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Analyzing Mitochondrial Morphology Through Simulation Supervised Learning
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Machine learning techniques for mitoses classification.

Shima Nofallah1, Sachin Mehta1, Ezgi Mercan1

  • 1University of Washington, Seattle WA 98195, USA.

Computerized Medical Imaging and Graphics : the Official Journal of the Computerized Medical Imaging Society
|December 10, 2020
PubMed
Summary
This summary is machine-generated.

Convolutional Neural Networks (CNNs) show promise in classifying mitotic figures for cancer diagnosis. DenseNet achieved high accuracy on melanoma and breast cancer datasets, outperforming other models in F-score and recall.

Keywords:
Convolutional neural networksMachine learningMelanomaMitosesPathology

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Area of Science:

  • Digital pathology
  • Computational biology
  • Oncology

Background:

  • Accurate cancer staging relies on precise analysis of biopsy material at cellular and structural levels.
  • Mitotic figures, as biomarkers of cellular proliferation, are crucial for prognostic information and clinical care.
  • Convolutional Neural Networks (CNNs) demonstrate significant potential for improving the accuracy of mitosis detection.

Purpose of the Study:

  • To evaluate the performance of state-of-the-art CNN models for mitosis classification in whole slide biopsy images.
  • To compare the quantitative performance of ESPNet and DenseNet on a primary melanoma dataset.
  • To benchmark four CNN architectures (ESPNet, DenseNet, ResNet, ShuffleNet) on the public MITOS breast cancer dataset.

Main Methods:

  • Two CNN models, ESPNet and DenseNet, were trained and evaluated on whole slide skin biopsy images.
  • Performance metrics including sensitivity, specificity, and F-score were used for comparison.
  • Four CNN architectures were further assessed on the MITOS breast cancer dataset using precision, recall, and F-score.

Main Results:

  • On the melanoma dataset, ESPNet and DenseNet achieved high sensitivity (0.976, 0.968) and specificity (0.987, 0.995).
  • On the MITOS dataset, DenseNet demonstrated superior F-score (0.927) and recall (0.916) compared to other models.
  • ResNet and ESPNet offered faster inference times (6s and 8s, respectively) compared to DenseNet (31s), presenting a trade-off between speed and accuracy.

Conclusions:

  • The study successfully evaluated CNNs for mitosis detection in whole slide biopsy images.
  • The proposed methodology and architectures are robust and applicable to various biopsy types for mitosis identification.
  • CNNs, particularly DenseNet, offer a powerful tool to aid pathologists in improving cancer diagnosis and staging accuracy.