Teerapon Jung (@TImp789) header
Teerapon Jung (@TImp789) profile picture

PhD in Bioinformatics and Pre-Cancer Immunology @ UCL Cancer Institute. Postdoctoral Researcher @ National Cancer Centre Japan

Tokyo-to, Japan
Joined May 2019
Photo by Teerapon Jung (@TImp789)Photo by Teerapon Jung (@TImp789)Photo by Teerapon Jung (@TImp789)
Congrats James!!
🎥 New interview from #ESMO26! We spoke with @JL_Reading about his latest research on how the T cell network is remodelled during early #LungCancer development 🫁 @myESMO #LCSM #ImmunoOnc
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In this @Nature paper, scientists reveal a conserved effector regulatory CD4+ T cell network that emerges across tissues during early pulmonary #tumorigenesis. Their work provides a theranostic framework to track and target preinvasive immune regulation for lung cancer interception. Read more in their #OpenAccess article. 👇 🫁 go.nature.com/4ipKD2d
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scRegulate: Single-Cell Regulatory-Embedded Variational Inference of Transcription Factor Activity from Gene Expression biorxiv.org/content/10.1101/…
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We developed a 3-gene signature to identify tumor-specific CD8 TIL, i.e. the cells targeted by #immunotherapy, from #singlecell data. Out now in @NatureComms. All data & code are public. Please use it! #WomenInSTEM #science #research #datascience #AI nature.com/articles/s41467-0…
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DeepSeek-R1 is great, but it still does not handle genomics yet :) 🚀 We’re thrilled to announce that IntegrAO (pronounced "integral") 🧬🔬—our new multi-omics integration framework—has been published in Nature Machine Intelligence! 📑 Paper: nature.com/articles/s42256-0… 💻 Code: github.com/bowang-lab/Integr… 🔬 What is IntegrAO? IntegrAO (Integrate Any Omics) is an unsupervised platform designed to tackle the challenges of incomplete multi-omics data. Crucially, it can be seamlessly transformed into a prediction model after integration, enabling robust classification of new patient samples—even when only partial omics data is available. 🧠 Why IntegrAO? Effective cancer stratification depends on comprehensive multiomics data, yet real-world clinical datasets are often incomplete. Accurately assigning new patients to predefined subtypes, even when only partial omics are available, is crucial for personalized care but remains a major barrier to the clinical adoption of multiomics. Existing methods struggle with missing data and rarely address the essential task of classifying patients with partial profiles. IntegrAO excels at overcoming these challenges. 🌟 IntegrAO Highlights: - Transductive Integration: Integrates patient graphs with partial overlaps across any omics sources. Utilizes GNNs to produce unified patient embeddings, preserving critical biological and clinical signals. - Resilience to Missing Data: Demonstrates robust performance on heterogeneous, incomplete datasets from multiple cancer cohorts. Maintains accuracy despite varying degrees of missing omics. - Inductive Prediction: Converts into a prediction model via supervised fine-tuning. Accurately classifying new samples with partial data into existing subtypes is crucial for precision medicine. - Real-World Impact: Comprehensive case study on acute myeloid leukemia, revealing clinically and biologically relevant subgroups. Shoutout to Rex Ma (@RexMa9), an incredible PhD student in the lab, for his exceptional leadership on this project! Huge thanks as well to our amazing collaborators: Andy G. X. Zeng, Benjamin Haibe-Kains, Anna Goldenberg, and John E. Dick! 👏🎉 @VectorInst @UHN_Research @UofTCompSci @UofT_TCAIREM
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Spatial dissimilarity analysis in single cell transcriptomics biorxiv.org/content/10.1101/…
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Simply Statistics: Biologists, stop putting UMAP plots in your papers simplystatistics.org/posts/2… from @rafalab 🧬🖥️🧪
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In many tumors, no driver mutations could be identified. We do not know why. Perhaps, it's an algorithmic failure. Perhaps, it reflects non genetic contributions to carcinogenesis. We should resist ...
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This really works wonders on Visium data. In our hands it is by far the best method to deconvolve spots.
This Post is from an account that no longer exists. Learn more
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PHALCON: phylogeny-aware variant calling from large-scale single-cell panel sequencing datasets biorxiv.org/content/10.1101/…
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tidyplots is an R package to generate publication-ready plots for scientific papers tidyplots.org/ #rstats
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scSurv: a deep generative model for single-cell survival analysis biorxiv.org/content/10.1101/…
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easySCF: A Tool for Enhancing Interoperability Between R and Python for Efficient Single-Cell Data Analysis academic.oup.com/bioinformat… 🧬🖥️🧪 github.com/xleizi/easySCF
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scE2G: Mapping enhancer-gene regulatory interactions from single-cell data biorxiv.org/content/10.1101/…
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1/ 🧬 Single-cell genomics reveals biological variations beyond cell types. Unveiling these in separate latent dimensions is known as disentanglement. Led by @AmirAliMoinfar, we introduce DRVI to learn nonlinear, disentangled & interpretable latent spaces. biorxiv.org/content/10.1101/…
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