Author

Meijie Du

Henan Normal UniversityORCID 0000-0002-9367-4199Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Research Focus:benchmarking· 1 Assay:DNA methylation· 1 Organism:human· 1

Frequent Co-Authors

Jianbin WangiD· 2 shared Lin Di· 2 shared Yanyi HuangiD· 2 shared Yuhong PangiD· 2 shared Chao LiuiD· 1 shared Cheng SuniD· 1 shared Chenghong YiniD· 1 shared Haifeng DuaniD· 1 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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2 shared papersGenomics

Jianbin WangORCID

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2 papers

Recent·Most cited

A fuzzy sequencer for rapid DNA fragment counting and genotyping

Wenxiong Zhou, Kang Li, Shuo Qiao, Haifeng Duan, Chenghong Yin, Chao Liu, Zhizhao Liao, Mingchuan Tang, Ruiying Zhang, Lei Li, Lei Shi, Meijie Du, Yipeng Wang, Wentao Yue, Yan Xiao, , Yanyi Huang

A fuzzy sequencer improves information efficiency and accuracy in DNA resequencing applications.

Nature Biomedical Engineering · Jul 2, 2025Peer-reviewedGenomics

Low frequency somatic copy number alterations in normal human lymphocytes revealed by large scale single-cell whole genome profiling

Lu Liu, He Chen, Cheng Sun, Jianyun Zhang, Juncheng Wang, Meijie Du, Lin Di, Jie Shen, Shuang Geng, Yuhong Pang, Yingying Luo, Yusi Fu, Zhe Zheng, Jianbin Wang, Yanyi Huang

The paper uses single-cell whole genome sequencing to identify low frequency somatic copy number alterations in normal human lymphocytes, finding 7.5% of cells have large-size copy number alterations.

Genome Research · Jan 1, 2022Peer-reviewedGenomics