Author

Meihong Li

The Jackson Laboratory for Genomic Medicine

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Cancer Biology· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:clustering· 1 Research Focus:database / resource· 1 Approach:deep learning· 1 Research Focus:differential expression· 1

Frequent Co-Authors

Chew Yee NganiD· 2 shared Abby LD Tadenev· 1 shared Belinda S. HarrisiD· 1 shared C. Shing Huang· 1 shared Chee‐Hong WongiD· 1 shared Chia‐Lin WeiiD· 1 shared Courtany Hanley· 1 shared George C Murray· 1 shared

Activity by Year

2021-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersCancer Biology

Chew Yee NganORCID

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2 papers

Recent·Most cited

An Atlas of Extrachromosomal DNA Structures Illuminates Its Evolution and Biogenesis in Cancer

Chee‐Hong Wong, Kuo‐Chen Wei, Kuan-Yu Kung, Li-Hao Yang, Yin-Cheng Huang, C. Shing Huang, I-Jiuan Chung, Huang Meng-fan, Pei‐Hua Peng, Meihong Li, Chew Yee Ngan, Kou-Juey Wu, Chia‐Lin Wei

The paper maps ecDNA structures in glioblastoma using long-read sequencing and ecLego3, revealing structural variation, evolutionary dynamics, and transcriptional links to tumor adaptation.

bioRxiv · Dec 25, 2025 · PreprintCancer Biology

An allelic series of spontaneous mutations in Rorb cause a gait phenotype, retinal abnormalities, and transcriptomic changes relevant to human neurodevelopmental conditions

George C Murray, Jason A. Bubier, Oraya J. Zinder, Belinda S. Harris, James Clark, Mia-Cara Christopher, Courtany Hanley, Harianto Tjong, Meihong Li, Chew Yee Ngan, Laura G. Reinholdt, Robert W. Burgess, Abby LD Tadenev

The paper describes five Rorb mutant mouse strains with gait and retinal abnormalities, showing transcriptomic changes linked to neurodevelopmental disorders.

bioRxiv · Nov 23, 2021 · PreprintGenetics