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Author Details

Wing Hung Wong
Stanford University
1991
206
67
PMIDPaper TitleJournal TitlePublished Year
37502861EpiGePT: a Pretrained Transformer model for epigenomics.bioRxiv2024
37502861EpiGePT: a Pretrained Transformer model for epigenomics.bioRxiv2024
36215037HiChIPdb: a comprehensive database of HiChIP regulatory interactions.Nucleic Acids Res2023
35503836Revealing Free Energy Landscape From MD Data via Conditional Angle Partition Tree.IEEE/ACM Trans Comput Biol Bioinform2023
36215037HiChIPdb: a comprehensive database of HiChIP regulatory interactions.Nucleic Acids Res2023
37584462Mutations in human DNA methyltransferase DNMT1 induce specific genome-wide epigenomic and transcriptomic changes in neurodevelopment.Hum Mol Genet2023
37399400Comprehensive tissue deconvolution of cell-free DNA by deep learning for disease diagnosis and monitoring.Proc Natl Acad Sci U S A2023
37023129NeuronMotif: Deciphering cis-regulatory codes by layer-wise demixing of deep neural networks.Proc Natl Acad Sci U S A2023
36494035CNEReg Interprets Ruminant-specific Conserved Non-coding Elements by Developmental Gene Regulatory Network.Genomics Proteomics Bioinformatics2023
37258665Deterministic evolution and stringent selection during preneoplasia.Nature2023
37053313The origins and functional effects of postzygotic mutations throughout the human life span.Science2023
37292801scTIE: data integration and inference of gene regulation using single-cell temporal multimodal data.bioRxiv2023
37584462Mutations in human DNA methyltransferase DNMT1 induce specific genome-wide epigenomic and transcriptomic changes in neurodevelopment.Hum Mol Genet2023
35503836Revealing Free Energy Landscape From MD Data via Conditional Angle Partition Tree.IEEE/ACM Trans Comput Biol Bioinform2023
37292801scTIE: data integration and inference of gene regulation using single-cell temporal multimodal data.bioRxiv2023
37258665Deterministic evolution and stringent selection during preneoplasia.Nature2023
37023129NeuronMotif: Deciphering cis-regulatory codes by layer-wise demixing of deep neural networks.Proc Natl Acad Sci U S A2023
37053313The origins and functional effects of postzygotic mutations throughout the human life span.Science2023
37399400Comprehensive tissue deconvolution of cell-free DNA by deep learning for disease diagnosis and monitoring.Proc Natl Acad Sci U S A2023
36494035CNEReg Interprets Ruminant-specific Conserved Non-coding Elements by Developmental Gene Regulatory Network.Genomics Proteomics Bioinformatics2023
34304711Loss of KMT2C reprograms the epigenomic landscape in hPSCs resulting in NODAL overexpression and a failure of hemogenic endothelium specification.Epigenetics2022
36175411Cost-effective methylome sequencing of cell-free DNA for accurately detecting and locating cancer.Nat Commun2022
35901781"Fateful" encounter: Lineage tracing meets phylogeny to unravel mysteries of cancer progression.Dev Cell2022
36229829Author Correction: Regulatory analysis of single cell multiome gene expression and chromatin accessibility data with scREG.Genome Biol2022
35578363Regulatory analysis of single cell multiome gene expression and chromatin accessibility data with scREG.Genome Biol2022
35951677Nested epistasis enhancer networks for robust genome regulation.Science2022
35992073Unfolding the genotype-to-phenotype black box of cardiovascular diseases through cross-scale modeling.iScience2022
36525361Heritability enrichment in context-specific regulatory networks improves phenotype-relevant tissue identification.Elife2022
34304711Loss of KMT2C reprograms the epigenomic landscape in hPSCs resulting in NODAL overexpression and a failure of hemogenic endothelium specification.Epigenetics2022
35293310DeepCAGE: Incorporating Transcription Factors in Genome-wide Prediction of Chromatin Accessibility.Genomics Proteomics Bioinformatics2022
34978563On the identifiability of the isoform deconvolution problem: application to select the proper fragment length in an RNA-seq library.Bioinformatics2022
