Evidence map›Paper›PMID 36464715›Full record

ArticleScientific reports2022

Graphlets in comparison of Petri net-based models of biological systems.

Bartłomiej Szawulak, Piotr Formanowicz

Abstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Bartłomiej SzawulakInstitute of Computing Science, Poznan University of Technology, 60-965, Poznań, Poland. bszawulak@cs.put.poznan.pl.
Piotr FormanowiczInstitute of Computing Science, Poznan University of Technology, 60-965, Poznań, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Capability to compare biological models is a crucial step needed in an analysis of complex organisms. Petri nets as a popular modelling technique, needs a possibility to determine the degree of structural similarities (e.g., comparison of metabolic or signaling pathways). However, existing comparison methods use matching invariants approach for establishing a degree of similarity, and because of that are vulnerable to the state explosion problem which may appear during calculation of a minimal invariants set. Its occurrence will block usage of existing methods. To find an alternative for this situation, we decided to adapt and tests in a Petri net environment a method based on finding a distribution of graphlets. First, we focused on adapting the original graphlets for notation of bipartite, directed graphs. As a result, 151 new graphlets with 592 orbits were created. The next step focused on evaluating a performance of the popular Graphlet Degree Distribution Agreement (GDDA) metric in the new environment. To do that, we decided to use randomly generated networks that share typical characteristics of biological models represented in Petri nets. Our results confirmed the usefulness of graphlets and GDDA in Petri net comparison and discovered its limitations.

Indexed as

Models, BiologicalReceptor Protein-Tyrosine KinasesReceptor Protein-Tyrosine Kinases

Identifiers

PMID36464715
PMCPMC9719902

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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.