# Efficient Auto-Interpretability of AI Models in Biology

arXiv: https://arxiv.org/abs/2608.27754 · HTML: https://mlsanity.com/paper/2608.27754/

## Key facts

- No citing papers in the map yet (data through 14 Oct 2026).
- Placed in Interpreting biomedical and science models, one of 13 directions in Mechanistic interpretability.
- Builds on 7 of its 13 references that are in the map.
- First posted on arXiv 27 Aug 2026.

## Placed in

- Mechanistic interpretability / [Interpreting biomedical and science models](https://mlsanity.com/mechinterp/interpreting-biomedical-and-science-models/)

## Builds on (most cited first, 7 of 7)

- [Sparse Autoencoders Trained on the Same Data Learn Different Features](https://mlsanity.com/paper/2501.16615/) (2025)
- [InterPLM: Discovering Interpretable Features in Protein Language Models via Sparse Autoencoders](https://mlsanity.com/paper/2412.12101/) (2024)
- [Do Sparse Autoencoders Capture Concept Manifolds?](https://mlsanity.com/paper/2604.28119/) (2026)
- [Evaluating SAE interpretability without explanations](https://mlsanity.com/paper/2507.08473/) (2025)
- [Stable and Steerable Sparse Autoencoders with Weight Regularization](https://mlsanity.com/paper/2603.04198/) (2026)
- [Automated Neuron Labelling Enables Generative Steering and Interpretability in Protein Language Models](https://mlsanity.com/paper/2507.06458/) (2025)
- [Probing and steering biology across Boltz-1s trunk-diffusion boundary](https://mlsanity.com/paper/2608.11475/) (2026)

## Abstract (arXiv)

Sparse autoencoders (SAEs), and other interpretability methods could turn AI models in Biology and other fields into engines of scientific discovery by explaining the superhuman capabilities of those models. However, a latent is only useful if we know three things: whether it is coherent, whether it can be described, and whether that description has predictive power. These questions are routinely conflated. We assemble them into a single pipeline and report the practical innovations each stage required. First, cross-seed dictionary stability prioritises which latents are worth spending resources to investigate. Second, an intruder-detection task asks whether a latents activating examples share a recognizable pattern. Third, a separate pass proposes a candidate biological description which we convert into falsifiable predictions which can be tested in silico. Deployed on the Boltz-1 Pairformer trunk, stability prioritisation finds interpretable latents using about 4.4 times fewer latent evaluations each, and at 5.2 times lower measured cost, while recovering over half of them, and the external check shows the surfaced motifs are significantly enriched for their claimed annotations. The results also suggest a possible tension: the cross- seed stability might be selecting for some types of features, like structure-related ones, much more than others, such as function-related features.
