Faculty Publications
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Item Efficient and robust deep learning architecture for segmentation of kidney and breast histopathology images(Elsevier Ltd, 2021) Chanchal, A.K.; Kumar, A.; Lal, S.; Kini, J.Image segmentation is consistently an important task for computer vision and the analysis of medical images. The analysis and diagnosis of histopathology images by using efficient algorithms that separate hematoxylin and eosin-stained nuclei was the purpose of our proposed method. In this paper, we propose a deep learning model that automatically segments the complex nuclei present in histology images by implementing an effective encoder–decoder architecture with a separable convolution pyramid pooling network (SCPP-Net). The SCPP unit focuses on two aspects: first, it increases the receptive field by varying four different dilation rates, keeping the kernel size fixed, and second, it reduces the trainable parameter by using depth-wise separable convolution. Our deep learning model experimented with three publicly available histopathology image datasets. The proposed SCPP-Net provides better experimental segmentation results compared to other existing deep learning models and is evaluated in terms of F1-score and aggregated Jaccard index. © 2021 Elsevier LtdItem Efficient deep learning architecture with dimension-wise pyramid pooling for nuclei segmentation of histopathology images(Elsevier Ltd, 2021) Aatresh, A.A.; Yatgiri, R.P.; Chanchal, A.K.; Kumar, A.; Ravi, A.; Das, D.; Raghavendra, B.S.; Lal, S.; Kini, J.Image segmentation remains to be one of the most vital tasks in the area of computer vision and more so in the case of medical image processing. Image segmentation quality is the main metric that is often considered with memory and computation efficiency overlooked, limiting the use of power hungry models for practical use. In this paper, we propose a novel framework (Kidney-SegNet) that combines the effectiveness of an attention based encoder-decoder architecture with atrous spatial pyramid pooling with highly efficient dimension-wise convolutions. The segmentation results of the proposed Kidney-SegNet architecture have been shown to outperform existing state-of-the-art deep learning methods by evaluating them on two publicly available kidney and TNBC breast H&E stained histopathology image datasets. Further, our simulation experiments also reveal that the computational complexity and memory requirement of our proposed architecture is very efficient compared to existing deep learning state-of-the-art methods for the task of nuclei segmentation of H&E stained histopathology images. The source code of our implementation will be available at https://github.com/Aaatresh/Kidney-SegNet. © 2021 Elsevier LtdItem Deep structured residual encoder-decoder network with a novel loss function for nuclei segmentation of kidney and breast histopathology images(Springer, 2022) Chanchal, A.K.; Lal, S.; Kini, J.To improve the process of diagnosis and treatment of cancer disease, automatic segmentation of haematoxylin and eosin (H & E) stained cell nuclei from histopathology images is the first step in digital pathology. The proposed deep structured residual encoder-decoder network (DSREDN) focuses on two aspects: first, it effectively utilized residual connections throughout the network and provides a wide and deep encoder-decoder path, which results to capture relevant context and more localized features. Second, vanished boundary of detected nuclei is addressed by proposing an efficient loss function that better train our proposed model and reduces the false prediction which is undesirable especially in healthcare applications. The proposed architecture experimented on three different publicly available H&E stained histopathological datasets namely: (I) Kidney (RCC) (II) Triple Negative Breast Cancer (TNBC) (III) MoNuSeg-2018. We have considered F1-score, Aggregated Jaccard Index (AJI), the total number of parameters, and FLOPs (Floating point operations), which are mostly preferred performance measure metrics for comparison of nuclei segmentation. The evaluated score of nuclei segmentation indicated that the proposed architecture achieved a considerable margin over five state-of-the-art deep learning models on three different histopathology datasets. Visual segmentation results show that the proposed DSREDN model accurately segment the nuclear regions than those of the state-of-the-art methods. © 2022, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.Item A novel deep classifier framework for automated molecular subtyping of breast carcinoma using immunohistochemistry image analysis(Elsevier Ltd, 2022) Mathew, T.; Niyas, S.; Johnpaul, C.I.; Kini, J.; Rajan, J.Breast carcinoma has various subtypes based on the genetic factors involved in the pathogenesis of the malignancy. Identifying the exact subtype and providing targeted treatment to the patient can improve the survival chances. Molecular subtyping through immunohistochemistry analysis is a pathology procedure to determine