Evidence map›Paper›PMID 33885735›Full record

ArticleBriefings in bioinformatics2021

New framework for recombination and adaptive evolution analysis with application to the novel coronavirus SARS-CoV-2.

Yinghan Wang, Jinfeng Zeng, Chi Zhang, Cai Chen, Zekai Qiu, Jiali Pang, Yutian Xu, Zhiqi Dong, Yanxin Song, Weiying Liu and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Briefings in bioinformatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 29% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
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  3. Article
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  5. Article
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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

15 authors at 1 institution in 1 country.

Yinghan WangSchool of Public Health (Shenzhen), Sun Yat-sen University, Guangzhou, China.
Jinfeng ZengSchool of Public Health (Shenzhen), Sun Yat-sen University, Guangzhou, China.
Chi ZhangSchool of Public Health (Shenzhen), Sun Yat-sen University, Guangzhou, China.
Cai ChenSchool of Public Health (Shenzhen), Sun Yat-sen University, Guangzhou, China.
Zekai QiuSchool of Public Health (Shenzhen), Sun Yat-sen University, Guangzhou, China.
Jiali PangSchool of Life Sciences, Sun Yat-sen University, Guangzhou, China.
Yutian XuSchool of Intelligent Systems Engineering, Sun Yat-sen University, Guangzhou, China.
Zhiqi DongSchool of Public Health (Shenzhen), Sun Yat-sen University, Guangzhou, China.
Yanxin SongLingnan College, Sun Yat-sen University, Guangzhou, China.
Weiying LiuSchool of Public Health (Shenzhen), Sun Yat-sen University, Guangzhou, China.
Peipei DongSchool of Public Health (Shenzhen), Sun Yat-sen University, Guangzhou, China.
Litao SunSchool of Public Health (Shenzhen), Sun Yat-sen University, Guangzhou, China.
Yao-Qing ChenSchool of Public Health (Shenzhen), Sun Yat-sen University, Guangzhou, China.
Yuelong ShuSchool of Public Health (Shenzhen), Sun Yat-sen University, Guangzhou, China.
Xiangjun DuSchool of Public Health (Shenzhen), Sun Yat-sen University, Guangzhou, China.
Sun Yat-sen University · CN

Funding

Guangdong Frontier and Key Tech Innovation Program 2019B111103001National Key Research and Development Program of China 2020YFC0840900Shenzhen Science and Technology Program KQTD20180411143323605
6 · The paper itself

Abstract

The 2019 novel coronavirus (SARS-CoV-2) has spread rapidly worldwide and was declared a pandemic by the WHO in March 2020. The evolution of SARS-CoV-2, either in its natural reservoir or in the human population, is still unclear, but this knowledge is essential for effective prevention and control. We propose a new framework to systematically identify recombination events, excluding those due to noise and convergent evolution. We found that several recombination events occurred for SARS-CoV-2 before its transfer to humans, including a more recent recombination event in the receptor-binding domain. We also constructed a probabilistic mutation network to explore the diversity and evolution of SARS-CoV-2 after human infection. Clustering results show that the novel coronavirus has diverged into several clusters that cocirculate over time in various regions and that several mutations across the genome are fixed during transmission throughout the human population, including D614G in the S gene and two accompanied mutations in ORF1ab. Together, these findings suggest that SARS-CoV-2 experienced a complicated evolution process in the natural environment and point to its continuous adaptation to humans. The new framework proposed in this study can help our understanding of and response to other emerging pathogens.

Indexed as

Evolution, MolecularRecombination, GeneticCOVID-19HumansPhylogenyReproducibility of ResultsSARS-CoV-2adaptationevolutionmutation networkrecombinationSARS-CoV-2

Identifiers

PMID33885735
PMCPMC8083196
OpenAlexW3156714702

What OpenQuestion holds

Textmetadata
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.