TEDDY: A Family Of Foundation Models For Understanding Single Cell Biology

Understanding the biological mechanism of disease is critical for medicine, and in particular drug discovery. AI-powered analysis of genome-scale biological data hold great potential in this regard. The increasing availability of single-cell RNA sequencing data has enabled the development of large foundation models for disease biology. However, existing foundation models either do not improve or only modestly improve over task-specific models in downstream applications. Here, we explored two avenues for improving the state-of-the-art. First, we scaled the pre-training dataset to 116 million cells, which is larger than those used by previous models. Second, we leveraged the availability of large-scale biological annotations as a form of supervision during pre-training. We trained the TEDDY family of models comprising six transformer-based state-of-the-art single-cell foundation models with 70 million, 160 million, and 400 million parameters. We vetted our models on two downstream evaluation tasks -- identifying the underlying disease state of held-out donors not seen during training and distinguishing healthy cells from diseased ones for disease conditions and donors not seen during training. Scaling experiments showed that performance improved predictably with both data volume and parameter count. Our models showed substantial improvement over existing work on the first task and more muted improvements on the second.

Graph-Based Retriever Captures the Long Tail of Biomedical Knowledge

Large language models (LLMs) are transforming the way information is retrieved with vast amounts of knowledge being summarized and presented via natural language conversations. Yet, LLMs are prone to highlight the most frequently seen pieces of information from the training set and to neglect the rare ones. In the field of biomedical research, latest discoveries are key to academic and industrial actors and are obscured by the abundance of an ever-increasing literature corpus (the information overload problem). Surfacing new associations between biomedical entities, e.g., drugs, genes, diseases, with LLMs becomes a challenge of capturing the long-tail knowledge of the biomedical scientific production. To overcome this challenge, Retrieval Augmented Generation (RAG) has been proposed to alleviate some of the shortcomings of LLMs by augmenting the prompts with context retrieved from external datasets. RAG methods typically select the context via maximum similarity search over text embeddings. In this study, we show that RAG methods leave out a significant proportion of relevant information due to clusters of over-represented concepts in the biomedical literature. We introduce a novel information-retrieval method that leverages a knowledge graph to downsample these clusters and mitigate the information overload problem. Its retrieval performance is about twice better than embedding similarity alternatives on both precision and recall. Finally, we demonstrate that both embedding similarity and knowledge graph retrieval methods can be advantageously combined into a hybrid model that outperforms both, enabling potential improvements to biomedical question-answering models.