# RIBOSPAN: A Long-Context RNA Foundation Model for Versatile RNA Modeling

arXiv: https://arxiv.org/abs/2608.22849 · HTML: https://mlsanity.com/paper/2608.22849/

## Key facts

- No citing papers in the map yet (data through 14 Oct 2026).
- Builds on 8 of its 29 references that are in the map.
- First posted on arXiv 24 Aug 2026.

## Builds on (most cited first, 8 of 8)

- [Attention Is All You Need](https://mlsanity.com/paper/1706.03762/) (2017)
- [BERT: Pre-training of Deep Bidirectional Transformers for Language Understanding](https://mlsanity.com/paper/1810.04805/) (2018)
- [RoFormer: Enhanced Transformer with Rotary Position Embedding](https://mlsanity.com/paper/2104.09864/) (2021)
- [Megatron-LM: Training Multi-Billion Parameter Language Models Using Model Parallelism](https://mlsanity.com/paper/1909.08053/) (2019)
- [Simple and Effective Masked Diffusion Language Models](https://mlsanity.com/paper/2406.07524/) (2024)
- [Extending Context Window of Large Language Models via Positional Interpolation](https://mlsanity.com/paper/2306.15595/) (2023)
- [RiNALMo: General-Purpose RNA Language Models Can Generalize Well on Structure Prediction Tasks](https://mlsanity.com/paper/2403.00043/) (2024)
- [mRNAutilus: Multi-Objective-Guided Discrete Generation of mRNA with Optimized Therapeutic Properties](https://mlsanity.com/paper/2605.31296/) (2026)

## Abstract (arXiv)

Full-length RNAs, particularly messenger RNAs, often exceed the context lengths used to pretrain existing RNA foundation models, limiting complete-transcript modeling at single-nucleotide resolution. We present RIBOSPAN, a 1.61-billion-parameter bidirectional RNA foundation model natively pretrained with context lengths up to 10,240 nt. RIBOSPAN combines dense bidirectional self-attention, single-nucleotide tokenization, and attention-isolated sequence packing to enable high-resolution modeling of complete long RNAs. Native 10K pretraining preserves strong reconstruction at 10,240 tokens and, in a controlled long-context benchmark, maintains strong contextual responsiveness and context-specific representation separation while keeping perturbation-induced changes highly localized. Inference-time YaRN scaling recovers much of the contextual organization lost by direct short-context extrapolation, but induces substantially greater distal representation diffusion. Frozen RNA-type evaluations show that RIBOSPAN learns state-of-the-art RNA representations, with a particularly clear advantage on long RNAs. Across downstream biological benchmarks, RIBOSPAN emerges as the strongest encoder-only RNA foundation model, achieving state-of-the-art performance in both full-transcript biological property prediction and zero-shot mutation-fitness modeling. Building on the same backbone, we develop a multidimensionally conditioned discrete-diffusion framework for full-length mRNA generation and redesign, including synonymous-codon diffusion for protein-preserving CDS optimization. Together, RIBOSPAN establishes a powerful long-context foundation for transferable RNA representation learning, biological prediction, and full-transcript mRNA design.