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InstanSeg: an embedding-based instance segmentation algorithm optimized for accurate, efficient and portable cell segmentation (2408.15954v1)

Published 28 Aug 2024 in cs.CV

Abstract: Cell and nucleus segmentation are fundamental tasks for quantitative bioimage analysis. Despite progress in recent years, biologists and other domain experts still require novel algorithms to handle increasingly large and complex real-world datasets. These algorithms must not only achieve state-of-the-art accuracy, but also be optimized for efficiency, portability and user-friendliness. Here, we introduce InstanSeg: a novel embedding-based instance segmentation pipeline designed to identify cells and nuclei in microscopy images. Using six public cell segmentation datasets, we demonstrate that InstanSeg can significantly improve accuracy when compared to the most widely used alternative methods, while reducing the processing time by at least 60%. Furthermore, InstanSeg is designed to be fully serializable as TorchScript and supports GPU acceleration on a range of hardware. We provide an open-source implementation of InstanSeg in Python, in addition to a user-friendly, interactive QuPath extension for inference written in Java. Our code and pre-trained models are available at https://github.com/instanseg/instanseg .

Citations (2)

Summary

  • The paper introduces InstanSeg, an embedding-based algorithm that clusters pixel embeddings from a modified U-Net for precise cell segmentation.
  • It achieves a 60% reduction in processing time and up to 45-fold improvements in accuracy compared to traditional methods.
  • The method’s efficient, portable design paves the way for broader applications in digital pathology and computational cell biology.

Insightful Overview of InstanSeg: An Embedding-Based Instance Segmentation Algorithm

The paper "InstanSeg: An Embedding-Based Instance Segmentation Algorithm Optimized for Accurate, Efficient and Portable Cell Segmentation" introduces InstanSeg, a cutting-edge approach to instance segmentation, specifically targeting cell and nucleus segmentation tasks in microscopy images. This research addresses the increasing need for algorithms that deliver not only state-of-the-art accuracy but also efficiency, portability, and user-friendliness. The paper tackles several significant challenges associated with current segmentation methods and presents InstanSeg as an effective solution.

Methodology

The principal innovation of InstanSeg lies in its embedding-based pipeline that clusters pixel embeddings around optimally selected seeds, using a modified U-Net backbone network. This technique differentiates pixels into individual instances, providing substantial improvements in segmentation accuracy and processing speed.

Crucially, InstanSeg eschews traditional proposal-based and proposal-free methods by introducing embedding-based segmentation, where the emphasis is on creating dense pixel embeddings that are clustered for instance resolution. This is facilitated by a lightweight neural network that leverages features such as seed pixels and conditional embeddings to enhance instance detection.

The algorithm operates through four key components: a feature encoder, and three auxiliary heads dedicated to seed mapping, positional embedding, and conditional embedding, complemented by an instance segmentation head that outputs the probability of each pixel belonging to a particular instance. This novel approach elegantly circumvents the inefficiencies inherent in existing methods, such as the computationally intensive binary mask prediction in proposal-based approaches and the challenges in seed sampling in proposal-free approaches.

Empirical Results

The authors empirically validate the superior performance of InstanSeg against existing segmentation algorithms, such as Stardist, CellPose, and HoVer-Net. InstanSeg achieves a notable reduction in processing time—by approximately 60%—across several public segmentation datasets while maintaining accuracy improvements of up to 2.5 to 45 times over the alternatives.

Statistical analysis through paired t-tests confirms that InstanSeg consistently yields higher F1 scores across various datasets, demonstrating its robustness and reliability. The paper also introduces test-time augmentations (TTA) to further refine accuracy, although the foundational model without TTA already establishes a new benchmark.

Implications and Future Developments

The implications of this research extend beyond the niche of cell segmentation. The methodology, featuring a non-restrictive approach to mapping embeddings to instance probabilities, could theoretically be adapted to other instances of segmentation problems across different domains. The improvements in computational efficiency and portability contribute to its potential utility in real-world applications, including widespread adoption in digital pathology and quantitative cell biology where scalability and integration ease are paramount.

Furthermore, integrating InstanSeg with user-friendly platforms like QuPath represents a significant step in bridging methods to applicable tools for domain scientists, dismantling traditional barriers presented by computational resource needs. It can lead to more efficient analytical pipelines and potentially foster more interdisciplinary collaborations, facilitating advanced research in computational pathology and related fields.

Conclusion

InstanSeg marks a significant advancement in instance segmentation technology by integrating an embedding-based approach that addresses many of the shortcomings of previous methodologies. Through a combination of accuracy, efficiency, and portability, InstanSeg has the potential to reshape practical applications in biomedical imaging. The research presented in this paper sets a compelling precedent for the development of future algorithms that focus on embedding-based segmentation tasks, potentially transforming the approaches in computational and applied sciences. Future work should explore the applicability of InstanSeg to other complex segmentation challenges outside the field of microscopy, paving the way for broader applications of this innovative approach.

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