Author

Ronghan Li

Washington University in St. Louis

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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Genomics· 2 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Assay:DNA methylation· 2 Research Focus:gene regulatory network inference· 2 Assay:long-read sequencing· 2 Assay:bulk RNA-seq· 1 Research Focus:database / resource· 1 Research Focus:eQTL / molecular QTL mapping· 1

Frequent Co-Authors

Daofeng LiiD· 3 shared Juan F. Macias-VelascoiD· 3 shared Juan JiangiD· 3 shared Xiaoyu ZhuoiD· 3 shared Zheng DongiD· 3 shared Edward A. BelteriD· 2 shared T -C Liu· 2 shared Ting WangiD· 2 shared

Activity by Year

2026-2026 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 43 mutual co-author links

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3 shared papersGenomics

Daofeng LiORCID

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Author profile →

3 papers

Recent·Most cited

Pangenome-resolved polymorphic transposable elements reveal human regulatory evolution in action

Juan Jiang, Xiaoyu Zhuo, Ronghan Li, Zheng Dong, Wenjin Zhang, Daofeng Li, Juan F Macias-Velasco, Ting Wang

The paper analyzes polymorphic transposable elements in human pangenomes to reveal regulatory evolution mechanisms before fixation.

bioRxiv · Sep 30, 2026 · PreprintGenetics

Human panepigenome represents epigenomic diversity

Zheng Dong, Juan F. Macias-Velasco, Xiaoyu Zhuo, Wenjin Zhang, Chad Tomlinson, Juan Jiang, Edward A. Belter, Saifur Rahman Jony, Ronghan Li, Robert S. Fulton, Shihua Dong, T -C Liu, Daofeng Li, Ting Wang

The paper presents a human panepigenome map of DNA methylation, revealing epigenomic diversity across populations and highlighting the role of genetic variation in CpG presence and absence.

bioRxiv · Aug 23, 2026 · PreprintGenomics

HPRC2: A human pangenome reference with near-complete coverage of common genetic variation

Julian Lucas, Prajna Hebbar, Wen‐Wei Liao, Juan F Macias-Velasco, Adam M. Novak, Mobin Asri, Jennifer Balacco, Andrew P. Blair, Jana Ebler, Joshua M.V. Gardner, Margarita Geleta, Cristian Groza, Andrea Guarracino, Peter Heringer, Glenn Hickey, , Jane E. Loveland

460 haplotypes from 230 genomes, selected to maximize common-variant coverage, capture 99.43% of All of Us common small variants and halve structurally unreliable regions and base errors versus HPRC1.

bioRxiv · Jul 22, 2026 · PreprintGenomics✦ In-depth digest