bioRxivBioinformaticsPreprint
scTransMIL Bridges Patient-Level Phenotypes and Single-Cell Transcriptomics for Cancer Screening and Heterogeneity Inference
Zhenchao TangiD, Fang WangiD, Fengtang YangiD, Jiangning SongiD, Calvin Yu‐Chian CheniD, Jianhua YaoiD
Abstract
Single-cell sequencing technology has revolutionized cancer research by revealing unprecedented insights into tumor heterogeneity. However, reliably connecting patient-level cancer phenotypes with single-cell transcriptomic profiles remains challenging, due to technical constraints and labeling ambiguity. This further hinders the precise cancer screening and intensive study of tumor mechanism based on single-cell sequencing. To bridge this gap, we introduce scTransMIL, a scRNA-seq Transformer-based Multi-Instance Learning framework that learns whole-genome context to deliver comprehensive cancer insights at the sample, cell, and gene levels across three biological scales: (1) accurate patient-level cancer phenotype prediction, (2) precise single-cell disease scoring (validated on 4 million single cells), and (3) genome-wide biomarker discovery. Benchmark experiments demonstrate scTransMILs exceptional performance, including robust out-of-distribution generalization and clinically relevant prediction of metastatic tissue-of-origin, a crucial capability for identifying cancers of unknow primary. At single-cell resolution, scTransMIL identified both known and novel biomarkers for tumor B cells that conventional differential expression analysis failed to detect while maintaining consistent concordance with malignant cell annotations. scTransMILs adaptability is exemplified in acute myelocytic leukemia, where minimal fine-tuning with only a few patient sample labels enabled: (i) discovery of novel disease subtypes with distinct clinical outcomes, (ii) reconstruction of differentiation trajectories at the single-cell resolution, and (iii) identification of subtype-specific gene signatures. In summary, by systematically linking cellular and molecular profiles with clinical disease phenotypes, scTransMIL emerges as a transformative tool poised to advance both basic cancer research and precision oncology applications.
- organism: human
- assay: scRNA-seq
- research focus: cell type annotation
- research focus: differential expression
- research focus: gene regulatory network inference
- approach: deep learning
- approach: transformer / foundation model
- Citations
- 3
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Pan-cancer classification of single cells in the tumour microenvironment
Ido Nofech-Mozes, David M. Soave, … Sagi Abelson·Nature CommunicationsPeer-reviewed·Mar 23, 2023
- Phenotype-guided subpopulation identification from single-cell sequencing data
Duanchen Sun, Xiangnan Guan, … Zheng Xia·bioRxiv·Jun 5, 2020
- scOPE identifies which driver-associated expression programs transfer from bulk tumors to single cells
Andrew J Ashford, Alex Lapadat, Emek Demir·bioRxiv·Aug 12, 2026
- Incorporating Hierarchical Information into Multiple Instance Learning for Patient Phenotype Prediction with scRNA-seq Data
Chau Do, Harri J Lähdesmäki·bioRxiv·Feb 10, 2025
- scSTAR2: a multiomics integration algorithm to reveal disease specific cellular signatures by bridging single-cell resolution features and clinical metadata
Xin Zou, Jiawei Zou, … Jie Hao·bioRxiv·Aug 12, 2025
- scCancer2: data-driven in-depth annotations of the tumor microenvironment at single-level resolution
Zeyu Chen, Yuxin Miao, … Jin Gu·BioinformaticsPeer-reviewed·Jan 15, 2024