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A 1-D Convolutional Neural Network with Gradient Mapped Intensity Features for Detection of Mitosis in Histopathological Images

Akarsh Jagadeesha, Devaraj Verma C., Panita Wannapiroon, Junjiraporn Thongprasit

Abstract


This paper proposes a mitosis detection algorithm that utilizes gradient-mapped intensity (GMI) features integrated into a one-dimensional convolutional neural network (1-D CNN) for the classification of mitotic cells in histopathological images. The proposed framework begins by preprocessing the input images through intensity compensation, followed by contrast enhancement using adaptive histogram equalization. Mitosis candidates are subsequently identified using adaptive thresholding techniques and morphological operations. From each detected candidate, GMI features are extracted through gradient estimation in both the x and y directions, construction of gradient histograms, and mapping of gradient magnitudes with corresponding intensity values. These features, derived from the red, green, and blue (RGB) channels, are used to train a 1-D CNN classifier that categorizes the inputs into two classes: mitosis and non-mitosis. The effectiveness of the proposed approach is evaluated using two benchmark datasets, ICPR 2012 and ICPR 2014, with performance measured via precision, recall, and F1-score metrics. The proposed model achieves an F1-score of 0.846, a recall of 0.859, and a precision of 0.863 on the ICPR 2012 dataset, demonstrating competitive performance compared to existing methods.

Keywords



[1]    C. W. Elston and I. O. Ellis, “Pathological prognostic factors in breast cancer. I. The value of histological grade in breast cancer: Experience from a large study with long-term follow-up,” Histopathology, vol. 19, no. 5, pp. 403–410, 1991.

[2]    C. Li, X. Wang, W. Liu, and L. J. Latecki, “DeepMitosis: Mitosis detection via deep detection, verification and segmentation networks,” Medical Image Analysis, vol. 45, pp. 121–133, Apr. 2018.

[3]    H. Chen, Q. Dou, X. Wang, J. Qin, and P. A. Heng, “Mitosis detection in breast cancer histology images via deep cascaded networks,” in Proceedings of the AAAI Conference on Artificial Intelligence, 2016, pp. 1160–1166.

[4]    D. C. Cireșan, A. Giusti, L. M. Gambardella, and J. Schmidhuber, “Mitosis detection in breast cancer histology images with deep neural networks,” in International Conference on Medical Image Computing and Computer-Assisted Intervention, 2013, pp. 411–418.

[5]    H. Lei, S. Liu, A. Elazab, X. Gong, and B. Lei, “Attention-guided multi-branch convolutional neural network for mitosis detection from histopathological images,” IEEE Journal of Biomedical and Health Informatics (JBHI), vol. 25, no. 2, pp. 358–370, 2020.

[6]    Y. Li, Y. Xue, L. Li, X. Zhang, and X. Qian, “Domain adaptive box-supervised instance segmentation network for mitosis detection,” IEEE Transactions on Medical Imaging, 2022.

[7]    N. Inoue, R. Furuta, T. Yamasaki, and K. Aizawa, “Cross-domain weakly-supervised object detection through progressive domain adaptation,” in the IEEE/CVF Conference on Computer Vision and Pattern Recognition, Jun. 2018, pp. 5001–5009.

[8]    Y. Chen, W. Li, C. Sakaridis, D. Dai, and L. Van Gool, “Domain adaptive faster R-CNN for object detection in the wild,” in Proc. IEEE/CVF Conf. Comput. Vis. Pattern Recognit., Jun. 2018, pp. 3339–3348.

[9]    M. Suchetha, N. S. Ganesh, R. Raman, and D. E. Dhas, “Region of interest-based predictive algorithm for subretinal hemorrhage detection using faster R-CNN,” Soft Computing, vol. 25, no. 24, pp. 15255–15268, 2021.

[10] Y. Xue, G. Bigras, J. Hugh, and N. Ray, “Training convolutional neural networks and compressed sensing end-to-end for microscopy cell detection,” IEEE Transactions on Medical Imaging, vol. 38, no. 11, pp. 2632–2641, Nov. 2019.

[11] X. Zhao, S. Liang, and Y. Wei, “Pseudo mask augmented object detection,” in the IEEE/CVF Conference on Computer Vision and Pattern Recognition, Jun. 2018, pp. 4061–4070.

[12] D. Tellez, M. Balkenhol, I. Otte-Höller, R. van de Loo, R. Vogels, and P. Bult, “Whole-slide mitosis detection in H&E breast histology using PHH3 as a reference to train distilled stain-invariant convolutional networks,” IEEE Transactions on Medical Imaging, vol. 37, no. 9, pp. 2126–2136, Sep. 2018.

[13] Y. Zhang, H. Chen, Y. Wei, P. Zhao, J. Cao, X. Fan, X. Lou, H. Liu, J. Hou, X. Han, J. Yao, Q. Wu, M. Tan, and J. Huang, “From whole slide imaging to microscopy: Deep microscopy adaptation network for histopathology cancer image classification,” in International Conference on Medical Image Computing and Computer-Assisted Intervention, 2019, pp. 360–368.

[14] C. Huang and H. Lee, “Automated mitosis detection based on exclusive independent component analysis,” in Proceedings of the 21st International Conference on Pattern Recognition (ICPR2012), 2012, pp. 1856–1859.

[15] A. M. Khan, H. El-Daly, and N. M. Rajpoot, “A gamma-gaussian mixture model for detection of mitotic cells in breast cancer histopathology images,” in Proceedings of the 21st International Conference on Pattern Recognition (ICPR2012), 2012, pp. 149–152.

