Evidence map›Paper›PMID 41462075›Full record

ArticleBMC bioinformatics2025

Improving protein interaction prediction in GenPPi: a novel interaction sampling approach preserving network topology.

Alisson Silva, Carlos Marquez, Iury Godoy, Lucas Silva, Matheus Prado, Murilo Beppler, Natanael Avila, Bruno Travençolo, Anderson R Santos

Abstract read
In one paragraph

Article in BMC bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Alisson SilvaFaculty of Computing (FACOM), Federal University of Uberlândia (UFU), Av. João Naves de Ávila, 2121, Campus Santa Mônica, Bloco B, Uberlândia, Minas Gerais, 38400-902, Brazil.
Carlos MarquezFaculty of Computing (FACOM), Federal University of Uberlândia (UFU), Av. João Naves de Ávila, 2121, Campus Santa Mônica, Bloco B, Uberlândia, Minas Gerais, 38400-902, Brazil.
Iury GodoyFaculty of Computing (FACOM), Federal University of Uberlândia (UFU), Av. João Naves de Ávila, 2121, Campus Santa Mônica, Bloco B, Uberlândia, Minas Gerais, 38400-902, Brazil.
Lucas SilvaFaculty of Computing (FACOM), Federal University of Uberlândia (UFU), Av. João Naves de Ávila, 2121, Campus Santa Mônica, Bloco B, Uberlândia, Minas Gerais, 38400-902, Brazil.
Matheus PradoFaculty of Computing (FACOM), Federal University of Uberlândia (UFU), Av. João Naves de Ávila, 2121, Campus Santa Mônica, Bloco B, Uberlândia, Minas Gerais, 38400-902, Brazil.
Murilo BepplerFaculty of Computing (FACOM), Federal University of Uberlândia (UFU), Av. João Naves de Ávila, 2121, Campus Santa Mônica, Bloco B, Uberlândia, Minas Gerais, 38400-902, Brazil.
Natanael AvilaFaculty of Computing (FACOM), Federal University of Uberlândia (UFU), Av. João Naves de Ávila, 2121, Campus Santa Mônica, Bloco B, Uberlândia, Minas Gerais, 38400-902, Brazil.
Bruno TravençoloFaculty of Computing (FACOM), Federal University of Uberlândia (UFU), Av. João Naves de Ávila, 2121, Campus Santa Mônica, Bloco B, Uberlândia, Minas Gerais, 38400-902, Brazil.
Anderson R SantosFaculty of Computing (FACOM), Federal University of Uberlândia (UFU), Av. João Naves de Ávila, 2121, Campus Santa Mônica, Bloco B, Uberlândia, Minas Gerais, 38400-902, Brazil. santosardr@ufu.br.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundComputational prediction of protein-protein interactions (PPIs) is crucial for understanding cell biology and drug development, offering an alternative to costly experimental methods. The original GenPPi software advanced ab initio PPI network prediction from bacterial genomes but was limited by its reliance on high sequence similarity. This work introduces GenPPi 1.5 to enhance these predictive capabilities.

resultsGenPPi 1.5 incorporates a Random Forest (RF) algorithm, trained on 60 biophysical features from amino acid propensity indices, to classify protein similarity even in low sequence identity scenarios (targeting >65% identity). To manage computational complexity from the increased interactions generated by the RF model, especially in extensive conserved phylogenetic profiles, we developed and integrated the Reduced Interaction Sampling (RIS) algorithm. RIS stochastically samples interactions within these profiles, optimizing performance for complete genome analysis. Extensive simulations across various configurations validated the methodology. RF integration significantly broadened GenPPi's predictive power; application to Buchnera aphidicola showed up to 62% overlap with STRING database interactions. Analysis of RIS demonstrated that while introducing some randomness, critical node identification remains robust, particularly for Top_N values ≥ 100, indicating minimal compromise to network integrity.

conclusionThe combination of Machine Learning (RF) and the RIS algorithm in GenPPi 1.5 represents a significant advancement. It overcomes the high-similarity dependency of the previous version while efficiently handling complex genomes. GenPPi 1.5 provides a robust and scalable alignment-free PPI prediction solution, enabling users to train custom models tailored to specific genomic contexts. GenPPi is freely available on our website https://genppi.facom.ufu.br/ , its source code is hosted on GitHub https://github.com/santosardr/genppi , and it can be easily installed via the Python Package Index using the command pip install genppi-py.

Indexed as

Computational BiologyProtein Interaction MappingSoftwareAlgorithmsDatabases, ProteinAlignment-freeGenomeInteractionProteinRandom ForestRIS algorithm

Identifiers

PMID41462075
PMCPMC12751606

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.