Evidence map›Paper›PMID 40636789›Full record

ArticleBioinformatics advances2025

A fast method for extracting essential and synthetic lethality genes in GEM models.

Francisco Guil, José M García

Abstract read
In one paragraph

Article in Bioinformatics advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Obtaining PDC and other high-added value products from lignin byJournal of integrative bioinformatics · 2025
    Article
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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

2 authors.

Francisco GuilParallel Computer Architecture Group, University of Murcia, CEIR Campus Mare Nostrum, Murcia 30100, Spain.ORCID https://orcid.org/0000-0002-6846-1888
José M GarcíaParallel Computer Architecture Group, University of Murcia, CEIR Campus Mare Nostrum, Murcia 30100, Spain.ORCID https://orcid.org/0000-0002-6388-2835

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Summary: Exploring and categorizing essential and synthetic lethality genes is crucial in developing effective and targeted therapies for various diseases. This endeavor hinges upon genetic minimal cut sets, which also find utility in metabolic engineering. Different methods have been suggested for calculating genetic minimal cut sets. Still, with the emergence of numerous new models and their increasing complexity, it has become essential to introduce new algorithms in this field. This paper presents a new algorithmic approach for computing genetic minimal cut sets, which utilizes linear programming techniques to improve temporal efficiency. The key concept of the method is to use a k-representative subset to replace the target set with a smaller, yet representative, one. We have analyzed its efficiency in terms of running times compared to gMCSPy, the most recent published research on computing genetic minimal cut sets. Availability and implementation: Software and additional material are freely available at https://github.com/biogacop/fastMethod.

Identifiers

PMID40636789
PMCPMC12240467

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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.