Evidence map›Paper›PMID 41557465›Full record

ArticleBioinformatics (Oxford, England)2026

MetaFX: feature extraction from whole-genome metagenomic sequencing data.

Artem Ivanov, Vladimir Popov, Maxim Morozov, Evgenii Olekhnovich, Vladimir Ulyantsev

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2026. 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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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Artem IvanovInformation Technology and Programming Department, ITMO University, St. Petersburg 197101, Russia.ORCID 0000-0002-7997-0637
Vladimir PopovSchool of Mathematics and Mechanics, St. Petersburg State University, St. Petersburg 199034, Russia.
Maxim MorozovGenome Research and Computational Biology Lab, Lopukhin Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency, Moscow 119435, Russia.
Evgenii OlekhnovichGenome Research and Computational Biology Lab, Lopukhin Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency, Moscow 119435, Russia.
Vladimir UlyantsevInformation Technology and Programming Department, ITMO University, St. Petersburg 197101, Russia.

Funding

Russian Science Foundation 23-75-10125
6 · The paper itself

Abstract

motivationMicrobial communities consist of thousands of microorganisms and viruses and have a tight connection with an environment, such as gut microbiota modulation of host body metabolism. However, the direct relationship between the presence of certain microorganism and the host state often remains unknown. Toolkits using reference-based approaches are limited to microbes present in databases. Reference-free methods often require enormous resources for metagenomic assembly or results in many poorly interpretable features based on k-mers.

resultsHere we present MetaFX-an open-source library for feature extraction from whole-genome metagenomic sequencing data and classification of groups of samples. Using a large volume of metagenomic samples deposited in databases, MetaFX compares samples grouped by metadata criteria (e.g. disease, treatment, etc.) and constructs genomic features distinct for certain types of communities. Features constructed based on statistical k-mer analysis and de Bruijn graphs partition. Those features are used in machine learning models for classification of novel samples. Extracted features can be visualized on de Bruijn graphs and annotated for providing biological insights. We demonstrate the utility of MetaFX by building classification models for 590 human gut samples with inflammatory bowel disease. Our results outperform the previous research disease prediction accuracy up to 17%, and improves classification results compared to taxonomic analysis by 9±10% on average. AVAILABILITY AND IMPLEMENTATION: MetaFX is a feature extraction toolkit applicable for metagenomic datasets analysis and samples classification. The source code, test data, and relevant information for MetaFX are freely accessible at https://github.com/ctlab/metafx under the MIT License. Alternatively, MetaFX can be obtained via http://doi.org/10.5281/zenodo.16949369.

Indexed as

MetagenomeMetagenomicsSoftwareWhole Genome SequencingAlgorithmsHumansInflammatory Bowel DiseasesMachine Learning

Identifiers

PMID41557465
PMCPMC12891910

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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.