At FullTilt: Real-Time Open-Set 3D Macromolecule Detection Directly from Tilted 2D Projections
Ming-Yang Ho, Alberto Bartesaghi

TL;DR
FullTilt is an innovative framework for real-time open-set 3D macromolecule detection from tilt-series in cryo-electron tomography, significantly reducing computational costs and enabling large-scale analysis.
Contribution
The paper introduces FullTilt, a novel end-to-end method that operates directly on 2D tilt-series, improving speed and efficiency over traditional volumetric approaches.
Findings
Achieves state-of-the-art zero-shot detection performance.
Reduces runtime and VRAM usage by orders of magnitude.
Enables large-scale, rapid proteomics analysis.
Abstract
Open-set 3D macromolecule detection in cryogenic electron tomography eliminates the need for target-specific model retraining. However, strict VRAM constraints prohibit processing an entire 3D tomogram, forcing current methods to rely on slow sliding-window inference over extracted subvolumes. To overcome this, we propose FullTilt, an end-to-end framework that redefines 3D detection by operating directly on aligned 2D tilt-series. Because a tilt-series contains significantly fewer images than slices in a reconstructed tomogram, FullTilt eliminates redundant volumetric computation, accelerating inference by orders of magnitude. To process the entire tilt-series simultaneously, we introduce a tilt-series encoder to efficiently fuse cross-view information. We further propose a multiclass visual prompt encoder for flexible prompting, a tilt-aware query initializer to effectively anchor 3D…
Peer Reviews
No public reviews on file for this paper yet. If you reviewed it on a platform where reviews are public (OpenReview, ICLR, NeurIPS, ICML), you can paste yours below so the community can read it here.
Videos
No videos yet. Explain this paper in a talk, walkthrough, or lecture? Add one.