[16] D. C. Cireșan, A. Giusti, L. M. Gambardella, and J. Schmidhuber, “Mitosis detection in breast cancer histology images with deep neural networks,” in International Conference on Medical Image Computing and Computer-Assisted Intervention, 2013, pp. 411–418.

[17] H. Chen, Q. Dou, X. Wang, J. Qin, and P. A. Heng, “Mitosis detection in breast cancer histology images via deep cascaded networks,” in Proceedings of the Thirtieth AAAI Conference on Artificial Intelligence, 2016, pp. 1160–1166.

[18] H. Wang, A. Cruz-Roa, A. Basavanhally, H. Gilmore, N. Shih, M. Feldman, J. Tomaszewski, F. Gonzalez, A. Madabhushi, “Mitosis detection in breast cancer pathology images by combining handcrafted and convolutional neural network features,” Journal of Medical Imaging, vol. 1, 2014, Art. no. 034003.

[19] S. Ren, K. He, R. Girshick, and J. Sun, “Faster R-CNN: Towards real-time object detection with region proposal networks,” in Advances in Neural Information Processing Systems (NeurIPS), 2015, pp. 91–99.

[20] J. Hu, L. Shen, S. Albanie, G. Sun, and E. Wu, “Squeeze-and-excitation networks,” in IEEE Conference on Computer Vision and Pattern Recognition (CVPR), 2018, pp. 7132–7141.

[21] M. Al-Imran, A. C. Das, M. A. Hasan, M. N. H. Mir, M. J. Ahmmed, T. Rahman, R. J. Bhuiyan, M. A. S. Mozumder, S. Akter, and M. E. Hossen, “Evaluating machine learning algorithms for breast cancer detection: A study on accurecy and predictive performance,” The American Journal of Engineering and Technology, vol. 6, pp. 22–33, 2024.

[22] S. M. Pizer, E. P. Amburn, J. D. Austin, R. Cromartie, A. Geselowitz, T. Greer, B. ter Haar Romeny, J. B. Zimmerman, and K. Zuiderveld, “Adaptive histogram equalization and its variations,” Computer Vision, Graphics, and Image Processing, vol. 39, no. 3, pp. 355–368, 1987.

[23] P. Roy, S. Dutta, N. Dey, G. Dey, S. Chakraborty, and R. Ray, “Adaptive thresholding: A comparative study,” in International Conference on Intelligent Computing, Instrumentation and Control Technologies (ICICICT), 2014, pp. 1182–1186.

[24] M. L. Comer and E. J. Delp III, “Morphological operations for color image processing,” Journal of Electronic Imaging, vol. 8, no. 3, pp. 279–289, 1999.

[25] S. Das, K. Kharbanda, M. Suchetha, R. Raman, and D. E. Dhas, “Deep learning architecture based on segmented fundus image features for classification of diabetic retinopathy,” Biomedical Signal Processing and Control, vol. 68, 2021, Art. no. 102600.

[26] C. Huang and H. Lee, “Automated mitosis detection based on exclusive independent component analysis,” in Proceedings of the 21st International Conference on Pattern Recognition (ICPR2012), 2012, pp. 1856–1859.

[27] ICPR. “ICPR 2014 Mitosis Detection Dataset.” mitos-atypia-14.grand-challenge.org. https://mitos-atypia-14.grand-challenge.org/home/ (accessed Nov. 19, 2022).

[28] H. Wang, A. Cruz-Roa, A. Basavanhally, H. Gilmore, N. Shih, M. Feldman, J. Tomaszewski, F. Gonzalez, A. Madabhushi, “Cascaded ensemble of convolutional neural networks and handcrafted features for mitosis detection,” in SPIE Conference Proceedings, 2014, vol. 9041.

[29] H. Irshad, “Automated mitosis detection in histopathology using morphological and multi-channel statistics features,” Journal of Pathology Informatics, vol. 4, pp. 10–17, 2013.

[30] A. Paul, A. Dey, D. P. Mukherjee, J. Sivaswamy, and V. Tourani, “Regenerative random forest with automatic feature selection to detect mitosis in histopathological breast cancer images,” in International Conference on Medical Image Computing and Computer-Assisted Intervention, 2015, pp. 94–102.

[31] Z. Tian, C. Shen, and H. Chen, “Conditional convolutions for instance segmentation,” in 16th European Conference on Computer Vision (ECCV), 2020, pp. 282–298.

[32] C. Li, X. Wang, W. Liu, L. J. Latecki, B. Wang, and J. Huang, “Weakly supervised mitosis detection in breast histopathology images using concentric loss,” Medical Image Analysis, vol. 53, pp. 165–178, 2019.

[33] Z. Tian, C. Shen, X. Wang, and H. Chen, “BoxInst: High-performance instance segmentation with box annotations,” in Proceedings of the IEEE conference on computer vision and pattern Recognition (CVPR), Jun. 2021, pp. 5443–5452.

[34] M. T. Imran, I. Shafi, J. Ahmad, M. F. U. Butt, S. G. Villar, E. G. Villena, T. Khurshaid, and I. Ashraf, “Virtual histopathology methods in medical imaging - A systematic review,” BMC Medical Imaging, vol. 24, no. 1, p. 318, Nov. 2004.

[35] J. Wang, T. Wang, R. Han, D. Shi, and B. Chen, “Artificial intelligence in cancer pathology: Applications, challenges, and future directions,” Cytojournal, vol. 22, p. 45, 2025.

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DOI: 10.14416/j.asep.2025.07.010

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