Deep scSTAR: leveraging deep learning for the extraction and enhancement of phenotype-associated features from single-cell RNA sequencing and spatial transcriptomics data

  • Lianchong Gao
  • , Yujun Liu
  • , Jiawei Zou
  • , Fulan Deng
  • , Zheqi Liu
  • , Zhen Zhang
  • , Xinran Zhao
  • , Lei Chen
  • , Henry H.Y. Tong
  • , Yuan Ji
  • , Huangying Le
  • , Xin Zou
  • , Jie Hao

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)

Abstract

Single-cell sequencing has advanced our understanding of cellular heterogeneity and disease pathology, offering insights into cellular behavior and immune mechanisms. However, extracting meaningful phenotype-related features is challenging due to noise, batch effects, and irrelevant biological signals. To address this, we introduce Deep scSTAR (DscSTAR), a deep learning-based tool designed to enhance phenotype-associated features. DscSTAR identified HSP+ FKBP4+ T cells in CD8+ T cells, which linked to immune dysfunction and resistance to immune checkpoint blockade in non-small cell lung cancer. It has also enhanced spatial transcriptomics analysis of renal cell carcinoma, revealing interactions between cancer cells, CD8+ T cells, and tumor-associated macrophages that may promote immune suppression and affect outcomes. In hepatocellular carcinoma, it highlighted the role of S100A12+ neutrophils and cancer-associated fibroblasts in forming tumor immune barriers and potentially contributing to immunotherapy resistance. These findings demonstrate DscSTAR’s capacity to model and extract phenotype-specific information, advancing our understanding of disease mechanisms and therapy resistance.

Original languageEnglish
Article numberbbaf160
JournalBriefings in Bioinformatics
Volume26
Issue number3
DOIs
Publication statusPublished - 1 May 2025

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • deep learning
  • phenotype-associated features
  • scRNA-seq
  • spatial transcriptomics
  • tumor microenvironment

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