Nuclear detection, segmentation and morphometric profiling are essential in helping us further understand the relationship between histology and patient outcome. To drive innovation in this area, we setup a community-wide challenge using the largest available dataset of its kind to assess nuclear segmentation and cellular composition. Our challenge, named CoNIC, stimulated the development of reproducible algorithms for cellular recognition with real-time result inspection on public leaderboards. We conducted an extensive post-challenge analysis based on the top-performing models using 1,658 whole-slide images of colon tissue. With around 700 million detected nuclei per model, associated features were used for dysplasia grading and survival analysis, where we demonstrated that the challenge's improvement over the previous state-ofthe-art led to significant boosts in downstream performance. Our findings also suggest that eosinophils and neutrophils play an important role in the tumour microevironment. We release challenge models and WSIlevel results to foster the development of further methods for biomarker discovery.

The diagnosis and surgical resection using Magnetic Resonance (MR) images in brain tumors is a challenging task to minimize the neurological defects after surgery owing to the non-linear nature of the size, shape, and textural variation. Radiologists, clinical experts, and brain surgeons examine brain MRI scans using the available methods, which are tedious, error-prone, time-consuming, and still exhibit positional accuracy up to 2–3 mm, which is very high in the case of brain cells. In this context, we propose an automated Ultra-Light Brain Tumor Detection (UL-BTD) system based on a novel Ultra-Light Deep Learning Architecture (UL-DLA) for deep features, integrated with highly distinctive textural features, extracted by Gray Level Co-occurrence Matrix (GLCM). It forms a Hybrid Feature Space (HFS), which is used for tumor detection using Support Vector Machine (SVM), culminating in high prediction accuracy and optimum false negatives with limited network size to fit within the average GPU resources of a modern PC system. The objective of this study is to categorize multi-class publicly available MRI brain tumor datasets with a minimum time thus real-time tumor detection can be carried out without compromising accuracy. Our proposed framework includes a sensitivity analysis of image size, One-versus-All and One-versus-One coding schemes with stringent efforts to assess the complexity and reliability performance of the proposed system with K-fold cross-validation as a part of the evaluation protocol. The best generalization achieved using SVM has an average detection rate of 99.23% (99.18%, 98.86%, and 99.67%), and F-measure of 0.99 (0.99, 0.98, and 0.99) for (glioma, meningioma, and pituitary tumors), respectively. Our results have been found to improve the state-of-the-art (97.30%) by 2%, indicating that the system exhibits capability for translation in modern hospitals during real-time surgical brain applications. The method needs 11.69 ms with an accuracy of 99.23% compared to 15 ms achieved by the state-of-the-art to earlier to detect tumors on a test image without any dedicated hardware providing a route for a desktop application in brain surgery.

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