the subtype of breast cancer. The existing manual procedure is tedious and involves assessing the status of the four vital molecular biomarkers present in the tumor tissues. In this paper, a deep learning-based framework for automated molecular subtyping of breast cancer is proposed. Digital slide images of the four biomarkers are separately processed by the proposed framework. In the preprocessing stage, the non-informative background regions from the images are separated. The patches extracted from the foreground regions are classified into target classes using convolutional neural network models trained for this purpose. Classification results are post-processed to predict the status of all the four biomarkers. The predictions for the individual biomarkers are finally consolidated as per clinical guidelines to determine the subtype of the cancer. The proposed system is evaluated for the performance of individual biomarker status prediction and patient-level subtype classification.For patient-level evaluation of biomarkers ER, PR, K67, and HER2, the proposed method gives F1 Scores 1.00, 1.00, 0.90, and 0.94 respectively, whereas for molecular subtyping an F1 score of 0.89 is obtained. In both these aspects, the proposed framework has given significant results that show the effectiveness of our approach. © 2022 Elsevier LtdItem Novel edge detection method for nuclei segmentation of liver cancer histopathology images(Springer Science and Business Media Deutschland GmbH, 2023) Roy, S.; Das, D.; Lal, S.; Kini, J.In automatic cancer detection, nuclei segmentation is a very essential step which enables the classification task simpler and computationally more efficient. However, automatic nuclei detection is fraught with the problems of inter-class variability of nuclei size and shapes. In this research article, a novel unsupervised edge detection technique, is proposed for segmenting the nuclei regions in liver cancer Hematoxylin and Eosin (H&E) stained histopathology images. In this novel edge detection technique, the notion of computing local standard deviation is incorporated, instead of computing gradients. Since, local standard deviation value is correlated with the edge information of image, this novel method can extract the nuclei edges efficiently, even at multiscale. The edge-detected image is further converted into a binary image by employing Ostu (IEEE Trans Syst Man Cybern 9(1):62–66, 1979)’s thresholding operation. Subsequently, an adaptive morphological filter is also employed in order to refine the final segmented image. The proposed nuclei segmentation method is also tested on a well-recognized multi-organ dataset, in order to check its effectiveness over wide variety of dataset. The visual results of both datasets indicate that the proposed segmentation method overcomes the limitations of existing unsupervised methods, moreover, its performance is comparable with the same of recent deep neural models like DIST, HoverNet, etc. Furthermore, three quality metrics are computed in order to measure the performance of several nuclei segmentation methods quantitatively. The mean value of quality metrics reveals that proposed segmentation method indeed outperformed other existing nuclei segmentation methods. © 2021, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.Item Evolution of LiverNet 2.x: Architectures for automated liver cancer grade classification from H&E stained liver histopathological images(Springer, 2024) Chanchal, A.K.; Lal, S.; Barnwal, D.; Sinha, P.; Arvavasu, S.; Kini, J.Recently, the automation of disease identification has been quite popular in the field of medical diagnosis. The rise of Convolutional Neural Networks (CNNs) for training and generalizing medical image data has proven to be quite efficient in detecting and identifying the types and sub-types of various diseases. Since the classification of large datasets of Hematoxylin & Eosin (H&E) stained histopathology images by experts can be expensive and time-consuming, automated processes using deep learning have been encouraged for the past decade. This paper introduces LiverNet 2.x model by modifying the previously encountered LiverNet architecture. The proposed model uses two different improvements of the Atrous Spatial Pyramid Pooling (ASPP) block to extract the clinically defined features of hepatocellular carcinoma (HCC) from liver histopathology images. LiverNet 2.0 uses a modified form of ASPP block known as DenseASPP, where all the atrous convolution outputs are densely connected. Whereas LiverNet 2.1 uses fewer concatenations while maintaining a large receptive field by stacking the dilated convolutional blocks in a tree-like fashion. This paper also discusses the trade-off between LiverNet 2.0 and LiverNet 2.1 in terms of accuracy and computational complexity. All comparison model and the proposed model is trained and tested on the patches of two different histopathological datasets. The experimental results show that the proposed model performs better compared to reference models. For the KMC Liver dataset, LiverNet 