Author

Qihui Wang

Chinese Academy of SciencesORCID 0000-0003-3768-0401Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Genomics· 1 Immunology· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Research Focus:variant effect prediction· 2 Assay:whole-genome sequencing· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Research Focus:GWAS / association mapping· 1

Frequent Co-Authors

Ana Tereza Ribeiro de VasconcelosiD· 1 shared Bo XieiD· 1 shared Caixia YuiD· 1 shared Chao SuiD· 1 shared Chunyue Yin· 1 shared George F. GaoiD· 1 shared Georgii A. BazykiniD· 1 shared Haoyi FuiD· 1 shared

Activity by Year

2021-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 14 mutual co-author links

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1 shared paperGenomics

Ana Tereza Ribeiro de VasconcelosORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

ImmunologyEBioMedicinePeer-reviewedAug 30, 2025

Rational design of respiratory syncytial virus dimeric F-subunit vaccines in protein and mRNA forms

Jing Li, Xuehui Ma, Zepeng Xu…·Jianxun Qi

This study designs and tests dimeric RSV F-subunit vaccines in protein and mRNA forms, showing enhanced immunogenicity and protection against RSV infection in rodent models.

3 citations

mouseprotein structure

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GenomicsGenomics Proteomics & BioinformaticsPeer-reviewedJan 13, 2022

Genomic perspectives on the emerging SARS-CoV-2 Omicron variant

Wentai Ma, Jing Yang, Haoyi Fu…·Mingkun Li

This study analyzes the genomic features of the SARS-CoV-2 Omicron variant, identifying its high mutation rate, spike protein alterations, and distinct evolutionary patterns.

66 citationstop 2%

viruswhole-genome sequencing

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BioinformaticsbioRxivPreprintMar 31, 2021

Emerging SARS-CoV-2 mutation hotspots associated with clinical outcomes

Xianwu Pang, Pu Li, Lifeng Zhang…·Yanling Hu

The paper identifies SARS-CoV-2 mutation hotspots linked to severe clinical outcomes using genomic and RNA-seq data from 209,551 sequences and 321 samples.

1 citation

whole-genome sequencingbulk RNA-seq

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