Evidence map›Paper›PMID 33935376›Full record

ArticleNeural computing & applications2022

Learning vector quantization as an interpretable classifier for the detection of SARS-CoV-2 types based on their RNA sequences.

Marika Kaden, Katrin Sophie Bohnsack, Mirko Weber, Mateusz Kudła, Kaja Gutowska, Jacek Blazewicz, Thomas Villmann

Abstract read
In one paragraph

Article in Neural computing & applications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Unsupervised identification of significant lineages of SARS-CoV-2 through scalable machine learning methods.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  3. Article
  4. Article
  5. Article
4 · The record

Corrections and comments

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

7 authors.

Marika Kaden *University of Applied Sciences Mittweida, Technikumplatz 17, 09648 Mittweida, Germany.
Katrin Sophie Bohnsack *University of Applied Sciences Mittweida, Technikumplatz 17, 09648 Mittweida, Germany.
Mirko Weber *University of Applied Sciences Mittweida, Technikumplatz 17, 09648 Mittweida, Germany.
Mateusz Kudła *University of Applied Sciences Mittweida, Technikumplatz 17, 09648 Mittweida, Germany.
Kaja Gutowska *Institute of Computing Science, Poznan University of Technology, Piotrowo 2, 60-965 Poznan, Poland.
Jacek Blazewicz *Institute of Computing Science, Poznan University of Technology, Piotrowo 2, 60-965 Poznan, Poland.
Thomas Villmann *University of Applied Sciences Mittweida, Technikumplatz 17, 09648 Mittweida, Germany.ORCID 0000-0001-6725-0141

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We present an approach to discriminate SARS-CoV-2 virus types based on their RNA sequence descriptions avoiding a sequence alignment. For that purpose, sequences are preprocessed by feature extraction and the resulting feature vectors are analyzed by prototype-based classification to remain interpretable. In particular, we propose to use variants of learning vector quantization (LVQ) based on dissimilarity measures for RNA sequence data. The respective matrix LVQ provides additional knowledge about the classification decisions like discriminant feature correlations and, additionally, can be equipped with easy to realize reject options for uncertain data. Those options provide self-controlled evidence, i.e., the model refuses to make a classification decision if the model evidence for the presented data is not sufficient. This model is first trained using a GISAID dataset with given virus types detected according to the molecular differences in coronavirus populations by phylogenetic tree clustering. In a second step, we apply the trained model to another but unlabeled SARS-CoV-2 virus dataset. For these data, we can either assign a virus type to the sequences or reject atypical samples. Those rejected sequences allow to speculate about new virus types with respect to nucleotide base mutations in the viral sequences. Moreover, this rejection analysis improves model robustness. Last but not least, the presented approach has lower computational complexity compared to methods based on (multiple) sequence alignment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00521-021-06018-2.

Indexed as

Genomic sequence analysisInterpretable modelsLearning vector quantizationReject options

Identifiers

PMID33935376
PMCPMC8076884

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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.