Author

Yin Tong

Queen Mary HospitalORCID 0000-0001-6521-1915Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Yin Tong2 papers

Biology Disciplines

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Cancer Biology· 2 Bioinformatics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 3 Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Organism:human· 2 Assay:scRNA-seq· 2 Assay:ATAC-seq· 1 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1

Frequent Co-Authors

Helen Y. N. YaniD· 2 shared Suet Yi LeungiD· 2 shared Yuanhua HuangiD· 2 shared Alice S.T. WongiD· 1 shared Annie S.Y. ChaniD· 1 shared April ChaniD· 1 shared Dessy ChaniD· 1 shared Frank Pui-Ling LaiiD· 1 shared

Activity by Year

2024-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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2 shared papersCancer Biology

Helen Y. N. YanORCID

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3 papers

Recent·Most cited

Cancer BiologyProtein & CellPeer-reviewedApr 7, 2025

Dynamin 1-mediated endocytic recycling of glycosylated N-cadherin sustains the plastic mesenchymal state to promote ovarian cancer metastasis

Yuee Cai, Zhangyan Guan, Yin Tong…·Alice S.T. Wong

This study identifies DNM1 as a master regulator of EMT in ovarian cancer, showing it sustains the mesenchymal state through N-cadherin endocytic recycling and promotes metastasis.

3 citations

humanbulk RNA-seq

𝕏 PostBluesky

Cancer BiologyGutPeer-reviewedNov 20, 2024

Divergent lineage trajectories and genetic landscapes in human gastric intestinal metaplasia organoids associated with early neoplastic progression

Sarah S K Yue, Yin Tong, Hoi Cheong Siu…·Helen H N Yan

44 citationstop 2%

𝕏 PostBluesky

BioinformaticsNature CommunicationsPeer-reviewedAug 6, 2024

Robust analysis of allele-specific copy number alterations from scRNA-seq data with XClone

Rongting Huang, Xianjie Huang, Yin Tong…·Yuanhua Huang

XClone detects allele-specific copy number alterations from scRNA-seq data by smoothing signals on cell and gene coordinate graphs, enabling robust identification of haplotype-aware CNAs and subclones.

8 citations

scRNA-seqstatistical model

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