A multistage, multitask transformer-based framework for multi-disease diagnosis and prediction using personal proteomes
Li, H.; Li, Y.; Liu, Y.; Cooper-Knock, J.; Gao, P.; Shen, X.; Chen, S.; Xing, X.; Zhang, S.
Show abstract
Recent advances in cohort-level proteomic profiling have offered unprecedented opportunities for discovering novel biomarkers and developing diagnostic and predictive tools for complex human diseases. However, the inherent complexity of proteomics data and the scarcity of phenotypic labels, particularly for rare diseases, pose significant challenges in modeling proteome-phenome relationships. Utilizing proteomics data from 2,924 plasma proteins measured in 53,014 UK Biobank participants, we introduce Prophet, an interpretable deep learning framework that combines transformer architecture with a multistage, multitask training strategy to improve disease prediction and biological discovery from personal proteomic profiles. Prophet begins with self-supervised pretraining to model protein interactions, followed by prompt-based fine-tuning for disease diagnosis, and concludes with continuous fine-tuning for disease prediction. Extensive benchmarking across more than 100 diseases demonstrates Prophets superior performance over multiple baseline methods, achieving the highest increase in the area under the precision-recall curve (AUPRC) by 132.71% for disease diagnosis and 60.29% for disease prediction. Specifically, Prophet enhances diagnostic accuracy for 95.83% of diseases and boosts predictive accuracy for 94.02% of diseases. Through model interpretation, Prophet identifies 21,549 and 25,915 protein-disease associations for prevalent and incident diseases, respectively, and uncovers prevailing proteomics-based similarities among diseases. Our work provides a powerful framework for proteomics-based disease diagnosis, prediction, and biomarker discovery.
Matching journals
The top 4 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- TrimNN: Characterizing cellular community motifs for studying multicellular topological organization in complex tissues 96%
- LEOPARD: missing view completion for multi-timepoints omics data via representation disentanglement and temporal knowledge transfer 96%
- Context-aware deconvolution of cell-cell communication with Tensor-cell2cell 95%
Similar papers in this journal
- A tissue-aware machine learning framework enhances the mechanistic understanding and genetic diagnosis of Mendelian and rare diseases 96%
- hu.MAP3.0: Atlas of human protein complexes by integration of > 25,000 proteomic experiments 95%
- PIFiA: Self-supervised Approach for Protein Functional Annotation from Single-Cell Imaging Data 95%
Similar papers in this journal
- The Interpretable Multimodal Machine Learning (IMML) framework reveals pathological signatures of distal sensorimotor polyneuropathy 96%
- Deep Proteome Profiling of Metabolic Dysfunction-Associated Steatotic Liver Disease 94%
- Complex patterns of multimorbidity associated with severe COVID-19 and Long COVID 93%
Similar papers in this journal
- Proteome-wide Mendelian randomization in global biobank meta-analysis reveals multi-ancestry drug targets for common diseases 95%
- Polygenic regression uncovers trait-relevant cellular contexts through pathway activation transformation of single-cell RNA sequencing data 94%
- Variant-resolved prediction of context-specific isoform variation with a graph-based attention model 94%
Similar papers in this journal
- Defining and predicting transdiagnostic categories of neurodegenerative disease 94%
- Neuroimaging-AI Endophenotypes of Brain Diseases in the General Population: Towards a Dimensional System of Vulnerability 94%
- Inferring Multi-Organ Genetic Causal Connections using Imaging and Clinical Data through Mendelian Randomization 92%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.