4.7 Article

Deep Consensus Network: Aggregating predictions to improve object detection in microscopy images

期刊

MEDICAL IMAGE ANALYSIS
卷 70, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.media.2021.102019

关键词

Microscopy; Detection; Deep Learning; Voting

资金

  1. BMBF [031A537C]
  2. DFG (German Research Foundation) [SFB 1129, 240245660, SPP 2202]
  3. BMBF within the project CancerTelSys (e:Med)

向作者/读者索取更多资源

The article presents a novel deep neural network for object detection in microscopy images, which includes a feature extractor, a centroid proposal network, and a layer for ensembling detection hypotheses over all image scales and anchors. Utilizing anchor regularization and a new loss function to address class imbalance, along with an improved non-maximum suppression algorithm, experiments demonstrate the method's outstanding performance on challenging data.
Detection of cells and particles in microscopy images is a common and challenging task. In recent years, detection approaches in computer vision achieved remarkable improvements by leveraging deep learning. Microscopy images pose challenges like small and clustered objects, low signal to noise, and complex shape and appearance, for which current approaches still struggle. We introduce Deep Consensus Network, a new deep neural network for object detection in microscopy images based on object centroids. Our network is trainable end-to-end and comprises a Feature Pyramid Network-based feature extractor, a Centroid Proposal Network, and a layer for ensembling detection hypotheses over all image scales and anchors. We suggest an anchor regularization scheme that favours prior anchors over regressed locations. We also propose a novel loss function based on Normalized Mutual Information to cope with strong class imbalance, which we derive within a Bayesian framework. In addition, we introduce an improved algorithm for Non-Maximum Suppression which significantly reduces the algorithmic complexity. Experiments on synthetic data are performed to provide insights into the properties of the proposed loss function and its robustness. We also applied our method to challenging data from the TUPAC16 mitosis detection challenge and the Particle Tracking Challenge, and achieved results competitive or better than state-of-the-art. ? 2021 Elsevier B.V. All rights reserved.

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