 · The paper itself

Abstract

summaryThe biomolecular networks underpinning cell function exhibit canalization, or the buffering of fluctuations required to function in a noisy environment. We present a new major release of CANA, v1.0.0, an open-source Python package for understanding canalization in automata network models, discrete dynamical systems in which activation of biomolecular entities (e.g. transcription of genes) is modeled as the activity of coupled automata. One understudied putative mechanism for canalization is the functional equivalence of biomolecular regulators (e.g. among the transcription factors for a gene). We study this mechanism using the theory of symmetry in discrete functions. We present a new exact method, schematodes, for finding maximal symmetry groups among the inputs to discrete functions, and integrate it into CANA. The schematodes method substantially outperforms the inexact method of previous CANA versions both in speed and accuracy. We apply CANA v1.0.0 to study symmetry in 74 experimentally supported automata network models from the Cell Collective (CC) repository. The symmetry distribution is significantly different in the CC than in random automata with the same in-degree (connectivity) and bias (average output) (Kolmogorov-Smirnov test, P ≪ .001). Its spread is much wider than in a null model (IQR 0.31 versus IQR 0.20 with equal medians), demonstrating that the CC is enriched in functions with extreme symmetry or asymmetry. AVAILABILITY AND IMPLEMENTATION: CANA source is on https://github.com/CASCI-lab/CANA and is installable via pip install cana. Source for schematodes is on https://github.com/CASCI-lab/schematodes. Analysis scripts are on https://github.com/CASCI-lab/symmetryInCellCollective.

Indexed as

Computational BiologyGene Regulatory NetworksModels, BiologicalSoftwareAlgorithms

Identifiers

PMID40848247
PMCPMC12512137

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.