Coronaviruses are a family of viruses that majorly cause respiratory disorders in humans. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a new strain of coronavirus that causes the coronavirus disease 2019 (COVID-19). WHO has identified COVID-19 as a pandemic as it has spread across the globe due to its highly contagious nature. For early diagnosis of COVID-19, the reverse transcription-polymerase chain reaction (RT-PCR) test is commonly done. However, it suffers from a high false-negative rate of up to 67% if the test is done during the first five days of exposure. As an alternative, research on the efficacy of deep learning techniques employed in the identification of COVID-19 disease using chest X-ray images is intensely pursued. As pneumonia and COVID-19 exhibit similar/ overlapping symptoms and affect the human lungs, a distinction between the chest X-ray images of pneumonia patients and COVID-19 patients becomes challenging. In this work, we have modeled the COVID-19 classification problem as a multiclass classification problem involving three classes, namely COVID-19, pneumonia, and normal. We have proposed a novel classification framework which combines a set of handpicked features with those obtained from a deep convolutional neural network. The proposed framework comprises of three modules. In the first module, we exploit the strength of transfer learning using ResNet-50 for training the network on a set of preprocessed images and obtain a vector of 2048 features. In the second module, we construct a pool of frequency and texture based 252 handpicked features that are further reduced to a set of 64 features using PCA. Subsequently, these are passed to a feed forward neural network to obtain a set of 16 features. The third module concatenates the features obtained from first and second modules, and passes them to a dense layer followed by the softmax layer to yield the desired classification model. We have used chest X-ray images of COVID-19 patients from four independent publicly available repositories, in addition to images from the Mendeley and Kaggle Chest X-Ray Datasets for pneumonia and normal cases. To establish the efficacy of the proposed model, 10-fold cross-validation is carried out. The model generated an overall classification accuracy of 0.974 0.02 and a sensitivity of 0.987 0.05, 0.963 0.05, and 0.973 0.04 at 95% confidence interval for COVID-19, normal, and pneumonia classes, respectively. To ensure the effectiveness of the proposed model, it was validated using an independent Chest X-ray cohort and an overall classification accuracy of 0.979 was achieved. Comparison of the proposed framework with state-of-the-art methods reveal that the proposed framework outperforms others in terms of accuracy and sensitivity. Since interpretability of results is crucial in the medical domain, the gradient-based localizations are captured using Gradient-weighted Class Activation Mapping (Grad-CAM). In su...
Coronaviruses constitute a family of viruses that gives rise to respiratory diseases. COVID-19 is an infectious disease caused by a newly discovered coronavirus also termed Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). As COVID-19 is highly contagious, early diagnosis of COVID-19 is crucial for an effective treatment strategy. However, the reverse transcription-polymerase chain reaction (RT-PCR) test which is considered to be a gold standard in the diagnosis of COVID-19 suffers from a high false-negative rate. Therefore, the research community is exploring alternative diagnostic mechanisms. Chest X-ray (CXR) image analysis has emerged as a feasible and effective diagnostic technique towards this objective. In this work, we propose the COVID-19 classification problem as a three-class classification problem to distinguish between COVID-19, normal, and pneumonia classes. We propose a three-stage framework, named COV-ELM based on extreme learning machine (ELM). Our dataset comprises CXR images in a frontal view, namely Posteroanterior (PA) and Erect anteroposterior (AP). Stage one deals with preprocessing and transformation while stage two deals with feature extraction. These extracted features are passed as an input to the ELM at the third stage, resulting in the identification of COVID-19. The choice of ELM in this work has been motivated by its faster convergence, better generalization capability, and shorter training time in comparison to the conventional gradient-based learning algorithms. As bigger and diverse datasets become available, ELM can be quickly retrained as compared to its gradient-based competitor models. We use 10-fold cross-validation to evaluate the results of COV-ELM. The proposed model achieved a macro average F1-score of 0.95 and the overall sensitivity of 0.94 ± 0.02 at a 95% confidence interval. When compared to state-of-the-art machine learning algorithms, the COV-ELM is found to outperform its competitors in this three-class classification scenario. Further, LIME has been integrated with the proposed COV-ELM model to generate annotated CXR images. The annotations are based on the superpixels that have contributed to distinguish between the different classes. It was observed that the superpixels correspond to the regions of the human lungs that are clinically observed in COVID-19 and Pneumonia cases.
Breast cancer being major death-leading cancer demands utmost attention. Recently, the nextgeneration sequencing techniques capable of capturing gene expression data have been used successfully for the detection of breast cancer. The proposed work identifies a small set of biomarker genes for molecular stratification of breast cancer subtypes. In this work, we have proposed Triphasic DeepBRCA -a novel deep learning framework, for breast cancer subtype detection and biomarker discovery. In the first phase, an autoencoder is used for extracting a compact representation of the gene expression data which is provided as an input to a supervised feed-forward neural network for classification of breast cancer subtypes in the second phase. In the third phase, the proposed Biomarker Gene Discovery Algorithm (BGDA) leverages the neural network classifier of the second phase to estimate the relevance of various genes. Next, Wilcoxon rank-sum test with False Discovery Rate (FDR) Correction is applied to identify the most differentiating genes. Using the TCGA BRCA RNASeq data, the proposed framework enabled us to discover a set of 54 most-variant genes. Using 10-fold cross-validation, we obtained a mean accuracy of 0.899 ± 0.04 at 95% confidence interval. We also validated our results on METABRIC dataset. Gene Set Analysis revealed statistically enriched pathways. Heatmap of the expression levels and t-SNE visualization reveals that these genes have an aggregated capability to distinguish amongst the different breast cancer subtypes. Further, the prognostic evaluation using 54 biomarkers revealed that over 30 genes out of 54 are significantly linked to the prognostic outcome.
Coronaviruses constitute a family of virus that gives rise to respiratory diseases. Coronavirus disease 2019 is an infectious disease caused by a newly discovered coronavirus also termed as Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Due to its rapid spread, WHO has declared COVID-19 outbreak a pandemic on 11th March 2020. Reverse transcription-polymerase chain reaction (RT-PCR) test is popularly used worldwide for the detection of COVID-19. However, due to the high false-negative rate of RT-PCR test, chest X-ray (CXR) imaging is emerging as a feasible alternative for the detection of COVID-19. In this work, we propose a multiclass classification model COV-ELM, based on the extreme learning machine which classifies the CXR images into one of the three classes, namely COVID-19, normal, and pneumonia. The choice of ELM in this work has been motivated by its significantly short training time as compared to conventional gradient-based learning algorithms. After some preprocessing, we extract a pool of features based on texture and frequency. This pool of features serves as an input to the ELM and a 10-fold cross-validation method is employed to evaluate the proposed model. For experimentation, we use chest X-ray (CXR) images from three publicly available sources. The results of applying COV-ELM on test data are quite promising. The COV-ELM achieved a macro average F1-score of 0.95 and the overall sensitivity of 0.94 ± 0.02 at 95% confidence interval. When compared to state-of-the-art machine learning algorithms, the COV-ELM is found to outperform in a three-class classification scenario. The main advantage of COV-ELM is that its training time being quite low, as bigger and diverse datasets become available, it can be quickly retrained as compared to its gradient-based competitor models.
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