Author

Weitao Wang

Peking UniversityORCID 0000-0003-3191-3980Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Assay:ChIP-seq· 1 Research Focus:clustering· 1 Research Focus:gene regulatory network inference· 1 Assay:Hi-C· 1

Frequent Co-Authors

Bingjie Dong· 2 shared Haichuan ZhuiD· 2 shared Hong WuiD· 2 shared Le‐Ping ZhangiD· 2 shared Lu YangiD· 2 shared Qian JiangiD· 2 shared Xiao‐Jun HuangiD· 2 shared Anqi YuiD· 1 shared

Activity by Year

2020-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Bingjie Dong

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2 papers

Recent·Most cited

Genetic & Genomic MedicineBlood SciencePeer-reviewedJan 1, 2022

Integrated Genomic Analyses Identify High-Risk Factors and Actionable Targets in T-Cell Acute Lymphoblastic Leukemia

Haichuan Zhu, Bingjie Dong, Yingchi Zhang…·Hong Wu

The paper identifies high-risk factors and actionable targets in T-ALL through integrated genomic and transcriptomic analyses of 165 patients, finding RAS pathway and PTEN mutations as poor survival factors and potential therapeutic targets.

15 citations

humanbulk RNA-seq

𝕏 PostBluesky

GenomicsbioRxivPreprintMar 11, 2020

3D Genome Analysis Identifies Enhancer Hijacking Mechanism for High-Risk Factors in Human T-Lineage Acute Lymphoblastic Leukemia

Lu Yang, Fengling Chen, Haichuan Zhu…·Hong Wu

The paper identifies 3D genome alterations and enhancer hijacking mechanisms in T-lineage acute lymphoblastic leukemia (T-ALL) using integrated analyses of 18 patients and 4 controls.

1 citation

humanChIP-seq

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