Evidence map›Paper›PMID 39715240›Full record

ArticlePloS one2024

Machine learning methods for predicting essential metabolic genes from Plasmodium falciparum genome-scale metabolic network.

Itunuoluwa Isewon, Stephen Binaansim, Faith Adegoke, Jerry Emmanuel, Jelili Oyelade

Abstract read
In one paragraph

Article in PloS one, 2024. 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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0cells of the map it votes in
0citing papers in PubMed
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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

5 authors.

Itunuoluwa IsewonDepartment of Computer and Information Sciences, Covenant University, Ota, Ogun State, Nigeria.
Stephen BinaansimDepartment of Computer and Information Sciences, Covenant University, Ota, Ogun State, Nigeria.ORCID 0009-0003-9178-8947
Faith AdegokeDepartment of Computer and Information Sciences, Covenant University, Ota, Ogun State, Nigeria.
Jerry EmmanuelDepartment of Computer and Information Sciences, Covenant University, Ota, Ogun State, Nigeria.
Jelili OyeladeDepartment of Computer and Information Sciences, Covenant University, Ota, Ogun State, Nigeria.ORCID 0000-0002-5476-4992

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Essential genes are those whose presence is vital for a cell's survival and growth. Detecting these genes in disease-causing organisms is critical for various biological studies, including understanding microbe metabolism, engineering genetically modified microorganisms, and identifying targets for treatment. When essential genes are expressed, they give rise to essential proteins. Identifying these genes, especially in complex organisms like Plasmodium falciparum, which causes malaria, is challenging due to the cost and time associated with experimental methods. Thus, computational approaches have emerged. Early research in this area prioritised the study of less intricate organisms, inadvertently neglecting the complexities of metabolite transport in metabolic networks. To overcome this, a Network-based Machine Learning framework was proposed. It assessed various network properties in Plasmodium falciparum, using a Genome-Scale Metabolic Model (iAM_Pf480) from the BiGG database and essentiality data from the Ogee database. The proposed approach substantially improved gene essentiality predictions as it considered the weighted and directed nature of metabolic networks and utilised network-based features, achieving a high accuracy rate of 0.85 and an AuROC of 0.7. Furthermore, this study enhanced the understanding of metabolic networks and their role in determining gene essentiality in Plasmodium falciparum. Notably, our model identified 9 genes previously considered non-essential in the Ogee database but now predicted to be essential, with some of them potentially serving as drug targets for malaria treatment, thereby opening exciting research avenues.

Indexed as

Genes, EssentialMachine LearningMetabolic Networks and PathwaysPlasmodium falciparumComputational BiologyGenome, Protozoan

Identifiers

PMID39715240
PMCPMC11666047

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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.