用冻结的预训练模型实现多组学数据的鲁棒对齐与嵌入。

Representation learning on multi-omics data is challenging due to extreme dimensionality, modality heterogeneity, and cohort-specific batch effects. While pre-trained transformer backbones have shown broad generalization capabilities in biological sequence modeling, their application to multi-omics integration remains underexplored. We present MoRE (Multi-Omics Representation Embedding), a framework that repurposes frozen pre-trained transformers to align heterogeneous assays into a shared latent space. Unlike purely generative approaches, MoRE employs a parameter-efficient fine-tuning (PEFT) strategy, prioritizing cross-sample and cross-modality alignment over simple sequence reconstruction. Specifically, MoRE attaches lightweight, modality-specific adapters and a task-adaptive fusion layer to the frozen backbone. It optimizes a masked modeling objective jointly with supervised contrastive and batch-invariant alignment losses, yielding structure-preserving embeddings that generalize across unseen cell types and platforms. We benchmark MoRE against established baselines, including scGPT, scVI, and Harmony with Scrublet, evaluating integration fidelity, rare population detection, and modality transfer. Our results demonstrate that MoRE achieves competitive batch robustness and biological conservation while significantly reducing trainable parameters compared to fully fine-tuned models. This work positions MoRE as a practical step toward general-purpose omics foundation models.