35058621scJoint integrates atlas-scale single-cell RNA-seq and ATAC-seq data with transfer learning.Nat Biotechnol2022
34930827Leveraging cell-type-specific regulatory networks to interpret genetic variants in abdominal aortic aneurysm.Proc Natl Acad Sci U S A2022
35578363Regulatory analysis of single cell multiome gene expression and chromatin accessibility data with scREG.Genome Biol2022
36525361Heritability enrichment in context-specific regulatory networks improves phenotype-relevant tissue identification.Elife2022
36175411Cost-effective methylome sequencing of cell-free DNA for accurately detecting and locating cancer.Nat Commun2022
35901781"Fateful" encounter: Lineage tracing meets phylogeny to unravel mysteries of cancer progression.Dev Cell2022
35992073Unfolding the genotype-to-phenotype black box of cardiovascular diseases through cross-scale modeling.iScience2022
36229829Author Correction: Regulatory analysis of single cell multiome gene expression and chromatin accessibility data with scREG.Genome Biol2022
35951677Nested epistasis enhancer networks for robust genome regulation.Science2022
34978563On the identifiability of the isoform deconvolution problem: application to select the proper fragment length in an RNA-seq library.Bioinformatics2022
35058621scJoint integrates atlas-scale single-cell RNA-seq and ATAC-seq data with transfer learning.Nat Biotechnol2022
34930827Leveraging cell-type-specific regulatory networks to interpret genetic variants in abdominal aortic aneurysm.Proc Natl Acad Sci U S A2022
35293310DeepCAGE: Incorporating Transcription Factors in Genome-wide Prediction of Chromatin Accessibility.Genomics Proteomics Bioinformatics2022
32919612Network Effects of the 15q13.3 Microdeletion on the Transcriptome and Epigenome in Human-Induced Neurons.Biol Psychiatry2021
34180954MIMIC: an optimization method to identify cell type-specific marker panel for cell sorting.Brief Bioinform2021
34179690Simultaneous deep generative modeling and clustering of single cell genomic data.Nat Mach Intell2021
34234141Sensitive detection of tumor mutations from blood and its application to immunotherapy prognosis.Nat Commun2021
34285077Dynamic chromatin regulatory landscape of human CAR T cell exhaustion.Proc Natl Acad Sci U S A2021
33990562Modeling regulatory network topology improves genome-wide analyses of complex human traits.Nat Commun2021
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Collaborators

Co-authored papers 14
Peking-Tsinghua Center for Life Sciences, College of Life Sciences, Peking University
Co-authored papers 9
Center for the Development of Therapeutics, Broad Institute of MIT and Harvard
Co-authored papers 9
University of Tennessee Health Science Center
Co-authored papers 7
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Icahn School of Medicine at Mount Sinai
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Yale University
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Washington State University
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Co-authored papers 5
David Geffen School of Medicine, University of California at Los Angeles
Co-authored papers 5
David Geffen School of Medicine, University of California at Los Angeles
Co-authored papers 4
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Harvard Medical School
Co-authored papers 4
Center for Personal Dynamic Regulomes, Stanford University
Co-authored papers 4
Co-authored papers 4
Korea University
Co-authored papers 3
Stanford University
Co-authored papers 3
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Co-authored papers 3
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Co-authored papers 3
Stanford University School of Medicine
Co-authored papers 3
University of Texas MD Anderson Cancer Center
Co-authored papers 3
David Geffen School of Medicine, University of California Los Angeles
Co-authored papers 3
The University of Texas MD Anderson Cancer Center
Co-authored papers 3
Co-authored papers 3
David Geffen School of Medicine at university of california los angeles
Co-authored papers 3