Advancements in dermatological artificial intelligence research require high-quality and comprehensive datasets that mirror real-world clinical scenarios. We introduce a collection of 18,946 dermoscopic images spanning from 2010 to 2016, collated at the Hospital Clínic in Barcelona, Spain. The BCN20000 dataset aims to address the problem of unconstrained classification of dermoscopic images of skin cancer, including lesions in hard-to-diagnose locations such as those found in nails and mucosa, large lesions which do not fit in the aperture of the dermoscopy device, and hypo-pigmented lesions. Our dataset covers eight key diagnostic categories in dermoscopy, providing a diverse range of lesions for artificial intelligence model training. Furthermore, a ninth out-of-distribution (OOD) class is also present on the test set, comprised of lesions which could not be distinctively classified as any of the others. By providing a comprehensive collection of varied images, BCN20000 helps bridge the gap between the training data for machine learning models and the day-to-day practice of medical practitioners. Additionally, we present a set of baseline classifiers based on state-of-the-art neural networks, which can be extended by other researchers for further experimentation.

Sentinel-2 satellites provide multi-spectral optical remote sensing images with four bands at 10 m of spatial resolution. These images, due to the open data distribution policy, are becoming an important resource for several applications. However, for small scale studies, the spatial detail of these images might not be sufficient. On the other hand, WorldView commercial satellites offer multi-spectral images with a very high spatial resolution, typically less than 2 m, but their use can be impractical for large areas or multi-temporal analysis due to their high cost. To exploit the free availability of Sentinel imagery, it is worth considering deep learning techniques for single-image super-resolution tasks, allowing the spatial enhancement of low-resolution (LR) images by recovering high-frequency details to produce high-resolution (HR) super-resolved images. In this work, we implement and train a model based on the Enhanced Super-Resolution Generative Adversarial Network (ESRGAN) with pairs of WorldView-Sentinel images to generate a super-resolved multispectral Sentinel-2 output with a scaling factor of 5. Our model, named RS-ESRGAN, removes the upsampling layers of the network to make it feasible to train with co-registered remote sensing images. Results obtained outperform state-of-the-art models using standard metrics like PSNR, SSIM, ERGAS, SAM and CC. Moreover, qualitative visual analysis shows spatial improvements as well as the preservation of the spectral information, allowing the super-resolved Sentinel-2 imagery to be used in studies requiring very high spatial resolution.

This paper discusses the use of binary partition trees (BPTs) for object detection. BPTs are hierarchical region-based representations of images. They define a reduced set of regions that covers the image support and that spans various levels of resolution. They are attractive for object detection as they tremendously reduce the search space. In this paper, several issues related to the use of BPT for object detection are studied. Concerning the tree construction, we analyze the compromise between computational complexity reduction and accuracy. This will lead us to define two parts in the BPT: one providing accuracy and one representing the search space for the object detection task. Then we analyze and objectively compare various similarity measures for the tree construction. We conclude that different similarity criteria should be used for the part providing accuracy in the BPT and for the part defining the search space and specific criteria are proposed for each case. Then we discuss the object detection strategy based on BPT. The notion of node extension is proposed and discussed. Finally, several object detection examples illustrating the generality of the approach and its efficiency are reported.

Brain-age can be inferred from structural neuroimaging and compared to chronological age (brain-age delta) as a marker of biological brain aging. Accelerated aging has been found in neurodegenerative disorders like Alzheimer’s disease (AD), but its validation against markers of neurodegeneration and AD is lacking. Here, imaging-derived measures from the UK Biobank dataset (N=22,661) were used to predict brain-age in 2,314 cognitively unimpaired (CU) individuals at higher risk of AD and mild cognitive impaired (MCI) patients from four independent cohorts with available biomarker data: ALFA+, ADNI, EPAD, and OASIS. Brain-age delta was associated with abnormal amyloid-β, more advanced stages (AT) of AD pathology and APOE-ε4 status. Brain-age delta was positively associated with plasma neurofilament light, a marker of neurodegeneration, and sex differences in the brain effects of this marker were found. These results validate brain-age delta as a non-invasive marker of biological brain aging in non-demented individuals with abnormal levels of biomarkers of AD and axonal injury.