Author

Shihui Yu

Kingmed DiagnosticsORCID 0000-0003-3672-4732Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:whole-genome sequencing· 2 Approach:benchmark study· 1 Research Focus:database / resource· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Research Focus:imputation· 1

Frequent Co-Authors

Beisha TangiD· 2 shared Geng TianiD· 2 shared Hou‐Feng ZhengiD· 2 shared Jianguo TaoiD· 2 shared Jinchen LiiD· 2 shared Jun-Quan LiuiD· 2 shared Mengyuan YangiD· 2 shared Mo-Chang Qiu· 2 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Beisha TangORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintDec 23, 2023

SEAD: an augmented reference panel with 22,134 haplotypes boosts the rare variants imputation and GWAS analysis in Asian population

Mengyuan Yang, Jia-Dong Zhong, Xin Li…·Hou‐Feng Zheng

The paper introduces SEAD, an Asian reference panel that improves rare variant imputation and GWAS analysis, identifying a novel association between SNTG1 and hip BMD.

1 citation

humanwhole-genome sequencing

𝕏 PostBluesky

GeneticsbioRxivPreprintFeb 6, 2021

Genomic analyses of 10,376 individuals provides comprehensive map of genetic variations, structure and reference haplotypes for Chinese population

Peikuan Cong, Wei-Yang Bai, Jinchen Li…·Hou‐Feng Zheng

The paper presents genomic analyses of 10,376 Chinese individuals, identifying novel genetic variations and providing a reference haplotype map, along with an imputation server for improved accuracy.

3 citations

humanwhole-genome sequencing

𝕏 PostBluesky