Evidence map›Paper›PMID 33647832›Full record

ArticleComputers in biology and medicine2021

UMAP-assisted K-means clustering of large-scale SARS-CoV-2 mutation datasets.

Yuta Hozumi, Rui Wang, Changchuan Yin, Guo-Wei Wei

Abstract read
In one paragraph

Article in Computers in biology and medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

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3 · Its place in the literature

Who cites it

31 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Yuta HozumiDepartment of Mathematics, Michigan State University, MI, 48824, USA.
Rui WangDepartment of Mathematics, Michigan State University, MI, 48824, USA.
Changchuan YinDepartment of Mathematics, Statistics, and Computer Science, University of Illinois at Chicago, Chicago, IL, 60607, USA.
Guo-Wei WeiDepartment of Mathematics, Michigan State University, MI, 48824, USA; Department of Electrical and Computer Engineering, Michigan State University, MI, 48824, USA; Department of Biochemistry and Molecular Biology, Michigan State University, MI, 48824, USA. Electronic address: weig@msu.edu.

Funding

Synergistic integration of topology and machine learning for the predictions of protein-ligand binding affinities and mutation impactsR01GM126189 · NIGMS · MICHIGAN STATE UNIVERSITY · PI WEI, GUOWEI · 2018 to 2021
$1.4M
NIGMS NIH HHS R01 GM126189
6 · The paper itself

Abstract

Coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has a worldwide devastating effect. Understanding the evolution and transmission of SARS-CoV-2 is of paramount importance for controlling, combating and preventing COVID-19. Due to the rapid growth in both the number of SARS-CoV-2 genome sequences and the number of unique mutations, the phylogenetic analysis of SARS-CoV-2 genome isolates faces an emergent large-data challenge. We introduce a dimension-reduced K-means clustering strategy to tackle this challenge. We examine the performance and effectiveness of three dimension-reduction algorithms: principal component analysis (PCA), t-distributed stochastic neighbor embedding (t-SNE), and uniform manifold approximation and projection (UMAP). By using four benchmark datasets, we found that UMAP is the best-suited technique due to its stable, reliable, and efficient performance, its ability to improve clustering accuracy, especially for large Jaccard distanced-based datasets, and its superior clustering visualization. The UMAP-assisted K-means clustering enables us to shed light on increasingly large datasets from SARS-CoV-2 genome isolates.

Indexed as

AlgorithmsDatabases, Nucleic AcidGenome, ViralMutationPhylogenyCOVID-19HumansSARS-CoV-2COVID-19PCASARS-CoV-2t-SNEUMAP

Identifiers

PMID33647832
PMCPMC7897976

What OpenQuestion holds

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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.