2.0 and LiverNet 2.1 achieved an accuracy of 97.50% and 97.14% respectively. Accuracy of 94.37% and 97.14% for the TCGA Liver dataset are achieved. © 2023, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.Item FPGA implementation of deep learning architecture for kidney cancer detection from histopathological images(Springer, 2024) Lal, S.; Chanchal, A.K.; Kini, J.; Upadhyay, G.K.Kidney cancer is the most common type of cancer, and designing an automated system to accurately classify the cancer grade is of paramount importance for a better prognosis of the disease from histopathological kidney cancer images. Application of deep learning neural networks (DLNNs) for histopathological image classification is thriving and implementation of these networks on edge devices has been gaining the ground correspondingly due to high computational power and low latency requirements. This paper designs an automated system that classifies histopathological kidney cancer images. For experimentation, we have collected Kidney histopathological images of Non-cancerous, cancerous, and their respective grade of Renal Cell Carcinoma (RCC) from Kasturba Medical College (KMC), Mangalore, Karnataka, India. We have implemented and analyzed performances of deep learning architectures on a Field Programmable Gate Array (FPGA) board. Results yield that the Inception-V3 network provides better accuracy for kidney cancer detection as compared to other deep learning models on Kidney histopathological images. Further, the DenseNet-169 network provides better accuracy for kidney cancer grading as compared to other existing deep learning architecture on the FPGA board. © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2023.Item An Efficient Parallel Branch Network for Multi-Class Classification of Prostate Cancer From Histopathological Images(John Wiley and Sons Inc, 2025) Srivastava, V.; Prabhu, A.; Sravya, S.; Vibha Damodara, K.; Lal, S.; Kini, J.Prostate cancer is one of the prevalent forms of cancer, posing a significant health concern for men. Accurate detection and classification of prostate cancer are crucial for effective diagnosis and treatment planning. Histopathological images play a pivotal role in identifying prostate cancer by enabling pathologists to identify cellular abnormalities and tumor characteristics. With the rapid advancements in deep learning, Convolutional Neural Networks (CNNs) have emerged as a powerful tool for tackling complex computer vision tasks, including object detection, classification, and segmentation. This paper proposes a Parallel Branch Network (PBN), a CNN architecture specifically designed for the automatic classification of prostate cancer into its subtypes from histopathological images. The paper introduces a novel Efficient Residual (ER) block that enhances feature representation using residual learning and multi-scale feature extraction. By utilizing multiple branches with different filter reduction ratios and dense attention mechanisms, the block captures diverse features while preserving essential information. The proposed PBN model achieved a classification accuracy of 93.16% on the Prostate Gleason dataset, outperforming all other comparison models. © 2025 Wiley Periodicals LLC.Item ProsGradNet: An effective and structured CNN approach for prostate cancer grading from histopathology images(Elsevier Ltd, 2025) Prabhu, A.; Sravya, N.; Lal, S.; Kini, J.Prostate cancer (PCa) is one of the most prevalent and potentially fatal malignancies affecting men globally. The incidence of prostate cancer is expected to double by 2040, posing significant health challenges. This anticipated increase underscores the urgent need for early and precise diagnosis to facilitate effective treatment and management. Histopathological analysis using Gleason grading system plays a pivotal role in clinical decision making by classifying cancer subtypes based on their cellular characteristics. This paper proposes a novel deep CNN model named as Prostate Grading Network (ProsGradNet), for the automatic grading of PCa from histopathological images. Central to the approach is the novel Context Guided Shared Channel Residual (CGSCR) block, that introduces structured methods for channel splitting and clustering, by varying group sizes. By grouping channels into 2, 4, and 8, it prioritizes deeper layer features, enhancing local semantic content and abstract feature representation. This methodological advancement significantly boosts classification accuracy, achieving an impressive 92.88% on Prostate Gleason dataset, outperforming other CNN models. To demonstrate the generalizability of ProsGradNet over different datasets, experiments are performed on Kasturba Medical College (KMC) Kidney dataset as well. The results further confirm the superiority of the proposed ProsGradNet model, with a classification accuracy of 92.68% on the KMC Kidney dataset. This demonstrates the model's potential to be applied effectively across various histopathological datasets, making it a valuable tool to fight against cancer. © 2025 Elsevier Ltd