Beyond Conditional Computation: Retrieval-Augmented Genomic Foundation Models with Gengram
On the map: Retrieval-augmented generation → Medical and biomedical RAG
Abstract (arXiv)
Current genomic foundation models (GFMs) rely on extensive neural computation to implicitly approximate conserved biological motifs from single-nucleotide inputs. We propose Gengram, a conditional memory module that introduces an explicit and highly efficient lookup primitive for multi-base motifs via a genomic-specific hashing scheme, establishing genomic "syntax". Integrated into the backbone of state-of-the-art GFMs, Gengram achieves substantial gains (up to 14%) across several functional genomics tasks. The module demonstrates robust architectural generalization, while further inspection of Gengram's latent space reveals the emergence of meaningful representations that align closely with fundamental biological knowledge. By establishing structured motif memory as a modeling primitive, Gengram simultaneously boosts empirical performance and mechanistic interpretability, providing a scalable and biology-aligned pathway for the next generation of GFMs. The code is available at https://github.com/zhejianglab/Genos, and the model checkpoint is available at https://huggingface.co/ZhejiangLab/Gengram.
Key facts. Cited by 1 paper in the map (data through 7 Oct 2026). Placed in Medical and biomedical RAG, one of 15 directions in Retrieval-augmented generation. Builds on 13 of its 36 references that are in the map. First posted on arXiv 29 Jan 2026.
Builds on
13 of 36 references.
References · 13
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Citing papers per year: 2026: 1.
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- 2025Gene42: Long-Range Genomic Foundation Model With Dense Attention
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- 2023PoET: A generative model of protein families as sequences-of-sequences
- 2025Genomic Next-Token Predictors are In-Context Learners
- 2026GenoMorph: Pathway-Grounded Genomic Disease Reasoning via Adaptive Latent Computation
- 2026SciHorizon-GENE: Benchmarking LLM for Life Sciences Inference from Gene Knowledge to Functional Understanding
- 2026Retrieval-Augmented Generation for Predicting Cellular Responses to Gene Perturbation