One Click per Cell Type Suffices: Training-free Group Interaction for Cell Instance Segmentation
Abstract
Group Prompting enables efficient cell instance segmentation by leveraging per-type prompting through a training-free framework that uses multi-scale encoder features and recursive prompt expansion.
Cell instance segmentation models trained on cell-specific datasets suffer severe performance drops on out-of-distribution cell types, while interactive foundation models overcome this through per-instance prompting at a cost that is prohibitively expensive for histopathology images containing hundreds to thousands of densely packed instances. We introduce Group Prompting, a new paradigm that shifts interactive segmentation from per-instance O(N) to per-type O(T), where a single click per cell type suffices to segment all instances of that type. Our key observation is that the frozen image encoder of the Segment Anything Model (SAM) already clusters same-type cells in its feature space before any prompt is given. Exploiting this property, we propose Chain-of-Prompts (CoP), a training-free framework that recursively expands a single user click by (1) identifying reliable same-type locations through non-parametric gating of multi-scale encoder features, and (2) selecting the most spatially distant reliable point as the next prompt to maximize coverage. On three cell-type-annotated benchmarks, CoP with one click per type retains over 90% of per-instance performance and surpasses fully-supervised methods without any additional training. On four morphologically homogeneous benchmarks, a single click retains over 99%. Project Page: https://shjo-april.github.io/Chain-of-Prompts/
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๐ฅ Early Accepted to MICCAI 2026 (Top 9%)
TL;DR: We introduce Chain-of-Prompts (CoP), a training-free framework that shifts the interaction cost for cell instance segmentation from per-instance O(N) to per-type O(T) using foundation models like SAM 3.
The Problem: While interactive foundation models generalize well, clicking hundreds to thousands of individual cells in digital pathology is highly unscalable.
The Solution: CoP requires only one click per cell type. It leverages the natural clustering within SAM's frozen image encoder to recursively propagate this single click to all same-type instances across the image.
Key Highlights:
- ๐ฑ๏ธ Cost Efficiency: Over 97% reduction in annotation cost (clicks).
- ๐ฏ High Performance: Retains >90% to 99% of per-instance performance across 7 diverse benchmarks.
- ๐ Training-Free: Surpasses fully-supervised methods requiring complete mask annotations for training.
- โก Fast, interactive speed on a single GPU with negligible memory overhead.
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