Author

Jiao Gong

Fudan UniversityORCID 0000-0003-3767-1636Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Jiao Gong1 paper · BGI Research

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:GWAS / association mapping· 1 Assay:long-read sequencing· 1 Research Focus:polygenic risk· 1

Frequent Co-Authors

Fritz Joachim SedlazeckiD· 2 shared Shaohua FaniD· 2 shared Dali LiiD· 1 shared Fang ZhouiD· 1 shared Feng QianiD· 1 shared Guoqing ZhangiD· 1 shared Hui Qiao· 1 shared Huiru Sun· 1 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Fritz Joachim SedlazeckORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineNature CommunicationsPeer-reviewedFeb 10, 2025

Long-read sequencing of 945 Han individuals identifies novel structural variants associated with phenotypic diversity and disease susceptibility

Jiao Gong, Huiru Sun, Kaiyuan Wang…·Shaohua Fan

The paper identifies novel structural variants in Han Chinese genomes using long-read sequencing and links them to phenotypic diversity and disease susceptibility.

18 citationstop 1%

humanwhole-genome sequencing

𝕏 PostBluesky

GenomicsbioRxivPreprintAug 3, 2022

Characterizing the genetic polymorphisms in 370 challenging medically relevant genes using long-read sequencing data from 41 human individuals among 19 global populations

Yanfeng Ji, Jiao Gong, Fritz Joachim Sedlazeck, Shaohua Fan

The paper uses long-read sequencing to analyze genetic polymorphisms in 370 medically relevant genes across 41 individuals from 19 populations, identifying CNVs and variants missed by short-read sequencing.

4 citations

humanlong-read sequencing

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