Author

Hongru Li

Nanjing Medical UniversityORCID 0009-0005-1527-4500Unclaimed ORCID profile · follow to get notified of new preprints

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Hongru Li1 paper

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Genetic & Genomic Medicine· 1

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

David C. ChristianiiD· 1 shared Dongfang YouiD· 1 shared Feng CheniD· 1 shared Hao HongiD· 1 shared Jinglan DaiiD· 1 shared Ruyang ZhangiD· 1 shared Sha DuiD· 1 shared Sipeng SheniD· 1 shared

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2025-2025 · peak 1/yr

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1 shared paperGenetic & Genomic Medicine

David C. ChristianiORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicineGenomics Proteomics & BioinformaticsPeer-reviewedSep 17, 2025

Boosting the power of rare variant association studies by imputation using large-scale sequencing population

Jinglan Dai, Yixin Zhang, Yuan Gao…·Sipeng Shen

This study evaluates how imputation from large-scale sequencing data improves the power of rare variant association studies, finding that TOPMed imputation increases detected variants and genes compared to whole-genome sequencing.

4 citations

humanwhole-genome sequencing

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