Wind energy is one of the most relevant clean energies today, so wind turbines must have good health and be reliable in operation. Current wind turbines have slender and elastic structures that can be easily damaged through vibrations and compromise their health; therefore, vibration monitoring is essential to ensure safe operation. Here, we present a method for simple wind turbine vibration monitoring in the laboratory by means of an accelerometer placed on a weathervane under different scenarios, with recording of different amplitudes of vibrations caused at a constant speed of 10 km/h. The variables, trends, and data captured during vibration monitoring were then used to implement a prediction system of synthetic failure using machine learning methods such as: Medium Trees, Cubic SVN, Logistic Regression Kernel, Optimized Neural Network, and Bagged Trees, with the last demonstrating an accuracy of up to 0.87%.

This paper investigates the impact of the amount of training data and the shape variability on the segmentation provided by the deep learning architecture U-Net. Further, the correctness of ground truth (GT) was also evaluated. The input data consisted of a three-dimensional set of images of HeLa cells observed with an electron microscope with dimensions $8192\times 8192\times 517$. From there, a smaller region of interest (ROI) of $2000\times 2000\times 300$ was cropped and manually delineated to obtain the ground truth necessary for a quantitative evaluation. A qualitative evaluation was performed on the $8192\times 8192$ slices due to the lack of ground truth. Pairs of patches of data and labels for the classes nucleus, nuclear envelope, cell and background were generated to train U-Net architectures from scratch. Several training strategies were followed, and the results were compared against a traditional image processing algorithm. The correctness of GT, that is, the inclusion of one or more nuclei within the region of interest was also evaluated. The impact of the extent of training data was evaluated by comparing results from 36,000 pairs of data and label patches extracted from the odd slices in the central region, to 135,000 patches obtained from every other slice in the set. Then, 135,000 patches from several cells from the $8192\times 8192$ slices were generated automatically using the image processing algorithm. Finally, the two sets of 135,000 pairs were combined to train once more with 270,000 pairs. As would be expected, the accuracy and Jaccard similarity index improved as the number of pairs increased for the ROI. This was also observed qualitatively for the $8192\times 8192$ slices. When the $8192\times 8192$ slices were segmented with U-Nets trained with 135,000 pairs, the architecture trained with automatically generated pairs provided better results than the architecture trained with the pairs from the manually segmented ground truths. This suggests that the pairs that were extracted automatically from many cells provided a better representation of the four classes of the various cells in the $8192\times 8192$ slice than those pairs that were manually segmented from a single cell. Finally, the two sets of 135,000 pairs were combined, and the U-Net trained with these provided the best results.

This paper describes a methodology that extracts key morphological features from histological breast cancer images in order to automatically assess Tumour Cellularity (TC) in Neo-Adjuvant treatment (NAT) patients. The response to NAT gives information on therapy efficacy and it is measured by the residual cancer burden index, which is composed of two metrics: TC and the assessment of lymph nodes. The data consist of whole slide images (WSIs) of breast tissue stained with Hematoxylin and Eosin (H&E) released in the 2019 SPIE Breast Challenge. The methodology proposed is based on traditional computer vision methods (K-means, watershed segmentation, Otsu’s binarisation, and morphological operations), implementing colour separation, segmentation, and feature extraction. Correlation between morphological features and the residual TC after a NAT treatment was examined. Linear regression and statistical methods were used and twenty-two key morphological parameters from the nuclei, epithelial region, and the full image were extracted. Subsequently, an automated TC assessment that was based on Machine Learning (ML) algorithms was implemented and trained with only selected key parameters. The methodology was validated with the score assigned by two pathologists through the intra-class correlation coefficient (ICC). The selection of key morphological parameters improved the results reported over other ML methodologies and it was very close to deep learning methodologies. These results are encouraging, as a traditionally-trained ML algorithm can be useful when limited training data are available preventing the use of deep learning approaches.

This paper describes a methodology that extracts morphological features from histological breast cancer images stained for Hematoxilyn and Eosin (H&E). Cellularity was estimated and the correlation between features and the residual tumour size cellularity after a Neo-Adjuvant treatment (NAT) was examined. Images from whole slide imaging (WSI) were processed automatically with traditional computer vision methods to extract twenty two morphological parameters from the nuclei, epithelial region and the global image. The methodology was applied to a set of images from breast cancer under NAT. The data came from the BreastPathQ Cancer Cellularity Challenge 2019, and consisted of 2579 patches of 255×255 pixels of H&E histopatological samples from NAT treatment patients. The methodology automatically implements colour separation, segmentation and morphological analysis using traditional algorithms (K-means grouping, watershed segmentation, Otsu’s binarisation). Linear regression methods were applied to determine strongest correlation between the parameters and the cancer cellularity. The morphological parameters showed correlation with the residual tumour cancer cellularity. The strongest correlations corresponded to the stroma concentration value (r = −0.9786) and value from HSV image colour space (r = −0.9728), both from a global image parameters.

This paper describes a multiclass semantic segmentation of breast cancer images into the following classes: Tumour, Stroma, Inflammatory, Necrosis and Other. The images were stained with Haematoxilin and Eosin and acquired from the Cancer Genome Atlas through the Breast Cancer Semantic Segmentation Challenge. Over 12,000 patches of data and classes were generated from training images with the use of data augmentation.The segmentation was obtained with a U-Net architecture for which the hyperparameters were explored systematically. Optimal values were obtained with batch size = 8, Loss function Adam and 50 epochs, which took over 50 hours to train. Due to this fact and limitations in time, the rest of the parameters were explored with 10 epochs and we speculate that values would increase if 50 epochs would be used. The trained U-Net was applied to unseen images, per-patch and the following metrics were obtained from full scale WSI; Accuracy, Mean Area Under the Curve and Dice Index. No post-processing was applied. The resulting segmentations outperformed the baseline in terms of accuracy for some tissues; Tumour from 0.804 to 0.913, Inflammatory from 0.743 to 0.8364. The data is available from the Grand Challenges website ( https://bcsegmentation.grand-challenge.org/ ) and the code is available from the following GitHub repository ( https://github.com/mauOrtRuiz/Breast_Cancer_Sem_Seg ).