Evidence map›Paper›PMID 37200352›Full record

ArticlePloS one2023

Unsupervised machine learning framework for discriminating major variants of concern during COVID-19.

Rohitash Chandra, Chaarvi Bansal, Mingyue Kang, Tom Blau, Vinti Agarwal, Pranjal Singh, Laurence O W Wilson, Seshadri Vasan

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.7field-weighted citation impact, top 16% of its field
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

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Rapid identification ofChinese herbal medicines · 2025
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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

8 authors at 5 institutions in 3 countries.

Rohitash ChandraTransitional Artificial Intelligence Research Group, School of Mathematics and Statistics, UNSW Sydney, Sydney, Australia.ORCID 0000-0001-6353-1464
Chaarvi BansalTransitional Artificial Intelligence Research Group, School of Mathematics and Statistics, UNSW Sydney, Sydney, Australia.ORCID 0000-0001-8080-9202
Mingyue KangTransitional Artificial Intelligence Research Group, School of Mathematics and Statistics, UNSW Sydney, Sydney, Australia.
Tom BlauData 61, CSIRO, Sydney, Australia.
Vinti AgarwalDepartment of Computer Science and Information Systems, Birla Institute of Technology and Science Pilani, Rajasthan, India.
Pranjal SinghDepartment of Computer Science and Engineering, Indian Institute of Technology Guwathi, Assam, India.
Laurence O W WilsonAustralian e-Health Research Centre, Commonwealth Scientific and Industrial Research Organisation, North Ryde, Australia.
Seshadri VasanDepartment of Health Sciences, University of York, York, United Kingdom.
UNSW Sydney · AUCommonwealth Scientific and Industrial Research Organisation · AUBirla Institute of Technology and Science, Pilani · INIndian Institute of Technology Guwahati · INUniversity of York · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Due to the high mutation rate of the virus, the COVID-19 pandemic evolved rapidly. Certain variants of the virus, such as Delta and Omicron emerged with altered viral properties leading to severe transmission and death rates. These variants burdened the medical systems worldwide with a major impact to travel, productivity, and the world economy. Unsupervised machine learning methods have the ability to compress, characterize, and visualize unlabelled data. This paper presents a framework that utilizes unsupervised machine learning methods to discriminate and visualize the associations between major COVID-19 variants based on their genome sequences. These methods comprise a combination of selected dimensionality reduction and clustering techniques. The framework processes the RNA sequences by performing a k-mer analysis on the data and further visualises and compares the results using selected dimensionality reduction methods that include principal component analysis (PCA), t-distributed stochastic neighbour embedding (t-SNE), and uniform manifold approximation projection (UMAP). Our framework also employs agglomerative hierarchical clustering to visualize the mutational differences among major variants of concern and country-wise mutational differences for selected variants (Delta and Omicron) using dendrograms. We also provide country-wise mutational differences for selected variants via dendrograms. We find that the proposed framework can effectively distinguish between the major variants and has the potential to identify emerging variants in the future.

Indexed as

COVID-19Unsupervised Machine LearningAlgorithmsHumansPandemicsSARS-CoV-2

Identifiers

PMID37200352
PMCPMC10194860
OpenAlexW4377046963

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.