Evidence map›Paper›PMID 37124703›Full record

ArticleVirus evolution2021

CoVizu: Rapid analysis and visualization of the global diversity of SARS-CoV-2 genomes.

Roux-Cil Ferreira, Emmanuel Wong, Gopi Gugan, Kaitlyn Wade, Molly Liu, Laura Muñoz Baena, Connor Chato, Bonnie Lu, Abayomi S Olabode, Art F Y Poon

Abstract read
In one paragraph

Article in Virus evolution, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Predicting pathogen evolution and immune evasion in the age of artificial intelligence.Computational and structural biotechnology journal · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Applying the digital data and the bioinformatics tools in SARS-CoV-2 research.Computational and structural biotechnology journal · 2023
    Review
  8. A scalable analytical approach from bacterial genomes to epidemiology.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Article
  9. Article
  10. Review
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

10 authors.

Roux-Cil FerreiraDepartment of Pathology and Laboratory Medicine, Western University, London, ON, Canada.ORCID https://orcid.org/0000-0002-8242-7862
Emmanuel WongDepartment of Pathology and Laboratory Medicine, Western University, London, ON, Canada.
Gopi GuganDepartment of Pathology and Laboratory Medicine, Western University, London, ON, Canada.
Kaitlyn WadeDepartment of Pathology and Laboratory Medicine, Western University, London, ON, Canada.
Molly LiuDepartment of Pathology and Laboratory Medicine, Western University, London, ON, Canada.
Laura Muñoz BaenaDepartment of Microbiology and Immunology, Western University, London, ON, Canada.
Connor ChatoDepartment of Pathology and Laboratory Medicine, Western University, London, ON, Canada.
Bonnie LuDepartment of Pathology and Laboratory Medicine, Western University, London, ON, Canada.
Abayomi S OlabodeDepartment of Pathology and Laboratory Medicine, Western University, London, ON, Canada.ORCID https://orcid.org/0000-0002-6620-8694
Art F Y PoonDepartment of Pathology and Laboratory Medicine, Western University, London, ON, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Phylogenetics has played a pivotal role in the genomic epidemiology of severe acute respiratory syndrome coronavirus 2, such as tracking the emergence and global spread of variants and scientific communication. However, the rapid accumulation of genomic data from around the world-with over two million genomes currently available in the Global Initiative on Sharing All Influenza Data database-is testing the limits of standard phylogenetic methods. Here, we describe a new approach to rapidly analyze and visualize large numbers of SARS-CoV-2 genomes. Using Python, genomes are filtered for problematic sites, incomplete coverage, and excessive divergence from a strict molecular clock. All differences from the reference genome, including indels, are extracted using minimap2 and compactly stored as a set of features for each genome. For each Pango lineage (https://cov-lineages.org), we collapse genomes with identical features into 'variants', generate 100 bootstrap samples of the feature set union to generate weights, and compute the symmetric differences between the weighted feature sets for every pair of variants. The resulting distance matrices are used to generate neighbor-joining trees in RapidNJ that are converted into a majority-rule consensus tree for each lineage. Branches with support values below 50 per cent or mean lengths below 0.5 differences are collapsed, and tip labels on affected branches are mapped to internal nodes as directly sampled ancestral variants. Currently, we process about 2 million genomes in approximately 9 h on 52 cores. The resulting trees are visualized using the JavaScript framework D3.js as 'beadplots', in which variants are represented by horizontal line segments, annotated with beads representing samples by collection date. Variants are linked by vertical edges to represent branches in the consensus tree. These visualizations are published at https://filogeneti.ca/CoVizu. All source code was released under an MIT license at https://github.com/PoonLab/covizu.

Indexed as

data visualizationgenomic epidemiologySARS-CoV-2

Identifiers

PMID37124703
PMCPMC10131274

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.