Evidence map›Paper›PMID 36533145›Full record

ArticleVirus evolution2022

covSampler: A subsampling method with balanced genetic diversity for large-scale SARS-CoV-2 genome data sets.

Yexiao Cheng, Chengyang Ji, Na Han, Jiaying Li, Lin Xu, Ziyi Chen, Rong Yang, Hang-Yu Zhou, Aiping Wu

Abstract read
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Article in Virus evolution, 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

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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.

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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

9 authors.

Yexiao ChengInstitute of Systems Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, 9 Dongdan Santiao, Dongcheng District, Beijing 100730, China.
Chengyang JiInstitute of Systems Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, 9 Dongdan Santiao, Dongcheng District, Beijing 100730, China.
Na HanInstitute of Systems Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, 9 Dongdan Santiao, Dongcheng District, Beijing 100730, China.
Jiaying LiInstitute of Systems Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, 9 Dongdan Santiao, Dongcheng District, Beijing 100730, China.
Lin XuInstitute of Systems Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, 9 Dongdan Santiao, Dongcheng District, Beijing 100730, China.
Ziyi ChenInstitute of Systems Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, 9 Dongdan Santiao, Dongcheng District, Beijing 100730, China.
Rong YangInstitute of Systems Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, 9 Dongdan Santiao, Dongcheng District, Beijing 100730, China.
Hang-Yu ZhouInstitute of Systems Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, 9 Dongdan Santiao, Dongcheng District, Beijing 100730, China.
Aiping WuInstitute of Systems Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, 9 Dongdan Santiao, Dongcheng District, Beijing 100730, China.ORCID https://orcid.org/0000-0002-5869-651X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Phylogenetic analysis has been widely used to describe, display, and infer the evolutionary patterns of viruses. The unprecedented accumulation of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) genomes has provided valuable materials for the real-time study of SARS-CoV-2 evolution. However, the large number of SARS-CoV-2 genome sequences also poses great challenges for data analysis. Several methods for subsampling these large data sets have been introduced. However, current methods mainly focus on the spatiotemporal distribution of genomes without considering their genetic diversity, which might lead to post-subsampling bias. In this study, a subsampling method named covSampler was developed for the subsampling of SARS-CoV-2 genomes with consideration of both their spatiotemporal distribution and their genetic diversity. First, covSampler clusters all genomes according to their spatiotemporal distribution and genetic variation into groups that we call divergent pathways. Then, based on these divergent pathways, two kinds of subsampling strategies, representative subsampling and comprehensive subsampling, were provided with adjustable parameters to meet different users' requirements. Our performance and validation tests indicate that covSampler is efficient and stable, with an abundance of options for user customization. Overall, our work has developed an easy-to-use tool and a webserver (https://www.covsampler.net) for the subsampling of SARS-CoV-2 genome sequences.

Indexed as

phylogeneticsSARS-CoV-2subsampling

Identifiers

PMID36533145
PMCPMC9384632

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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.