Evidence map›Paper›PMID 42304231›Full record

ArticleBMC bioinformatics2026

GnnDebugger: GNN based error correction in De Bruijn Graphs.

Marijo Šimunović, Lovro Vrček, Mile Šikić, Anton Bankevich

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Article in BMC bioinformatics, 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

What it found

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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

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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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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Marijo ŠimunovićFaculty of Electrical Engineering and Computing, University of Zagreb, Zagreb, Croatia. marijo.simunovic@fer.hr.ORCID http://orcid.org/0009-0006-8681-5869
Lovro VrčekGenome Institute of Singapore, A*STAR, Singapore, Singapore.ORCID http://orcid.org/0000-0001-6977-4002
Mile ŠikićFaculty of Electrical Engineering and Computing, University of Zagreb, Zagreb, Croatia.ORCID http://orcid.org/0000-0002-8370-0891
Anton BankevichDepartment of Computer Science and Engineering, Pennsylvania State University, University Park, PA, USA. anton.bankevich@psu.edu.ORCID http://orcid.org/0000-0003-0609-9542

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundModern sequencing technologies have enabled the reconstruction of complete mammalian genomes from telomere to telomere. However, scaling this achievement to thousands of species and population-level studies remains a challenge. Key bottlenecks include the low quality of the draft assemblies and the high coverage requirements. In particular, reconstructing complete and accurate sequences of both haplotypes in diploid genomes is especially difficult since the sequencing depth is not always sufficient to properly reconstruct diverged regions. We aim to explore the use of machine learning, specifically graph neural networks, for scalable error correction in De Bruijn Graphs, addressing the limitations of existing heuristic methods in genome assembly.

resultsInspired by the success of neural networks in extracting patterns from the data on a massive scale, we introduce a method for correcting errors in De Bruijn Graphs using Graph Neural Networks. Our model provides a reliable classification of edges into correct and erroneous, especially for diploid genomes with coverage depth 35 and lower. We demonstrate that these predictions can guide the downstream read error correction algorithm and genome assembly, ultimately allowing for more accurate genome assembly.

conclusionsMachine learning methods have the potential to replace heuristic methods commonly used in genome assembly. Learning-based approaches can enhance the performance of existing assemblers in challenging scenarios and facilitate adaptation to newly sequenced species.

Indexed as

GenomicsSequence Analysis, DNASoftwareAlgorithmsAnimalsGenomeGraph Neural NetworksMachine Learningde Bruijn GraphError correctionGenome assemblyGNNsPacBio HiFi

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What Socratic holds

Textmetadata
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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 Socratic graph.