Evidence map›Paper›PMID 38617261›Full record

ArticlebioRxiv : the preprint server for biology2024

Predicting The Pathway Involvement Of Metabolites Based on Combined Metabolite and Pathway Features.

Erik D Huckvale, Hunter N B Moseley

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Erik D HuckvaleMarkey Cancer Center, University of Kentucky, Lexington, KY 40506, USA.ORCID 0000-0002-6994-8831
Hunter N B MoseleyMarkey Cancer Center, University of Kentucky, Lexington, KY 40506, USA.ORCID 0000-0003-3995-5368

Funding

Vascular Mechanisms of PCB-Induced Brain MetastasesP42ES007380 · NIEHS · UNIVERSITY OF KENTUCKY · PI MORRIS, ANDREW J · 1997 to 2024
$47.8M
NIEHS NIH HHS P42 ES007380
6 · The paper itself

Abstract

A major limitation of most metabolomics datasets is the sparsity of pathway annotations of detected metabolites. It is common for less than half of identified metabolites in these datasets to have known metabolic pathway involvement. Trying to address this limitation, machine learning models have been developed to predict the association of a metabolite with a "pathway category", as defined by one of the metabolic knowledgebases like the Kyoto Encyclopedia of Gene and Genomes. Most of these models are implemented as a single binary classifier specific to a single pathway category, requiring a set of binary classifiers for generating predictions for multiple pathway categories. This single binary classifier per pathway category approach both multiplies the computational resources necessary for training while diluting the positive entries in gold standard datasets needed for training. To address the limitations of training separate classifiers, we propose a generalization of the metabolic pathway prediction problem using a single binary classifier that accepts both features representing a metabolite and features representing a generic pathway category and then predicts whether the given metabolite is involved in the corresponding pathway category. We demonstrate that this metabolite-pathway features-pair approach is not only competitive with the combined performance of training separate binary classifiers, but it outperforms the previous benchmark models.

Indexed as

Binary classificationDeep learningMachine learningMetabolic pathwayMetabolismMetaboliteMulti-layer perceptronSupervised learningXGBoost

Identifiers

PMID38617261
PMCPMC11014601

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.