RAGCell: Retrieval-Augmented Generation as Supervision for Versatile Single-cell Analysis
Tianyu Liu, Fan Zhang, Jiayuan Chen, Kun Wang, Haoxuan Li, Shengju Qian, Zhihong Zhu, Donghao Zhou, Hao Wu, Ziheng Zhang, Zhenxi Lin, Xian Wu, Yefeng Zheng
Abstract
Single-cell foundation models (scFMs) are transforming computational biology by enabling generalizable, task-agnostic representations for versatile single-cell analysis. Despite their progress in facilitating rapid deployment for downstream tasks, off-the-shelf scFMs still have some overlooked concerns: (I) (Pretraining Cost.) Pretrain-based scFMs necessitate pretraining on a vast volume of cells, rendering it draining resources in applications. (II) (Heterogeneous Gap.) Large Language Models (LLM)-based scFMs ignore the tremendous heterogeneous gap between LLM textual and raw cellular spaces, leading to insufficient capability when facing downstream tasks. To this end, we introduce RAGCell, a versatile single-cell analysis framework that achieves a double-win in both cost-effectiveness and high performance. The success of RAGCell lies in two key aspects: Leveraging LLMs to construct cell-level and feature-level knowledge databases, which serve as supervision signals for training the cell model and significantly reduce the training cost (>pretrain-based scFMs). Aligning cell representations with text embeddings from the bi-level knowledge databases, enabling knowledge transfer from textual spaces to cellular spaces and effectively mitigating the heterogeneous gap (>LLM-based scFMs). Through extensive experiments on six downstream single-cell analysis tasks, we demonstrate that RAGCell achieves outstanding performance compared to state-of-the-art scFMs while operating at less than 1/10 the cost of pretrain-based scFMs.
Create a lesson
Related papers
PlainMap: a lightweight, restartable mapping pipeline for ancient and modern DNA
Michael V. Westbury
Democratizing Clinical Tumor Whole Genome Sequencing: 18-hour End-to-end Analysis via Trillion-parameter Large Language Models Locally Deployed on Consumer-grade Hardware
Rui Xiao, Yili Xu
Structure is not mechanism: high-gain gated-FFN rows across text and genomic foundation models
Alexandros Tzanakakis, Aris Karatzikos, Ilias Georgakopoulos-Soares
A Transformer-Based Delta Expression Encoder for Psilocybin Transcriptional Response: Architecture, Representations, and Biological Validation
Sai Jayakumar
Human mutation field reveals an equilibrium-like structure with irreversible circulation
Isabella Caranzano, Daniel Maria Busiello, Stefano Priorelli et al.
Enhancer-promoter proximity predicts transcriptional competence but not transcriptional output in the Drosophila brain
Olivier Messina, Loucif Remini, Christopher H. Bohrer et al.