Evidence map›Paper›PMID 42435050›Full record

ArticleJournal of molecular evolution2026

Classification of SARS-CoV-2 Variants Through the Epistatic Circos Plots with Convolutional Neural Networks.

Bo Jing, Kai-Rui Zhang, Hong-Li Zeng, Erik Aurell

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Article in Journal of molecular evolution, 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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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

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

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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

4 authors.

Bo JingSchool of Science, Nanjing University of Posts and Telecommunications, Nanjing, 210023, China.
Kai-Rui ZhangSchool of Science, Nanjing University of Posts and Telecommunications, Nanjing, 210023, China.
Hong-Li ZengSchool of Science, Nanjing University of Posts and Telecommunications, Nanjing, 210023, China. hlzeng@njupt.edu.cn.
Erik AurellDepartment of Computational Science and Technology, AlbaNova University Center, Stockholm, SE-106 91, Sweden. eaurell@kth.se.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The COVID-19 pandemic has profoundly affected global health, driven by the remarkable transmissibility and mutational adaptability of the SARS-CoV-2 virus. Although five variants of concern, Alpha, Beta, Gamma, Delta, and Omicron, have been identified, the classification task in this study is formulated using four classes: Alpha, Delta, Omicron, and Else, reflecting the sequence availability and temporal coverage of the dataset. Here, we develop an integrative framework that combines direct coupling analysis (DCA), Circos-based visualization, and convolutional neural networks (CNNs) to characterize lineage-specific epistatic signatures from large-scale SARS-CoV-2 genomic sequences. DCA-inferred pairwise mutational couplings were transformed into Circos images, which were then used as inputs for CNN-based classification models. The proposed framework achieved robust variant classification, with the best-performing model reaching a weighted-average [Formula: see text] of [Formula: see text] and an AUC close to 1. Additional temporal holdout analyses showed that the framework retained reasonable predictive capability across evolutionary time, yielding a weighted-average [Formula: see text] of 87.85%.

Indexed as

Circos plotsConvolution neural networkDirect coupling analysis (DCA)EpistasisSARS-CoV-2

Identifiers

What OpenQuestion 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 OpenQuestion graph.