Retrieval-Augmented Generation for Predicting Cellular Responses to Gene Perturbation
- URL: http://arxiv.org/abs/2603.07233v1
- Date: Sat, 07 Mar 2026 14:31:27 GMT
- Title: Retrieval-Augmented Generation for Predicting Cellular Responses to Gene Perturbation
- Abstract summary: PT-RAG (Perturbation-aware Two-stage Retrieval-Augmented Generation) is a novel framework that extends Retrieval-Augmented Generation beyond traditional language-model applications to cellular biology.<n>Our results establish retrieval-augmented generation as a promising paradigm for modelling cellular responses to gene perturbation.
- Score: 11.439588896862155
- License: http://creativecommons.org/licenses/by/4.0/
- Abstract: Predicting how cells respond to genetic perturbations is fundamental to understanding gene function, disease mechanisms, and therapeutic development. While recent deep learning approaches have shown promise in modeling single-cell perturbation responses, they struggle to generalize across cell types and perturbation contexts due to limited contextual information during generation. We introduce PT-RAG (Perturbation-aware Two-stage Retrieval-Augmented Generation), a novel framework that extends Retrieval-Augmented Generation beyond traditional language-model applications to cellular biology. Unlike standard RAG systems designed for text retrieval with pre-trained LLMs, perturbation retrieval lacks established similarity metrics and requires learning what constitutes relevant context, making differentiable retrieval essential. PT-RAG addresses this through a two-stage pipeline: first, retrieving candidate perturbations $K$ using GenePT embeddings, then adaptively refining the selection through Gumbel-Softmax discrete sampling conditioned on both the cell state and the input perturbation. This cell-type-aware differentiable retrieval enables end-to-end optimization of the retrieval objective jointly with generation. On the Replogle-Nadig single-gene perturbation dataset, we demonstrate that PT-RAG outperforms both STATE and vanilla RAG under identical experimental conditions, with the strongest gains in distributional similarity metrics ($W_1$, $W_2$). Notably, vanilla RAG's dramatic failure is itself a key finding: it demonstrates that differentiable, cell-type-aware retrieval is essential in this domain, and that naive retrieval can actively harm performance. Our results establish retrieval-augmented generation as a promising paradigm for modelling cellular responses to gene perturbation. The code to reproduce our experiments is available at https://github.com/difra100/PT-RAG_ICLR.
Related papers
- Influence-Guided Symbolic Regression: Scientific Discovery via LLM-Driven Equation Search with Granular Feedback [56.69850045068714]
We introduce textitInfluence-Guided Regression (IGSR), a method that frames equation discovery as an iterative two-step process.<n>We demonstrate IGSRs effectiveness on a diverse suite of benchmarks, including LLM-SRBench, pharmacological PKPD models, an epidemiological simulation, and real-world genomic data.
arXiv Detail & Related papers (2026-05-27T23:48:01Z) - MAT-Cell: A Multi-Agent Tree-Structured Reasoning Framework for Batch-Level Single-Cell Annotation [81.82645086402366]
We propose MAT-Cell, a neuro-symbolic reasoning framework that reframes single-cell analysis into constructive, verifiable proof generation.<n> MAT-Cell injects symbolic constraints through adaptive Retrieval-Augmented Generation (RAG) to ground neural reasoning in biological axioms and reduce transcriptomic noise.<n>It significantly outperforms state-of-the-art (SOTA) models and maintains robust per-formance in challenging scenarios.
arXiv Detail & Related papers (2026-04-07T04:56:06Z) - Lingshu-Cell: A generative cellular world model for transcriptome modeling toward virtual cells [48.885716676667776]
Lingshu-Cell is a discrete diffusion model that learns transcriptomic state distributions and supports conditional simulation under perturbations.<n>It captures complex transcriptome-wide expression dependencies across approximately 18,000 genes without relying on prior gene selection.<n>It achieves leading performance on the Virtual Cell Challenge H1 genetic perturbation benchmark and in predicting cytokine-induced responses in human PBMCs.
arXiv Detail & Related papers (2026-03-26T09:46:27Z) - Scalable Single-Cell Gene Expression Generation with Latent Diffusion Models [11.343106383645441]
We introduce a scalable latent diffusion model for single-cell gene expression data, which we refer to as scLDM.<n>We show its superior performance in a variety of experiments for both observational and perturbational single-cell data, as well as downstream tasks like cell-level classification.
arXiv Detail & Related papers (2025-11-04T20:44:12Z) - Unlasting: Unpaired Single-Cell Multi-Perturbation Estimation by Dual Conditional Diffusion Implicit Bridges [68.98973318553983]
We propose a framework based on Dual Diffusion Implicit Bridges (DDIB) to learn the mapping between different data distributions.<n>We integrate gene regulatory network (GRN) information to propagate perturbation signals in a biologically meaningful way.<n>We also incorporate a masking mechanism to predict silent genes, improving the quality of generated profiles.
arXiv Detail & Related papers (2025-06-26T09:05:38Z) - ImpRAG: Retrieval-Augmented Generation with Implicit Queries [34.72864597562907]
ImpRAG is a query-free RAG system that integrates retrieval and generation into a unified model.<n>We show that ImpRAG achieves 3.6-11.5 improvements in exact match scores on unseen tasks with diverse formats.
arXiv Detail & Related papers (2025-06-02T21:38:21Z) - Ext2Gen: Alignment through Unified Extraction and Generation for Robust Retrieval-Augmented Generation [18.570899885235104]
We propose Ext2Gen, a novel extract-then-generate model that enhances RAG by extracting query-relevant sentences before generating answers.<n>Experiments demonstrate that Ext2Gen effectively identifies query-relevant sentences with high precision and recall, leading to highly reliable answers.
arXiv Detail & Related papers (2025-02-28T06:46:53Z) - Multi-Modal and Multi-Attribute Generation of Single Cells with CFGen [76.02070962797794]
This work introduces CellFlow for Generation (CFGen), a flow-based conditional generative model that preserves the inherent discreteness of single-cell data.<n>CFGen generates whole-genome multi-modal single-cell data reliably, improving the recovery of crucial biological data characteristics.
arXiv Detail & Related papers (2024-07-16T14:05:03Z) - Learning Causal Representations of Single Cells via Sparse Mechanism
Shift Modeling [3.2435888122704037]
We propose a deep generative model of single-cell gene expression data for which each perturbation is treated as an intervention targeting an unknown, but sparse, subset of latent variables.
We benchmark these methods on simulated single-cell data to evaluate their performance at latent units recovery, causal target identification and out-of-domain generalization.
arXiv Detail & Related papers (2022-11-07T15:47:40Z) - CausalBench: A Large-scale Benchmark for Network Inference from
Single-cell Perturbation Data [61.088705993848606]
We introduce CausalBench, a benchmark suite for evaluating causal inference methods on real-world interventional data.
CaulBench incorporates biologically-motivated performance metrics, including new distribution-based interventional metrics.
arXiv Detail & Related papers (2022-10-31T13:04:07Z) - Granger causal inference on DAGs identifies genomic loci regulating
transcription [77.58911272503771]
GrID-Net is a framework based on graph neural networks with lagged message passing for Granger causal inference on DAG-structured systems.
Our application is the analysis of single-cell multimodal data to identify genomic loci that mediate the regulation of specific genes.
arXiv Detail & Related papers (2022-10-18T21:15:10Z)
This list is automatically generated from the titles and abstracts of the papers in this site.
This site does not guarantee the quality of this site (including all information) and is not responsible for any consequences.